MiMeDB: Showing metabocard for Chloropestolide F (MMDBc0002630)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:54:53 UTC

Update Date

2025-10-07 16:04:36 UTC

Metabolite ID

MMDBc0002630

Metabolite Identification

Common Name

Chloropestolide F

Description

Chloropestolide F is a chlorinated natural product belonging to the class of secondary metabolites. There is little literature available on this metabolite, indicating that further research may be necessary to fully understand its properties and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142122542D          

 49 54  0  0  1  0            999 V2000
    8.9631   -0.8132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8157   -1.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5141   -0.1694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7854   -2.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9746    2.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6518   -0.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8322   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3532   -1.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6624   -1.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -0.0054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8263    0.9780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9337   -1.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1504   -1.8918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1435   -0.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6907   -1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2585   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210    0.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0946   -1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4888    1.4698    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6624   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5921   -1.2844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7571   -1.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5015   -0.0054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6498    1.1419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4068    0.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6780   -0.1694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9873    0.6502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2458    1.1419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5141   -1.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -0.4972    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3405    0.3224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0819   -0.1694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5551    1.9615    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -2.6790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1893   -2.4641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3941    2.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8819   -1.7042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7727   -0.9889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    0.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088   -2.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0693    1.3058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3249    0.1585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0029    0.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1766   -0.9889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1512    1.9615    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7444    0.3224    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156   -0.6611    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5834    0.6502    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  6  2  0  0  0  0
 15  3  1  0  0  0  0
 15  9  2  0  0  0  0
 15 10  1  0  0  0  0
 16  4  1  0  0  0  0
 16  8  2  0  0  0  0
 16 12  1  0  0  0  0
 17  8  1  0  0  0  0
 18 11  1  0  0  0  0
 18 17  2  0  0  0  0
 19  9  1  0  0  0  0
 20 11  1  0  0  0  0
 21 10  2  0  0  0  0
 22 13  1  0  0  0  0
 23 19  2  0  0  0  0
 23 21  1  0  0  0  0
 24 17  1  0  0  0  0
 26 24  1  0  0  0  0
 26 25  2  0  0  0  0
 27 18  1  0  0  0  0
 28 25  1  0  0  0  0
 29 20  1  0  0  0  0
 30 23  1  0  0  0  0
 31 12  1  0  0  0  0
 31 22  1  1  0  0  0
 31 24  1  0  0  0  0
 32  7  1  1  0  0  0
 32 27  1  0  0  0  0
 32 29  1  0  0  0  0
 33 28  1  0  0  0  0
 33 31  1  0  0  0  0
 34 25  1  0  0  0  0
 35 13  1  0  0  0  0
 36 19  1  0  0  0  0
 20 37  1  6  0  0  0
 38 22  2  0  0  0  0
 27 39  1  6  0  0  0
 40 28  2  0  0  0  0
 41 30  2  0  0  0  0
 42  5  1  0  0  0  0
 42 26  1  0  0  0  0
 43 21  1  0  0  0  0
 33 43  1  6  0  0  0
 44 29  1  0  0  0  0
 44 32  1  0  0  0  0
 45 30  1  0  0  0  0
 45 33  1  0  0  0  0
 20 46  1  1  0  0  0
 24 47  1  1  0  0  0
 27 48  1  1  0  0  0
 29 49  1  1  0  0  0
M  END


  Mrv1652305142122542D          

 49 54  0  0  1  0            999 V2000
    8.9631   -0.8132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8157   -1.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5141   -0.1694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7854   -2.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9746    2.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6518   -0.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8322   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3532   -1.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6624   -1.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -0.0054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8263    0.9780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9337   -1.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1504   -1.8918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1435   -0.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6907   -1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2585   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210    0.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0946   -1.6446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4888    1.4698    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6624   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5921   -1.2844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7571   -1.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5015   -0.0054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6498    1.1419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4068    0.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6780   -0.1694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9873    0.6502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2458    1.1419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5141   -1.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8390   -0.4972    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3405    0.3224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0819   -0.1694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5551    1.9615    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -2.6790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1893   -2.4641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3941    2.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8819   -1.7042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7727   -0.9889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302    0.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088   -2.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0693    1.3058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3249    0.1585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0029    0.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1766   -0.9889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1512    1.9615    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7444    0.3224    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156   -0.6611    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5834    0.6502    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  6  2  0  0  0  0
 15  3  1  0  0  0  0
 15  9  2  0  0  0  0
 15 10  1  0  0  0  0
 16  4  1  0  0  0  0
 16  8  2  0  0  0  0
 16 12  1  0  0  0  0
 17  8  1  0  0  0  0
 18 11  1  0  0  0  0
 18 17  2  0  0  0  0
 19  9  1  0  0  0  0
 20 11  1  0  0  0  0
 21 10  2  0  0  0  0
 22 13  1  0  0  0  0
 23 19  2  0  0  0  0
 23 21  1  0  0  0  0
 24 17  1  0  0  0  0
 26 24  1  0  0  0  0
 26 25  2  0  0  0  0
 27 18  1  0  0  0  0
 28 25  1  0  0  0  0
 29 20  1  0  0  0  0
 30 23  1  0  0  0  0
 31 12  1  0  0  0  0
 31 22  1  1  0  0  0
 31 24  1  0  0  0  0
 32  7  1  1  0  0  0
 32 27  1  0  0  0  0
 32 29  1  0  0  0  0
 33 28  1  0  0  0  0
 33 31  1  0  0  0  0
 34 25  1  0  0  0  0
 35 13  1  0  0  0  0
 36 19  1  0  0  0  0
 20 37  1  6  0  0  0
 38 22  2  0  0  0  0
 27 39  1  6  0  0  0
 40 28  2  0  0  0  0
 41 30  2  0  0  0  0
 42  5  1  0  0  0  0
 42 26  1  0  0  0  0
 43 21  1  0  0  0  0
 33 43  1  6  0  0  0
 44 29  1  0  0  0  0
 44 32  1  0  0  0  0
 45 30  1  0  0  0  0
 45 33  1  0  0  0  0
 20 46  1  1  0  0  0
 24 47  1  1  0  0  0
 27 48  1  1  0  0  0
 29 49  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0002630

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12O[C@]1(CC=C(C)C)[C@]([H])(O)\C(C[C@]2([H])O)=C1/C=C(C)C[C@@]2(C(=O)CO)[C@]1([H])C(OC)=C(Cl)C(=O)[C@]21OC(=O)C2=C(O)C=C(C)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C33H35ClO11/c1-14(2)6-7-32-27(39)18(11-20(37)29(32)44-32)17-8-16(4)12-31(22(38)13-35)24(17)26(42-5)25(34)28(40)33(31)43-21-10-15(3)9-19(36)23(21)30(41)45-33/h6,8-10,20,24,27,29,35-37,39H,7,11-13H2,1-5H3/b18-17+/t20-,24-,27+,29-,31+,32+,33-/m0/s1

> <INCHI_KEY>
BETJPYMBAGJTRK-RCCJNJTDSA-N

> <FORMULA>
C33H35ClO11

> <MOLECULAR_WEIGHT>
643.08

> <EXACT_MASS>
642.1867896

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
64.11709963367582

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4'aR,8'aS)-3'-chloro-5'-[(1R,2R,3E,5S,6S)-2,5-dihydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]heptan-3-ylidene]-5-hydroxy-8'a-(2-hydroxyacetyl)-4'-methoxy-7,7'-dimethyl-4'a,5',8',8'a-tetrahydro-2'H,4H-spiro[1,3-benzodioxine-2,1'-naphthalene]-2',4-dione

> <ALOGPS_LOGP>
2.51

> <JCHEM_LOGP>
3.6066190333333323

> <ALOGPS_LOGS>
-4.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.79418601093135

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2313700236906904

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2247978241782986

> <JCHEM_POLAR_SURFACE_AREA>
172.34999999999997

> <JCHEM_REFRACTIVITY>
164.25540000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.50e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4'aR,8'aS)-3'-chloro-5'-[(1R,2R,3E,5S,6S)-2,5-dihydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]heptan-3-ylidene]-5-hydroxy-8'a-(2-hydroxyacetyl)-4'-methoxy-7,7'-dimethyl-4'a,8'-dihydrospiro[1,3-benzodioxine-2,1'-naphthalene]-2',4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0      16.731  -1.518   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.589  -3.108   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.826  -0.316   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.066  -4.600   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.419   3.967   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.283  -0.458   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.753  -0.635   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.126  -2.152   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.237  -2.458   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.177  -0.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.009   1.826   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.476  -2.458   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.881  -3.531   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.201  -1.695   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.413  -0.928   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.889  -3.070   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.949  -0.622   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.186   0.296   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.177  -3.070   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.246   2.744   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.237  -0.622   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.839  -2.397   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.413  -2.152   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.536  -0.010   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.946   2.132   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.359   1.520   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.599  -0.316   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.710   1.214   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.659   2.132   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.826  -2.764   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.300  -0.928   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.836   0.602   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.886  -0.316   0.000  0.00  0.00           C+0
HETATM   34 Cl   UNK     0       4.770   3.661   0.000  0.00  0.00          Cl+0
HETATM   35  O   UNK     0       5.420  -5.001   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       0.353  -4.600   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      10.069   4.273   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       3.513  -3.181   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      10.776  -1.846   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       2.296   1.826   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       3.003  -4.294   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       7.596   2.438   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       2.473   0.296   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      13.072   1.520   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       4.063  -1.846   0.000  0.00  0.00           O+0
HETATM   46  H   UNK     0      11.482   3.661   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.123   0.602   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0       9.362  -1.234   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0      10.422   1.214   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5   42                                                            
CONECT    6    7   14                                                       
CONECT    7    6   32                                                       
CONECT    8   16   17                                                       
CONECT    9   15   19                                                       
CONECT   10   15   21                                                       
CONECT   11   18   20                                                       
CONECT   12   16   31                                                       
CONECT   13   22   35                                                       
CONECT   14    1    2    6                                                  
CONECT   15    3    9   10                                                  
CONECT   16    4    8   12                                                  
CONECT   17    8   18   24                                                  
CONECT   18   11   17   27                                                  
CONECT   19    9   23   36                                                  
CONECT   20   11   29   37   46                                             
CONECT   21   10   23   43                                                  
CONECT   22   13   31   38                                                  
CONECT   23   19   21   30                                                  
CONECT   24   17   26   31   47                                             
CONECT   25   26   28   34                                                  
CONECT   26   24   25   42                                                  
CONECT   27   18   32   39   48                                             
CONECT   28   25   33   40                                                  
CONECT   29   20   32   44   49                                             
CONECT   30   23   41   45                                                  
CONECT   31   12   22   24   33                                             
CONECT   32    7   27   29   44                                             
CONECT   33   28   31   43   45                                             
CONECT   34   25                                                            
CONECT   35   13                                                            
CONECT   36   19                                                            
CONECT   37   20                                                            
CONECT   38   22                                                            
CONECT   39   27                                                            
CONECT   40   28                                                            
CONECT   41   30                                                            
CONECT   42    5   26                                                       
CONECT   43   21   33                                                       
CONECT   44   29   32                                                       
CONECT   45   30   33                                                       
CONECT   46   20                                                            
CONECT   47   24                                                            
CONECT   48   27                                                            
CONECT   49   29                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  108    0
END

Synonyms

Not Available

Molecular Formula

C₃₃H₃₅ClO₁₁

Average Mass

643.08

Monoisotopic Mass

642.1867896

IUPAC Name

(2R,4'aR,8'aS)-3'-chloro-5'-[(1R,2R,3E,5S,6S)-2,5-dihydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]heptan-3-ylidene]-5-hydroxy-8'a-(2-hydroxyacetyl)-4'-methoxy-7,7'-dimethyl-4'a,5',8',8'a-tetrahydro-2'H,4H-spiro[1,3-benzodioxine-2,1'-naphthalene]-2',4-dione

Traditional Name

(2R,4'aR,8'aS)-3'-chloro-5'-[(1R,2R,3E,5S,6S)-2,5-dihydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]heptan-3-ylidene]-5-hydroxy-8'a-(2-hydroxyacetyl)-4'-methoxy-7,7'-dimethyl-4'a,8'-dihydrospiro[1,3-benzodioxine-2,1'-naphthalene]-2',4-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12O[C@]1(CC=C(C)C)[C@]([H])(O)\C(C[C@]2([H])O)=C1/C=C(C)C[C@@]2(C(=O)CO)[C@]1([H])C(OC)=C(Cl)C(=O)[C@]21OC(=O)C2=C(O)C=C(C)C=C2O1

InChI Identifier

InChI=1S/C33H35ClO11/c1-14(2)6-7-32-27(39)18(11-20(37)29(32)44-32)17-8-16(4)12-31(22(38)13-35)24(17)26(42-5)25(34)28(40)33(31)43-21-10-15(3)9-19(36)23(21)30(41)45-33/h6,8-10,20,24,27,29,35-37,39H,7,11-13H2,1-5H3/b18-17+/t20-,24-,27+,29-,31+,32+,33-/m0/s1

InChI Key

BETJPYMBAGJTRK-RCCJNJTDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Ketal
Cyclohexenone
Oxepane
Benzenoid
Alpha-haloketone
Alpha-chloroketone
Vinylogous ester
Vinylogous acid
Cyclic alcohol
Alpha-hydroxy ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Chloroalkene
Haloalkene
Vinyl halide
Vinyl chloride
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.035 g/L	ALOGPS
logP	2.51	ALOGPS
logP	3.61	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	3.23	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	172.35 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	164.26 m³·mol⁻¹	ChemAxon
Polarizability	64.12 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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_3_6) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	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

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

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

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

78436460

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583606

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

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 Chloropestolide F (MMDBc0002630)

MOL for #<Metabolite:0x00007fd421666aa0>

3D MOL for #<Metabolite:0x00007fd421666aa0>

3D SDF for #<Metabolite:0x00007fd421666aa0>

3D-SDF for #<Metabolite:0x00007fd421666aa0>

PDB for #<Metabolite:0x00007fd421666aa0>

3D PDB for #<Metabolite:0x00007fd421666aa0>

SMILES for #<Metabolite:0x00007fd421666aa0>

INCHI for #<Metabolite:0x00007fd421666aa0>

Structure for #<Metabolite:0x00007fd421666aa0>

3D Structure for #<Metabolite:0x00007fd421666aa0>