NP-MRD: Showing NP-Card for Garcinisidone H (NP0085853)

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Record Information

Version

2.0

Created at

2022-04-29 06:18:04 UTC

Updated at

2022-04-29 06:18:04 UTC

NP-MRD ID

NP0085853

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Garcinisidone H

Description

Garcinisidone H belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). Garcinisidone H is found in Garcinia celebiva. Based on a literature review very few articles have been published on Garcinisidone H.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292208182D          

 26 28  0  0  0  0            999 V2000
    5.7025   -0.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5448    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3332    1.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9682    2.7028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7846    3.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3893    4.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1638    2.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7725    2.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    2.7028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  8 11  1  0  0  0  0
  8 12  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  2  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 17 24  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 25  1  0  0  0  0
 15 26  2  0  0  0  0
M  END

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
   -2.5173   -1.8376   -1.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6468   -1.4537    0.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4501   -0.9546    0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4112   -2.0121    0.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9322   -0.7073    2.4001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420    0.3673    0.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466    1.3625    0.5662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2818    1.0373    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2412    2.0644    1.2232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7526    2.6119    0.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5417    2.9281   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2379    4.2009   -0.9130 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146    1.9220   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1828    0.6159   -0.0922 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0869   -0.4377   -0.1501 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3394   -0.5452   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9412    0.4147   -1.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1886    0.1333   -2.0563 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8264   -1.0381   -1.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2329   -1.9912   -0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8995   -3.1897   -0.7258 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9693   -1.7306   -0.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4506   -2.7238    0.3171 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5045    1.6884   -1.9670 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6172    2.4597   -1.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8546    3.6815   -1.0409 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3642   -2.1940   -1.6342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5526   -1.7925   -1.5481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6109   -1.4940    0.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8115   -2.9513    1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4275   -1.7094    1.6387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1432   -2.3527   -0.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7325    0.3304    2.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959   -1.4288    3.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0249   -0.8656    2.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1615    1.7421    1.7288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5389    2.4419    0.2103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8480    2.9462    1.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5387    3.3715    0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9074    4.9565   -0.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6498    0.9002   -2.6909 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8125   -1.2525   -2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5416   -3.9186   -0.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7918   -3.5958    0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6 14  1  0
 14 13  2  0
 13 11  1  0
 11 12  1  0
 11 10  2  0
 13 25  1  0
 25 26  2  0
 25 24  1  0
 24 17  1  0
 17 16  2  0
 16 15  1  0
 16 22  1  0
 22 23  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 18  2  0
  6  3  1  0
  3  4  1  1
  3  5  1  0
  3  2  1  0
  2  1  2  3
 10  7  1  0
 18 17  1  0
 15 14  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 12 40  1  0
 10 39  1  0
 23 44  1  0
 21 43  1  0
 19 42  1  0
 18 41  1  0
  4 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  5 35  1  0
  2 29  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652304292208182D          

 26 28  0  0  0  0            999 V2000
    5.7025   -0.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5448    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3332    1.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9682    2.7028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7846    3.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3893    4.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1638    2.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7725    2.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    2.7028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  8 11  1  0  0  0  0
  8 12  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  2  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 17 24  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 25  1  0  0  0  0
 15 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0085853

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C2=C(C(O)=C1)C(=O)OC1=C(O2)C(O)=C(O)C=C1)C(C)(C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O7/c1-5-19(2,3)14-12(24-4)8-10(21)13-17(14)26-16-11(25-18(13)23)7-6-9(20)15(16)22/h5-8,20-22H,1H2,2-4H3

> <INCHI_KEY>
MLYWDYGJDFQKDY-UHFFFAOYSA-N

> <FORMULA>
C19H18O7

> <MOLECULAR_WEIGHT>
358.346

> <EXACT_MASS>
358.10525292

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.37921100027055

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,5,12-trihydroxy-14-methoxy-15-(2-methylbut-3-en-2-yl)-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

> <ALOGPS_LOGP>
3.81

> <JCHEM_LOGP>
4.2289923143333334

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.260004780742557

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.156173706361608

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8111161271888716

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
93.7606

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.77e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,12-trihydroxy-14-methoxy-15-(2-methylbut-3-en-2-yl)-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      10.645  -0.960   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.302   0.541   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.431   1.588   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.088   3.090   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.217   4.137   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      13.689   3.683   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.617   3.544   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.274   5.045   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.931   6.547   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.060   7.594   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.772   4.703   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.775   5.388   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.488   2.496   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.830   0.995   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.870  -0.209   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.330  -0.209   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.370   0.995   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.898   0.541   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.770   1.588   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.112   3.090   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.983   4.137   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.584   3.544   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.926   5.045   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.713   2.496   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.100   3.165   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.538  -1.597   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8   13                                                  
CONECT    8    7    9   11   12                                             
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8                                                            
CONECT   12    8                                                            
CONECT   13    7   14   25                                                  
CONECT   14   13    2   15                                                  
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   17   22   25                                                  
CONECT   25   24   13                                                       
CONECT   26   15                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₇

Average Mass

358.3460 Da

Monoisotopic Mass

358.10525 Da

IUPAC Name

4,5,12-trihydroxy-14-methoxy-15-(2-methylbut-3-en-2-yl)-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

Traditional Name

4,5,12-trihydroxy-14-methoxy-15-(2-methylbut-3-en-2-yl)-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-10-one

CAS Registry Number

Not Available

SMILES

COC1=C(C2=C(C(O)=C1)C(=O)OC1=C(O2)C(O)=C(O)C=C1)C(C)(C)C=C

InChI Identifier

InChI=1S/C19H18O7/c1-5-19(2,3)14-12(24-4)8-10(21)13-17(14)26-16-11(25-18(13)23)7-6-9(20)15(16)22/h5-8,20-22H,1H2,2-4H3

InChI Key

MLYWDYGJDFQKDY-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Garcinia celebiva	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depsidone
Diaryl ether
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Dioxepine
Alkyl aryl ether
1,4-dioxepine
Benzenoid
Vinylogous acid
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.81	ALOGPS
logP	4.23	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	8.16	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	93.76 m³·mol⁻¹	ChemAxon
Polarizability	35.38 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00055886

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

132538121

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Garcinisidone H (NP0085853)

MOL for NP0085853 (Garcinisidone H)

3D MOL for NP0085853 (Garcinisidone H)

3D SDF for NP0085853 (Garcinisidone H)

3D-SDF for NP0085853 (Garcinisidone H)

PDB for NP0085853 (Garcinisidone H)

3D PDB for NP0085853 (Garcinisidone H)

SMILES for NP0085853 (Garcinisidone H)

INCHI for NP0085853 (Garcinisidone H)

Structure for NP0085853 (Garcinisidone H)

3D Structure for NP0085853 (Garcinisidone H)