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Sarcaglaboside A

PubChem CID: 11546034

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Compound Synonyms Sarcaglaboside A, (4aS,8S,8aR,9aS)-3,8a-dimethyl-5-methylidene-8-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy-4a,6,7,8,9,9a-hexahydro-4H-benzo(f)(1)benzofuran-2-one, (4aS,8S,8aR,9aS)-3,8a-dimethyl-5-methylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one, CHEMBL482227, 882652-77-9
Topological Polar Surface Area 126.0
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 29.0
Isotope Atom Count 0.0
Molecular Complexity 732.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 9.0
Uniprot Id n.a.
Iupac Name (4aS,8S,8aR,9aS)-3,8a-dimethyl-5-methylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one
Prediction Hob 1.0
Xlogp -0.1
Molecular Formula C21H30O8
Prediction Swissadme 1.0
Inchi Key IGLQJWTUCUZHTP-BVFXZANDSA-N
Fcsp3 0.7619047619047619
Logs -2.547
Rotatable Bond Count 3.0
Logd 1.354
Compound Name Sarcaglaboside A
Prediction Hob Swissadme 1.0
Exact Mass 410.194
Formal Charge 0.0
Monoisotopic Mass 410.194
Hydrogen Bond Acceptor Count 8.0
Molecular Weight 410.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 9.0
Total Bond Stereocenter Count 0.0
Esol -2.1364706
Inchi InChI=1S/C21H30O8/c1-9-4-5-15(29-20-18(25)17(24)16(23)14(8-22)28-20)21(3)7-13-11(6-12(9)21)10(2)19(26)27-13/h12-18,20,22-25H,1,4-8H2,2-3H3/t12-,13-,14+,15-,16+,17-,18+,20-,21+/m0/s1
Smiles CC1=C2C[C@H]3C(=C)CC[C@@H]([C@@]3(C[C@@H]2OC1=O)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
Nring 4.0
Defined Bond Stereocenter Count 0.0