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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:15:04 UTC

Update Date

2022-03-07 02:55:59 UTC

HMDB ID

HMDB0038903

Secondary Accession Numbers

HMDB38903

Metabolite Identification

Common Name

Gancaonin M

Description

Gancaonin M belongs to the class of organic compounds known as 4'-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone. Thus, gancaonin m is considered to be a flavonoid. Gancaonin M has been detected, but not quantified in, herbs and spices. This could make gancaonin m a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Gancaonin M.

Structure

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


  Mrv0541 05061310432D          

 26 28  0  0  0  0            999 V2000
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    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
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
  9  4  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  4  2  0  0  0  0
 13  5  2  0  0  0  0
 13  6  1  0  0  0  0
 14  7  2  0  0  0  0
 14  8  1  0  0  0  0
 15  9  1  0  0  0  0
 16 11  2  0  0  0  0
 16 13  1  0  0  0  0
 17 10  2  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 19 18  2  0  0  0  0
 20 16  1  0  0  0  0
 20 19  1  0  0  0  0
 21 15  2  0  0  0  0
 21 19  1  0  0  0  0
 22 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 20  2  0  0  0  0
 25  3  1  0  0  0  0
 25 14  1  0  0  0  0
 26 11  1  0  0  0  0
 26 21  1  0  0  0  0
M  END

HMDB0038903
     RDKit          3D
Gancaonin M
 46 48  0  0  0  0  0  0  0  0999 V2000
    7.6496    1.3820    1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1239    0.4830    0.6460 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7368    0.3033    0.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2928   -0.5991   -0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9522   -0.7994   -0.6400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9924   -0.1093    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5658   -0.3439   -0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.5246    0.8895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6262   -0.7344    0.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1246   -0.7888   -0.5554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -1.0139   -0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3451   -1.1893    0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6312    0.0935    1.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169    0.6088    1.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9660    1.9176    2.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0439   -0.0831    0.8513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9530   -1.0617   -2.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3007   -1.2842   -2.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1527   -0.8986   -3.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7809   -0.6714   -2.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0279   -0.5159   -4.0524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -0.6165   -1.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -0.3937   -1.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8707   -0.2366   -2.3649 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4708    0.7853    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8237    0.9961    1.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1942    1.3032    2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7531    1.1565    1.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5446    2.4431    1.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559   -1.1326   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6283   -1.5084   -1.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075   -0.4886    1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2969   -1.6873    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8563   -1.9005    1.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7539    0.6383    1.4693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9151    2.7119    1.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9567    1.9472    2.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2049    2.0786    2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0383   -1.1666    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1347    0.1599   -0.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9566    0.4036    1.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0333   -1.4246   -1.6471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5478   -0.9405   -4.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8919   -0.3555   -4.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    1.3470    1.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1683    1.7098    1.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
 11 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
  6 25  1  0
 25 26  2  0
 26  3  1  0
 23  7  1  0
 22 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
 25 45  1  0
 26 46  1  0
M  END


  Mrv0541 05061310432D          

 26 28  0  0  0  0            999 V2000
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    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
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
  9  4  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  4  2  0  0  0  0
 13  5  2  0  0  0  0
 13  6  1  0  0  0  0
 14  7  2  0  0  0  0
 14  8  1  0  0  0  0
 15  9  1  0  0  0  0
 16 11  2  0  0  0  0
 16 13  1  0  0  0  0
 17 10  2  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 19 18  2  0  0  0  0
 20 16  1  0  0  0  0
 20 19  1  0  0  0  0
 21 15  2  0  0  0  0
 21 19  1  0  0  0  0
 22 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 20  2  0  0  0  0
 25  3  1  0  0  0  0
 25 14  1  0  0  0  0
 26 11  1  0  0  0  0
 26 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038903

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC=C(C=C1)C1=COC2=C(CC=C(C)C)C(O)=CC(O)=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O5/c1-12(2)4-9-15-17(22)10-18(23)19-20(24)16(11-26-21(15)19)13-5-7-14(25-3)8-6-13/h4-8,10-11,22-23H,9H2,1-3H3

> <INCHI_KEY>
DDLPIQXHEKZHQX-UHFFFAOYSA-N

> <FORMULA>
C21H20O5

> <MOLECULAR_WEIGHT>
352.3805

> <EXACT_MASS>
352.13107375

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
38.239549484733985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-3-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

> <ALOGPS_LOGP>
4.26

> <JCHEM_LOGP>
4.951333445

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.259977890219908

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.423542161774479

> <JCHEM_PKA_STRONGEST_BASIC>
-4.71815282072926

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
100.40799999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
gancanin M

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038903
     RDKit          3D
Gancaonin M
 46 48  0  0  0  0  0  0  0  0999 V2000
    7.6496    1.3820    1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1239    0.4830    0.6460 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7368    0.3033    0.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2928   -0.5991   -0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9522   -0.7994   -0.6400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9924   -0.1093    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5658   -0.3439   -0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.5246    0.8895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6262   -0.7344    0.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1246   -0.7888   -0.5554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -1.0139   -0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3451   -1.1893    0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6312    0.0935    1.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169    0.6088    1.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9660    1.9176    2.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0439   -0.0831    0.8513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9530   -1.0617   -2.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3007   -1.2842   -2.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1527   -0.8986   -3.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7809   -0.6714   -2.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0279   -0.5159   -4.0524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -0.6165   -1.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -0.3937   -1.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8707   -0.2366   -2.3649 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4708    0.7853    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8237    0.9961    1.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1942    1.3032    2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7531    1.1565    1.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5446    2.4431    1.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559   -1.1326   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6283   -1.5084   -1.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075   -0.4886    1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2969   -1.6873    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8563   -1.9005    1.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7539    0.6383    1.4693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9151    2.7119    1.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9567    1.9472    2.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2049    2.0786    2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0383   -1.1666    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1347    0.1599   -0.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9566    0.4036    1.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0333   -1.4246   -1.6471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5478   -0.9405   -4.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8919   -0.3555   -4.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    1.3470    1.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1683    1.7098    1.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
 11 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
  6 25  1  0
 25 26  2  0
 26  3  1  0
 23  7  1  0
 22 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
 25 45  1  0
 26 46  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   25                                                            
CONECT    4    9   12                                                       
CONECT    5    7   13                                                       
CONECT    6    8   13                                                       
CONECT    7    5   14                                                       
CONECT    8    6   14                                                       
CONECT    9    4   15                                                       
CONECT   10   17   18                                                       
CONECT   11   16   26                                                       
CONECT   12    1    2    4                                                  
CONECT   13    5    6   16                                                  
CONECT   14    7    8   25                                                  
CONECT   15    9   17   21                                                  
CONECT   16   11   13   20                                                  
CONECT   17   10   15   22                                                  
CONECT   18   10   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   16   19   24                                                  
CONECT   21   15   19   26                                                  
CONECT   22   17                                                            
CONECT   23   18                                                            
CONECT   24   20                                                            
CONECT   25    3   14                                                       
CONECT   26   11   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0038903
HETATM    1  C1  UNL     1       7.650   1.382   1.583  1.00  0.00           C  
HETATM    2  O1  UNL     1       7.124   0.483   0.646  1.00  0.00           O  
HETATM    3  C2  UNL     1       5.737   0.303   0.486  1.00  0.00           C  
HETATM    4  C3  UNL     1       5.293  -0.599  -0.457  1.00  0.00           C  
HETATM    5  C4  UNL     1       3.952  -0.799  -0.640  1.00  0.00           C  
HETATM    6  C5  UNL     1       2.992  -0.109   0.108  1.00  0.00           C  
HETATM    7  C6  UNL     1       1.566  -0.344  -0.114  1.00  0.00           C  
HETATM    8  C7  UNL     1       0.646  -0.525   0.890  1.00  0.00           C  
HETATM    9  O2  UNL     1      -0.626  -0.734   0.653  1.00  0.00           O  
HETATM   10  C8  UNL     1      -1.125  -0.789  -0.555  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.483  -1.014  -0.759  1.00  0.00           C  
HETATM   12  C10 UNL     1      -3.345  -1.189   0.428  1.00  0.00           C  
HETATM   13  C11 UNL     1      -3.631   0.094   1.111  1.00  0.00           C  
HETATM   14  C12 UNL     1      -4.817   0.609   1.312  1.00  0.00           C  
HETATM   15  C13 UNL     1      -4.966   1.918   2.018  1.00  0.00           C  
HETATM   16  C14 UNL     1      -6.044  -0.083   0.851  1.00  0.00           C  
HETATM   17  C15 UNL     1      -2.953  -1.062  -2.044  1.00  0.00           C  
HETATM   18  O3  UNL     1      -4.301  -1.284  -2.285  1.00  0.00           O  
HETATM   19  C16 UNL     1      -2.153  -0.899  -3.143  1.00  0.00           C  
HETATM   20  C17 UNL     1      -0.781  -0.671  -2.932  1.00  0.00           C  
HETATM   21  O4  UNL     1      -0.028  -0.516  -4.052  1.00  0.00           O  
HETATM   22  C18 UNL     1      -0.265  -0.616  -1.629  1.00  0.00           C  
HETATM   23  C19 UNL     1       1.080  -0.394  -1.426  1.00  0.00           C  
HETATM   24  O5  UNL     1       1.871  -0.237  -2.365  1.00  0.00           O  
HETATM   25  C20 UNL     1       3.471   0.785   1.041  1.00  0.00           C  
HETATM   26  C21 UNL     1       4.824   0.996   1.235  1.00  0.00           C  
HETATM   27  H1  UNL     1       7.194   1.303   2.586  1.00  0.00           H  
HETATM   28  H2  UNL     1       8.753   1.156   1.647  1.00  0.00           H  
HETATM   29  H3  UNL     1       7.545   2.443   1.263  1.00  0.00           H  
HETATM   30  H4  UNL     1       6.056  -1.133  -1.036  1.00  0.00           H  
HETATM   31  H5  UNL     1       3.628  -1.508  -1.381  1.00  0.00           H  
HETATM   32  H6  UNL     1       1.008  -0.489   1.904  1.00  0.00           H  
HETATM   33  H7  UNL     1      -4.297  -1.687   0.167  1.00  0.00           H  
HETATM   34  H8  UNL     1      -2.856  -1.901   1.169  1.00  0.00           H  
HETATM   35  H9  UNL     1      -2.754   0.638   1.469  1.00  0.00           H  
HETATM   36  H10 UNL     1      -4.915   2.712   1.239  1.00  0.00           H  
HETATM   37  H11 UNL     1      -5.957   1.947   2.523  1.00  0.00           H  
HETATM   38  H12 UNL     1      -4.205   2.079   2.792  1.00  0.00           H  
HETATM   39  H13 UNL     1      -6.038  -1.167   1.036  1.00  0.00           H  
HETATM   40  H14 UNL     1      -6.135   0.160  -0.248  1.00  0.00           H  
HETATM   41  H15 UNL     1      -6.957   0.404   1.305  1.00  0.00           H  
HETATM   42  H16 UNL     1      -5.033  -1.425  -1.647  1.00  0.00           H  
HETATM   43  H17 UNL     1      -2.548  -0.940  -4.149  1.00  0.00           H  
HETATM   44  H18 UNL     1       0.892  -0.355  -4.232  1.00  0.00           H  
HETATM   45  H19 UNL     1       2.762   1.347   1.649  1.00  0.00           H  
HETATM   46  H20 UNL     1       5.168   1.710   1.980  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3
CONECT    3    4    4   26
CONECT    4    5   30
CONECT    5    6    6   31
CONECT    6    7   25
CONECT    7    8    8   23
CONECT    8    9   32
CONECT    9   10
CONECT   10   11   11   22
CONECT   11   12   17
CONECT   12   13   33   34
CONECT   13   14   14   35
CONECT   14   15   16
CONECT   15   36   37   38
CONECT   16   39   40   41
CONECT   17   18   19   19
CONECT   18   42
CONECT   19   20   43
CONECT   20   21   22   22
CONECT   21   44
CONECT   22   23
CONECT   23   24   24
CONECT   25   26   26   45
CONECT   26   46
END

HMDB0038903
     RDKit          3D
Gancaonin M
 46 48  0  0  0  0  0  0  0  0999 V2000
    7.6496    1.3820    1.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1239    0.4830    0.6460 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7368    0.3033    0.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2928   -0.5991   -0.4568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9522   -0.7994   -0.6400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9924   -0.1093    0.1079 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5658   -0.3439   -0.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.5246    0.8895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6262   -0.7344    0.6534 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1246   -0.7888   -0.5554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -1.0139   -0.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3451   -1.1893    0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6312    0.0935    1.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169    0.6088    1.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9660    1.9176    2.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0439   -0.0831    0.8513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9530   -1.0617   -2.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3007   -1.2842   -2.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1527   -0.8986   -3.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7809   -0.6714   -2.9316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0279   -0.5159   -4.0524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -0.6165   -1.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -0.3937   -1.4261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8707   -0.2366   -2.3649 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4708    0.7853    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8237    0.9961    1.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1942    1.3032    2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7531    1.1565    1.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5446    2.4431    1.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559   -1.1326   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6283   -1.5084   -1.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0075   -0.4886    1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2969   -1.6873    0.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8563   -1.9005    1.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7539    0.6383    1.4693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9151    2.7119    1.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9567    1.9472    2.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2049    2.0786    2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0383   -1.1666    1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1347    0.1599   -0.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9566    0.4036    1.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0333   -1.4246   -1.6471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5478   -0.9405   -4.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8919   -0.3555   -4.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    1.3470    1.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1683    1.7098    1.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
 11 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
  6 25  1  0
 25 26  2  0
 26  3  1  0
 23  7  1  0
 22 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 16 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  0
 25 45  1  0
 26 46  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
5,7-Dihydroxy-4'-methoxy-8-prenylisoflavone	HMDB
Gancanin m	HMDB

Chemical Formula

C₂₁H₂₀O₅

Average Molecular Weight

352.3805

Monoisotopic Molecular Weight

352.13107375

IUPAC Name

5,7-dihydroxy-3-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

Traditional Name

gancanin M

CAS Registry Number

129145-51-3

SMILES

COC1=CC=C(C=C1)C1=COC2=C(CC=C(C)C)C(O)=CC(O)=C2C1=O

InChI Identifier

InChI=1S/C21H20O5/c1-12(2)4-9-15-17(22)10-18(23)19-20(24)16(11-26-21(15)19)13-5-7-14(25-3)8-6-13/h4-8,10-11,22-23H,9H2,1-3H3

InChI Key

DDLPIQXHEKZHQX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4'-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C4' atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

4'-O-methylisoflavones

Alternative Parents

Substituents

4p-o-methylisoflavone
Isoflavone
Hydroxyisoflavonoid
Chromone
Benzopyran
1-benzopyran
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Alkyl aryl ether
Pyranone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyran
Monocyclic benzene moiety
Vinylogous acid
Heteroaromatic compound
Ether
Organoheterocyclic compound
Oxacycle
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Isoflavonoids (LMPK12050226 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0038903)

Cellular substructure

Membrane (HMDB: HMDB0038903)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038903)

Source

Exogenous

Food

Food (HMDB: HMDB0038903)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Endogenous

Plant

Plant (HMDB: HMDB0038903)

Not Available

Nutrient (HMDB: HMDB0038903)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	139 - 141 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.28 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0077 g/L	ALOGPS
logP	4.26	ALOGPS
logP	4.95	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	6.42	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.41 m³·mol⁻¹	ChemAxon
Polarizability	38.24 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	184.301	30932474
DeepCCS	[M-H]-	181.943	30932474
DeepCCS	[M-2H]-	216.146	30932474
DeepCCS	[M+Na]+	192.066	30932474
AllCCS	[M+H]+	185.7	32859911
AllCCS	[M+H-H2O]+	182.5	32859911
AllCCS	[M+NH4]+	188.7	32859911
AllCCS	[M+Na]+	189.6	32859911
AllCCS	[M-H]-	184.6	32859911
AllCCS	[M+Na-2H]-	184.1	32859911
AllCCS	[M+HCOO]-	183.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Gancaonin M	COC1=CC=C(C=C1)C1=COC2=C(CC=C(C)C)C(O)=CC(O)=C2C1=O	4670.7	Standard polar	33892256
Gancaonin M	COC1=CC=C(C=C1)C1=COC2=C(CC=C(C)C)C(O)=CC(O)=C2C1=O	3171.5	Standard non polar	33892256
Gancaonin M	COC1=CC=C(C=C1)C1=COC2=C(CC=C(C)C)C(O)=CC(O)=C2C1=O	3243.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Gancaonin M,1TMS,isomer #1	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2=O)C=C1	3278.6	Semi standard non polar	33892256
Gancaonin M,1TMS,isomer #2	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2=O)C=C1	3286.2	Semi standard non polar	33892256
Gancaonin M,2TMS,isomer #1	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C=C1	3159.6	Semi standard non polar	33892256
Gancaonin M,1TBDMS,isomer #1	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C=C1	3535.3	Semi standard non polar	33892256
Gancaonin M,1TBDMS,isomer #2	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C=C1	3533.5	Semi standard non polar	33892256
Gancaonin M,2TBDMS,isomer #1	COC1=CC=C(C2=COC3=C(CC=C(C)C)C(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C=C1	3654.2	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 - Gancaonin M GC-MS (Non-derivatized) - 70eV, Positive	splash10-00dr-1119000000-7c1ecd2d7c4ee947fa0a	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gancaonin M GC-MS (2 TMS) - 70eV, Positive	splash10-001i-1001900000-9a66ff2229aded95639f	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gancaonin M GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gancaonin M GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - Gancaonin M 10V, Positive-QTOF	splash10-0udi-0009000000-096d527bd47d10cd5c7a	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 20V, Positive-QTOF	splash10-0fr2-3049000000-96eaca6c82e81ea82f22	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 40V, Positive-QTOF	splash10-0gb9-9463000000-3e1a955437c055d1bba1	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 10V, Negative-QTOF	splash10-0udi-0009000000-640f10348af0e3c5b33b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 20V, Negative-QTOF	splash10-0udi-0019000000-9a03caedf8b06588727b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 40V, Negative-QTOF	splash10-0a6r-4988000000-9a92ab6fbd3218d30d69	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 10V, Positive-QTOF	splash10-0udi-0029000000-488e4c27eacd654b3bc1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 20V, Positive-QTOF	splash10-0002-0091000000-de6862f8c02a9db64957	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 40V, Positive-QTOF	splash10-0gc0-0391000000-5185da686417094f1651	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 10V, Negative-QTOF	splash10-0udi-0009000000-05df88930ebcf3252a3c	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 20V, Negative-QTOF	splash10-0udi-0009000000-a90a383bbe6eaf8f8f3e	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gancaonin M 40V, Negative-QTOF	splash10-0gkc-1393000000-1a48ee247e97d98d82ef	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB018367

KNApSAcK ID

C00009897

Chemspider ID

10211354

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14604078

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1872571

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for Gancaonin M (HMDB0038903)

MOL for HMDB0038903 (Gancaonin M)

3D MOL for HMDB0038903 (Gancaonin M)

3D SDF for HMDB0038903 (Gancaonin M)

3D-SDF for HMDB0038903 (Gancaonin M)

PDB for HMDB0038903 (Gancaonin M)

3D PDB for HMDB0038903 (Gancaonin M)

SMILES for HMDB0038903 (Gancaonin M)

INCHI for HMDB0038903 (Gancaonin M)

Structure for HMDB0038903 (Gancaonin M)

3D Structure for HMDB0038903 (Gancaonin M)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra