MiMeDB: Showing metabocard for Ketocytochalasin (MMDBc0012532)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:02:32 UTC

Update Date

2025-10-07 16:06:00 UTC

Metabolite ID

MMDBc0012532

Metabolite Identification

Common Name

Ketocytochalasin

Description

Ketocytochalasin is a member of the cytochalasin chemical class, which consists of a group of fungal metabolites known for their ability to disrupt cytoskeletal dynamics. This compound was identified as a novel natural product isolated from the fungus Arthrinium arundinis ZSDS1-F3, which was sourced from the sponge Phakellia fusca. The discovery of ketocytochalasin, along with four new cytochalasins (arthriniumnins A-D) and five known cytochalasin analogues, highlights its potential significance in the study of cellular processes, particularly in relation to actin filament dynamics and cell motility. The structural characteristics of ketocytochalasin contribute to its biological activity, making it a valuable compound for further research in both chemistry and biology. The exploration of such metabolites can provide insights into their mechanisms of action and potential applications in therapeutic contexts, particularly in cancer research and other fields where modulation of the cytoskeleton is relevant (PMID:25626143 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106022D          

 42 45  0  0  1  0            999 V2000
    4.4087   -0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5093   -2.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829   -1.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601   -3.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9927   -6.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6396   -6.1346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2258   -6.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4820   -1.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1495   -0.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5196   -5.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1059   -5.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7070   -2.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3949   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6221   -3.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0128   -1.2012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6328   -4.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0041   -0.9755    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6852   -2.5323    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3865   -1.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4876   -2.5589    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7528   -5.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8023   -1.4411    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2797   -3.6859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9610   -2.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2707   -2.8514    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4671   -1.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5130   -3.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0558   -2.4454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0791   -3.8837    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2518   -1.6988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2230   -1.3701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3380   -3.1737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6351   -2.3230    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259   -1.7897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7321   -4.0790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0429   -2.3095    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5958   -0.2586    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2044   -1.8912    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2754   -2.2452    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660   -0.6325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5352   -3.3306    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9778   -3.2766    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  5  1  0  0  0  0
  9  8  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  2  0  0  0  0
 12  8  2  0  0  0  0
 14 13  2  0  0  0  0
 17  1  1  6  0  0  0
 17  9  1  0  0  0  0
 18  2  1  1  0  0  0
 18 13  1  0  0  0  0
 19  3  1  0  0  0  0
 19 15  2  0  0  0  0
 20  4  1  6  0  0  0
 20 19  1  0  0  0  0
 21 10  2  0  0  0  0
 21 11  1  0  0  0  0
 21 16  1  0  0  0  0
 22 12  1  0  0  0  0
 22 15  1  0  0  0  0
 23 16  1  1  0  0  0
 24 14  1  0  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 17  1  0  0  0  0
 26 18  1  0  0  0  0
 28 22  1  0  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 28 27  1  1  0  0  0
 29 23  1  0  0  0  0
 29 27  2  0  0  0  0
 30 24  2  0  0  0  0
 31 26  2  0  0  0  0
 32 27  1  0  0  0  0
 33  8  1  0  0  0  0
 34 12  1  0  0  0  0
 35 13  1  0  0  0  0
 36 14  1  0  0  0  0
 17 37  1  1  0  0  0
 18 38  1  6  0  0  0
 20 39  1  1  0  0  0
 22 40  1  6  0  0  0
 23 41  1  6  0  0  0
 25 42  1  1  0  0  0
M  END


  Mrv1652305152106022D          

 42 45  0  0  1  0            999 V2000
    4.4087   -0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5093   -2.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829   -1.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601   -3.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9927   -6.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6396   -6.1346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2258   -6.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4820   -1.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1495   -0.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5196   -5.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1059   -5.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7070   -2.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3949   -3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6221   -3.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0128   -1.2012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6328   -4.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0041   -0.9755    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6852   -2.5323    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3865   -1.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4876   -2.5589    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7528   -5.0142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8023   -1.4411    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2797   -3.6859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9610   -2.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2707   -2.8514    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4671   -1.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5130   -3.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0558   -2.4454    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0791   -3.8837    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2518   -1.6988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2230   -1.3701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3380   -3.1737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6351   -2.3230    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9259   -1.7897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7321   -4.0790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0429   -2.3095    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5958   -0.2586    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2044   -1.8912    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2754   -2.2452    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9660   -0.6325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5352   -3.3306    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9778   -3.2766    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  5  1  0  0  0  0
  9  8  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  2  0  0  0  0
 12  8  2  0  0  0  0
 14 13  2  0  0  0  0
 17  1  1  6  0  0  0
 17  9  1  0  0  0  0
 18  2  1  1  0  0  0
 18 13  1  0  0  0  0
 19  3  1  0  0  0  0
 19 15  2  0  0  0  0
 20  4  1  6  0  0  0
 20 19  1  0  0  0  0
 21 10  2  0  0  0  0
 21 11  1  0  0  0  0
 21 16  1  0  0  0  0
 22 12  1  0  0  0  0
 22 15  1  0  0  0  0
 23 16  1  1  0  0  0
 24 14  1  0  0  0  0
 25 20  1  0  0  0  0
 25 23  1  0  0  0  0
 26 17  1  0  0  0  0
 26 18  1  0  0  0  0
 28 22  1  0  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 28 27  1  1  0  0  0
 29 23  1  0  0  0  0
 29 27  2  0  0  0  0
 30 24  2  0  0  0  0
 31 26  2  0  0  0  0
 32 27  1  0  0  0  0
 33  8  1  0  0  0  0
 34 12  1  0  0  0  0
 35 13  1  0  0  0  0
 36 14  1  0  0  0  0
 17 37  1  1  0  0  0
 18 38  1  6  0  0  0
 20 39  1  1  0  0  0
 22 40  1  6  0  0  0
 23 41  1  6  0  0  0
 25 42  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012532

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C1=C([H])[C@@]2([H])C=C(C)[C@@]([H])(C)[C@@]3([H])[C@]([H])(CC4=CC=CC=C4)N=C(O)[C@]23C(=O)C([H])=C([H])[C@]([H])(C)C(=O)[C@@]([H])(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H33NO3/c1-17-9-8-12-22-15-19(3)20(4)25-23(16-21-10-6-5-7-11-21)29-27(32)28(22,25)24(30)14-13-18(2)26(17)31/h5-8,10-15,17-18,20,22-23,25H,9,16H2,1-4H3,(H,29,32)/b12-8-,14-13+/t17-,18-,20+,22-,23-,25-,28-/m0/s1

> <INCHI_KEY>
MZRDRLOYHFZNCS-ORMYONGWSA-N

> <FORMULA>
C28H33NO3

> <MOLECULAR_WEIGHT>
431.576

> <EXACT_MASS>
431.246043927

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
48.75591615994768

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4S,6aS,10S,12S,15aS,15bR)-3-benzyl-1-hydroxy-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindole-11,15-dione

> <ALOGPS_LOGP>
4.79

> <JCHEM_LOGP>
4.977877666133787

> <ALOGPS_LOGS>
-5.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.16072926243212

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8168429071005843

> <JCHEM_PKA_STRONGEST_BASIC>
5.530132635744658

> <JCHEM_POLAR_SURFACE_AREA>
66.73

> <JCHEM_REFRACTIVITY>
130.3584

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.50e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,6aS,10S,12S,15aS,15bR)-3-benzyl-1-hydroxy-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,12H,15bH-cycloundeca[e]isoindole-11,15-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       8.230  -0.479   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.284  -4.800   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.715  -2.690   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.299  -5.731   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.853 -12.407   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.061 -11.451   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.422 -11.839   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.633  -2.823   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.879  -1.785   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.837  -9.928   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.198 -10.316   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.186  -3.836   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.204  -6.209   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.761  -5.636   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.891  -2.242   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.181  -7.836   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.474  -1.821   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.746  -4.727   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.722  -3.246   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.910  -4.777   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.405  -9.360   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.364  -2.690   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.389  -6.880   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.527  -4.612   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.372  -5.323   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.339  -3.175   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.691  -5.930   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.838  -4.565   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       3.881  -7.250   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0       6.070  -3.171   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       9.750  -2.558   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.231  -5.924   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0       4.919  -4.336   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.728  -3.341   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       8.833  -7.614   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       7.547  -4.311   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.712  -0.483   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       9.715  -3.530   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.514  -4.191   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.670  -1.181   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.999  -6.217   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.692  -6.116   0.000  0.00  0.00           H+0
CONECT    1   17                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    6    7                                                       
CONECT    6    5   10                                                       
CONECT    7    5   11                                                       
CONECT    8    9   12   33                                                  
CONECT    9    8   17                                                       
CONECT   10    6   21                                                       
CONECT   11    7   21                                                       
CONECT   12    8   22   34                                                  
CONECT   13   14   18   35                                                  
CONECT   14   13   24   36                                                  
CONECT   15   19   22                                                       
CONECT   16   21   23                                                       
CONECT   17    1    9   26   37                                             
CONECT   18    2   13   26   38                                             
CONECT   19    3   15   20                                                  
CONECT   20    4   19   25   39                                             
CONECT   21   10   11   16                                                  
CONECT   22   12   15   28   40                                             
CONECT   23   16   25   29   41                                             
CONECT   24   14   28   30                                                  
CONECT   25   20   23   28   42                                             
CONECT   26   17   18   31                                                  
CONECT   27   28   29   32                                                  
CONECT   28   22   24   25   27                                             
CONECT   29   23   27                                                       
CONECT   30   24                                                            
CONECT   31   26                                                            
CONECT   32   27                                                            
CONECT   33    8                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   17                                                            
CONECT   38   18                                                            
CONECT   39   20                                                            
CONECT   40   22                                                            
CONECT   41   23                                                            
CONECT   42   25                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₃NO₃

Average Mass

431.576

Monoisotopic Mass

431.246043927

IUPAC Name

(3S,4S,6aS,10S,12S,15aS,15bR)-3-benzyl-1-hydroxy-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindole-11,15-dione

Traditional Name

(3S,4S,6aS,10S,12S,15aS,15bR)-3-benzyl-1-hydroxy-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,12H,15bH-cycloundeca[e]isoindole-11,15-dione

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])[C@@]2([H])C=C(C)[C@@]([H])(C)[C@@]3([H])[C@]([H])(CC4=CC=CC=C4)N=C(O)[C@]23C(=O)C([H])=C([H])[C@]([H])(C)C(=O)[C@@]([H])(C)C1

InChI Identifier

InChI=1S/C28H33NO3/c1-17-9-8-12-22-15-19(3)20(4)25-23(16-21-10-6-5-7-11-21)29-27(32)28(22,25)24(30)14-13-18(2)26(17)31/h5-8,10-15,17-18,20,22-23,25H,9,16H2,1-4H3,(H,29,32)/b12-8-,14-13+/t17-,18-,20+,22-,23-,25-,28-/m0/s1

InChI Key

MZRDRLOYHFZNCS-ORMYONGWSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00095 g/L	ALOGPS
logP	4.79	ALOGPS
logP	4.98	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	2.82	ChemAxon
pKa (Strongest Basic)	5.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.73 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.36 m³·mol⁻¹	ChemAxon
Polarizability	48.76 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

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	2		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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for Ketocytochalasin (MMDBc0012532)

MOL for #<Metabolite:0x00007f28ac92ee48>

3D MOL for #<Metabolite:0x00007f28ac92ee48>

3D SDF for #<Metabolite:0x00007f28ac92ee48>

3D-SDF for #<Metabolite:0x00007f28ac92ee48>

PDB for #<Metabolite:0x00007f28ac92ee48>

3D PDB for #<Metabolite:0x00007f28ac92ee48>

SMILES for #<Metabolite:0x00007f28ac92ee48>

INCHI for #<Metabolite:0x00007f28ac92ee48>

Structure for #<Metabolite:0x00007f28ac92ee48>

3D Structure for #<Metabolite:0x00007f28ac92ee48>