MiMeDB: Showing metabocard for Anhydroisocochlioquinone A (MMDBc0015335)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:10:58 UTC

Update Date

2022-08-31 06:39:09 UTC

Metabolite ID

MMDBc0015335

Metabolite Identification

Common Name

Anhydroisocochlioquinone A

Description

Anhydroisocochlioquinone A belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds. Anhydroisocochlioquinone A is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108102D          

 42 45  0  0  1  0            999 V2000
    3.8743   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4118  -11.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138   -9.9217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1743   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993   -8.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -8.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1118   -3.9039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7618   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -9.6197    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3493   -8.9052    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1118   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -3.1895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5243   -6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993  -10.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -8.1908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5243   -7.4763    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849  -10.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -9.6197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -6.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -1.7605    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -4.6184    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1743  -10.3342    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368   -8.1908    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -3.1895    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  1  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 16  2  1  6  0  0  0
 16  9  1  0  0  0  0
 17  3  1  6  0  0  0
 18  4  1  0  0  0  0
 19 14  2  0  0  0  0
 19 17  1  0  0  0  0
 20 15  1  0  0  0  0
 21 14  1  0  0  0  0
 21 20  1  0  0  0  0
 22 15  2  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 19  1  0  0  0  0
 26 16  1  0  0  0  0
 26 17  1  0  0  0  0
 27 20  2  0  0  0  0
 27 25  1  0  0  0  0
 28  5  1  0  0  0  0
 28  6  1  0  0  0  0
 23 28  1  6  0  0  0
 29  7  1  6  0  0  0
 29 12  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30  8  1  6  0  0  0
 30 13  1  0  0  0  0
 30 22  1  0  0  0  0
 31 18  2  0  0  0  0
 32 21  2  0  0  0  0
 33 25  2  0  0  0  0
 34 28  1  0  0  0  0
 35 18  1  0  0  0  0
 26 35  1  6  0  0  0
 36 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 27  1  0  0  0  0
 37 30  1  0  0  0  0
 16 38  1  1  0  0  0
 17 39  1  1  0  0  0
 23 40  1  1  0  0  0
 24 41  1  1  0  0  0
 26 42  1  6  0  0  0
M  END


  Mrv1652305152108102D          

 42 45  0  0  1  0            999 V2000
    3.8743   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4118  -11.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138   -9.9217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1743   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993   -8.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -8.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1118   -3.9039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7618   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -9.6197    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3493   -8.9052    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1118   -5.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243   -3.1895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5243   -6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993  -10.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -8.1908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5243   -7.4763    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849  -10.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3493   -3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618   -9.6197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1118   -6.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -1.7605    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -4.6184    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1743  -10.3342    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368   -8.1908    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993   -3.1895    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  1  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 16  2  1  6  0  0  0
 16  9  1  0  0  0  0
 17  3  1  6  0  0  0
 18  4  1  0  0  0  0
 19 14  2  0  0  0  0
 19 17  1  0  0  0  0
 20 15  1  0  0  0  0
 21 14  1  0  0  0  0
 21 20  1  0  0  0  0
 22 15  2  0  0  0  0
 23 10  1  0  0  0  0
 24 11  1  0  0  0  0
 25 19  1  0  0  0  0
 26 16  1  0  0  0  0
 26 17  1  0  0  0  0
 27 20  2  0  0  0  0
 27 25  1  0  0  0  0
 28  5  1  0  0  0  0
 28  6  1  0  0  0  0
 23 28  1  6  0  0  0
 29  7  1  6  0  0  0
 29 12  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30  8  1  6  0  0  0
 30 13  1  0  0  0  0
 30 22  1  0  0  0  0
 31 18  2  0  0  0  0
 32 21  2  0  0  0  0
 33 25  2  0  0  0  0
 34 28  1  0  0  0  0
 35 18  1  0  0  0  0
 26 35  1  6  0  0  0
 36 23  1  0  0  0  0
 36 24  1  0  0  0  0
 37 27  1  0  0  0  0
 37 30  1  0  0  0  0
 16 38  1  1  0  0  0
 17 39  1  1  0  0  0
 23 40  1  1  0  0  0
 24 41  1  1  0  0  0
 26 42  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015335

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)[C@@]([H])(OC(C)=O)[C@@]([H])(C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@@]4([H])O[C@]([H])(CC[C@]4(C)C3=C2)C(C)(C)O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O7/c1-9-16(2)26(35-18(4)31)17(3)19-14-21(32)20-15-22-29(7)12-10-23(28(5,6)34)36-24(29)11-13-30(22,8)37-27(20)25(19)33/h14-17,23-24,26,34H,9-13H2,1-8H3/t16-,17-,23+,24+,26+,29+,30+/m0/s1

> <INCHI_KEY>
VJUNTOKUTJFPFE-NMBYGHSTSA-N

> <FORMULA>
C30H42O7

> <MOLECULAR_WEIGHT>
514.659

> <EXACT_MASS>
514.293053692

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
57.948543356412415

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S)-2-[(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-6,9-dioxo-2,3,4,4a,6,9,10a,11,12,12a-decahydro-1,10-dioxatetraphen-8-yl]-4-methylhexan-3-yl acetate

> <ALOGPS_LOGP>
4.39

> <JCHEM_LOGP>
4.218145587333333

> <ALOGPS_LOGS>
-5.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.326080039959791

> <JCHEM_PKA_STRONGEST_BASIC>
-3.093572590521588

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
142.30290000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.56e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S)-2-[(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-6,9-dioxo-2,3,4,11,12,12a-hexahydro-1,10-dioxatetraphen-8-yl]-4-methylhexan-3-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       7.232  -3.286   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.312  -3.286   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  -7.287   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.852  -3.286   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.702 -20.624   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.266 -18.520   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.392 -13.956   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.772 -13.956   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.932 -16.623   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.312 -16.623   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.162 -15.289   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.542 -15.289   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.852  -8.621   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.622 -12.622   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.542  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.542  -7.287   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.622  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.312  -8.621   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.852 -11.288   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.622  -9.955   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.852 -13.956   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.162 -17.957   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.852 -16.623   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.542  -9.955   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.312  -5.954   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.312 -11.288   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.932 -19.290   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.622 -15.289   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.312 -13.956   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.162  -4.620   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      14.162  -9.955   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       8.002  -9.955   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      13.598 -20.060   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      11.852  -5.954   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      12.622 -17.957   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       9.542 -12.622   0.000  0.00  0.00           O+0
HETATM   38  H   UNK     0       8.772  -3.286   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       8.772  -8.621   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0      13.392 -19.290   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      11.082 -15.289   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       8.772  -5.954   0.000  0.00  0.00           H+0
CONECT    1    9                                                            
CONECT    2   16                                                            
CONECT    3   17                                                            
CONECT    4   18                                                            
CONECT    5   28                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8   30                                                            
CONECT    9    1   16                                                       
CONECT   10   12   23                                                       
CONECT   11   13   24                                                       
CONECT   12   10   29                                                       
CONECT   13   11   30                                                       
CONECT   14   19   21                                                       
CONECT   15   20   22                                                       
CONECT   16    2    9   26   38                                             
CONECT   17    3   19   26   39                                             
CONECT   18    4   31   35                                                  
CONECT   19   14   17   25                                                  
CONECT   20   15   21   27                                                  
CONECT   21   14   20   32                                                  
CONECT   22   15   29   30                                                  
CONECT   23   10   28   36   40                                             
CONECT   24   11   29   36   41                                             
CONECT   25   19   27   33                                                  
CONECT   26   16   17   35   42                                             
CONECT   27   20   25   37                                                  
CONECT   28    5    6   23   34                                             
CONECT   29    7   12   22   24                                             
CONECT   30    8   13   22   37                                             
CONECT   31   18                                                            
CONECT   32   21                                                            
CONECT   33   25                                                            
CONECT   34   28                                                            
CONECT   35   18   26                                                       
CONECT   36   23   24                                                       
CONECT   37   27   30                                                       
CONECT   38   16                                                            
CONECT   39   17                                                            
CONECT   40   23                                                            
CONECT   41   24                                                            
CONECT   42   26                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₃₀H₄₂O₇

Average Mass

514.659

Monoisotopic Mass

514.293053692

IUPAC Name

(2S,3R,4S)-2-[(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-6,9-dioxo-2,3,4,4a,6,9,10a,11,12,12a-decahydro-1,10-dioxatetraphen-8-yl]-4-methylhexan-3-yl acetate

Traditional Name

(2S,3R,4S)-2-[(2R,4aR,10aR,12aR)-2-(2-hydroxypropan-2-yl)-4a,10a-dimethyl-6,9-dioxo-2,3,4,11,12,12a-hexahydro-1,10-dioxatetraphen-8-yl]-4-methylhexan-3-yl acetate

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@@]([H])(OC(C)=O)[C@@]([H])(C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@@]4([H])O[C@]([H])(CC[C@]4(C)C3=C2)C(C)(C)O)C1=O

InChI Identifier

InChI=1S/C30H42O7/c1-9-16(2)26(35-18(4)31)17(3)19-14-21(32)20-15-22-29(7)12-10-23(28(5,6)34)36-24(29)11-13-30(22,8)37-27(20)25(19)33/h14-17,23-24,26,34H,9-13H2,1-8H3/t16-,17-,23+,24+,26+,29+,30+/m0/s1

InChI Key

VJUNTOKUTJFPFE-NMBYGHSTSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Not Available

Direct Parent

Pyrans

Alternative Parents

Substituents

Oxane
Pyran
Tertiary alcohol
Vinylogous ester
Carboxylic acid ester
Ketone
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organic oxide
Organic oxygen compound
Organooxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0016 g/L	ALOGPS
logP	4.39	ALOGPS
logP	4.22	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	142.3 m³·mol⁻¹	ChemAxon
Polarizability	57.95 Å³	ChemAxon
Number of Rings	4	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_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

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

28284319

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16757100

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 Anhydroisocochlioquinone A (MMDBc0015335)

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