MiMeDB: Showing metabocard for Chaetocochin I (MMDBc0010538)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:40:59 UTC

Update Date

2025-10-07 16:05:45 UTC

Metabolite ID

MMDBc0010538

Metabolite Identification

Common Name

Chaetocochin I

Description

Chaetocochin I is a sulfur-containing metabolite belonging to the class of polythioether compounds. This compound is characterized by its unique structural features, including two sulfur bridges: one formed by three sulfur atoms connecting C-3 and C-11a, and another formed by four sulfur atoms linking C-3' and C-6' (PMID:26125976 ). The presence of these sulfur bridges contributes to its chemical stability and reactivity. Biologically, Chaetocochin I can undergo transformations, readily converting into several related metabolites, including chetomin (2), chetoseminudin A (3), chaetocochin D (4), chaetocochin G (5), and chaetocochin H (6) through the loss of sulfur atoms (PMID:26125976 ). This metabolic versatility suggests potential roles in various biological processes and highlights the importance of sulfur in the structural integrity and function of these metabolites.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104412D          

 51 59  0  0  1  0            999 V2000
    7.6391   -3.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1719   -4.5532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1863    1.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7880   -2.9607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6694   -0.0564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8073    0.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2502   -2.3351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5987   -2.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8960   -0.3436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1718    1.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5230   -1.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4053   -2.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5653   -0.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7695   -0.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5634   -5.5525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3842    2.4088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6327   -1.7110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8716   -2.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2605    0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3985    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3337   -1.4036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0778    0.8015    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0734   -3.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2664    0.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533   -4.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7344    1.5690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4443    0.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3187   -2.9646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0004   -0.0728    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0385   -4.8217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8343    1.6465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6675    1.3785    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7133   -3.5236    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3716   -4.0669    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2444    0.9957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7625   -0.6988    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    0.8087    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4883   -6.4007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5900    2.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5070   -2.4748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5896   -0.5234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9170   -3.8672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8541    2.4549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5494   -3.2627    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -0.4723    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3099    0.9232    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.2692   -5.1198    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.4443    0.0448    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.2163   -4.0175    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.5145   -4.7867    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.7695    1.5667    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 17 12  1  0  0  0  0
 17 13  2  0  0  0  0
 18  8  2  0  0  0  0
 18 17  1  0  0  0  0
 19  9  2  0  0  0  0
 20 10  2  0  0  0  0
 20 19  1  0  0  0  0
 21 11  2  0  0  0  0
 21 18  1  0  0  0  0
 27 14  1  0  0  0  0
 27 19  1  0  0  0  0
 27 22  1  0  0  0  0
 28 12  1  6  0  0  0
 28 23  1  0  0  0  0
 29 14  1  0  0  0  0
 29 24  1  0  0  0  0
 30 15  1  6  0  0  0
 30 25  1  0  0  0  0
 31 16  1  6  0  0  0
 31 26  1  0  0  0  0
 32 20  1  0  0  0  0
 32 22  1  0  0  0  0
 33  1  1  0  0  0  0
 33 25  1  0  0  0  0
 33 28  1  0  0  0  0
 34  2  1  0  0  0  0
 34 23  1  0  0  0  0
 34 30  1  0  0  0  0
 35  3  1  0  0  0  0
 35 24  1  0  0  0  0
 35 31  1  0  0  0  0
 36 13  1  0  0  0  0
 36 21  1  0  0  0  0
 36 27  1  0  0  0  0
 37 22  1  0  0  0  0
 37 26  1  0  0  0  0
 29 37  1  1  0  0  0
 38 15  1  0  0  0  0
 39 16  1  0  0  0  0
 40 23  2  0  0  0  0
 41 24  2  0  0  0  0
 42 25  2  0  0  0  0
 43 26  2  0  0  0  0
 44 28  1  0  0  0  0
 45 29  1  0  0  0  0
 46 31  1  0  0  0  0
 47 30  1  0  0  0  0
 48 45  1  0  0  0  0
 48 46  1  0  0  0  0
 49 44  1  0  0  0  0
 50 47  1  0  0  0  0
 50 49  1  0  0  0  0
 22 51  1  6  0  0  0
M  END


  Mrv1652305152104412D          

 51 59  0  0  1  0            999 V2000
    7.6391   -3.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1719   -4.5532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1863    1.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7880   -2.9607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6694   -0.0564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8073    0.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2502   -2.3351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5987   -2.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8960   -0.3436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1718    1.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5230   -1.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4053   -2.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5653   -0.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7695   -0.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5634   -5.5525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3842    2.4088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6327   -1.7110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8716   -2.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2605    0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3985    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3337   -1.4036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0778    0.8015    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0734   -3.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2664    0.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533   -4.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7344    1.5690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4443    0.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3187   -2.9646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0004   -0.0728    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0385   -4.8217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8343    1.6465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6675    1.3785    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7133   -3.5236    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3716   -4.0669    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2444    0.9957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7625   -0.6988    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2240    0.8087    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4883   -6.4007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5900    2.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5070   -2.4748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5896   -0.5234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9170   -3.8672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8541    2.4549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5494   -3.2627    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -0.4723    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3099    0.9232    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.2692   -5.1198    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.4443    0.0448    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.2163   -4.0175    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.5145   -4.7867    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.7695    1.5667    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 17 12  1  0  0  0  0
 17 13  2  0  0  0  0
 18  8  2  0  0  0  0
 18 17  1  0  0  0  0
 19  9  2  0  0  0  0
 20 10  2  0  0  0  0
 20 19  1  0  0  0  0
 21 11  2  0  0  0  0
 21 18  1  0  0  0  0
 27 14  1  0  0  0  0
 27 19  1  0  0  0  0
 27 22  1  0  0  0  0
 28 12  1  6  0  0  0
 28 23  1  0  0  0  0
 29 14  1  0  0  0  0
 29 24  1  0  0  0  0
 30 15  1  6  0  0  0
 30 25  1  0  0  0  0
 31 16  1  6  0  0  0
 31 26  1  0  0  0  0
 32 20  1  0  0  0  0
 32 22  1  0  0  0  0
 33  1  1  0  0  0  0
 33 25  1  0  0  0  0
 33 28  1  0  0  0  0
 34  2  1  0  0  0  0
 34 23  1  0  0  0  0
 34 30  1  0  0  0  0
 35  3  1  0  0  0  0
 35 24  1  0  0  0  0
 35 31  1  0  0  0  0
 36 13  1  0  0  0  0
 36 21  1  0  0  0  0
 36 27  1  0  0  0  0
 37 22  1  0  0  0  0
 37 26  1  0  0  0  0
 29 37  1  1  0  0  0
 38 15  1  0  0  0  0
 39 16  1  0  0  0  0
 40 23  2  0  0  0  0
 41 24  2  0  0  0  0
 42 25  2  0  0  0  0
 43 26  2  0  0  0  0
 44 28  1  0  0  0  0
 45 29  1  0  0  0  0
 46 31  1  0  0  0  0
 47 30  1  0  0  0  0
 48 45  1  0  0  0  0
 48 46  1  0  0  0  0
 49 44  1  0  0  0  0
 50 47  1  0  0  0  0
 50 49  1  0  0  0  0
 22 51  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0010538

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12NC3=CC=CC=C3C1(C[C@]13SSS[C@](CO)(N(C)C1=O)C(=O)N23)N1C=C(C[C@]23SSSS[C@](CO)(N(C)C2=O)C(=O)N3C)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C31H30N6O6S7/c1-33-25(42)30(15-38)34(2)23(40)28(33,44-49-50-47-30)12-17-13-36(21-11-7-4-8-18(17)21)27-14-29-24(41)35(3)31(16-39,46-48-45-29)26(43)37(29)22(27)32-20-10-6-5-9-19(20)27/h4-11,13,22,32,38-39H,12,14-16H2,1-3H3/t22-,27?,28+,29+,30+,31+/m1/s1

> <INCHI_KEY>
YISUSQYDZYMJHH-QBFIAXCUSA-N

> <FORMULA>
C31H30N6O6S7

> <MOLECULAR_WEIGHT>
807.04

> <EXACT_MASS>
806.027180928

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
76.18953085040444

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,11R,14S)-14-(hydroxymethyl)-3-(3-{[(1S,6S)-6-(hydroxymethyl)-7,9-dimethyl-8,10-dioxo-2,3,4,5-tetrathia-7,9-diazabicyclo[4.2.2]decan-1-yl]methyl}-1H-indol-1-yl)-19-methyl-15,16,17-trithia-10,12,19-triazapentacyclo[12.3.2.0^{1,12}.0^{3,11}.0^{4,9}]nonadeca-4,6,8-triene-13,18-dione

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
5.408601863666668

> <ALOGPS_LOGS>
-3.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.770760052400625

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.751896195719773

> <JCHEM_PKA_STRONGEST_BASIC>
1.0228485250524766

> <JCHEM_POLAR_SURFACE_AREA>
138.66

> <JCHEM_REFRACTIVITY>
199.82899999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11R,14S)-14-(hydroxymethyl)-3-(3-{[(1S,6S)-6-(hydroxymethyl)-7,9-dimethyl-8,10-dioxo-2,3,4,5-tetrathia-7,9-diazabicyclo[4.2.2]decan-1-yl]methyl}indol-1-yl)-19-methyl-15,16,17-trithia-10,12,19-triazapentacyclo[12.3.2.0^{1,12}.0^{3,11}.0^{4,9}]nonadeca-4,6,8-triene-13,18-dione

> <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      14.260  -5.900   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.254  -8.499   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.948   2.581   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.071  -5.527   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.449  -0.105   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.707   1.413   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.067  -4.359   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.584  -5.241   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.006  -0.641   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.521   2.395   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.576  -2.906   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.957  -3.950   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.389  -1.659   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.036  -0.833   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.118 -10.365   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.584   4.496   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.514  -3.194   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.094  -3.788   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.820   0.341   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.077   1.859   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.090  -2.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.612   1.496   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.204  -6.156   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.231   0.417   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.979  -7.733   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.104   2.929   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.296   0.116   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.795  -5.534   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.601  -0.136   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.138  -9.000   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.424   3.074   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       8.713   2.573   0.000  0.00  0.00           N+0
HETATM   33  N   UNK     0      12.532  -6.577   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0      13.760  -7.592   0.000  0.00  0.00           N+0
HETATM   35  N   UNK     0       4.190   1.859   0.000  0.00  0.00           N+0
HETATM   36  N   UNK     0       8.890  -1.304   0.000  0.00  0.00           N+0
HETATM   37  N   UNK     0       6.018   1.510   0.000  0.00  0.00           N+0
HETATM   38  O   UNK     0      13.978 -11.948   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       1.101   5.066   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      14.013  -4.620   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       2.967  -0.977   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      14.778  -7.219   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.328   4.583   0.000  0.00  0.00           O+0
HETATM   44  S   UNK     0      10.359  -6.090   0.000  0.00  0.00           S+0
HETATM   45  S   UNK     0       4.073  -0.882   0.000  0.00  0.00           S+0
HETATM   46  S   UNK     0       2.445   1.723   0.000  0.00  0.00           S+0
HETATM   47  S   UNK     0      11.703  -9.557   0.000  0.00  0.00           S+0
HETATM   48  S   UNK     0       2.696   0.084   0.000  0.00  0.00           S+0
HETATM   49  S   UNK     0       9.737  -7.499   0.000  0.00  0.00           S+0
HETATM   50  S   UNK     0      10.294  -8.935   0.000  0.00  0.00           S+0
HETATM   51  H   UNK     0       7.036   2.925   0.000  0.00  0.00           H+0
CONECT    1   33                                                            
CONECT    2   34                                                            
CONECT    3   35                                                            
CONECT    4    7    8                                                       
CONECT    5    6    9                                                       
CONECT    6    5   10                                                       
CONECT    7    4   11                                                       
CONECT    8    4   18                                                       
CONECT    9    5   19                                                       
CONECT   10    6   20                                                       
CONECT   11    7   21                                                       
CONECT   12   17   28                                                       
CONECT   13   17   36                                                       
CONECT   14   27   29                                                       
CONECT   15   30   38                                                       
CONECT   16   31   39                                                       
CONECT   17   12   13   18                                                  
CONECT   18    8   17   21                                                  
CONECT   19    9   20   27                                                  
CONECT   20   10   19   32                                                  
CONECT   21   11   18   36                                                  
CONECT   22   27   32   37   51                                             
CONECT   23   28   34   40                                                  
CONECT   24   29   35   41                                                  
CONECT   25   30   33   42                                                  
CONECT   26   31   37   43                                                  
CONECT   27   14   19   22   36                                             
CONECT   28   12   23   33   44                                             
CONECT   29   14   24   37   45                                             
CONECT   30   15   25   34   47                                             
CONECT   31   16   26   35   46                                             
CONECT   32   20   22                                                       
CONECT   33    1   25   28                                                  
CONECT   34    2   23   30                                                  
CONECT   35    3   24   31                                                  
CONECT   36   13   21   27                                                  
CONECT   37   22   26   29                                                  
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   23                                                            
CONECT   41   24                                                            
CONECT   42   25                                                            
CONECT   43   26                                                            
CONECT   44   28   49                                                       
CONECT   45   29   48                                                       
CONECT   46   31   48                                                       
CONECT   47   30   50                                                       
CONECT   48   45   46                                                       
CONECT   49   44   50                                                       
CONECT   50   47   49                                                       
CONECT   51   22                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  118    0
END

Synonyms

Not Available

Molecular Formula

C₃₁H₃₀N₆O₆S₇

Average Mass

807.04

Monoisotopic Mass

806.027180928

IUPAC Name

(1S,11R,14S)-14-(hydroxymethyl)-3-(3-{[(1S,6S)-6-(hydroxymethyl)-7,9-dimethyl-8,10-dioxo-2,3,4,5-tetrathia-7,9-diazabicyclo[4.2.2]decan-1-yl]methyl}-1H-indol-1-yl)-19-methyl-15,16,17-trithia-10,12,19-triazapentacyclo[12.3.2.0^{1,12}.0^{3,11}.0^{4,9}]nonadeca-4,6,8-triene-13,18-dione

Traditional Name

(1S,11R,14S)-14-(hydroxymethyl)-3-(3-{[(1S,6S)-6-(hydroxymethyl)-7,9-dimethyl-8,10-dioxo-2,3,4,5-tetrathia-7,9-diazabicyclo[4.2.2]decan-1-yl]methyl}indol-1-yl)-19-methyl-15,16,17-trithia-10,12,19-triazapentacyclo[12.3.2.0^{1,12}.0^{3,11}.0^{4,9}]nonadeca-4,6,8-triene-13,18-dione

CAS Registry Number

Not Available

SMILES

[H][C@]12NC3=CC=CC=C3C1(C[C@]13SSS[C@](CO)(N(C)C1=O)C(=O)N23)N1C=C(C[C@]23SSSS[C@](CO)(N(C)C2=O)C(=O)N3C)C2=CC=CC=C12

InChI Identifier

InChI=1S/C31H30N6O6S7/c1-33-25(42)30(15-38)34(2)23(40)28(33,44-49-50-47-30)12-17-13-36(21-11-7-4-8-18(17)21)27-14-29-24(41)35(3)31(16-39,46-48-45-29)26(43)37(29)22(27)32-20-10-6-5-9-19(20)27/h4-11,13,22,32,38-39H,12,14-16H2,1-3H3/t22-,27?,28+,29+,30+,31+/m1/s1

InChI Key

YISUSQYDZYMJHH-QBFIAXCUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
N-alkylindole
3-alkylindole
Alpha-amino acid or derivatives
Thiodioxopiperazine
Dihydroindole
Indole
2,5-dioxopiperazine
Dioxopiperazine
N-alkylpiperazine
N-methylpiperazine
Secondary aliphatic/aromatic amine
Benzenoid
Substituted pyrrole
Piperazine
1,4-diazinane
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Organic trisulfide
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Secondary amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	0.49 g/L	ALOGPS
logP	3.18	ALOGPS
logP	5.41	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	1.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	138.66 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	199.83 m³·mol⁻¹	ChemAxon
Polarizability	76.19 Å³	ChemAxon
Number of Rings	9	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 (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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View 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

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

78441109

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585884

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 Chaetocochin I (MMDBc0010538)

MOL for #<Metabolite:0x00007f8dd002b650>

3D MOL for #<Metabolite:0x00007f8dd002b650>

3D SDF for #<Metabolite:0x00007f8dd002b650>

3D-SDF for #<Metabolite:0x00007f8dd002b650>

PDB for #<Metabolite:0x00007f8dd002b650>

3D PDB for #<Metabolite:0x00007f8dd002b650>

SMILES for #<Metabolite:0x00007f8dd002b650>

INCHI for #<Metabolite:0x00007f8dd002b650>

Structure for #<Metabolite:0x00007f8dd002b650>

3D Structure for #<Metabolite:0x00007f8dd002b650>