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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:38:58 UTC

Update Date

2022-03-07 02:52:41 UTC

HMDB ID

HMDB0030778

Secondary Accession Numbers

HMDB30778

Metabolite Identification

Common Name

Mammea A/AB

Description

Mammea A/AB, also known as MAB 1, belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone. Thus, mammea a/ab is considered to be a flavonoid. Based on a literature review very few articles have been published on Mammea A/AB.

Structure

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


  Mrv0541 05061305302D          

 30 32  0  0  0  0            999 V2000
    5.0013    2.0625    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
    1.4289   -1.6500    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
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    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
    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
    0.7145   -1.2375    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
    0.0000    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
    0.0000    2.4750    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
    0.7145    2.0625    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
    1.4289    2.4750    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    0.8250    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
    2.8579    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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 12 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 11  2  0  0  0  0
 15  4  1  0  0  0  0
 15  5  1  0  0  0  0
 16  9  2  0  0  0  0
 16 10  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  2  0  0  0  0
 18 16  1  0  0  0  0
 19 13  1  0  0  0  0
 20 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 23 21  2  0  0  0  0
 24 20  2  0  0  0  0
 24 21  1  0  0  0  0
 25 17  2  0  0  0  0
 25 20  1  0  0  0  0
 26 19  2  0  0  0  0
 27 22  2  0  0  0  0
 28 23  1  0  0  0  0
 29 24  1  0  0  0  0
 30 19  1  0  0  0  0
 30 25  1  0  0  0  0
M  END

HMDB0030778
     RDKit          3D
Mammea A/AB
 56 58  0  0  0  0  0  0  0  0999 V2000
   -0.3376    5.0103    1.2951 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5455    4.9630    0.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501    3.5093   -0.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9119    3.6174   -1.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0995    2.6369   -0.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2305    3.2905   -0.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2257    1.2203   -0.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5051    0.6645   -0.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5642    1.5299   -0.6618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7472   -0.6710   -0.6997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1336   -1.2268   -0.8757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8999   -1.2179    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3882   -2.3474    0.8661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2036   -3.6348    0.1793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1575   -2.3106    2.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6985   -1.5580   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -2.8566   -0.7411 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0481   -3.7398   -0.6930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1933   -4.9727   -0.7979 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3308   -3.3188   -0.5257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331   -1.9452   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0137   -1.5645   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9634   -1.7000   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3024   -1.3967   -0.9189 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7135   -0.9481    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7750   -0.8085    1.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4414   -1.1166    1.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678   -1.0870   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126    0.3152   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0737    0.6705   -0.2007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637    5.3280    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3906    4.0483    1.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0252    5.7592    2.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0454    5.3340   -0.8391 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    5.6147    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313    3.2826    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7864    4.5726   -1.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9720    3.5676   -1.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411    2.7378   -2.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4867    1.2161   -0.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587   -2.2734   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6502   -0.6065   -1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0700   -0.2883    0.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5133   -3.6130   -0.8820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1658   -4.0247    0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8923   -4.3990    0.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0398   -2.9852    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4745   -1.2788    2.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5122   -2.6933    2.9858 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736   -3.9927   -0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.0466   -2.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0523   -1.5009   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7750   -0.7124    0.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890   -0.4567    2.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7016   -1.0086    1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6150    1.4122   -0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 13 15  1  0
 10 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 21 28  1  0
 28 29  2  0
 29 30  1  0
 29  7  1  0
 28 16  1  0
 27 22  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  9 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 20 50  1  0
 23 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 30 56  1  0
M  END


  Mrv0541 05061305302D          

 30 32  0  0  0  0            999 V2000
    5.0013    2.0625    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
    1.4289   -1.6500    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
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    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
    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
    0.7145   -1.2375    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
    0.0000    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
    0.0000    2.4750    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
    0.7145    2.0625    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
    1.4289    2.4750    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    0.8250    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
    2.8579    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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 12 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 11  2  0  0  0  0
 15  4  1  0  0  0  0
 15  5  1  0  0  0  0
 16  9  2  0  0  0  0
 16 10  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  2  0  0  0  0
 18 16  1  0  0  0  0
 19 13  1  0  0  0  0
 20 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 23 21  2  0  0  0  0
 24 20  2  0  0  0  0
 24 21  1  0  0  0  0
 25 17  2  0  0  0  0
 25 20  1  0  0  0  0
 26 19  2  0  0  0  0
 27 22  2  0  0  0  0
 28 23  1  0  0  0  0
 29 24  1  0  0  0  0
 30 19  1  0  0  0  0
 30 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030778

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O5/c1-5-15(4)22(27)21-23(28)17(12-11-14(2)3)25-20(24(21)29)18(13-19(26)30-25)16-9-7-6-8-10-16/h6-11,13,15,28-29H,5,12H2,1-4H3

> <INCHI_KEY>
YALRCXHVQYBSJC-UHFFFAOYSA-N

> <FORMULA>
C25H26O5

> <MOLECULAR_WEIGHT>
406.4709

> <EXACT_MASS>
406.178023942

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
44.8694889066183

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-4-phenyl-2H-chromen-2-one

> <ALOGPS_LOGP>
5.12

> <JCHEM_LOGP>
6.883732858

> <ALOGPS_LOGS>
-4.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.12656350387106

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.953907025586881

> <JCHEM_PKA_STRONGEST_BASIC>
-5.205489124478103

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
127.51109999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.75e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-4-phenylchromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030778
     RDKit          3D
Mammea A/AB
 56 58  0  0  0  0  0  0  0  0999 V2000
   -0.3376    5.0103    1.2951 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5455    4.9630    0.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501    3.5093   -0.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9119    3.6174   -1.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0995    2.6369   -0.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2305    3.2905   -0.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2257    1.2203   -0.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5051    0.6645   -0.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5642    1.5299   -0.6618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7472   -0.6710   -0.6997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1336   -1.2268   -0.8757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8999   -1.2179    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3882   -2.3474    0.8661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2036   -3.6348    0.1793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1575   -2.3106    2.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6985   -1.5580   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -2.8566   -0.7411 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0481   -3.7398   -0.6930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1933   -4.9727   -0.7979 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3308   -3.3188   -0.5257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331   -1.9452   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0137   -1.5645   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9634   -1.7000   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3024   -1.3967   -0.9189 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7135   -0.9481    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7750   -0.8085    1.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4414   -1.1166    1.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678   -1.0870   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126    0.3152   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0737    0.6705   -0.2007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637    5.3280    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3906    4.0483    1.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0252    5.7592    2.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0454    5.3340   -0.8391 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    5.6147    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313    3.2826    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7864    4.5726   -1.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9720    3.5676   -1.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411    2.7378   -2.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4867    1.2161   -0.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587   -2.2734   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6502   -0.6065   -1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0700   -0.2883    0.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5133   -3.6130   -0.8820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1658   -4.0247    0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8923   -4.3990    0.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0398   -2.9852    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4745   -1.2788    2.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5122   -2.6933    2.9858 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736   -3.9927   -0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.0466   -2.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0523   -1.5009   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7750   -0.7124    0.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890   -0.4567    2.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7016   -1.0086    1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6150    1.4122   -0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 13 15  1  0
 10 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 21 28  1  0
 28 29  2  0
 29 30  1  0
 29  7  1  0
 28 16  1  0
 27 22  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  9 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 20 50  1  0
 23 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 30 56  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       9.336   3.850   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       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    5                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    1   15                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   16                                                       
CONECT   10    8   16                                                       
CONECT   11   12   14                                                       
CONECT   12   11   17                                                       
CONECT   13   18   19                                                       
CONECT   14    2    3   11                                                  
CONECT   15    4    5   22                                                  
CONECT   16    9   10   18                                                  
CONECT   17   12   23   25                                                  
CONECT   18   13   16   20                                                  
CONECT   19   13   26   30                                                  
CONECT   20   18   24   25                                                  
CONECT   21   22   23   24                                                  
CONECT   22   15   21   27                                                  
CONECT   23   17   21   28                                                  
CONECT   24   20   21   29                                                  
CONECT   25   17   20   30                                                  
CONECT   26   19                                                            
CONECT   27   22                                                            
CONECT   28   23                                                            
CONECT   29   24                                                            
CONECT   30   19   25                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

COMPND    HMDB0030778
HETATM    1  C1  UNL     1      -0.338   5.010   1.295  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.546   4.963   0.071  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.050   3.509  -0.163  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.912   3.617  -1.408  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.100   2.637  -0.310  1.00  0.00           C  
HETATM    6  O1  UNL     1      -1.230   3.291  -0.350  1.00  0.00           O  
HETATM    7  C6  UNL     1      -0.226   1.220  -0.423  1.00  0.00           C  
HETATM    8  C7  UNL     1      -1.505   0.664  -0.595  1.00  0.00           C  
HETATM    9  O2  UNL     1      -2.564   1.530  -0.662  1.00  0.00           O  
HETATM   10  C8  UNL     1      -1.747  -0.671  -0.700  1.00  0.00           C  
HETATM   11  C9  UNL     1      -3.134  -1.227  -0.876  1.00  0.00           C  
HETATM   12  C10 UNL     1      -3.900  -1.218   0.393  1.00  0.00           C  
HETATM   13  C11 UNL     1      -4.388  -2.347   0.866  1.00  0.00           C  
HETATM   14  C12 UNL     1      -4.204  -3.635   0.179  1.00  0.00           C  
HETATM   15  C13 UNL     1      -5.157  -2.311   2.151  1.00  0.00           C  
HETATM   16  C14 UNL     1      -0.699  -1.558  -0.637  1.00  0.00           C  
HETATM   17  O3  UNL     1      -0.904  -2.857  -0.741  1.00  0.00           O  
HETATM   18  C15 UNL     1       0.048  -3.740  -0.693  1.00  0.00           C  
HETATM   19  O4  UNL     1      -0.193  -4.973  -0.798  1.00  0.00           O  
HETATM   20  C16 UNL     1       1.331  -3.319  -0.526  1.00  0.00           C  
HETATM   21  C17 UNL     1       1.633  -1.945  -0.405  1.00  0.00           C  
HETATM   22  C18 UNL     1       3.014  -1.565  -0.162  1.00  0.00           C  
HETATM   23  C19 UNL     1       3.963  -1.700  -1.147  1.00  0.00           C  
HETATM   24  C20 UNL     1       5.302  -1.397  -0.919  1.00  0.00           C  
HETATM   25  C21 UNL     1       5.714  -0.948   0.315  1.00  0.00           C  
HETATM   26  C22 UNL     1       4.775  -0.809   1.307  1.00  0.00           C  
HETATM   27  C23 UNL     1       3.441  -1.117   1.060  1.00  0.00           C  
HETATM   28  C24 UNL     1       0.568  -1.087  -0.469  1.00  0.00           C  
HETATM   29  C25 UNL     1       0.813   0.315  -0.361  1.00  0.00           C  
HETATM   30  O5  UNL     1       2.074   0.671  -0.201  1.00  0.00           O  
HETATM   31  H1  UNL     1      -1.364   5.328   0.972  1.00  0.00           H  
HETATM   32  H2  UNL     1      -0.391   4.048   1.814  1.00  0.00           H  
HETATM   33  H3  UNL     1       0.025   5.759   2.044  1.00  0.00           H  
HETATM   34  H4  UNL     1       0.045   5.334  -0.839  1.00  0.00           H  
HETATM   35  H5  UNL     1       1.414   5.615   0.262  1.00  0.00           H  
HETATM   36  H6  UNL     1       1.631   3.283   0.724  1.00  0.00           H  
HETATM   37  H7  UNL     1       1.786   4.573  -1.935  1.00  0.00           H  
HETATM   38  H8  UNL     1       2.972   3.568  -1.083  1.00  0.00           H  
HETATM   39  H9  UNL     1       1.741   2.738  -2.066  1.00  0.00           H  
HETATM   40  H10 UNL     1      -3.487   1.216  -0.782  1.00  0.00           H  
HETATM   41  H11 UNL     1      -3.059  -2.273  -1.232  1.00  0.00           H  
HETATM   42  H12 UNL     1      -3.650  -0.606  -1.645  1.00  0.00           H  
HETATM   43  H13 UNL     1      -4.070  -0.288   0.954  1.00  0.00           H  
HETATM   44  H14 UNL     1      -4.513  -3.613  -0.882  1.00  0.00           H  
HETATM   45  H15 UNL     1      -3.166  -4.025   0.234  1.00  0.00           H  
HETATM   46  H16 UNL     1      -4.892  -4.399   0.646  1.00  0.00           H  
HETATM   47  H17 UNL     1      -6.040  -2.985   2.117  1.00  0.00           H  
HETATM   48  H18 UNL     1      -5.474  -1.279   2.393  1.00  0.00           H  
HETATM   49  H19 UNL     1      -4.512  -2.693   2.986  1.00  0.00           H  
HETATM   50  H20 UNL     1       2.174  -3.993  -0.477  1.00  0.00           H  
HETATM   51  H21 UNL     1       3.700  -2.047  -2.133  1.00  0.00           H  
HETATM   52  H22 UNL     1       6.052  -1.501  -1.689  1.00  0.00           H  
HETATM   53  H23 UNL     1       6.775  -0.712   0.481  1.00  0.00           H  
HETATM   54  H24 UNL     1       5.089  -0.457   2.279  1.00  0.00           H  
HETATM   55  H25 UNL     1       2.702  -1.009   1.852  1.00  0.00           H  
HETATM   56  H26 UNL     1       2.615   1.412  -0.085  1.00  0.00           H  
CONECT    1    2   31   32   33
CONECT    2    3   34   35
CONECT    3    4    5   36
CONECT    4   37   38   39
CONECT    5    6    6    7
CONECT    7    8    8   29
CONECT    8    9   10
CONECT    9   40
CONECT   10   11   16   16
CONECT   11   12   41   42
CONECT   12   13   13   43
CONECT   13   14   15
CONECT   14   44   45   46
CONECT   15   47   48   49
CONECT   16   17   28
CONECT   17   18
CONECT   18   19   19   20
CONECT   20   21   21   50
CONECT   21   22   28
CONECT   22   23   23   27
CONECT   23   24   51
CONECT   24   25   25   52
CONECT   25   26   53
CONECT   26   27   27   54
CONECT   27   55
CONECT   28   29   29
CONECT   29   30
CONECT   30   56
END

HMDB0030778
     RDKit          3D
Mammea A/AB
 56 58  0  0  0  0  0  0  0  0999 V2000
   -0.3376    5.0103    1.2951 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5455    4.9630    0.0711 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501    3.5093   -0.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9119    3.6174   -1.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0995    2.6369   -0.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2305    3.2905   -0.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2257    1.2203   -0.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5051    0.6645   -0.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5642    1.5299   -0.6618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7472   -0.6710   -0.6997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1336   -1.2268   -0.8757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8999   -1.2179    0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3882   -2.3474    0.8661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2036   -3.6348    0.1793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1575   -2.3106    2.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6985   -1.5580   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9036   -2.8566   -0.7411 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0481   -3.7398   -0.6930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1933   -4.9727   -0.7979 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3308   -3.3188   -0.5257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331   -1.9452   -0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0137   -1.5645   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9634   -1.7000   -1.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3024   -1.3967   -0.9189 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7135   -0.9481    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7750   -0.8085    1.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4414   -1.1166    1.0598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678   -1.0870   -0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8126    0.3152   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0737    0.6705   -0.2007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637    5.3280    0.9722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3906    4.0483    1.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0252    5.7592    2.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0454    5.3340   -0.8391 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4144    5.6147    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313    3.2826    0.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7864    4.5726   -1.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9720    3.5676   -1.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411    2.7378   -2.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4867    1.2161   -0.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587   -2.2734   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6502   -0.6065   -1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0700   -0.2883    0.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5133   -3.6130   -0.8820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1658   -4.0247    0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8923   -4.3990    0.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0398   -2.9852    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4745   -1.2788    2.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5122   -2.6933    2.9858 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736   -3.9927   -0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.0466   -2.1327 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0523   -1.5009   -1.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7750   -0.7124    0.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890   -0.4567    2.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7016   -1.0086    1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6150    1.4122   -0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 13 15  1  0
 10 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 21 28  1  0
 28 29  2  0
 29 30  1  0
 29  7  1  0
 28 16  1  0
 27 22  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  9 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 20 50  1  0
 23 51  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 27 55  1  0
 30 56  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methyl-1-oxobutyl)-4-phenyl-2H-1-benzopyran-2-one, 9ci	HMDB
5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylbutyryl)-4-phenylcoumarin, 8ci	HMDB
MAB 1	HMDB

Chemical Formula

C₂₅H₂₆O₅

Average Molecular Weight

406.4709

Monoisotopic Molecular Weight

406.178023942

IUPAC Name

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-4-phenyl-2H-chromen-2-one

Traditional Name

5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-4-phenylchromen-2-one

CAS Registry Number

7058-70-0

SMILES

CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O

InChI Identifier

InChI=1S/C25H26O5/c1-5-15(4)22(27)21-23(28)17(12-11-14(2)3)25-20(24(21)29)18(13-19(26)30-25)16-9-7-6-8-10-16/h6-11,13,15,28-29H,5,12H2,1-4H3

InChI Key

YALRCXHVQYBSJC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
4-phenylcoumarin
7-hydroxycoumarin
Hydroxycoumarin
Butyrophenone
Coumarin
Benzopyran
1-benzopyran
Aryl alkyl ketone
Aryl ketone
Pyranone
Monocyclic benzene moiety
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Lactone
Ketone
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Neoflavonoids (LMPK12100018 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0030778)

Cellular substructure

Membrane (HMDB: HMDB0030778)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030778)

Source

Endogenous

Endogenous (HMDB: HMDB0030778)

Plant

Plant (HMDB: HMDB0030778)

Exogenous

Food

Food (HMDB: HMDB0030778)

Fruit

Fruits (FooDB: FOOD00871)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	107 - 108 °C	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
Water Solubility	0.0048 g/L	ALOGPS
logP	5.12	ALOGPS
logP	6.88	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	7.95	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	127.51 m³·mol⁻¹	ChemAxon
Polarizability	44.87 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	197.236	31661259
DarkChem	[M-H]-	196.756	31661259
DeepCCS	[M+H]+	201.351	30932474
DeepCCS	[M-H]-	198.969	30932474
DeepCCS	[M-2H]-	232.704	30932474
DeepCCS	[M+Na]+	207.806	30932474
AllCCS	[M+H]+	198.4	32859911
AllCCS	[M+H-H2O]+	195.7	32859911
AllCCS	[M+NH4]+	200.9	32859911
AllCCS	[M+Na]+	201.6	32859911
AllCCS	[M-H]-	203.0	32859911
AllCCS	[M+Na-2H]-	203.1	32859911
AllCCS	[M+HCOO]-	203.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Mammea A/AB	CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O	4072.8	Standard polar	33892256
Mammea A/AB	CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O	2875.0	Standard non polar	33892256
Mammea A/AB	CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O	3269.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Mammea A/AB,1TMS,isomer #1	CCC(C)C(=O)C1=C(O[Si](C)(C)C)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O	3239.1	Semi standard non polar	33892256
Mammea A/AB,1TMS,isomer #2	CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O[Si](C)(C)C	3253.1	Semi standard non polar	33892256
Mammea A/AB,2TMS,isomer #1	CCC(C)C(=O)C1=C(O[Si](C)(C)C)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O[Si](C)(C)C	3265.1	Semi standard non polar	33892256
Mammea A/AB,1TBDMS,isomer #1	CCC(C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O	3463.4	Semi standard non polar	33892256
Mammea A/AB,1TBDMS,isomer #2	CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O[Si](C)(C)C(C)(C)C	3476.2	Semi standard non polar	33892256
Mammea A/AB,2TBDMS,isomer #1	CCC(C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(CC=C(C)C)=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O[Si](C)(C)C(C)(C)C	3646.1	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 - Mammea A/AB GC-MS (Non-derivatized) - 70eV, Positive	splash10-0pi3-3109000000-d305eecd40988a3813e4	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS (2 TMS) - 70eV, Positive	splash10-0udr-6902770000-1926159470c068eb5dfd	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mammea A/AB GC-MS ("Mammea A/AB,1TBDMS,#2" TMS) - 70eV, Positive	Not Available	2021-10-14	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 - Mammea A/AB 10V, Positive-QTOF	splash10-0a4i-2009800000-2d7f012742f6b6a653cb	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 20V, Positive-QTOF	splash10-05n1-5009100000-23f896d7b512c856c0ef	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 40V, Positive-QTOF	splash10-0aor-9012000000-317388c90698a90195bd	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 10V, Negative-QTOF	splash10-0a4i-0003900000-dab2bc511c1a21436433	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 20V, Negative-QTOF	splash10-05fr-4029200000-6031c2c876436e4376c4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 40V, Negative-QTOF	splash10-002u-9365000000-e64a05289e04050b794b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 10V, Positive-QTOF	splash10-0a4i-0000900000-dfb39e832785760ae7f7	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 20V, Positive-QTOF	splash10-0a4i-0025900000-732844d8fcd8ee145fab	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 40V, Positive-QTOF	splash10-0002-3089000000-fe204e605df440e409c1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 10V, Negative-QTOF	splash10-0a4i-0000900000-7b5974fd53d3ffdb29ad	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 20V, Negative-QTOF	splash10-0a4i-0027900000-9fea58bb1d643b9c70fe	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mammea A/AB 40V, Negative-QTOF	splash10-004i-4259000000-c5506d004fd49e04601b	2021-09-22	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

FDB002715

KNApSAcK ID

C00046114

Chemspider ID

4983774

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6483317

PDB ID

Not Available

ChEBI ID

429966

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

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

Enzymes

Enzyme Details

1. UDP-glucuronosyltransferase 1-1

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:: UGT1A1
Uniprot ID:: P22309
Molecular weight:: 59590.91

Reactions

Mammea A/AB → 3,4,5-trihydroxy-6-{[7-hydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-2-oxo-4-phenyl-2H-chromen-5-yl]oxy}oxane-2-carboxylic acid	details
Mammea A/AB → 3,4,5-trihydroxy-6-{[5-hydroxy-8-(3-methylbut-2-en-1-yl)-6-(2-methylbutanoyl)-2-oxo-4-phenyl-2H-chromen-7-yl]oxy}oxane-2-carboxylic acid	details

Showing metabocard for Mammea A/AB (HMDB0030778)

MOL for HMDB0030778 (Mammea A/AB)

3D MOL for HMDB0030778 (Mammea A/AB)

3D SDF for HMDB0030778 (Mammea A/AB)

3D-SDF for HMDB0030778 (Mammea A/AB)

PDB for HMDB0030778 (Mammea A/AB)

3D PDB for HMDB0030778 (Mammea A/AB)

SMILES for HMDB0030778 (Mammea A/AB)

INCHI for HMDB0030778 (Mammea A/AB)

Structure for HMDB0030778 (Mammea A/AB)

3D Structure for HMDB0030778 (Mammea A/AB)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions