MiMeDB: Showing metabocard for 1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene (MMDBc0029959)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-17 23:48:21 UTC

Update Date

2022-08-31 17:38:00 UTC

MiMeDB ID

MMDBc0029959

Metabolite Identification

Common Name

1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene

Description

1-nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene belongs to the class of Peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. (inferred from compound structure)

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 08131209222D          

 38 39  0  0  0  0            999 V2000
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  6  4  2  0  0  0  0
  7  5  1  0  0  0  0
 10  4  1  0  0  0  0
 11  2  1  0  0  0  0
 11 10  2  0  0  0  0
 12  5  1  0  0  0  0
 13  9  1  0  0  0  0
 14  3  2  0  0  0  0
 14 10  1  0  0  0  0
 15  6  1  0  0  0  0
 16  7  1  0  0  0  0
 17  8  1  0  0  0  0
 18 11  1  0  0  0  0
 18 15  1  0  0  0  0
 19 13  1  0  0  0  0
 20 12  1  0  0  0  0
 12 21  1  1  0  0  0
 22  8  1  4  0  0  0
 22 19  2  0  0  0  0
 13 23  1  6  0  0  0
 23 16  2  0  0  0  0
 24 14  1  0  0  0  0
 25 15  1  0  0  0  0
 16 26  1  4  0  0  0
 27 17  2  0  0  0  0
 28 17  1  0  0  0  0
 29 19  1  0  0  0  0
 30 20  2  0  0  0  0
 31 20  1  0  0  0  0
 32 24  2  0  0  0  0
 33 24  2  0  0  0  0
 34  9  1  0  0  0  0
 34 18  1  0  0  0  0
 12 35  1  1  0  0  0
 13 36  1  6  0  0  0
 37 15  1  0  0  0  0
 38 18  1  0  0  0  0
M  END

HMDB0060326
     RDKit          3D
1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene
 58 59  0  0  0  0  0  0  0  0999 V2000
    4.6726   -3.8815    0.3060 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -2.7403   -0.4269 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3391   -1.4981   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025   -1.6376   -0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -0.3006   -0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.8336   -1.0803 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2717   -0.1932    0.3800 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6376    1.0720    0.6240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2691    0.9037    1.8448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.3524    1.5506 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6239    0.2220    0.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958   -0.8636    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0834   -2.1754    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9547   -3.1952   -0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768   -2.9814   -0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7877   -1.6759   -0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1501   -1.4729   -0.7356 N   0  0  0  0  0  4  0  0  0  0  0  0
   -7.6802   -2.3365   -1.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8878   -0.4604   -0.2416 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.9208   -0.6342   -0.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3712    0.7578   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5635    1.7370    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1575    1.5546    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9417    1.8606    1.8508 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922    2.1326    0.9866 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    1.9522    2.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6493    3.2042    0.3127 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8940    3.5972   -0.8233 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    5.1013   -0.8768 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2689    5.7111   -1.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095    5.8425    0.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5500   -2.4079    0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1346   -3.0871    0.8643 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1173   -1.3122   -0.6255 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4285   -4.6156    0.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495   -4.2758   -0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1956   -2.9925   -1.5057 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7982   -0.7115   -0.8852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1555    0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -1.9360   -1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4298   -2.4122   -0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6867    1.0968   -1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0363    1.3187   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6420    1.8923    2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144    0.5841    2.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029    0.2623   -0.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0397   -2.3148    0.2400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5642   -4.2060   -0.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9737   -3.7740   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4242    0.9765   -0.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0299    2.7443    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6067    2.3600   -0.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0642    1.0107    2.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685    1.3982    2.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2539    3.1871   -1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776    3.2968   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    6.4634   -0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5485   -1.4731   -1.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
 20 12  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  6
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  6
  9 44  1  0
  9 45  1  0
 11 46  1  0
 13 47  1  0
 14 48  1  0
 15 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 24 53  1  0
 26 54  1  0
 28 55  1  0
 28 56  1  0
 31 57  1  0
 34 58  1  0
M  CHG  2  17   1  19  -1
M  END


  Mrv0541 08131209222D          

 38 39  0  0  0  0            999 V2000
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579   -4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  6  4  2  0  0  0  0
  7  5  1  0  0  0  0
 10  4  1  0  0  0  0
 11  2  1  0  0  0  0
 11 10  2  0  0  0  0
 12  5  1  0  0  0  0
 13  9  1  0  0  0  0
 14  3  2  0  0  0  0
 14 10  1  0  0  0  0
 15  6  1  0  0  0  0
 16  7  1  0  0  0  0
 17  8  1  0  0  0  0
 18 11  1  0  0  0  0
 18 15  1  0  0  0  0
 19 13  1  0  0  0  0
 20 12  1  0  0  0  0
 12 21  1  1  0  0  0
 22  8  1  4  0  0  0
 22 19  2  0  0  0  0
 13 23  1  6  0  0  0
 23 16  2  0  0  0  0
 24 14  1  0  0  0  0
 25 15  1  0  0  0  0
 16 26  1  4  0  0  0
 27 17  2  0  0  0  0
 28 17  1  0  0  0  0
 29 19  1  0  0  0  0
 30 20  2  0  0  0  0
 31 20  1  0  0  0  0
 32 24  2  0  0  0  0
 33 24  2  0  0  0  0
 34  9  1  0  0  0  0
 34 18  1  0  0  0  0
 12 35  1  1  0  0  0
 13 36  1  6  0  0  0
 37 15  1  0  0  0  0
 38 18  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0029959

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C2=C(C=CC1([H])O)C(=CC=C2)N(=O)=O)C(O)=NCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H24N4O9S/c21-12(20(30)31)5-7-16(26)23-13(19(29)22-8-17(27)28)9-34-18-11-2-1-3-14(24(32)33)10(11)4-6-15(18)25/h1-4,6,12-13,15,18,25H,5,7-9,21H2,(H,22,29)(H,23,26)(H,27,28)(H,30,31)/t12-,13-,15?,18?/m0/s1

> <INCHI_KEY>
ASZHPHJDCUIIBF-RJXQQRCHSA-N

> <FORMULA>
C20H24N4O9S

> <MOLECULAR_WEIGHT>
496.491

> <EXACT_MASS>
496.126399076

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
47.24907762113102

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-hydroxy-5-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <ALOGPS_LOGP>
-1.46

> <JCHEM_LOGP>
-1.7545124615894483

> <ALOGPS_LOGS>
-4.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.413189824292793

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8304299860583901

> <JCHEM_PKA_STRONGEST_BASIC>
9.53750999249938

> <JCHEM_POLAR_SURFACE_AREA>
231.84999999999994

> <JCHEM_REFRACTIVITY>
121.42789999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.85e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-4-{[(1R)-1-(carboxymethyl-C-hydroxycarbonimidoyl)-2-[(2-hydroxy-5-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060326
     RDKit          3D
1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene
 58 59  0  0  0  0  0  0  0  0999 V2000
    4.6726   -3.8815    0.3060 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -2.7403   -0.4269 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3391   -1.4981   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025   -1.6376   -0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -0.3006   -0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.8336   -1.0803 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2717   -0.1932    0.3800 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6376    1.0720    0.6240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2691    0.9037    1.8448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.3524    1.5506 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6239    0.2220    0.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958   -0.8636    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0834   -2.1754    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9547   -3.1952   -0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768   -2.9814   -0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7877   -1.6759   -0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1501   -1.4729   -0.7356 N   0  0  0  0  0  4  0  0  0  0  0  0
   -7.6802   -2.3365   -1.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8878   -0.4604   -0.2416 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.9208   -0.6342   -0.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3712    0.7578   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5635    1.7370    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1575    1.5546    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9417    1.8606    1.8508 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922    2.1326    0.9866 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    1.9522    2.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6493    3.2042    0.3127 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8940    3.5972   -0.8233 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    5.1013   -0.8768 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2689    5.7111   -1.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095    5.8425    0.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5500   -2.4079    0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1346   -3.0871    0.8643 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1173   -1.3122   -0.6255 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4285   -4.6156    0.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495   -4.2758   -0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1956   -2.9925   -1.5057 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7982   -0.7115   -0.8852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1555    0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -1.9360   -1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4298   -2.4122   -0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6867    1.0968   -1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0363    1.3187   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6420    1.8923    2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144    0.5841    2.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029    0.2623   -0.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0397   -2.3148    0.2400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5642   -4.2060   -0.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9737   -3.7740   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4242    0.9765   -0.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0299    2.7443    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6067    2.3600   -0.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0642    1.0107    2.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685    1.3982    2.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2539    3.1871   -1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776    3.2968   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    6.4634   -0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5485   -1.4731   -1.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
 20 12  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  6
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  6
  9 44  1  0
  9 45  1  0
 11 46  1  0
 13 47  1  0
 14 48  1  0
 15 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 24 53  1  0
 26 54  1  0
 28 55  1  0
 28 56  1  0
 31 57  1  0
 34 58  1  0
M  CHG  2  17   1  19  -1
M  END

HEADER    PROTEIN                                 13-AUG-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-AUG-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   34  S   UNK     0       0.000   0.000   0.000  0.00  0.00           S+0
HETATM   35  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
CONECT    1    2    3                                                       
CONECT    2    1   11                                                       
CONECT    3    1   14                                                       
CONECT    4    6   10                                                       
CONECT    5    7   12                                                       
CONECT    6    4   15                                                       
CONECT    7    5   16                                                       
CONECT    8   17   22                                                       
CONECT    9   13   34                                                       
CONECT   10    4   11   14                                                  
CONECT   11    2   10   18                                                  
CONECT   12    5   20   21   35                                             
CONECT   13    9   19   23   36                                             
CONECT   14    3   10   24                                                  
CONECT   15    6   18   25   37                                             
CONECT   16    7   23   26                                                  
CONECT   17    8   27   28                                                  
CONECT   18   11   15   34   38                                             
CONECT   19   13   22   29                                                  
CONECT   20   12   30   31                                                  
CONECT   21   12                                                            
CONECT   22    8   19                                                       
CONECT   23   13   16                                                       
CONECT   24   14   32   33                                                  
CONECT   25   15                                                            
CONECT   26   16                                                            
CONECT   27   17                                                            
CONECT   28   17                                                            
CONECT   29   19                                                            
CONECT   30   20                                                            
CONECT   31   20                                                            
CONECT   32   24                                                            
CONECT   33   24                                                            
CONECT   34    9   18                                                       
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   15                                                            
CONECT   38   18                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

COMPND    HMDB0060326
HETATM    1  N1  UNL     1       4.673  -3.881   0.306  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.145  -2.740  -0.427  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.339  -1.498  -0.247  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.902  -1.638  -0.671  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.249  -0.301  -0.426  1.00  0.00           C  
HETATM    6  O1  UNL     1       2.708   0.834  -1.080  1.00  0.00           O  
HETATM    7  N2  UNL     1       1.272  -0.193   0.380  1.00  0.00           N  
HETATM    8  C5  UNL     1       0.638   1.072   0.624  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.269   0.904   1.845  1.00  0.00           C  
HETATM   10  S1  UNL     1      -1.503  -0.352   1.551  1.00  0.00           S  
HETATM   11  C7  UNL     1      -2.624   0.222   0.215  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.596  -0.864   0.032  1.00  0.00           C  
HETATM   13  C9  UNL     1      -3.083  -2.175   0.040  1.00  0.00           C  
HETATM   14  C10 UNL     1      -3.955  -3.195  -0.210  1.00  0.00           C  
HETATM   15  C11 UNL     1      -5.277  -2.981  -0.461  1.00  0.00           C  
HETATM   16  C12 UNL     1      -5.788  -1.676  -0.467  1.00  0.00           C  
HETATM   17  N3  UNL     1      -7.150  -1.473  -0.736  1.00  0.00           N1+
HETATM   18  O2  UNL     1      -7.680  -2.337  -1.511  1.00  0.00           O  
HETATM   19  O3  UNL     1      -7.888  -0.460  -0.242  1.00  0.00           O1-
HETATM   20  C13 UNL     1      -4.921  -0.634  -0.216  1.00  0.00           C  
HETATM   21  C14 UNL     1      -5.371   0.758  -0.134  1.00  0.00           C  
HETATM   22  C15 UNL     1      -4.563   1.737   0.173  1.00  0.00           C  
HETATM   23  C16 UNL     1      -3.158   1.555   0.469  1.00  0.00           C  
HETATM   24  O4  UNL     1      -2.942   1.861   1.851  1.00  0.00           O  
HETATM   25  C17 UNL     1       1.592   2.133   0.987  1.00  0.00           C  
HETATM   26  O5  UNL     1       2.423   1.952   2.065  1.00  0.00           O  
HETATM   27  N4  UNL     1       1.649   3.204   0.313  1.00  0.00           N  
HETATM   28  C18 UNL     1       0.894   3.597  -0.823  1.00  0.00           C  
HETATM   29  C19 UNL     1       0.869   5.101  -0.877  1.00  0.00           C  
HETATM   30  O6  UNL     1       0.269   5.711  -1.792  1.00  0.00           O  
HETATM   31  O7  UNL     1       1.510   5.843   0.085  1.00  0.00           O  
HETATM   32  C20 UNL     1       6.550  -2.408   0.003  1.00  0.00           C  
HETATM   33  O8  UNL     1       7.135  -3.087   0.864  1.00  0.00           O  
HETATM   34  O9  UNL     1       7.117  -1.312  -0.626  1.00  0.00           O  
HETATM   35  H1  UNL     1       5.429  -4.616   0.221  1.00  0.00           H  
HETATM   36  H2  UNL     1       3.849  -4.276  -0.184  1.00  0.00           H  
HETATM   37  H3  UNL     1       5.196  -2.992  -1.506  1.00  0.00           H  
HETATM   38  H4  UNL     1       4.798  -0.712  -0.885  1.00  0.00           H  
HETATM   39  H5  UNL     1       4.374  -1.156   0.810  1.00  0.00           H  
HETATM   40  H6  UNL     1       2.799  -1.936  -1.725  1.00  0.00           H  
HETATM   41  H7  UNL     1       2.430  -2.412  -0.043  1.00  0.00           H  
HETATM   42  H8  UNL     1       3.687   1.097  -1.009  1.00  0.00           H  
HETATM   43  H9  UNL     1       0.036   1.319  -0.279  1.00  0.00           H  
HETATM   44  H10 UNL     1      -0.642   1.892   2.134  1.00  0.00           H  
HETATM   45  H11 UNL     1       0.414   0.584   2.661  1.00  0.00           H  
HETATM   46  H12 UNL     1      -2.003   0.262  -0.746  1.00  0.00           H  
HETATM   47  H13 UNL     1      -2.040  -2.315   0.240  1.00  0.00           H  
HETATM   48  H14 UNL     1      -3.564  -4.206  -0.206  1.00  0.00           H  
HETATM   49  H15 UNL     1      -5.974  -3.774  -0.661  1.00  0.00           H  
HETATM   50  H16 UNL     1      -6.424   0.976  -0.358  1.00  0.00           H  
HETATM   51  H17 UNL     1      -5.030   2.744   0.193  1.00  0.00           H  
HETATM   52  H18 UNL     1      -2.607   2.360  -0.119  1.00  0.00           H  
HETATM   53  H19 UNL     1      -3.064   1.011   2.341  1.00  0.00           H  
HETATM   54  H20 UNL     1       3.269   1.398   2.058  1.00  0.00           H  
HETATM   55  H21 UNL     1       1.254   3.187  -1.782  1.00  0.00           H  
HETATM   56  H22 UNL     1      -0.178   3.297  -0.657  1.00  0.00           H  
HETATM   57  H23 UNL     1       2.276   6.463  -0.040  1.00  0.00           H  
HETATM   58  H24 UNL     1       7.548  -1.473  -1.527  1.00  0.00           H  
CONECT    1    2   35   36
CONECT    2    3   32   37
CONECT    3    4   38   39
CONECT    4    5   40   41
CONECT    5    6    7    7
CONECT    6   42
CONECT    7    8
CONECT    8    9   25   43
CONECT    9   10   44   45
CONECT   10   11
CONECT   11   12   23   46
CONECT   12   13   13   20
CONECT   13   14   47
CONECT   14   15   15   48
CONECT   15   16   49
CONECT   16   17   20   20
CONECT   17   18   18   19
CONECT   20   21
CONECT   21   22   22   50
CONECT   22   23   51
CONECT   23   24   52
CONECT   24   53
CONECT   25   26   27   27
CONECT   26   54
CONECT   27   28
CONECT   28   29   55   56
CONECT   29   30   30   31
CONECT   31   57
CONECT   32   33   33   34
CONECT   34   58
END

HMDB0060326
     RDKit          3D
1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene
 58 59  0  0  0  0  0  0  0  0999 V2000
    4.6726   -3.8815    0.3060 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1451   -2.7403   -0.4269 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3391   -1.4981   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9025   -1.6376   -0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -0.3006   -0.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.8336   -1.0803 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2717   -0.1932    0.3800 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6376    1.0720    0.6240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2691    0.9037    1.8448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -0.3524    1.5506 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6239    0.2220    0.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5958   -0.8636    0.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0834   -2.1754    0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9547   -3.1952   -0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768   -2.9814   -0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7877   -1.6759   -0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1501   -1.4729   -0.7356 N   0  0  0  0  0  4  0  0  0  0  0  0
   -7.6802   -2.3365   -1.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8878   -0.4604   -0.2416 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.9208   -0.6342   -0.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3712    0.7578   -0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5635    1.7370    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1575    1.5546    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9417    1.8606    1.8508 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922    2.1326    0.9866 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    1.9522    2.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6493    3.2042    0.3127 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8940    3.5972   -0.8233 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    5.1013   -0.8768 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2689    5.7111   -1.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095    5.8425    0.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5500   -2.4079    0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1346   -3.0871    0.8643 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1173   -1.3122   -0.6255 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4285   -4.6156    0.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495   -4.2758   -0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1956   -2.9925   -1.5057 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7982   -0.7115   -0.8852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3745   -1.1555    0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7990   -1.9360   -1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4298   -2.4122   -0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6867    1.0968   -1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0363    1.3187   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6420    1.8923    2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144    0.5841    2.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0029    0.2623   -0.7465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0397   -2.3148    0.2400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5642   -4.2060   -0.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9737   -3.7740   -0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4242    0.9765   -0.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0299    2.7443    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6067    2.3600   -0.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0642    1.0107    2.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685    1.3982    2.0578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2539    3.1871   -1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776    3.2968   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    6.4634   -0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5485   -1.4731   -1.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
  8 25  1  0
 25 26  1  0
 25 27  2  3
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
  2 32  1  0
 32 33  2  0
 32 34  1  0
 23 11  1  0
 20 12  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  6
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  8 43  1  6
  9 44  1  0
  9 45  1  0
 11 46  1  0
 13 47  1  0
 14 48  1  0
 15 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 24 53  1  0
 26 54  1  0
 28 55  1  0
 28 56  1  0
 31 57  1  0
 34 58  1  0
M  CHG  2  17   1  19  -1
M  END

Synonyms

Not Available

Chemical Formula

C₂₀H₂₄N₄O₉S

Average Molecular Weight

496.491

Monoisotopic Molecular Weight

496.126399076

IUPAC Name

(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-hydroxy-5-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

Traditional Name

(2S)-2-amino-4-{[(1R)-1-(carboxymethyl-C-hydroxycarbonimidoyl)-2-[(2-hydroxy-5-nitro-1,2-dihydronaphthalen-1-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C2=C(C=CC1([H])O)C(=CC=C2)N(=O)=O)C(O)=NCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C20H24N4O9S/c21-12(20(30)31)5-7-16(26)23-13(19(29)22-8-17(27)28)9-34-18-11-2-1-3-14(24(32)33)10(11)4-6-15(18)25/h1-4,6,12-13,15,18,25H,5,7-9,21H2,(H,22,29)(H,23,26)(H,27,28)(H,30,31)/t12-,13-,15?,18?/m0/s1

InChI Key

ASZHPHJDCUIIBF-RJXQQRCHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Gamma-glutamyl alpha peptide
Glutamine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
1-nitronaphthalene
Alpha-amino acid amide
Cysteine or derivatives
Alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
L-alpha-amino acid
Naphthalene
Nitroaromatic compound
Dicarboxylic acid or derivatives
Fatty amide
N-acyl-amine
Fatty acyl
Benzenoid
Secondary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
C-nitro compound
Carboxamide group
Organic nitro compound
Amino acid
Sulfenyl compound
Thioether
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Allyl-type 1,3-dipolar organic compound
Organic oxoazanium
Dialkylthioether
Carboxylic acid
Primary amine
Primary aliphatic amine
Organic oxygen compound
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Amine
Organic zwitterion
Organic oxide
Organooxygen compound
Organosulfur compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

peptide (CHEBI:34102 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.048 g/L	ALOGPS
logP	-1.5	ALOGPS
logP	-1.8	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	1.83	ChemAxon
pKa (Strongest Basic)	9.54	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	231.85 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	121.43 m³·mol⁻¹	ChemAxon
Polarizability	47.25 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-2600900000-79279688cfbc687d3a3a	2017-09-20	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positive	splash10-0006-5901144000-e9732e07c907c537f5f0	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_3) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_6) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_10) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS ("1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene,2TBDMS,#4" TMS) - 70eV, Positive	Not Available	2021-10-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0002-0000900000-ff4921fa4db2226179f3	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-006t-3000900000-a5bdd09564bea0dcd157	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-00di-9210000000-bc0198c4e44217ca1bdd	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0002-0000900000-6cac03836a1b55f7d257	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0002-2110900000-9b223f0ded26f56446d3	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-001i-9840000000-193d3a6346b816a51d2d	2015-09-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

#<MetaboliteProteinLink:0x00007f08f0d72440>

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
	Proteobacteria	1	Human	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB		details

External Links

HMDB ID

HMDB0060326

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10128352

KEGG Compound ID

C14806

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11954057

PDB ID

Not Available

ChEBI ID

34100

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Showing metabocard for 1-Nitro-5-glutathionyl-6-hydroxy-5,6-dihydronaphthalene (MMDBc0029959)

MOL for #<Metabolite:0x00007f08ec1f8ed8>

3D MOL for #<Metabolite:0x00007f08ec1f8ed8>

3D SDF for #<Metabolite:0x00007f08ec1f8ed8>

3D-SDF for #<Metabolite:0x00007f08ec1f8ed8>

PDB for #<Metabolite:0x00007f08ec1f8ed8>

3D PDB for #<Metabolite:0x00007f08ec1f8ed8>

SMILES for #<Metabolite:0x00007f08ec1f8ed8>

INCHI for #<Metabolite:0x00007f08ec1f8ed8>

Structure for #<Metabolite:0x00007f08ec1f8ed8>

3D Structure for #<Metabolite:0x00007f08ec1f8ed8>