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12S,13S-Hydroxyandrographilide

PubChem CID: 24879274

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Compound Synonyms 12S,13S-Hydroxyandrographilide, (3S,4S)-3-((1S)-2-((1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-1-hydroxyethyl)-4-hydroxyoxolan-2-one, (3S,4S)-3-[(1S)-2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-4-hydroxyoxolan-2-one, CHEMBL467963
Topological Polar Surface Area 107.0
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 26.0
Isotope Atom Count 0.0
Molecular Complexity 577.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (3S,4S)-3-[(1S)-2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-4-hydroxyoxolan-2-one
Prediction Hob 0.0
Xlogp 1.9
Molecular Formula C20H32O6
Prediction Swissadme 1.0
Inchi Key NLYQWYLWLQBMPF-AWAUATEUSA-N
Fcsp3 0.85
Logs -2.129
Rotatable Bond Count 4.0
Logd 1.138
Compound Name 12S,13S-Hydroxyandrographilide
Prediction Hob Swissadme 0.0
Exact Mass 368.22
Formal Charge 0.0
Monoisotopic Mass 368.22
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 368.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Esol -3.0764140000000006
Inchi InChI=1S/C20H32O6/c1-11-4-5-15-19(2,7-6-16(24)20(15,3)10-21)12(11)8-13(22)17-14(23)9-26-18(17)25/h12-17,21-24H,1,4-10H2,2-3H3/t12-,13+,14-,15+,16-,17+,19+,20+/m1/s1
Smiles C[C@@]12CC[C@H]([C@@]([C@H]1CCC(=C)[C@H]2C[C@@H]([C@H]3[C@@H](COC3=O)O)O)(C)CO)O
Nring 3.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Andrographis Paniculata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all