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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:07:36 UTC

Update Date

2022-03-07 02:56:17 UTC

HMDB ID

HMDB0039622

Secondary Accession Numbers

HMDB39622

Metabolite Identification

Common Name

Gibberellin A90

Description

Gibberellin A90 (GA90) belongs to the class of organic compounds known as C19-gibberellin 6-carboxylic acids. These are C19-gibberellins with a carboxyl group at the 6-position. Gibberellin A90 is found in cereals and cereal products. Gibberellin A90 is a constituent of Triticum aestivum (wheat).

Structure

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

  Mrv1652307272022332D          

 27 31  0  0  1  0            999 V2000
    0.1402   -0.5591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0861    0.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767    1.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399    1.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1453    0.7794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8608    1.4823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4440    0.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9958    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6203    0.1046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7879    0.4371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3958   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2032   -1.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553   -1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433    0.5212    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6433   -0.3038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6433    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3619    0.9319    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3619   -0.7261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8031   -0.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0732    0.5212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0732   -0.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659   -1.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1984    0.0230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433   -1.1253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1144   -0.0036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7876    0.9336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637    1.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  8  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9  2  1  6  0  0  0
  6  2  1  6  0  0  0
  8 10  2  0  0  0  0
  1  9  1  0  0  0  0
  1 11  1  1  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  6  0  0  0
 14 17  1  0  0  0  0
 15 18  1  0  0  0  0
 16 19  1  0  0  0  0
 17 20  1  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
 19 23  2  0  0  0  0
 18 19  1  6  0  0  0
 20 21  1  0  0  0  0
 15 24  1  1  0  0  0
 14  5  1  0  0  0  0
 15  1  1  0  0  0  0
  5 25  1  1  0  0  0
 17 27  1  1  0  0  0
 20 26  1  1  0  0  0
M  END

HMDB0039622
     RDKit          3D
Gibberellin A90
 49 53  0  0  0  0  0  0  0  0999 V2000
   -4.6316   -0.5951    0.9557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4665   -0.2086    0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -0.4524    1.1068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1474    0.2621    0.2454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9869    1.3599   -0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    0.5525   -0.7565 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8440   -0.3156   -1.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3484   -0.4459   -2.0839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -0.7406   -0.7875 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7917   -0.4608   -0.8439 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0302    0.6845   -1.6451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9739    1.5140   -1.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281    2.6247   -1.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4234    0.8069    0.1749 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8736    1.7968    1.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5025   -0.1609   -0.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -1.5403   -0.5121 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9778   -2.3393    0.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -1.5748   -1.2339 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0825   -2.8369   -1.0826 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    0.0221    0.5531 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0225    0.8631    0.9182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1831    0.9044    2.3785 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    0.1886    3.1084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1302    1.6477    3.0297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5527   -0.3587    0.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7662   -1.1516    1.8717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1059   -0.2355    2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9899   -1.5743    1.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5577    1.7995   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2140    2.0762    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0220    1.2759   -0.9877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2299    0.1813   -2.8449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3110   -1.2953   -1.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1824   -1.3389   -2.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8701    0.4014   -2.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8874   -1.7771   -0.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0131    1.3651    2.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.6423    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8340    2.2232    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0422    0.2026   -1.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2862   -0.2499    0.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7399   -2.0403   -1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6343   -2.0155    1.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8764   -1.4857   -2.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837   -3.5336   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465   -0.7824    1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    1.9203    0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9112    2.1947    3.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  4  3  1  1
  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  6
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 14 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21 10  1  0
 22  4  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  6
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  1
 15 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  6
 18 44  1  0
 19 45  1  6
 20 46  1  0
 21 47  1  1
 22 48  1  6
 25 49  1  0
M  END

  Mrv1652307272022332D          

 27 31  0  0  1  0            999 V2000
    0.1402   -0.5591    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0861    0.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767    1.5712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1399    1.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1453    0.7794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8608    1.4823    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4440    0.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9958    0.6683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6203    0.1046    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7879    0.4371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3958   -1.3435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2032   -1.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553   -1.9571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433    0.5212    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6433   -0.3038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6433    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3619    0.9319    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3619   -0.7261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8031   -0.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0732    0.5212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0732   -0.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659   -1.5436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1984    0.0230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433   -1.1253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1144   -0.0036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7876    0.9336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637    1.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  8  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9  2  1  6  0  0  0
  6  2  1  6  0  0  0
  8 10  2  0  0  0  0
  1  9  1  0  0  0  0
  1 11  1  1  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  6  0  0  0
 14 17  1  0  0  0  0
 15 18  1  0  0  0  0
 16 19  1  0  0  0  0
 17 20  1  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
 19 23  2  0  0  0  0
 18 19  1  6  0  0  0
 20 21  1  0  0  0  0
 15 24  1  1  0  0  0
 14  5  1  0  0  0  0
 15  1  1  0  0  0  0
  5 25  1  1  0  0  0
 17 27  1  1  0  0  0
 20 26  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0039622

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@]1([H])[C@@]3(C)C[C@@H](O)[C@@H](O)[C@@]21OC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O6/c1-8-5-18-6-9(8)3-4-11(18)19-13(12(18)15(22)23)17(2,16(24)25-19)7-10(20)14(19)21/h9-14,20-21H,1,3-7H2,2H3,(H,22,23)/t9-,10-,11-,12-,13-,14-,17-,18+,19-/m1/s1

> <INCHI_KEY>
ZRNQDBNUGCCKBO-KEPMMDNUSA-N

> <FORMULA>
C19H24O6

> <MOLECULAR_WEIGHT>
348.395

> <EXACT_MASS>
348.157288493

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.53872709642607

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,5R,8R,9S,10R,11R,13R,14R)-13,14-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

> <ALOGPS_LOGP>
0.48

> <JCHEM_LOGP>
0.6413236383333337

> <ALOGPS_LOGS>
-1.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.986746870504263

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.195142302450583

> <JCHEM_PKA_STRONGEST_BASIC>
-3.203007941645157

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
85.28629999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.69e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5R,8R,9S,10R,11R,13R,14R)-13,14-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039622
     RDKit          3D
Gibberellin A90
 49 53  0  0  0  0  0  0  0  0999 V2000
   -4.6316   -0.5951    0.9557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4665   -0.2086    0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -0.4524    1.1068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1474    0.2621    0.2454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9869    1.3599   -0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    0.5525   -0.7565 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8440   -0.3156   -1.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3484   -0.4459   -2.0839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -0.7406   -0.7875 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7917   -0.4608   -0.8439 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0302    0.6845   -1.6451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9739    1.5140   -1.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281    2.6247   -1.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4234    0.8069    0.1749 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8736    1.7968    1.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5025   -0.1609   -0.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -1.5403   -0.5121 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9778   -2.3393    0.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -1.5748   -1.2339 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0825   -2.8369   -1.0826 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    0.0221    0.5531 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0225    0.8631    0.9182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1831    0.9044    2.3785 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    0.1886    3.1084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1302    1.6477    3.0297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5527   -0.3587    0.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7662   -1.1516    1.8717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1059   -0.2355    2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9899   -1.5743    1.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5577    1.7995   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2140    2.0762    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0220    1.2759   -0.9877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2299    0.1813   -2.8449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3110   -1.2953   -1.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1824   -1.3389   -2.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8701    0.4014   -2.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8874   -1.7771   -0.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0131    1.3651    2.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.6423    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8340    2.2232    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0422    0.2026   -1.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2862   -0.2499    0.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7399   -2.0403   -1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6343   -2.0155    1.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8764   -1.4857   -2.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837   -3.5336   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465   -0.7824    1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    1.9203    0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9112    2.1947    3.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  4  3  1  1
  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  6
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 14 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21 10  1  0
 22  4  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  6
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  1
 15 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  6
 18 44  1  0
 19 45  1  6
 20 46  1  0
 21 47  1  1
 22 48  1  6
 25 49  1  0
M  END

HEADER    PROTEIN                                 27-JUL-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-JUL-20         0                                  
HETATM    1  C   UNK     0       0.262  -1.044   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.027   1.750   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.703   2.933   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.128   3.517   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.271   1.455   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.473   2.767   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.695   0.103   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.725   1.247   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.158   0.195   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.204   0.816   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.739  -2.508   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.246  -2.827   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.290  -3.653   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.201   0.973   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.201  -0.567   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.201   2.506   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.542   1.740   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.542  -1.355   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.366  -0.134   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.870   0.973   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.870  -0.567   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.550  -2.881   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.237   0.043   0.000  0.00  0.00           O+0
HETATM   24  H   UNK     0      -1.201  -2.101   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.214  -0.007   0.000  0.00  0.00           H+0
HETATM   26  O   UNK     0      -5.204   1.743   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.546   3.279   0.000  0.00  0.00           O+0
CONECT    1    9   11   15                                                  
CONECT    2    9    6                                                       
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    9   14   25                                             
CONECT    6    4    8    2                                                  
CONECT    7    8    9                                                       
CONECT    8    6    7   10                                                  
CONECT    9    5    7    2    1                                             
CONECT   10    8                                                            
CONECT   11    1   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   15   16   17    5                                             
CONECT   15   14   18   24    1                                             
CONECT   16   14   19                                                       
CONECT   17   14   20   27                                                  
CONECT   18   15   21   22   19                                             
CONECT   19   16   23   18                                                  
CONECT   20   17   21   26                                                  
CONECT   21   18   20                                                       
CONECT   22   18                                                            
CONECT   23   19                                                            
CONECT   24   15                                                            
CONECT   25    5                                                            
CONECT   26   20                                                            
CONECT   27   17                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

COMPND    HMDB0039622
HETATM    1  C1  UNL     1      -4.632  -0.595   0.956  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.467  -0.209   0.488  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.138  -0.452   1.107  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.147   0.262   0.245  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.987   1.360  -0.374  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.228   0.553  -0.756  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.844  -0.316  -1.931  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.348  -0.446  -2.084  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.655  -0.741  -0.787  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.792  -0.461  -0.844  1.00  0.00           C  
HETATM   11  O1  UNL     1       1.030   0.684  -1.645  1.00  0.00           O  
HETATM   12  C11 UNL     1       1.974   1.514  -1.055  1.00  0.00           C  
HETATM   13  O2  UNL     1       2.328   2.625  -1.523  1.00  0.00           O  
HETATM   14  C12 UNL     1       2.423   0.807   0.175  1.00  0.00           C  
HETATM   15  C13 UNL     1       2.874   1.797   1.195  1.00  0.00           C  
HETATM   16  C14 UNL     1       3.502  -0.161  -0.245  1.00  0.00           C  
HETATM   17  C15 UNL     1       2.983  -1.540  -0.512  1.00  0.00           C  
HETATM   18  O3  UNL     1       2.978  -2.339   0.649  1.00  0.00           O  
HETATM   19  C16 UNL     1       1.677  -1.575  -1.234  1.00  0.00           C  
HETATM   20  O4  UNL     1       1.083  -2.837  -1.083  1.00  0.00           O  
HETATM   21  C17 UNL     1       1.218   0.022   0.553  1.00  0.00           C  
HETATM   22  C18 UNL     1       0.022   0.863   0.918  1.00  0.00           C  
HETATM   23  C19 UNL     1      -0.183   0.904   2.379  1.00  0.00           C  
HETATM   24  O5  UNL     1       0.583   0.189   3.108  1.00  0.00           O  
HETATM   25  O6  UNL     1      -1.130   1.648   3.030  1.00  0.00           O  
HETATM   26  H1  UNL     1      -5.553  -0.359   0.413  1.00  0.00           H  
HETATM   27  H2  UNL     1      -4.766  -1.152   1.872  1.00  0.00           H  
HETATM   28  H3  UNL     1      -2.106  -0.235   2.170  1.00  0.00           H  
HETATM   29  H4  UNL     1      -1.990  -1.574   1.028  1.00  0.00           H  
HETATM   30  H5  UNL     1      -1.558   1.800  -1.270  1.00  0.00           H  
HETATM   31  H6  UNL     1      -2.214   2.076   0.429  1.00  0.00           H  
HETATM   32  H7  UNL     1      -4.022   1.276  -0.988  1.00  0.00           H  
HETATM   33  H8  UNL     1      -3.230   0.181  -2.845  1.00  0.00           H  
HETATM   34  H9  UNL     1      -3.311  -1.295  -1.847  1.00  0.00           H  
HETATM   35  H10 UNL     1      -1.182  -1.339  -2.750  1.00  0.00           H  
HETATM   36  H11 UNL     1      -0.870   0.401  -2.584  1.00  0.00           H  
HETATM   37  H12 UNL     1      -0.887  -1.777  -0.445  1.00  0.00           H  
HETATM   38  H13 UNL     1       3.013   1.365   2.192  1.00  0.00           H  
HETATM   39  H14 UNL     1       2.141   2.642   1.192  1.00  0.00           H  
HETATM   40  H15 UNL     1       3.834   2.223   0.866  1.00  0.00           H  
HETATM   41  H16 UNL     1       4.042   0.203  -1.145  1.00  0.00           H  
HETATM   42  H17 UNL     1       4.286  -0.250   0.554  1.00  0.00           H  
HETATM   43  H18 UNL     1       3.740  -2.040  -1.187  1.00  0.00           H  
HETATM   44  H19 UNL     1       3.634  -2.015   1.313  1.00  0.00           H  
HETATM   45  H20 UNL     1       1.876  -1.486  -2.343  1.00  0.00           H  
HETATM   46  H21 UNL     1       1.784  -3.534  -1.068  1.00  0.00           H  
HETATM   47  H22 UNL     1       1.346  -0.782   1.265  1.00  0.00           H  
HETATM   48  H23 UNL     1       0.193   1.920   0.604  1.00  0.00           H  
HETATM   49  H24 UNL     1      -0.911   2.195   3.844  1.00  0.00           H  
CONECT    1    2    2   26   27
CONECT    2    3    6
CONECT    3    4   28   29
CONECT    4    5    9   22
CONECT    5    6   30   31
CONECT    6    7   32
CONECT    7    8   33   34
CONECT    8    9   35   36
CONECT    9   10   37
CONECT   10   11   19   21
CONECT   11   12
CONECT   12   13   13   14
CONECT   14   15   16   21
CONECT   15   38   39   40
CONECT   16   17   41   42
CONECT   17   18   19   43
CONECT   18   44
CONECT   19   20   45
CONECT   20   46
CONECT   21   22   47
CONECT   22   23   48
CONECT   23   24   24   25
CONECT   25   49
END

HMDB0039622
     RDKit          3D
Gibberellin A90
 49 53  0  0  0  0  0  0  0  0999 V2000
   -4.6316   -0.5951    0.9557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4665   -0.2086    0.4877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378   -0.4524    1.1068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1474    0.2621    0.2454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9869    1.3599   -0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    0.5525   -0.7565 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8440   -0.3156   -1.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3484   -0.4459   -2.0839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -0.7406   -0.7875 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7917   -0.4608   -0.8439 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0302    0.6845   -1.6451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9739    1.5140   -1.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281    2.6247   -1.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4234    0.8069    0.1749 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8736    1.7968    1.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5025   -0.1609   -0.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9835   -1.5403   -0.5121 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9778   -2.3393    0.6495 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -1.5748   -1.2339 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0825   -2.8369   -1.0826 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    0.0221    0.5531 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0225    0.8631    0.9182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1831    0.9044    2.3785 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    0.1886    3.1084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1302    1.6477    3.0297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5527   -0.3587    0.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7662   -1.1516    1.8717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1059   -0.2355    2.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9899   -1.5743    1.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5577    1.7995   -1.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2140    2.0762    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0220    1.2759   -0.9877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2299    0.1813   -2.8449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3110   -1.2953   -1.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1824   -1.3389   -2.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8701    0.4014   -2.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8874   -1.7771   -0.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0131    1.3651    2.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.6423    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8340    2.2232    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0422    0.2026   -1.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2862   -0.2499    0.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7399   -2.0403   -1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6343   -2.0155    1.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8764   -1.4857   -2.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7837   -3.5336   -1.0680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3465   -0.7824    1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    1.9203    0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9112    2.1947    3.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  4  3  1  1
  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  6
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 14 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
  6  2  1  0
 19 10  1  0
  9  4  1  0
 21 10  1  0
 22  4  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  6
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  1
 15 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  6
 18 44  1  0
 19 45  1  6
 20 46  1  0
 21 47  1  1
 22 48  1  6
 25 49  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(1R,2R,5R,8R,9S,10R,11R,13R,14R)-13,14-Dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1,.0,.0,]heptadecane-9-carboxylate	HMDB
GA90	HMDB
GBA90	HMDB
Gibberellin A90	HMDB

Chemical Formula

C₁₉H₂₄O₆

Average Molecular Weight

348.395

Monoisotopic Molecular Weight

348.157288493

IUPAC Name

(1R,2R,5R,8R,9S,10R,11R,13R,14R)-13,14-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

Traditional Name

(1R,2R,5R,8R,9S,10R,11R,13R,14R)-13,14-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

CAS Registry Number

152110-34-4

SMILES

[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@]1([H])[C@@]3(C)C[C@@H](O)[C@@H](O)[C@@]21OC3=O

InChI Identifier

InChI=1S/C19H24O6/c1-8-5-18-6-9(8)3-4-11(18)19-13(12(18)15(22)23)17(2,16(24)25-19)7-10(20)14(19)21/h9-14,20-21H,1,3-7H2,2H3,(H,22,23)/t9-,10-,11-,12-,13-,14-,17-,18+,19-/m1/s1

InChI Key

ZRNQDBNUGCCKBO-KEPMMDNUSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

C19-gibberellin 6-carboxylic acids

Alternative Parents

Substituents

20-norgibberellane-6-carboxylic acid
2-hydroxy,20-norgibberellane
Diterpene lactone
Caprolactone
Oxepane
Gamma butyrolactone
Dicarboxylic acid or derivatives
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
1,2-diol
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039622)

Source

Endogenous

Endogenous (HMDB: HMDB0039622)

Plant

Poaceae (HMDB: HMDB0039622)

Animal

Animal (HMDB: HMDB0039622)

Exogenous

Food

Food (HMDB: HMDB0039622)

Cereal and cereal product

Cereal product

Breakfast cereal (FooDB: FOOD00270)

Cereal

Wheat (FooDB: FOOD00561)
Common wheat (FooDB: FOOD00187)

Cereals and cereal products (FooDB: FOOD00858)

Exogenous (HMDB: HMDB0039622)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0039622)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0039622)

Lipid metabolism pathway (HMDB: HMDB0039622)

Cellular process

Cell signaling (HMDB: HMDB0039622)

Biochemical process

Lipid transport (HMDB: HMDB0039622)

Role

Biological role

Energy source (HMDB: HMDB0039622)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0039622)

Physical Properties

State

Solid

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
Water Solubility	5.69 g/L	ALOGPS
logP	0.48	ALOGPS
logP	0.64	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	4.2	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	85.29 m³·mol⁻¹	ChemAxon
Polarizability	35.54 Å³	ChemAxon
Number of Rings	5	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-2H]-	212.298	30932474
DeepCCS	[M+Na]+	186.488	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Gibberellin A90	[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@]1([H])[C@@]3(C)C[C@@H](O)[C@@H](O)[C@@]21OC3=O	4341.5	Standard polar	33892256
Gibberellin A90	[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@]1([H])[C@@]3(C)C[C@@H](O)[C@@H](O)[C@@]21OC3=O	2649.0	Standard non polar	33892256
Gibberellin A90	[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@]1([H])[C@@]3(C)C[C@@H](O)[C@@H](O)[C@@]21OC3=O	3013.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Gibberellin A90,1TMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C	2680.9	Semi standard non polar	33892256
Gibberellin A90,1TMS,isomer #2	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C)[C@H]1O)[C@H]2[C@@H]3C(=O)O	2710.8	Semi standard non polar	33892256
Gibberellin A90,1TMS,isomer #3	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O[Si](C)(C)C)[C@H]2[C@@H]3C(=O)O	2719.9	Semi standard non polar	33892256
Gibberellin A90,2TMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C)[C@H]1O)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C	2707.5	Semi standard non polar	33892256
Gibberellin A90,2TMS,isomer #2	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O[Si](C)(C)C)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C	2729.0	Semi standard non polar	33892256
Gibberellin A90,2TMS,isomer #3	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[C@H]2[C@@H]3C(=O)O	2729.4	Semi standard non polar	33892256
Gibberellin A90,3TMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C	2740.8	Semi standard non polar	33892256
Gibberellin A90,1TBDMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C	2920.2	Semi standard non polar	33892256
Gibberellin A90,1TBDMS,isomer #2	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[C@H]2[C@@H]3C(=O)O	2922.3	Semi standard non polar	33892256
Gibberellin A90,1TBDMS,isomer #3	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[C@H]2[C@@H]3C(=O)O	2934.5	Semi standard non polar	33892256
Gibberellin A90,2TBDMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C	3151.1	Semi standard non polar	33892256
Gibberellin A90,2TBDMS,isomer #2	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C	3168.4	Semi standard non polar	33892256
Gibberellin A90,2TBDMS,isomer #3	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[C@H]2[C@@H]3C(=O)O	3152.2	Semi standard non polar	33892256
Gibberellin A90,3TBDMS,isomer #1	C=C1C[C@]23C[C@H]1CC[C@H]2[C@]12OC(=O)[C@](C)(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[C@H]2[C@@H]3C(=O)O[Si](C)(C)C(C)(C)C	3376.6	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 - Gibberellin A90 GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Gibberellin A90 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 - Gibberellin A90 10V, Positive-QTOF	splash10-0002-0009000000-6c4f279f6373b0323d55	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gibberellin A90 20V, Positive-QTOF	splash10-0udj-0129000000-41b78bfc969e521b5a9d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gibberellin A90 40V, Positive-QTOF	splash10-0fmj-2669000000-f52a23a96c091c0c9555	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gibberellin A90 10V, Negative-QTOF	splash10-0002-0009000000-920d3a938afe0bb10527	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gibberellin A90 20V, Negative-QTOF	splash10-0002-0009000000-c67ff0bfa77e0da3f58b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Gibberellin A90 40V, Negative-QTOF	splash10-003b-3933000000-cf0f937991bdd55ead50	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
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

FDB019250

KNApSAcK ID

C00000090

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

156908051

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Gibberellin A90 (HMDB0039622)

MOL for HMDB0039622 (Gibberellin A90)

3D MOL for HMDB0039622 (Gibberellin A90)

3D SDF for HMDB0039622 (Gibberellin A90)

3D-SDF for HMDB0039622 (Gibberellin A90)

PDB for HMDB0039622 (Gibberellin A90)

3D PDB for HMDB0039622 (Gibberellin A90)

SMILES for HMDB0039622 (Gibberellin A90)

INCHI for HMDB0039622 (Gibberellin A90)

Structure for HMDB0039622 (Gibberellin A90)

3D Structure for HMDB0039622 (Gibberellin A90)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra