MiMeDB: Showing metabocard for Pneumocandin B1 (MMDBc0007520)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:40:50 UTC

Update Date

2022-08-31 06:27:23 UTC

Metabolite ID

MMDBc0007520

Metabolite Identification

Common Name

Pneumocandin B1

Description

Pneumocandin B1 belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. Based on a literature review very few articles have been published on Pneumocandin B1.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102402D          

 89 92  0  0  1  0            999 V2000
  -10.4787   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0498   -1.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6209   -1.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3318   -2.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7643   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7630   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0485   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4774   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3340   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1919   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6196   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9064   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9700    0.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8632    1.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7927    0.3192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6859    1.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0381    5.2523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703    4.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3353   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1703   -1.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2178    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631    0.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4817    4.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674   -1.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0498   -0.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6209   -0.5056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0997   -2.2618    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5052    0.9392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1506    1.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8920   -2.0194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2383   -0.0931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3951    1.4976    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5177   -0.7381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4504    4.6733    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6826    0.8776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6590    4.2591    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1247    1.4976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9464    4.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1906   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2227   -1.4460    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1943    3.5775    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8194    3.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7527   -0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2115    2.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0321   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0588    2.3019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0761    3.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0477   -1.4460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4510    3.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5885    5.6224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4762   -0.5056    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3335    0.6749    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4343   -1.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7990    3.0164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4713    3.0164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6352    4.0584    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8360   -1.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7447   -2.7762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9733    1.1242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3568   -2.7011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365    4.8085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3011    5.0024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9474    1.5592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7691    4.8175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1906    0.7319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1916   -1.3429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9795    2.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7465   -0.5056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7091    2.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6114    4.2591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1707   -2.2618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942    4.7238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7643   -0.9181    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9064   -0.9181    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4547   -1.7474    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4957   -2.7430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9528    0.3194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5724    1.4359    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9565   -0.1333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2013    5.4598    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0405    1.6209    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170    3.5158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980    1.4359    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3457   -0.6302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7295    2.8959    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626    3.1471    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8268    2.0005    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  2  0  0  0  0
 19 18  1  0  0  0  0
 26  2  1  1  0  0  0
 26  5  1  0  0  0  0
 26 20  1  0  0  0  0
 27  3  1  1  0  0  0
 27 12  1  0  0  0  0
 27 20  1  0  0  0  0
 28  4  1  0  0  0  0
 29 14  2  0  0  0  0
 29 15  1  0  0  0  0
 30 16  2  0  0  0  0
 30 17  1  0  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
 32 23  1  0  0  0  0
 33 22  1  1  0  0  0
 34 21  1  0  0  0  0
 35 18  1  0  0  0  0
 36 22  1  0  0  0  0
 36 29  1  0  0  0  0
 37 24  1  0  0  0  0
 38 23  1  0  0  0  0
 39 24  1  0  0  0  0
 40 13  1  0  0  0  0
 41 28  1  1  0  0  0
 42 37  1  1  0  0  0
 43 35  1  0  0  0  0
 44 32  1  0  0  0  0
 45 33  1  0  0  0  0
 46 34  1  0  0  0  0
 47 38  1  0  0  0  0
 48 43  1  0  0  0  0
 49 41  1  0  0  0  0
 50 42  1  0  0  0  0
 51 39  2  0  0  0  0
 32 52  1  1  0  0  0
 52 40  2  0  0  0  0
 53 33  1  0  0  0  0
 53 46  2  0  0  0  0
 54 41  1  0  0  0  0
 54 44  2  0  0  0  0
 55 42  1  0  0  0  0
 55 45  2  0  0  0  0
 56 47  1  0  0  0  0
 56 48  2  0  0  0  0
 57 19  1  0  0  0  0
 57 43  1  0  0  0  0
 57 50  1  0  0  0  0
 58 25  1  0  0  0  0
 58 34  1  0  0  0  0
 58 49  1  0  0  0  0
 28 59  1  1  0  0  0
 60 30  1  0  0  0  0
 31 61  1  1  0  0  0
 35 62  1  1  0  0  0
 36 63  1  1  0  0  0
 37 64  1  1  0  0  0
 38 65  1  6  0  0  0
 66 39  1  0  0  0  0
 40 67  1  4  0  0  0
 44 68  1  4  0  0  0
 45 69  1  4  0  0  0
 46 70  1  4  0  0  0
 47 71  1  6  0  0  0
 48 72  1  4  0  0  0
 73 49  2  0  0  0  0
 74 50  2  0  0  0  0
 26 75  1  6  0  0  0
 27 76  1  6  0  0  0
 28 77  1  1  0  0  0
 31 78  1  6  0  0  0
 32 79  1  1  0  0  0
 33 80  1  1  0  0  0
 34 81  1  1  0  0  0
 35 82  1  6  0  0  0
 36 83  1  1  0  0  0
 37 84  1  1  0  0  0
 38 85  1  6  0  0  0
 41 86  1  1  0  0  0
 42 87  1  1  0  0  0
 43 88  1  1  0  0  0
 47 89  1  6  0  0  0
M  END


  Mrv1652305152102402D          

 89 92  0  0  1  0            999 V2000
  -10.4787   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0498   -1.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6209   -1.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3318   -2.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7643   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7630   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0485   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4774   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3340   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1919   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6196   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9064   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051   -0.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9700    0.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8632    1.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7927    0.3192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6859    1.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0381    5.2523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7703    4.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3353   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1703   -1.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2178    1.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0631    0.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4817    4.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0674   -1.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0498   -0.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6209   -0.5056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0997   -2.2618    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5052    0.9392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1506    1.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8920   -2.0194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2383   -0.0931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3951    1.4976    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5177   -0.7381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4504    4.6733    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6826    0.8776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6590    4.2591    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1247    1.4976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9464    4.8791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1906   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2227   -1.4460    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1943    3.5775    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8194    3.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7527   -0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2115    2.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0321   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0588    2.3019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0761    3.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0477   -1.4460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4510    3.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5885    5.6224    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4762   -0.5056    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3335    0.6749    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4343   -1.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7990    3.0164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4713    3.0164    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6352    4.0584    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8360   -1.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7447   -2.7762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9733    1.1242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3568   -2.7011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365    4.8085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3011    5.0024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9474    1.5592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7691    4.8175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1906    0.7319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1916   -1.3429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9795    2.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7465   -0.5056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7091    2.6033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6114    4.2591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1707   -2.2618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942    4.7238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7643   -0.9181    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9064   -0.9181    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4547   -1.7474    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4957   -2.7430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9528    0.3194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5724    1.4359    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9565   -0.1333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2013    5.4598    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0405    1.6209    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0170    3.5158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980    1.4359    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3457   -0.6302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7295    2.8959    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626    3.1471    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8268    2.0005    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  2  0  0  0  0
 19 18  1  0  0  0  0
 26  2  1  1  0  0  0
 26  5  1  0  0  0  0
 26 20  1  0  0  0  0
 27  3  1  1  0  0  0
 27 12  1  0  0  0  0
 27 20  1  0  0  0  0
 28  4  1  0  0  0  0
 29 14  2  0  0  0  0
 29 15  1  0  0  0  0
 30 16  2  0  0  0  0
 30 17  1  0  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
 32 23  1  0  0  0  0
 33 22  1  1  0  0  0
 34 21  1  0  0  0  0
 35 18  1  0  0  0  0
 36 22  1  0  0  0  0
 36 29  1  0  0  0  0
 37 24  1  0  0  0  0
 38 23  1  0  0  0  0
 39 24  1  0  0  0  0
 40 13  1  0  0  0  0
 41 28  1  1  0  0  0
 42 37  1  1  0  0  0
 43 35  1  0  0  0  0
 44 32  1  0  0  0  0
 45 33  1  0  0  0  0
 46 34  1  0  0  0  0
 47 38  1  0  0  0  0
 48 43  1  0  0  0  0
 49 41  1  0  0  0  0
 50 42  1  0  0  0  0
 51 39  2  0  0  0  0
 32 52  1  1  0  0  0
 52 40  2  0  0  0  0
 53 33  1  0  0  0  0
 53 46  2  0  0  0  0
 54 41  1  0  0  0  0
 54 44  2  0  0  0  0
 55 42  1  0  0  0  0
 55 45  2  0  0  0  0
 56 47  1  0  0  0  0
 56 48  2  0  0  0  0
 57 19  1  0  0  0  0
 57 43  1  0  0  0  0
 57 50  1  0  0  0  0
 58 25  1  0  0  0  0
 58 34  1  0  0  0  0
 58 49  1  0  0  0  0
 28 59  1  1  0  0  0
 60 30  1  0  0  0  0
 31 61  1  1  0  0  0
 35 62  1  1  0  0  0
 36 63  1  1  0  0  0
 37 64  1  1  0  0  0
 38 65  1  6  0  0  0
 66 39  1  0  0  0  0
 40 67  1  4  0  0  0
 44 68  1  4  0  0  0
 45 69  1  4  0  0  0
 46 70  1  4  0  0  0
 47 71  1  6  0  0  0
 48 72  1  4  0  0  0
 73 49  2  0  0  0  0
 74 50  2  0  0  0  0
 26 75  1  6  0  0  0
 27 76  1  6  0  0  0
 28 77  1  1  0  0  0
 31 78  1  6  0  0  0
 32 79  1  1  0  0  0
 33 80  1  1  0  0  0
 34 81  1  1  0  0  0
 35 82  1  6  0  0  0
 36 83  1  1  0  0  0
 37 84  1  1  0  0  0
 38 85  1  6  0  0  0
 41 86  1  1  0  0  0
 42 87  1  1  0  0  0
 43 88  1  1  0  0  0
 47 89  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007520

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)C[C@]([H])(C)CCCCCCCCC(O)=N[C@]1([H])C[C@@]([H])(O)[C@@]([H])(O)N=C(O)[C@@]2([H])N(CC[C@]2([H])O)C(=O)[C@@]([H])(N=C(O)[C@]([H])(C[C@@]([H])(O)C2=CC=C(O)C=C2)N=C(O)[C@]2([H])C[C@@]([H])(O)CN2C(=O)[C@@]([H])(N=C1O)[C@@]([H])(C)O)[C@]([H])(O)CC(O)=N

> <INCHI_IDENTIFIER>
InChI=1S/C50H80N8O16/c1-5-26(2)20-27(3)12-10-8-6-7-9-11-13-40(67)52-32-23-38(65)47(71)56-48(72)43-35(62)18-19-57(43)50(74)42(37(64)24-39(51)66)55-45(69)33(22-36(63)29-14-16-30(60)17-15-29)53-46(70)34-21-31(61)25-58(34)49(73)41(28(4)59)54-44(32)68/h14-17,26-28,31-38,41-43,47,59-65,71H,5-13,18-25H2,1-4H3,(H2,51,66)(H,52,67)(H,53,70)(H,54,68)(H,55,69)(H,56,72)/t26-,27+,28+,31+,32+,33-,34-,35-,36+,37+,38+,41-,42-,43-,47+/m0/s1

> <INCHI_KEY>
UBEYULPDJZYEFA-AVMWGXBGSA-N

> <FORMULA>
C50H80N8O16

> <MOLECULAR_WEIGHT>
1049.23

> <EXACT_MASS>
1048.569228528

> <JCHEM_ACCEPTOR_COUNT>
22

> <JCHEM_ATOM_COUNT>
154

> <JCHEM_AVERAGE_POLARIZABILITY>
109.95124632730395

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
15

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(10R,12S)-10,12-dimethyl-N-[(3S,6S,9S,11R,15S,18R,20R,21R,24S,25S)-5,8,11,17,20,21,23,25-octahydroxy-6-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-[(1R)-1-hydroxy-2-(C-hydroxycarbonimidoyl)ethyl]-15-[(1R)-1-hydroxyethyl]-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0^{9,13}]heptacosa-4,7,16,22-tetraen-18-yl]tetradecanimidic acid

> <ALOGPS_LOGP>
1.36

> <JCHEM_LOGP>
-1.023037039312751

> <ALOGPS_LOGS>
-3.96

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.028089673691498

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.2309098076781089

> <JCHEM_PKA_STRONGEST_BASIC>
12.460144411934175

> <JCHEM_POLAR_SURFACE_AREA>
409.49

> <JCHEM_REFRACTIVITY>
276.6368

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(10R,12S)-10,12-dimethyl-N-[(3S,6S,9S,11R,15S,18R,20R,21R,24S,25S)-5,8,11,17,20,21,23,25-octahydroxy-6-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-[(1R)-1-hydroxy-2-(C-hydroxycarbonimidoyl)ethyl]-15-[(1R)-1-hydroxyethyl]-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0^{9,13}]heptacosa-4,7,16,22-tetraen-18-yl]tetradecanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0     -19.560  -0.944   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -16.893  -2.484   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -14.226  -2.484   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.486  -4.785   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -18.227  -0.174   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.891  -0.944   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.557  -0.174   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.225  -0.174   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.224  -0.944   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.558  -0.944   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.890  -0.174   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -12.892  -0.174   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.556  -0.944   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.877   0.481   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.678   3.141   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.413   0.596   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.214   3.256   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.804   9.804   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.171   9.095   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -15.559  -0.174   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.651  -2.320   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.607   2.911   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.118   1.260   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.233   7.835   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.592  -3.724   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -16.893  -0.944   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -14.226  -0.944   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.919  -4.222   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.010   1.753   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.081   1.983   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.132  -3.770   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.445  -0.174   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.071   2.795   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.433  -1.378   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.707   8.724   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.474   1.638   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.697   7.950   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.233   2.795   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.100   9.108   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.222  -0.174   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.149  -2.699   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.829   6.678   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.396   7.346   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.405  -1.378   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.728   4.297   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.393  -0.174   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       0.110   4.297   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       2.009   6.678   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.689  -2.699   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.442   7.346   0.000  0.00  0.00           C+0
HETATM   51  N   UNK     0      10.432  10.495   0.000  0.00  0.00           N+0
HETATM   52  N   UNK     0      -0.889  -0.944   0.000  0.00  0.00           N+0
HETATM   53  N   UNK     0       9.956   1.260   0.000  0.00  0.00           N+0
HETATM   54  N   UNK     0       2.677  -2.245   0.000  0.00  0.00           N+0
HETATM   55  N   UNK     0       8.958   5.631   0.000  0.00  0.00           N+0
HETATM   56  N   UNK     0       0.880   5.631   0.000  0.00  0.00           N+0
HETATM   57  N   UNK     0       4.919   7.576   0.000  0.00  0.00           N+0
HETATM   58  N   UNK     0       7.161  -2.245   0.000  0.00  0.00           N+0
HETATM   59  O   UNK     0       5.124  -5.182   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      18.617   2.098   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0       9.999  -5.042   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       1.188   8.976   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      11.806   0.251   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0       8.029   9.338   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0      -1.769   2.911   0.000  0.00  0.00           O+0
HETATM   66  O   UNK     0      12.636   8.993   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0      -2.222   1.366   0.000  0.00  0.00           O+0
HETATM   68  O   UNK     0       0.358  -2.507   0.000  0.00  0.00           O+0
HETATM   69  O   UNK     0      11.162   4.859   0.000  0.00  0.00           O+0
HETATM   70  O   UNK     0      10.727  -0.944   0.000  0.00  0.00           O+0
HETATM   71  O   UNK     0      -1.324   4.859   0.000  0.00  0.00           O+0
HETATM   72  O   UNK     0       1.141   7.950   0.000  0.00  0.00           O+0
HETATM   73  O   UNK     0       5.919  -4.222   0.000  0.00  0.00           O+0
HETATM   74  O   UNK     0       6.896   8.818   0.000  0.00  0.00           O+0
HETATM   75  H   UNK     0     -18.227  -1.714   0.000  0.00  0.00           H+0
HETATM   76  H   UNK     0     -12.892  -1.714   0.000  0.00  0.00           H+0
HETATM   77  H   UNK     0       2.715  -3.262   0.000  0.00  0.00           H+0
HETATM   78  H   UNK     0       8.392  -5.120   0.000  0.00  0.00           H+0
HETATM   79  H   UNK     0       1.779   0.596   0.000  0.00  0.00           H+0
HETATM   80  H   UNK     0       8.535   2.680   0.000  0.00  0.00           H+0
HETATM   81  H   UNK     0       7.386  -0.249   0.000  0.00  0.00           H+0
HETATM   82  H   UNK     0       2.242  10.192   0.000  0.00  0.00           H+0
HETATM   83  H   UNK     0      13.142   3.026   0.000  0.00  0.00           H+0
HETATM   84  H   UNK     0       9.365   6.563   0.000  0.00  0.00           H+0
HETATM   85  H   UNK     0       1.303   2.680   0.000  0.00  0.00           H+0
HETATM   86  H   UNK     0       4.379  -1.176   0.000  0.00  0.00           H+0
HETATM   87  H   UNK     0       6.962   5.406   0.000  0.00  0.00           H+0
HETATM   88  H   UNK     0       3.850   5.875   0.000  0.00  0.00           H+0
HETATM   89  H   UNK     0       1.543   3.734   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   26                                                            
CONECT    3   27                                                            
CONECT    4   28                                                            
CONECT    5    1   26                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   27                                                       
CONECT   13   11   40                                                       
CONECT   14   16   29                                                       
CONECT   15   17   29                                                       
CONECT   16   14   30                                                       
CONECT   17   15   30                                                       
CONECT   18   19   35                                                       
CONECT   19   18   57                                                       
CONECT   20   26   27                                                       
CONECT   21   31   34                                                       
CONECT   22   33   36                                                       
CONECT   23   32   38                                                       
CONECT   24   37   39                                                       
CONECT   25   31   58                                                       
CONECT   26    2    5   20   75                                             
CONECT   27    3   12   20   76                                             
CONECT   28    4   41   59   77                                             
CONECT   29   14   15   36                                                  
CONECT   30   16   17   60                                                  
CONECT   31   21   25   61   78                                             
CONECT   32   23   44   52   79                                             
CONECT   33   22   45   53   80                                             
CONECT   34   21   46   58   81                                             
CONECT   35   18   43   62   82                                             
CONECT   36   22   29   63   83                                             
CONECT   37   24   42   64   84                                             
CONECT   38   23   47   65   85                                             
CONECT   39   24   51   66                                                  
CONECT   40   13   52   67                                                  
CONECT   41   28   49   54   86                                             
CONECT   42   37   50   55   87                                             
CONECT   43   35   48   57   88                                             
CONECT   44   32   54   68                                                  
CONECT   45   33   55   69                                                  
CONECT   46   34   53   70                                                  
CONECT   47   38   56   71   89                                             
CONECT   48   43   56   72                                                  
CONECT   49   41   58   73                                                  
CONECT   50   42   57   74                                                  
CONECT   51   39                                                            
CONECT   52   32   40                                                       
CONECT   53   33   46                                                       
CONECT   54   41   44                                                       
CONECT   55   42   45                                                       
CONECT   56   47   48                                                       
CONECT   57   19   43   50                                                  
CONECT   58   25   34   49                                                  
CONECT   59   28                                                            
CONECT   60   30                                                            
CONECT   61   31                                                            
CONECT   62   35                                                            
CONECT   63   36                                                            
CONECT   64   37                                                            
CONECT   65   38                                                            
CONECT   66   39                                                            
CONECT   67   40                                                            
CONECT   68   44                                                            
CONECT   69   45                                                            
CONECT   70   46                                                            
CONECT   71   47                                                            
CONECT   72   48                                                            
CONECT   73   49                                                            
CONECT   74   50                                                            
CONECT   75   26                                                            
CONECT   76   27                                                            
CONECT   77   28                                                            
CONECT   78   31                                                            
CONECT   79   32                                                            
CONECT   80   33                                                            
CONECT   81   34                                                            
CONECT   82   35                                                            
CONECT   83   36                                                            
CONECT   84   37                                                            
CONECT   85   38                                                            
CONECT   86   41                                                            
CONECT   87   42                                                            
CONECT   88   43                                                            
CONECT   89   47                                                            
MASTER        0    0    0    0    0    0    0    0   89    0  184    0
END

Synonyms

Not Available

Molecular Formula

C₅₀H₈₀N₈O₁₆

Average Mass

1049.23

Monoisotopic Mass

1048.569228528

IUPAC Name

(10R,12S)-10,12-dimethyl-N-[(3S,6S,9S,11R,15S,18R,20R,21R,24S,25S)-5,8,11,17,20,21,23,25-octahydroxy-6-[(2R)-2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-[(1R)-1-hydroxy-2-(C-hydroxycarbonimidoyl)ethyl]-15-[(1R)-1-hydroxyethyl]-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0^{9,13}]heptacosa-4,7,16,22-tetraen-18-yl]tetradecanimidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)C[C@]([H])(C)CCCCCCCCC(O)=N[C@]1([H])C[C@@]([H])(O)[C@@]([H])(O)N=C(O)[C@@]2([H])N(CC[C@]2([H])O)C(=O)[C@@]([H])(N=C(O)[C@]([H])(C[C@@]([H])(O)C2=CC=C(O)C=C2)N=C(O)[C@]2([H])C[C@@]([H])(O)CN2C(=O)[C@@]([H])(N=C1O)[C@@]([H])(C)O)[C@]([H])(O)CC(O)=N

InChI Identifier

InChI=1S/C50H80N8O16/c1-5-26(2)20-27(3)12-10-8-6-7-9-11-13-40(67)52-32-23-38(65)47(71)56-48(72)43-35(62)18-19-57(43)50(74)42(37(64)24-39(51)66)55-45(69)33(22-36(63)29-14-16-30(60)17-15-29)53-46(70)34-21-31(61)25-58(34)49(73)41(28(4)59)54-44(32)68/h14-17,26-28,31-38,41-43,47,59-65,71H,5-13,18-25H2,1-4H3,(H2,51,66)(H,52,67)(H,53,70)(H,54,68)(H,55,69)(H,56,72)/t26-,27+,28+,31+,32+,33-,34-,35-,36+,37+,38+,41-,42-,43-,47+/m0/s1

InChI Key

UBEYULPDJZYEFA-AVMWGXBGSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Alpha-amino acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Secondary alcohol
Lactam
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Carboximidic acid derivative
Carboximidic acid
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.12 g/L	ALOGPS
logP	1.36	ALOGPS
logP	-1	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	-1.2	ChemAxon
pKa (Strongest Basic)	12.46	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	22	ChemAxon
Hydrogen Donor Count	15	ChemAxon
Polar Surface Area	409.49 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	276.64 m³·mol⁻¹	ChemAxon
Polarizability	109.95 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78436162

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585057

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Pneumocandin B1 (MMDBc0007520)

MOL for #<Metabolite:0x0000560be1ecedf0>

3D MOL for #<Metabolite:0x0000560be1ecedf0>

3D SDF for #<Metabolite:0x0000560be1ecedf0>

3D-SDF for #<Metabolite:0x0000560be1ecedf0>

PDB for #<Metabolite:0x0000560be1ecedf0>

3D PDB for #<Metabolite:0x0000560be1ecedf0>

SMILES for #<Metabolite:0x0000560be1ecedf0>

INCHI for #<Metabolite:0x0000560be1ecedf0>

Structure for #<Metabolite:0x0000560be1ecedf0>

3D Structure for #<Metabolite:0x0000560be1ecedf0>