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Cypellocarpin B

PubChem CID: 10506563

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Compound Synonyms cypellocarpin B, [(2R,3S,4S,5R,6S)-6-[(2,5-dihydroxy-2-methyl-4-oxo-3H-chromen-7-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate, ((2R,3S,4S,5R,6S)-6-((2,5-dihydroxy-2-methyl-4-oxo-3H-chromen-7-yl)oxy)-3,4,5-trihydroxyoxan-2-yl)methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate, CHEMBL520205, 294856-65-8
Topological Polar Surface Area 192.0
Hydrogen Bond Donor Count 6.0
Heavy Atom Count 38.0
Isotope Atom Count 0.0
Molecular Complexity 920.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 6.0
Iupac Name [(2R,3S,4S,5R,6S)-6-[(2,5-dihydroxy-2-methyl-4-oxo-3H-chromen-7-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate
Prediction Hob 0.0
Xlogp 0.5
Molecular Formula C26H34O12
Prediction Swissadme 0.0
Inchi Key BNOXWGIIFHBMQJ-UOCJQAADSA-N
Fcsp3 0.6153846153846154
Logs -3.117
Rotatable Bond Count 7.0
Logd 0.846
Compound Name Cypellocarpin B
Prediction Hob Swissadme 0.0
Exact Mass 538.205
Formal Charge 0.0
Monoisotopic Mass 538.205
Hydrogen Bond Acceptor Count 12.0
Molecular Weight 538.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 7.0
Total Bond Stereocenter Count 0.0
Esol -3.1362273052631604
Inchi InChI=1S/C26H34O12/c1-25(2,33)13-6-4-12(5-7-13)23(32)35-11-18-20(29)21(30)22(31)24(37-18)36-14-8-15(27)19-16(28)10-26(3,34)38-17(19)9-14/h4,8-9,13,18,20-22,24,27,29-31,33-34H,5-7,10-11H2,1-3H3/t13-,18+,20+,21-,22+,24+,26?/m0/s1
Smiles CC1(CC(=O)C2=C(C=C(C=C2O1)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)COC(=O)C4=CC[C@@H](CC4)C(C)(C)O)O)O)O)O)O
Nring 4.0
Defined Bond Stereocenter Count 0.0