MiMeDB: Showing metabocard for Cytochalasin K (MMDBc0017278)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 07:42:24 UTC

Update Date

2022-08-31 06:42:04 UTC

Metabolite ID

MMDBc0017278

Metabolite Identification

Common Name

Cytochalasin K

Description

Based on a literature review very few articles have been published on (1S,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-19-benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0¹,¹⁸.0¹⁴,¹⁶]henicosa-3,7,11,20-tetraen-6-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152109422D          

 51 55  0  0  1  0            999 V2000
    5.9806    3.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7145    5.3981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    4.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9706    5.6799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0876    3.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143    4.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9594    3.5423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    4.9400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303    1.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0259    2.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1524    3.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447    4.7685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7850    1.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    4.2263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7389    3.4674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970    4.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2066    3.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1583    3.3296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3020    4.6836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    3.1853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2733    6.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3997    3.9838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    1.5353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4616    3.0277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7013    4.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8052    2.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2462    2.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5096    4.9131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6751    1.9478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4616    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6751    2.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2462    1.9478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9766    2.3603    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3066    6.9452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3476    5.4935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803    2.6384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2066    0.9082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5428    5.7375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896    2.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0521    1.2167    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9500    0.6937    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6186    4.9219    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5585    3.5612    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5943    4.5530    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3360    3.2632    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6751    3.5978    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7311    0.7428    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6706    3.2622    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    2.3603    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4764    4.0888    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8501    1.9478    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  2  0  0  0  0
 13  9  2  0  0  0  0
 15 14  2  0  0  0  0
 18  1  1  6  0  0  0
 18 10  1  0  0  0  0
 18 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19 16  2  0  0  0  0
 20  3  1  6  0  0  0
 21  4  1  0  0  0  0
 22 11  2  0  0  0  0
 22 12  1  0  0  0  0
 22 17  1  0  0  0  0
 23 13  1  0  0  0  0
 24 17  1  1  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27 20  1  0  0  0  0
 27 24  1  0  0  0  0
 28 19  1  0  0  0  0
 28 25  1  0  0  0  0
 29 23  1  0  0  0  0
 31  5  1  6  0  0  0
 31 20  1  0  0  0  0
 31 29  1  0  0  0  0
 32 23  1  0  0  0  0
 32 26  1  0  0  0  0
 32 27  1  0  0  0  0
 32 30  1  6  0  0  0
 33 24  1  0  0  0  0
 33 30  2  0  0  0  0
 34 21  2  0  0  0  0
 35 25  2  0  0  0  0
 36 26  2  0  0  0  0
 37 30  1  0  0  0  0
 38 21  1  0  0  0  0
 28 38  1  1  0  0  0
 39 29  1  0  0  0  0
 39 31  1  0  0  0  0
 40  9  1  0  0  0  0
 41 13  1  0  0  0  0
 42 14  1  0  0  0  0
 43 15  1  0  0  0  0
 44 16  1  0  0  0  0
 18 45  1  6  0  0  0
 20 46  1  1  0  0  0
 23 47  1  1  0  0  0
 24 48  1  6  0  0  0
 27 49  1  1  0  0  0
 28 50  1  1  0  0  0
 29 51  1  6  0  0  0
M  END


  Mrv1652305152109422D          

 51 55  0  0  1  0            999 V2000
    5.9806    3.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7145    5.3981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    4.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9706    5.6799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0876    3.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143    4.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9594    3.5423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623    4.9400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303    1.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0259    2.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1524    3.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447    4.7685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7850    1.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    4.2263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7389    3.4674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970    4.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2066    3.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1583    3.3296    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3020    4.6836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    3.1853    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2733    6.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3997    3.9838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    1.5353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4616    3.0277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7013    4.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8052    2.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2462    2.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5096    4.9131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6751    1.9478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4616    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6751    2.7728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2462    1.9478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9766    2.3603    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3066    6.9452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3476    5.4935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803    2.6384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2066    0.9082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5428    5.7375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896    2.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0521    1.2167    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9500    0.6937    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6186    4.9219    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5585    3.5612    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5943    4.5530    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3360    3.2632    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6751    3.5978    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7311    0.7428    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6706    3.2622    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607    2.3603    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4764    4.0888    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8501    1.9478    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
 10  9  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  2  0  0  0  0
 13  9  2  0  0  0  0
 15 14  2  0  0  0  0
 18  1  1  6  0  0  0
 18 10  1  0  0  0  0
 18 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19 16  2  0  0  0  0
 20  3  1  6  0  0  0
 21  4  1  0  0  0  0
 22 11  2  0  0  0  0
 22 12  1  0  0  0  0
 22 17  1  0  0  0  0
 23 13  1  0  0  0  0
 24 17  1  1  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27 20  1  0  0  0  0
 27 24  1  0  0  0  0
 28 19  1  0  0  0  0
 28 25  1  0  0  0  0
 29 23  1  0  0  0  0
 31  5  1  6  0  0  0
 31 20  1  0  0  0  0
 31 29  1  0  0  0  0
 32 23  1  0  0  0  0
 32 26  1  0  0  0  0
 32 27  1  0  0  0  0
 32 30  1  6  0  0  0
 33 24  1  0  0  0  0
 33 30  2  0  0  0  0
 34 21  2  0  0  0  0
 35 25  2  0  0  0  0
 36 26  2  0  0  0  0
 37 30  1  0  0  0  0
 38 21  1  0  0  0  0
 28 38  1  1  0  0  0
 39 29  1  0  0  0  0
 39 31  1  0  0  0  0
 40  9  1  0  0  0  0
 41 13  1  0  0  0  0
 42 14  1  0  0  0  0
 43 15  1  0  0  0  0
 44 16  1  0  0  0  0
 18 45  1  6  0  0  0
 20 46  1  1  0  0  0
 23 47  1  1  0  0  0
 24 48  1  6  0  0  0
 27 49  1  1  0  0  0
 28 50  1  1  0  0  0
 29 51  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0017278

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C32H37NO6/c1-18-10-9-13-23-29-31(5,39-29)20(3)27-24(17-22-11-7-6-8-12-22)33-30(37)32(23,27)26(36)15-14-25(35)28(19(2)16-18)38-21(4)34/h6-9,11-16,18,20,23-24,27-29H,10,17H2,1-5H3,(H,33,37)/b13-9-,15-14+,19-16-/t18-,20-,23-,24-,27-,28+,29-,31+,32+/m0/s1

> <INCHI_KEY>
AZWOSJCABFILKS-YEDZSSQDSA-N

> <FORMULA>
C32H37NO6

> <MOLECULAR_WEIGHT>
531.649

> <EXACT_MASS>
531.262087915

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
57.63714578607075

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraen-6-yl acetate

> <ALOGPS_LOGP>
4.53

> <JCHEM_LOGP>
4.328404419361514

> <ALOGPS_LOGS>
-5.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.93075159960236

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.556509475182443

> <JCHEM_PKA_STRONGEST_BASIC>
5.245063324982398

> <JCHEM_POLAR_SURFACE_AREA>
105.56

> <JCHEM_REFRACTIVITY>
149.43150000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.25e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraen-6-yl acetate

> <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      11.164   6.339   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.800  10.076   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.527   7.486   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.278  10.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.630   6.509   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.267   8.077   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.791   6.612   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.236   9.221   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.457   3.464   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.382   4.695   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.284   6.292   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.270   8.901   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.065   2.804   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.850   7.889   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.246   6.472   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.141   7.676   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.252   7.116   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.629   6.215   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.030   8.743   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.527   5.946   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.977  11.426   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.746   7.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.527   2.866   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.728   5.652   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.042   8.863   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.370   4.937   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.193   5.176   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.551   9.171   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.860   3.636   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.728   3.160   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.860   5.176   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.193   3.636   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       1.823   4.406   0.000  0.00  0.00           N+0
HETATM   34  O   UNK     0       8.039  12.964   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       4.382  10.254   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       1.830   4.925   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       2.252   1.695   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       6.613  10.710   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       8.194   4.406   0.000  0.00  0.00           O+0
HETATM   40  H   UNK     0       9.431   2.271   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       7.373   1.295   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.021   9.188   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0       4.776   6.648   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      10.443   8.499   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0       8.094   6.091   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0       6.860   6.716   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.098   1.387   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.252   6.089   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0       5.527   4.406   0.000  0.00  0.00           H+0
HETATM   50  H   UNK     0       6.489   7.632   0.000  0.00  0.00           H+0
HETATM   51  H   UNK     0       5.320   3.636   0.000  0.00  0.00           H+0
CONECT    1   18                                                            
CONECT    2   19                                                            
CONECT    3   20                                                            
CONECT    4   21                                                            
CONECT    5   31                                                            
CONECT    6    7    8                                                       
CONECT    7    6   11                                                       
CONECT    8    6   12                                                       
CONECT    9   10   13   40                                                  
CONECT   10    9   18                                                       
CONECT   11    7   22                                                       
CONECT   12    8   22                                                       
CONECT   13    9   23   41                                                  
CONECT   14   15   25   42                                                  
CONECT   15   14   26   43                                                  
CONECT   16   18   19   44                                                  
CONECT   17   22   24                                                       
CONECT   18    1   10   16   45                                             
CONECT   19    2   16   28                                                  
CONECT   20    3   27   31   46                                             
CONECT   21    4   34   38                                                  
CONECT   22   11   12   17                                                  
CONECT   23   13   29   32   47                                             
CONECT   24   17   27   33   48                                             
CONECT   25   14   28   35                                                  
CONECT   26   15   32   36                                                  
CONECT   27   20   24   32   49                                             
CONECT   28   19   25   38   50                                             
CONECT   29   23   31   39   51                                             
CONECT   30   32   33   37                                                  
CONECT   31    5   20   29   39                                             
CONECT   32   23   26   27   30                                             
CONECT   33   24   30                                                       
CONECT   34   21                                                            
CONECT   35   25                                                            
CONECT   36   26                                                            
CONECT   37   30                                                            
CONECT   38   21   28                                                       
CONECT   39   29   31                                                       
CONECT   40    9                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   15                                                            
CONECT   44   16                                                            
CONECT   45   18                                                            
CONECT   46   20                                                            
CONECT   47   23                                                            
CONECT   48   24                                                            
CONECT   49   27                                                            
CONECT   50   28                                                            
CONECT   51   29                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

Synonyms

Value	Source
(1S,6R,7Z,9S,11Z,13R,14S,16R,17S,18R,19S)-19-Benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0,.0,]henicosa-3,7,11,20-tetraen-6-yl acetic acid	Generator

Molecular Formula

C₃₂H₃₇NO₆

Average Mass

531.649

Monoisotopic Mass

531.262087915

IUPAC Name

(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraen-6-yl acetate

Traditional Name

(1S,3E,6R,7E,9S,11E,13R,14S,16R,17S,18R,19S)-19-benzyl-21-hydroxy-7,9,16,17-tetramethyl-2,5-dioxo-15-oxa-20-azatetracyclo[11.8.0.0^{1,18}.0^{14,16}]henicosa-3,7,11,20-tetraen-6-yl acetate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C32H37NO6/c1-18-10-9-13-23-29-31(5,39-29)20(3)27-24(17-22-11-7-6-8-12-22)33-30(37)32(23,27)26(36)15-14-25(35)28(19(2)16-18)38-21(4)34/h6-9,11-16,18,20,23-24,27-29H,10,17H2,1-5H3,(H,33,37)/b13-9-,15-14+,19-16-/t18-,20-,23-,24-,27-,28+,29-,31+,32+/m0/s1

InChI Key

AZWOSJCABFILKS-YEDZSSQDSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00072 g/L	ALOGPS
logP	4.53	ALOGPS
logP	4.33	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	2.56	ChemAxon
pKa (Strongest Basic)	5.25	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	105.56 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	149.43 m³·mol⁻¹	ChemAxon
Polarizability	57.64 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

Metabolic Reactions

Not Available

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	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	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

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 Cytochalasin K (MMDBc0017278)

MOL for #<Metabolite:0x00005634c282b818>

3D MOL for #<Metabolite:0x00005634c282b818>

3D SDF for #<Metabolite:0x00005634c282b818>

3D-SDF for #<Metabolite:0x00005634c282b818>

PDB for #<Metabolite:0x00005634c282b818>

3D PDB for #<Metabolite:0x00005634c282b818>

SMILES for #<Metabolite:0x00005634c282b818>

INCHI for #<Metabolite:0x00005634c282b818>

Structure for #<Metabolite:0x00005634c282b818>

3D Structure for #<Metabolite:0x00005634c282b818>