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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 13:32:22 UTC

Update Date

2021-09-26 23:08:13 UTC

HMDB ID

HMDB0254307

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Malabaricone B

Description

Malabaricone B belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Malabaricone B is an extremely weak basic (essentially neutral) compound (based on its pKa). This compound has been identified in human blood as reported by (PMID: 31557052 ). Malabaricone b is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Malabaricone B is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0254307
     RDKit          3D
Malabaricone B
 51 52  0  0  0  0  0  0  0  0999 V2000
    3.4356   -1.4644   -1.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9544   -0.8212   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -0.0905    0.2349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6053   -0.2744   -0.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7898    0.4881    0.8288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6996    0.3653    0.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0669    0.8915   -0.8221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5466    0.7759   -1.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9672   -0.6479   -0.9855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4560   -0.8262   -1.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2873   -0.1035   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7269   -0.6417    0.9218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5051    0.0931    1.7904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8751    1.3884    1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6589    2.1184    2.3956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4320    1.9260    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6528    1.2069   -0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966   -0.8050   -0.5584 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2477   -1.4801   -1.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7674   -2.2043   -2.4726 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425   -1.4284   -1.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251   -0.7328   -0.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3923   -0.0642    0.6450 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0239   -0.1046    0.4703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1876    0.5869    1.3595 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3091    0.9846    0.1702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1716   -0.4056    1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388    0.0861   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3726   -1.3547   -0.1197 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0976    1.5534    0.8415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9275    0.0782    1.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2911    0.8238    1.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -0.7418    0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7118    1.9325   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5294    0.2392   -1.5750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0343    1.4080   -0.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8155    1.2197   -2.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4270   -1.2313   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -1.0489    0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6585   -1.9180   -1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7283   -0.5483   -2.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4323   -1.6712    1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8389   -0.3598    2.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9576    1.6840    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7394    2.9558    0.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3237    1.6787   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9359   -2.4359   -2.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2898   -1.9693   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3164   -0.7139   -0.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8476    0.4910    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5911    1.1121    2.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 17 11  1  0
 24 18  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 23 50  1  0
 25 51  1  0
M  END


  Mrv1533004161502142D          

 25 26  0  0  0  0            999 V2000
    0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 24  1  0  0  0  0
 24 25  2  0  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0254307

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1=CC=C(CCCCCCCCC(=O)C2=C(O)C=CC=C2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O4/c22-17-14-12-16(13-15-17)8-5-3-1-2-4-6-9-18(23)21-19(24)10-7-11-20(21)25/h7,10-15,22,24-25H,1-6,8-9H2

> <INCHI_KEY>
KOAPDMKKECXPHX-UHFFFAOYSA-N

> <FORMULA>
C21H26O4

> <MOLECULAR_WEIGHT>
342.435

> <EXACT_MASS>
342.183109317

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.6603585266171

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one

> <ALOGPS_LOGP>
4.78

> <JCHEM_LOGP>
6.866517844333334

> <ALOGPS_LOGS>
-4.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.016534148055852

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.949703056913167

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8962175388258204

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
99.3324

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0254307
     RDKit          3D
Malabaricone B
 51 52  0  0  0  0  0  0  0  0999 V2000
    3.4356   -1.4644   -1.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9544   -0.8212   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -0.0905    0.2349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6053   -0.2744   -0.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7898    0.4881    0.8288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6996    0.3653    0.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0669    0.8915   -0.8221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5466    0.7759   -1.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9672   -0.6479   -0.9855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4560   -0.8262   -1.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2873   -0.1035   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7269   -0.6417    0.9218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5051    0.0931    1.7904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8751    1.3884    1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6589    2.1184    2.3956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4320    1.9260    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6528    1.2069   -0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966   -0.8050   -0.5584 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2477   -1.4801   -1.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7674   -2.2043   -2.4726 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425   -1.4284   -1.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251   -0.7328   -0.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3923   -0.0642    0.6450 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0239   -0.1046    0.4703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1876    0.5869    1.3595 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3091    0.9846    0.1702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1716   -0.4056    1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388    0.0861   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3726   -1.3547   -0.1197 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0976    1.5534    0.8415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9275    0.0782    1.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2911    0.8238    1.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -0.7418    0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7118    1.9325   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5294    0.2392   -1.5750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0343    1.4080   -0.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8155    1.2197   -2.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4270   -1.2313   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -1.0489    0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6585   -1.9180   -1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7283   -0.5483   -2.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4323   -1.6712    1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8389   -0.3598    2.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9576    1.6840    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7394    2.9558    0.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3237    1.6787   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9359   -2.4359   -2.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2898   -1.9693   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3164   -0.7139   -0.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8476    0.4910    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5911    1.1121    2.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 17 11  1  0
 24 18  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 23 50  1  0
 25 51  1  0
M  END

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  O   UNK     0       1.334 -14.630   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      17.338 -10.010   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      20.005 -10.010   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      17.338 -14.630   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
CONECT   24    5   25                                                       
CONECT   25   24    2                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

COMPND    HMDB0254307
HETATM    1  O1  UNL     1       3.436  -1.464  -1.650  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.954  -0.821  -0.707  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.077  -0.090   0.235  1.00  0.00           C  
HETATM    4  C3  UNL     1       1.605  -0.274  -0.164  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.790   0.488   0.829  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.700   0.365   0.529  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.067   0.891  -0.822  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.547   0.776  -1.058  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.967  -0.648  -0.986  1.00  0.00           C  
HETATM   10  C9  UNL     1      -4.456  -0.826  -1.237  1.00  0.00           C  
HETATM   11  C10 UNL     1      -5.287  -0.103  -0.264  1.00  0.00           C  
HETATM   12  C11 UNL     1      -5.727  -0.642   0.922  1.00  0.00           C  
HETATM   13  C12 UNL     1      -6.505   0.093   1.790  1.00  0.00           C  
HETATM   14  C13 UNL     1      -6.875   1.388   1.513  1.00  0.00           C  
HETATM   15  O2  UNL     1      -7.659   2.118   2.396  1.00  0.00           O  
HETATM   16  C14 UNL     1      -6.432   1.926   0.322  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.653   1.207  -0.560  1.00  0.00           C  
HETATM   18  C16 UNL     1       5.397  -0.805  -0.558  1.00  0.00           C  
HETATM   19  C17 UNL     1       6.248  -1.480  -1.424  1.00  0.00           C  
HETATM   20  O3  UNL     1       5.767  -2.204  -2.473  1.00  0.00           O  
HETATM   21  C18 UNL     1       7.642  -1.428  -1.231  1.00  0.00           C  
HETATM   22  C19 UNL     1       8.225  -0.733  -0.213  1.00  0.00           C  
HETATM   23  C20 UNL     1       7.392  -0.064   0.645  1.00  0.00           C  
HETATM   24  C21 UNL     1       6.024  -0.105   0.470  1.00  0.00           C  
HETATM   25  O4  UNL     1       5.188   0.587   1.359  1.00  0.00           O  
HETATM   26  H1  UNL     1       3.309   0.985   0.170  1.00  0.00           H  
HETATM   27  H2  UNL     1       3.172  -0.406   1.286  1.00  0.00           H  
HETATM   28  H3  UNL     1       1.439   0.086  -1.195  1.00  0.00           H  
HETATM   29  H4  UNL     1       1.373  -1.355  -0.120  1.00  0.00           H  
HETATM   30  H5  UNL     1       1.098   1.553   0.842  1.00  0.00           H  
HETATM   31  H6  UNL     1       0.928   0.078   1.848  1.00  0.00           H  
HETATM   32  H7  UNL     1      -1.291   0.824   1.341  1.00  0.00           H  
HETATM   33  H8  UNL     1      -0.904  -0.742   0.582  1.00  0.00           H  
HETATM   34  H9  UNL     1      -0.712   1.933  -0.976  1.00  0.00           H  
HETATM   35  H10 UNL     1      -0.529   0.239  -1.575  1.00  0.00           H  
HETATM   36  H11 UNL     1      -3.034   1.408  -0.261  1.00  0.00           H  
HETATM   37  H12 UNL     1      -2.815   1.220  -2.047  1.00  0.00           H  
HETATM   38  H13 UNL     1      -2.427  -1.231  -1.732  1.00  0.00           H  
HETATM   39  H14 UNL     1      -2.777  -1.049   0.042  1.00  0.00           H  
HETATM   40  H15 UNL     1      -4.658  -1.918  -1.108  1.00  0.00           H  
HETATM   41  H16 UNL     1      -4.728  -0.548  -2.261  1.00  0.00           H  
HETATM   42  H17 UNL     1      -5.432  -1.671   1.141  1.00  0.00           H  
HETATM   43  H18 UNL     1      -6.839  -0.360   2.723  1.00  0.00           H  
HETATM   44  H19 UNL     1      -7.958   1.684   3.251  1.00  0.00           H  
HETATM   45  H20 UNL     1      -6.739   2.956   0.125  1.00  0.00           H  
HETATM   46  H21 UNL     1      -5.324   1.679  -1.498  1.00  0.00           H  
HETATM   47  H22 UNL     1       4.936  -2.436  -2.867  1.00  0.00           H  
HETATM   48  H23 UNL     1       8.290  -1.969  -1.927  1.00  0.00           H  
HETATM   49  H24 UNL     1       9.316  -0.714  -0.092  1.00  0.00           H  
HETATM   50  H25 UNL     1       7.848   0.491   1.457  1.00  0.00           H  
HETATM   51  H26 UNL     1       5.591   1.112   2.125  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   18
CONECT    3    4   26   27
CONECT    4    5   28   29
CONECT    5    6   30   31
CONECT    6    7   32   33
CONECT    7    8   34   35
CONECT    8    9   36   37
CONECT    9   10   38   39
CONECT   10   11   40   41
CONECT   11   12   12   17
CONECT   12   13   42
CONECT   13   14   14   43
CONECT   14   15   16
CONECT   15   44
CONECT   16   17   17   45
CONECT   17   46
CONECT   18   19   19   24
CONECT   19   20   21
CONECT   20   47
CONECT   21   22   22   48
CONECT   22   23   49
CONECT   23   24   24   50
CONECT   24   25
CONECT   25   51
END

HMDB0254307
     RDKit          3D
Malabaricone B
 51 52  0  0  0  0  0  0  0  0999 V2000
    3.4356   -1.4644   -1.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9544   -0.8212   -0.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -0.0905    0.2349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6053   -0.2744   -0.1639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7898    0.4881    0.8288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6996    0.3653    0.5286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0669    0.8915   -0.8221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5466    0.7759   -1.0576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9672   -0.6479   -0.9855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4560   -0.8262   -1.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2873   -0.1035   -0.2641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7269   -0.6417    0.9218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5051    0.0931    1.7904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8751    1.3884    1.5133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6589    2.1184    2.3956 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4320    1.9260    0.3217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6528    1.2069   -0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966   -0.8050   -0.5584 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2477   -1.4801   -1.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7674   -2.2043   -2.4726 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425   -1.4284   -1.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2251   -0.7328   -0.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3923   -0.0642    0.6450 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0239   -0.1046    0.4703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1876    0.5869    1.3595 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3091    0.9846    0.1702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1716   -0.4056    1.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4388    0.0861   -1.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3726   -1.3547   -0.1197 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0976    1.5534    0.8415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9275    0.0782    1.8485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2911    0.8238    1.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -0.7418    0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7118    1.9325   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5294    0.2392   -1.5750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0343    1.4080   -0.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8155    1.2197   -2.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4270   -1.2313   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -1.0489    0.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6585   -1.9180   -1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7283   -0.5483   -2.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4323   -1.6712    1.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8389   -0.3598    2.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9576    1.6840    3.2513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7394    2.9558    0.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3237    1.6787   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9359   -2.4359   -2.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2898   -1.9693   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3164   -0.7139   -0.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8476    0.4910    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5911    1.1121    2.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 17 11  1  0
 24 18  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 12 42  1  0
 13 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 23 50  1  0
 25 51  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆O₄

Average Molecular Weight

342.435

Monoisotopic Molecular Weight

342.183109317

IUPAC Name

1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one

Traditional Name

1-(2,6-dihydroxyphenyl)-9-(4-hydroxyphenyl)nonan-1-one

CAS Registry Number

Not Available

SMILES

OC1=CC=C(CCCCCCCCC(=O)C2=C(O)C=CC=C2O)C=C1

InChI Identifier

InChI=1S/C21H26O4/c22-17-14-12-16(13-15-17)8-5-3-1-2-4-6-9-18(23)21-19(24)10-7-11-20(21)25/h7,10-15,22,24-25H,1-6,8-9H2

InChI Key

KOAPDMKKECXPHX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Butyrophenone
Aryl alkyl ketone
Resorcinol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	4.78	ALOGPS
logP	6.87	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	8.95	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	99.33 m³·mol⁻¹	ChemAxon
Polarizability	39.66 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	188.18	30932474
DeepCCS	[M-H]-	185.669	30932474
DeepCCS	[M-2H]-	219.016	30932474
DeepCCS	[M+Na]+	194.523	30932474
AllCCS	[M+H]+	184.1	32859911
AllCCS	[M+H-H2O]+	181.2	32859911
AllCCS	[M+NH4]+	186.7	32859911
AllCCS	[M+Na]+	187.5	32859911
AllCCS	[M-H]-	184.1	32859911
AllCCS	[M+Na-2H]-	184.7	32859911
AllCCS	[M+HCOO]-	185.4	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	19.7076 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.33 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	3304.6 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	480.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	234.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	246.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	638.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	1051.8 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	1025.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	84.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1899.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	693.4 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1853.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	689.5 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	578.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	498.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	169.5 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	45.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Malabaricone B	OC1=CC=C(CCCCCCCCC(=O)C2=C(O)C=CC=C2O)C=C1	3976.7	Standard polar	33892256
Malabaricone B	OC1=CC=C(CCCCCCCCC(=O)C2=C(O)C=CC=C2O)C=C1	3056.5	Standard non polar	33892256
Malabaricone B	OC1=CC=C(CCCCCCCCC(=O)C2=C(O)C=CC=C2O)C=C1	3164.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (Non-derivatized) - 70eV, Positive	splash10-000i-0900000000-bf011bf30b626f696326	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Malabaricone B GC-MS (TBDMS_3_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 10V, Positive-QTOF	splash10-0006-0329000000-0d862a3ad38aa0bab60e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 20V, Positive-QTOF	splash10-059i-0940000000-612340975db469e9e0df	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 40V, Positive-QTOF	splash10-0a4i-1900000000-54a810d7ea6a293b9c1e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 10V, Negative-QTOF	splash10-0006-0109000000-929f568076805cf6a31d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 20V, Negative-QTOF	splash10-052f-0907000000-492d5da835293f4b092a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Malabaricone B 40V, Negative-QTOF	splash10-07pl-7910000000-7bf8c6d1c982ab8bc4ae	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163001

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Malabaricone B (HMDB0254307)

MOL for HMDB0254307 (Malabaricone B)

3D MOL for HMDB0254307 (Malabaricone B)

3D SDF for HMDB0254307 (Malabaricone B)

3D-SDF for HMDB0254307 (Malabaricone B)

PDB for HMDB0254307 (Malabaricone B)

3D PDB for HMDB0254307 (Malabaricone B)

SMILES for HMDB0254307 (Malabaricone B)

INCHI for HMDB0254307 (Malabaricone B)

Structure for HMDB0254307 (Malabaricone B)

3D Structure for HMDB0254307 (Malabaricone B)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra