MiMeDB: Showing metabocard for Ergonornorine (MMDBc0007780)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:50:52 UTC

Update Date

2022-08-31 06:27:43 UTC

MiMeDB ID

MMDBc0007780

Metabolite Identification

Common Name

Ergonornorine

Description

Ergonornorine belongs to the class of organic compounds known as ergopeptines. These are ergoline derivatives that contain a tripeptide structure attached to the basic ergoline ring in the same location as the amide group of the lysergic acid derivatives. Based on a literature review very few articles have been published on Ergonornorine.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102502D          

 45 51  0  0  1  0            999 V2000
    3.5100    5.9337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9139    0.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2947    5.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5784    1.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9761    4.7744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4662    4.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6405    4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7579    1.7213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3630    5.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7486    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2508    4.6168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8201    4.1070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8639    5.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9374    3.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2070    3.5549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6485    4.9139    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    3.8099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6924    5.9759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124    3.1424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9606    3.2194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2070    2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0793    5.4238    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0354    4.3619    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  2  1  0  0  0  0
  8  4  1  0  0  0  0
  9  6  2  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  5  1  0  0  0  0
 13  7  1  0  0  0  0
 18 15  1  0  0  0  0
 18 16  2  0  0  0  0
 19 14  1  0  0  0  0
 19 17  1  0  0  0  0
 20  9  1  0  0  0  0
 21 14  2  0  0  0  0
 21 20  1  0  0  0  0
 22 10  2  0  0  0  0
 23  8  1  1  0  0  0
 24 15  1  0  0  0  0
 24 21  1  0  0  0  0
 25 11  1  0  0  0  0
 26 18  1  0  0  0  0
 26 20  2  0  0  0  0
 26 22  1  0  0  0  0
 19 27  1  1  0  0  0
 28 23  1  0  0  0  0
 30 12  1  6  0  0  0
 30 29  1  0  0  0  0
 31 25  1  0  0  0  0
 32 16  1  0  0  0  0
 32 22  1  0  0  0  0
 33 27  2  0  0  0  0
 30 33  1  1  0  0  0
 34  3  1  0  0  0  0
 34 17  1  0  0  0  0
 34 24  1  0  0  0  0
 35 13  1  0  0  0  0
 35 25  1  0  0  0  0
 35 28  1  0  0  0  0
 36 23  1  0  0  0  0
 36 29  1  0  0  0  0
 36 31  1  0  0  0  0
 27 37  1  4  0  0  0
 38 28  2  0  0  0  0
 39 29  2  0  0  0  0
 31 40  1  1  0  0  0
 41 30  1  0  0  0  0
 41 31  1  0  0  0  0
 19 42  1  6  0  0  0
 23 43  1  6  0  0  0
 24 44  1  1  0  0  0
 25 45  1  6  0  0  0
M  END


  Mrv1652305152102502D          

 45 51  0  0  1  0            999 V2000
    3.5100    5.9337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9139    0.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2947    5.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5784    1.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7925    2.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9761    4.7744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4662    4.8718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6405    4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7579    1.7213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3630    5.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7486    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3509    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2508    4.6168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8201    4.1070    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1355    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8639    5.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9374    3.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2070    3.5549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1340    0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6485    4.9139    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    3.8099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6924    5.9759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124    3.1424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9606    3.2194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2070    2.7299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0793    5.4238    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0354    4.3619    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  2  1  0  0  0  0
  8  4  1  0  0  0  0
  9  6  2  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  5  1  0  0  0  0
 13  7  1  0  0  0  0
 18 15  1  0  0  0  0
 18 16  2  0  0  0  0
 19 14  1  0  0  0  0
 19 17  1  0  0  0  0
 20  9  1  0  0  0  0
 21 14  2  0  0  0  0
 21 20  1  0  0  0  0
 22 10  2  0  0  0  0
 23  8  1  1  0  0  0
 24 15  1  0  0  0  0
 24 21  1  0  0  0  0
 25 11  1  0  0  0  0
 26 18  1  0  0  0  0
 26 20  2  0  0  0  0
 26 22  1  0  0  0  0
 19 27  1  1  0  0  0
 28 23  1  0  0  0  0
 30 12  1  6  0  0  0
 30 29  1  0  0  0  0
 31 25  1  0  0  0  0
 32 16  1  0  0  0  0
 32 22  1  0  0  0  0
 33 27  2  0  0  0  0
 30 33  1  1  0  0  0
 34  3  1  0  0  0  0
 34 17  1  0  0  0  0
 34 24  1  0  0  0  0
 35 13  1  0  0  0  0
 35 25  1  0  0  0  0
 35 28  1  0  0  0  0
 36 23  1  0  0  0  0
 36 29  1  0  0  0  0
 36 31  1  0  0  0  0
 27 37  1  4  0  0  0
 38 28  2  0  0  0  0
 39 29  2  0  0  0  0
 31 40  1  1  0  0  0
 41 30  1  0  0  0  0
 41 31  1  0  0  0  0
 19 42  1  6  0  0  0
 23 43  1  6  0  0  0
 24 44  1  1  0  0  0
 25 45  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007780

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@]([H])(CCC)N1C(=O)[C@@](CCC)(O[C@@]21O)N=C(O)[C@@]1([H])CN(C)[C@]2([H])CC3=CNC4=CC=CC(=C34)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C31H39N5O5/c1-4-8-23-28(38)35-13-7-11-25(35)31(40)36(23)29(39)30(41-31,12-5-2)33-27(37)19-14-21-20-9-6-10-22-26(20)18(16-32-22)15-24(21)34(3)17-19/h6,9-10,14,16,19,23-25,32,40H,4-5,7-8,11-13,15,17H2,1-3H3,(H,33,37)/t19-,23+,24-,25+,30-,31+/m1/s1

> <INCHI_KEY>
MORHLKHASYRXLL-QIOPVHFHSA-N

> <FORMULA>
C31H39N5O5

> <MOLECULAR_WEIGHT>
561.683

> <EXACT_MASS>
561.295119376

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
62.08125444727551

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R,7R)-N-[(1S,2S,4R,7S)-2-hydroxy-5,8-dioxo-4,7-dipropyl-3-oxa-6,9-diazatricyclo[7.3.0.0^{2,6}]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),2,9,12,14-pentaene-4-carboximidic acid

> <ALOGPS_LOGP>
2.93

> <JCHEM_LOGP>
1.3250127431174117

> <ALOGPS_LOGS>
-3.55

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
9.718595063867411

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.478903769169541

> <JCHEM_PKA_STRONGEST_BASIC>
8.084328456501941

> <JCHEM_POLAR_SURFACE_AREA>
121.70000000000002

> <JCHEM_REFRACTIVITY>
154.2653

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.58e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,7R)-N-[(1S,2S,4R,7S)-2-hydroxy-5,8-dioxo-4,7-dipropyl-3-oxa-6,9-diazatricyclo[7.3.0.0^{2,6}]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),2,9,12,14-pentaene-4-carboximidic 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       6.552  11.076   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.906   1.645   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.121  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.017  10.600   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.280   3.052   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.479   4.553   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.889   8.912   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.337   9.094   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.944   4.077   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.335   3.522   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.262   7.505   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.748   3.213   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.744   9.943   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.453  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.655  -0.476   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.120   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.264   2.570   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.655   2.016   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.802   8.618   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.787  -0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.731   7.666   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.120   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.946   9.649   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.217   5.866   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.122   4.620   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.586   6.636   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      -0.250   0.770   0.000  0.00  0.00           N+0
HETATM   33  N   UNK     0       8.788   3.850   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0       6.121  -0.770   0.000  0.00  0.00           N+0
HETATM   35  N   UNK     0      12.411   9.173   0.000  0.00  0.00           N+0
HETATM   36  N   UNK     0      10.122   7.112   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0      10.122   1.540   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      10.626  11.155   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       7.677   5.866   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      12.993   6.010   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      11.586   5.096   0.000  0.00  0.00           O+0
HETATM   42  H   UNK     0       8.788   0.770   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0       9.481  10.124   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.787  -1.540   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      11.266   8.142   0.000  0.00  0.00           H+0
CONECT    1    4                                                            
CONECT    2    5                                                            
CONECT    3   34                                                            
CONECT    4    1    8                                                       
CONECT    5    2   12                                                       
CONECT    6    9   10                                                       
CONECT    7   11   13                                                       
CONECT    8    4   23                                                       
CONECT    9    6   20                                                       
CONECT   10    6   22                                                       
CONECT   11    7   25                                                       
CONECT   12    5   30                                                       
CONECT   13    7   35                                                       
CONECT   14   19   21                                                       
CONECT   15   18   24                                                       
CONECT   16   18   32                                                       
CONECT   17   19   34                                                       
CONECT   18   15   16   26                                                  
CONECT   19   14   17   27   42                                             
CONECT   20    9   21   26                                                  
CONECT   21   14   20   24                                                  
CONECT   22   10   26   32                                                  
CONECT   23    8   28   36   43                                             
CONECT   24   15   21   34   44                                             
CONECT   25   11   31   35   45                                             
CONECT   26   18   20   22                                                  
CONECT   27   19   33   37                                                  
CONECT   28   23   35   38                                                  
CONECT   29   30   36   39                                                  
CONECT   30   12   29   33   41                                             
CONECT   31   25   36   40   41                                             
CONECT   32   16   22                                                       
CONECT   33   27   30                                                       
CONECT   34    3   17   24                                                  
CONECT   35   13   25   28                                                  
CONECT   36   23   29   31                                                  
CONECT   37   27                                                            
CONECT   38   28                                                            
CONECT   39   29                                                            
CONECT   40   31                                                            
CONECT   41   30   31                                                       
CONECT   42   19                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

Synonyms

Not Available

Chemical Formula

C₃₁H₃₉N₅O₅

Average Molecular Weight

561.683

Monoisotopic Molecular Weight

561.295119376

IUPAC Name

(4R,7R)-N-[(1S,2S,4R,7S)-2-hydroxy-5,8-dioxo-4,7-dipropyl-3-oxa-6,9-diazatricyclo[7.3.0.0^{2,6}]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),2,9,12,14-pentaene-4-carboximidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@]([H])(CCC)N1C(=O)[C@@](CCC)(O[C@@]21O)N=C(O)[C@@]1([H])CN(C)[C@]2([H])CC3=CNC4=CC=CC(=C34)C2=C1

InChI Identifier

InChI=1S/C31H39N5O5/c1-4-8-23-28(38)35-13-7-11-25(35)31(40)36(23)29(39)30(41-31,12-5-2)33-27(37)19-14-21-20-9-6-10-22-26(20)18(16-32-22)15-24(21)34(3)17-19/h6,9-10,14,16,19,23-25,32,40H,4-5,7-8,11-13,15,17H2,1-3H3,(H,33,37)/t19-,23+,24-,25+,30-,31+/m1/s1

InChI Key

MORHLKHASYRXLL-QIOPVHFHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergopeptines. These are ergoline derivatives that contain a tripeptide structure attached to the basic ergoline ring in the same location as the amide group of the lysergic acid derivatives.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ergoline and derivatives

Sub Class

Lysergic acids and derivatives

Direct Parent

Ergopeptines

Alternative Parents

Substituents

Hybrid peptide
Ergopeptine
Alpha-dipeptide
Lysergic acid amide
Indoloquinoline
Benzoquinoline
Quinoline-3-carboxamide
N-acyl-alpha amino acid or derivatives
Pyrroloquinoline
Quinoline
Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Isoindole or derivatives
Aralkylamine
N-alkylpiperazine
1,4-diazinane
Benzenoid
Oxazolidinone
Piperazine
Pyrrolidine
Pyrrole
Heteroaromatic compound
Tertiary carboxylic acid amide
Oxazolidine
Carboxamide group
Amino acid or derivatives
Lactam
Tertiary aliphatic amine
Tertiary amine
Orthocarboxylic acid derivative
Secondary carboxylic acid amide
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Azacycle
Alkanolamine
Amine
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
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	0.16 g/L	ALOGPS
logP	2.93	ALOGPS
logP	1.33	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	4.48	ChemAxon
pKa (Strongest Basic)	8.08	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	121.7 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	154.27 m³·mol⁻¹	ChemAxon
Polarizability	62.08 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum

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

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

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
Fungi	Ascomycota	1	Human Feces	Metabolic reconstruction

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

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

78439929

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585119

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

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 Ergonornorine (MMDBc0007780)

MOL for #<Metabolite:0x000055b76d2de3d8>

3D MOL for #<Metabolite:0x000055b76d2de3d8>

3D SDF for #<Metabolite:0x000055b76d2de3d8>

3D-SDF for #<Metabolite:0x000055b76d2de3d8>

PDB for #<Metabolite:0x000055b76d2de3d8>

3D PDB for #<Metabolite:0x000055b76d2de3d8>

SMILES for #<Metabolite:0x000055b76d2de3d8>

INCHI for #<Metabolite:0x000055b76d2de3d8>

Structure for #<Metabolite:0x000055b76d2de3d8>

3D Structure for #<Metabolite:0x000055b76d2de3d8>