MiMeDB: Showing metabocard for Chloropupukeanone A (MMDBc0018208)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 08:26:53 UTC

Update Date

2022-08-31 06:43:36 UTC

Metabolite ID

MMDBc0018208

Metabolite Identification

Common Name

Chloropupukeanone A

Description

Chloropupukeanone A belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group. Based on a literature review very few articles have been published on Chloropupukeanone A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152110262D          

 47 52  0  0  1  0            999 V2000
   -3.3661   -3.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9526   -3.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5038    2.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2391    1.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6671    0.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8408   -1.9444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1945   -1.4317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1750    1.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2944    0.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -1.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3503    0.6770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195    0.8378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3517    0.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7198   -2.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9911    1.4965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3078   -0.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0045   -0.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6622    0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7816    0.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0984   -2.2604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9852    1.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9655    0.2039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1239   -0.9678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9145   -2.3813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4528   -0.4424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3951   -0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6959   -0.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772    0.8873    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0907    0.1026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4272   -1.7350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7965    0.2488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1968    1.1391    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8900    1.9050    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.8461    1.0920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0849   -0.6842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144   -2.9067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748    2.2992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561   -1.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3112   -1.1983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5129   -1.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0678    0.6355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841   -0.2144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6367   -0.3215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7306   -2.5022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4017   -3.0276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8206   -0.2006    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6112   -1.6141    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  8  2  0  0  0  0
 15  9  1  0  0  0  0
 16 10  2  0  0  0  0
 17 11  2  0  0  0  0
 17 16  1  0  0  0  0
 18  8  1  0  0  0  0
 19  9  2  0  0  0  0
 20 10  1  0  0  0  0
 21 12  1  0  0  0  0
 22 18  2  0  0  0  0
 22 19  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  1  0  0  0  0
 25 22  1  0  0  0  0
 28  4  1  1  0  0  0
 28 11  1  0  0  0  0
 28 13  1  0  0  0  0
 29 12  1  0  0  0  0
 29 13  1  0  0  0  0
 29 26  1  0  0  0  0
 29 27  1  1  0  0  0
 30  7  1  1  0  0  0
 30 23  1  0  0  0  0
 30 24  1  0  0  0  0
 31 17  1  0  0  0  0
 31 26  1  0  0  0  0
 32 21  1  0  0  0  0
 32 28  1  0  0  0  0
 32 31  1  0  0  0  0
 32 33  1  6  0  0  0
 34 18  1  0  0  0  0
 35 19  1  0  0  0  0
 20 36  1  6  0  0  0
 37 21  2  0  0  0  0
 38 25  2  0  0  0  0
 39 26  2  0  0  0  0
 40 27  2  0  0  0  0
 31 41  1  6  0  0  0
 42  5  1  0  0  0  0
 42 27  1  0  0  0  0
 23 43  1  6  0  0  0
 43 25  1  0  0  0  0
 44 24  1  0  0  0  0
 44 30  1  0  0  0  0
 20 45  1  1  0  0  0
 23 46  1  1  0  0  0
 24 47  1  1  0  0  0
M  END


  Mrv1652305152110262D          

 47 52  0  0  1  0            999 V2000
   -3.3661   -3.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9526   -3.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5038    2.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2391    1.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6671    0.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8408   -1.9444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1945   -1.4317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1750    1.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2944    0.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -1.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3503    0.6770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195    0.8378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3517    0.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7198   -2.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9911    1.4965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3078   -0.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0045   -0.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6622    0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7816    0.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0984   -2.2604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9852    1.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9655    0.2039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1239   -0.9678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9145   -2.3813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4528   -0.4424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3951   -0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6959   -0.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772    0.8873    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0907    0.1026    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4272   -1.7350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7965    0.2488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1968    1.1391    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8900    1.9050    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.8461    1.0920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0849   -0.6842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144   -2.9067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748    2.2992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561   -1.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3112   -1.1983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5129   -1.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0678    0.6355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841   -0.2144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6367   -0.3215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7306   -2.5022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4017   -3.0276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8206   -0.2006    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6112   -1.6141    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  8  2  0  0  0  0
 15  9  1  0  0  0  0
 16 10  2  0  0  0  0
 17 11  2  0  0  0  0
 17 16  1  0  0  0  0
 18  8  1  0  0  0  0
 19  9  2  0  0  0  0
 20 10  1  0  0  0  0
 21 12  1  0  0  0  0
 22 18  2  0  0  0  0
 22 19  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  1  0  0  0  0
 25 22  1  0  0  0  0
 28  4  1  1  0  0  0
 28 11  1  0  0  0  0
 28 13  1  0  0  0  0
 29 12  1  0  0  0  0
 29 13  1  0  0  0  0
 29 26  1  0  0  0  0
 29 27  1  1  0  0  0
 30  7  1  1  0  0  0
 30 23  1  0  0  0  0
 30 24  1  0  0  0  0
 31 17  1  0  0  0  0
 31 26  1  0  0  0  0
 32 21  1  0  0  0  0
 32 28  1  0  0  0  0
 32 31  1  0  0  0  0
 32 33  1  6  0  0  0
 34 18  1  0  0  0  0
 35 19  1  0  0  0  0
 20 36  1  6  0  0  0
 37 21  2  0  0  0  0
 38 25  2  0  0  0  0
 39 26  2  0  0  0  0
 40 27  2  0  0  0  0
 31 41  1  6  0  0  0
 42  5  1  0  0  0  0
 42 27  1  0  0  0  0
 23 43  1  6  0  0  0
 43 25  1  0  0  0  0
 44 24  1  0  0  0  0
 44 30  1  0  0  0  0
 20 45  1  1  0  0  0
 23 46  1  1  0  0  0
 24 47  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0018208

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12O[C@]1(CC=C(C)C)[C@]([H])(OC(=O)C1=C(O)C=C(C)C=C1O)C(=C[C@]2([H])O)C1=C[C@@]2(C)C[C@@]3(CC(=O)[C@@]2(Cl)[C@@]1(O)C3=O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C32H33ClO11/c1-14(2)6-7-30-23(43-25(38)22-18(34)8-15(3)9-19(22)35)16(10-20(36)24(30)44-30)17-11-28(4)13-29(27(40)42-5)12-21(37)32(28,33)31(17,41)26(29)39/h6,8-11,20,23-24,34-36,41H,7,12-13H2,1-5H3/t20-,23+,24-,28-,29+,30+,31-,32-/m0/s1

> <INCHI_KEY>
OREOZQNTHRYERA-VNELKZGHSA-N

> <FORMULA>
C32H33ClO11

> <MOLECULAR_WEIGHT>
629.06

> <EXACT_MASS>
628.1711396

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
61.83741718168142

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,3S,6R,7S)-7-chloro-4-[(1R,2R,5S,6S)-2-(2,6-dihydroxy-4-methylbenzoyloxy)-5-hydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-3-hydroxy-6-methyl-2,8-dioxotricyclo[4.3.1.0^{3,7}]dec-4-ene-1-carboxylate

> <ALOGPS_LOGP>
2.62

> <JCHEM_LOGP>
4.877491007

> <ALOGPS_LOGS>
-4.35

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.757506627105977

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.639923014416615

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3740664385764294

> <JCHEM_POLAR_SURFACE_AREA>
180.18999999999994

> <JCHEM_REFRACTIVITY>
156.48460000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.84e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,3S,6R,7S)-7-chloro-4-[(1R,2R,5S,6S)-2-(2,6-dihydroxy-4-methylbenzoyloxy)-5-hydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-3-hydroxy-6-methyl-2,8-dioxotricyclo[4.3.1.0^{3,7}]dec-4-ene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      -6.283  -6.110   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.645  -5.719   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.407   4.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.446   3.131   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.845   1.102   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.303  -3.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.096  -2.672   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.927   3.019   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.016   1.361   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.383  -2.787   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.654   1.264   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.703   1.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.523   1.003   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.077  -5.153   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -7.450   2.793   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.575  -1.581   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.008  -0.149   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.969   1.813   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.059   0.155   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.184  -4.219   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.706   2.793   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.536   0.381   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.098  -1.807   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.707  -4.445   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.578  -0.826   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.604  -0.705   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.032  -0.855   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.891   1.656   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.903   0.192   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.664  -3.239   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.487   0.464   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.234   2.126   0.000  0.00  0.00           C+0
HETATM   33 Cl   UNK     0       1.661   3.556   0.000  0.00  0.00          Cl+0
HETATM   34  O   UNK     0      -3.446   2.038   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -7.625  -1.277   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       0.773  -5.426   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       4.060   4.292   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -5.145  -2.258   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       2.448  -2.237   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       4.691  -2.357   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       0.127   1.186   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       6.504  -0.400   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      -3.055  -0.600   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      -3.230  -4.671   0.000  0.00  0.00           O+0
HETATM   45  H   UNK     0      -0.750  -5.652   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.532  -0.374   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.141  -3.013   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   28                                                            
CONECT    5   42                                                            
CONECT    6    7   14                                                       
CONECT    7    6   30                                                       
CONECT    8   15   18                                                       
CONECT    9   15   19                                                       
CONECT   10   16   20                                                       
CONECT   11   17   28                                                       
CONECT   12   21   29                                                       
CONECT   13   28   29                                                       
CONECT   14    1    2    6                                                  
CONECT   15    3    8    9                                                  
CONECT   16   10   17   23                                                  
CONECT   17   11   16   31                                                  
CONECT   18    8   22   34                                                  
CONECT   19    9   22   35                                                  
CONECT   20   10   24   36   45                                             
CONECT   21   12   32   37                                                  
CONECT   22   18   19   25                                                  
CONECT   23   16   30   43   46                                             
CONECT   24   20   30   44   47                                             
CONECT   25   22   38   43                                                  
CONECT   26   29   31   39                                                  
CONECT   27   29   40   42                                                  
CONECT   28    4   11   13   32                                             
CONECT   29   12   13   26   27                                             
CONECT   30    7   23   24   44                                             
CONECT   31   17   26   32   41                                             
CONECT   32   21   28   31   33                                             
CONECT   33   32                                                            
CONECT   34   18                                                            
CONECT   35   19                                                            
CONECT   36   20                                                            
CONECT   37   21                                                            
CONECT   38   25                                                            
CONECT   39   26                                                            
CONECT   40   27                                                            
CONECT   41   31                                                            
CONECT   42    5   27                                                       
CONECT   43   23   25                                                       
CONECT   44   24   30                                                       
CONECT   45   20                                                            
CONECT   46   23                                                            
CONECT   47   24                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₃₃ClO₁₁

Average Mass

629.06

Monoisotopic Mass

628.1711396

IUPAC Name

methyl (1S,3S,6R,7S)-7-chloro-4-[(1R,2R,5S,6S)-2-(2,6-dihydroxy-4-methylbenzoyloxy)-5-hydroxy-1-(3-methylbut-2-en-1-yl)-7-oxabicyclo[4.1.0]hept-3-en-3-yl]-3-hydroxy-6-methyl-2,8-dioxotricyclo[4.3.1.0^{3,7}]dec-4-ene-1-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@@]12O[C@]1(CC=C(C)C)[C@]([H])(OC(=O)C1=C(O)C=C(C)C=C1O)C(=C[C@]2([H])O)C1=C[C@@]2(C)C[C@@]3(CC(=O)[C@@]2(Cl)[C@@]1(O)C3=O)C(=O)OC

InChI Identifier

InChI=1S/C32H33ClO11/c1-14(2)6-7-30-23(43-25(38)22-18(34)8-15(3)9-19(22)35)16(10-20(36)24(30)44-30)17-11-28(4)13-29(27(40)42-5)12-21(37)32(28,33)31(17,41)26(29)39/h6,8-11,20,23-24,34-36,41H,7,12-13H2,1-5H3/t20-,23+,24-,28-,29+,30+,31-,32-/m0/s1

InChI Key

OREOZQNTHRYERA-VNELKZGHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

o-Hydroxybenzoic acid esters

Alternative Parents

Substituents

O-hydroxybenzoic acid ester
Salicylic acid or derivatives
M-cresol
Resorcinol
Benzoyl
Toluene
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Dicarboxylic acid or derivatives
Cyclic alcohol
Vinylogous acid
Methyl ester
Tertiary alcohol
Alpha-haloketone
Alpha-chloroketone
Halohydrin
Carboxylic acid ester
Chlorohydrin
Secondary alcohol
Ketone
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Organoheterocyclic compound
Oxirane
Ether
Alkyl halide
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organochloride
Organohalogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.028 g/L	ALOGPS
logP	2.62	ALOGPS
logP	4.88	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	9.64	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	180.19 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	156.48 m³·mol⁻¹	ChemAxon
Polarizability	61.84 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	Yes	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	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	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

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	1	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

78438437

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45102453

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 Chloropupukeanone A (MMDBc0018208)

MOL for #<Metabolite:0x00007fecdcb7e0f0>

3D MOL for #<Metabolite:0x00007fecdcb7e0f0>

3D SDF for #<Metabolite:0x00007fecdcb7e0f0>

3D-SDF for #<Metabolite:0x00007fecdcb7e0f0>

PDB for #<Metabolite:0x00007fecdcb7e0f0>

3D PDB for #<Metabolite:0x00007fecdcb7e0f0>

SMILES for #<Metabolite:0x00007fecdcb7e0f0>

INCHI for #<Metabolite:0x00007fecdcb7e0f0>

Structure for #<Metabolite:0x00007fecdcb7e0f0>

3D Structure for #<Metabolite:0x00007fecdcb7e0f0>