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Gibberellin A29

PubChem CID: 14605548

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Compound Synonyms Gibberellin A29, 29774-53-6, (1R,2R,5S,8S,9S,10R,11R,13R)-5,13-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid, CHEBI:28040, (1R,2R,5S,8S,9S,10R,11R,13R)-5,13-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, 3beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibbane-10beta-carboxylic acid, 2-Epi-Gibberellin A29, GA29, (1R,2R,5S,8S,9S,10R,11R,13R)-5,13-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, (1R,2R,5S,8S,9S,10R,11R,13R)-5,13-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo(9.3.2.15,8.01,10.02,8)heptadecane-9-carboxylic acid, (1R,2R,5S,8S,9S,10R,13R)-5,13-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo(9.3.2.15,8.01,10.02,8)heptadecane-9-carboxylic acid, (1R,2R,5S,8S,9S,10R,13R)-5,13-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid, (2E,6Z)-2,6-Nonadien-1-yl acetic acid, C06096, Q27103470
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 104.0
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC23CC1CCC2C12CCCC(C(C)C1)C2C3
Np Classifier Class Gibberellins
Deep Smiles O[C@H]C[C@]OC=O)[C@]C7)[C@H]5[C@@H][C@][C@H]8CC[C@]C6)C=C)C7))O))))))C=O)O))))C
Heavy Atom Count 25.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CC23CC1CCC2C12CCCC(C(O)O1)C2C3
Classyfire Subclass Diterpenoids
Isotope Atom Count 0.0
Molecular Complexity 731.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (1R,2R,5S,8S,9S,10R,11R,13R)-5,13-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 0.2
Gsk 4 400 Rule True
Molecular Formula C19H24O6
Scaffold Graph Node Bond Level C=C1CC23CC1CCC2C12CCCC(C(=O)O1)C2C3
Prediction Swissadme 1.0
Inchi Key BKBYHSYZKIAJDA-WWSAFQOPSA-N
Silicos It Class Soluble
Fcsp3 0.7894736842105263
Logs -3.186
Rotatable Bond Count 1.0
Logd -0.26
Synonyms gibberellin a(ga29), gibberellin a29, gibberellin ga29
Esol Class Soluble
Functional Groups C=C(C)C, CC(=O)O, CO, COC(C)=O
Compound Name Gibberellin A29
Prediction Hob Swissadme 1.0
Exact Mass 348.157
Formal Charge 0.0
Monoisotopic Mass 348.157
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 348.4
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -2.0789490000000006
Inchi InChI=1S/C19H24O6/c1-9-5-17-8-18(9,24)4-3-11(17)19-7-10(20)6-16(2,15(23)25-19)13(19)12(17)14(21)22/h10-13,20,24H,1,3-8H2,2H3,(H,21,22)/t10-,11-,12-,13-,16-,17+,18+,19-/m1/s1
Smiles C[C@@]12C[C@H](C[C@@]3([C@@H]1[C@@H]([C@]45[C@H]3CC[C@](C4)(C(=C)C5)O)C(=O)O)OC2=O)O
Nring 5.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Diterpenoids

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