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Triptersinin G

PubChem CID: 71524360

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Compound Synonyms Triptersinin G, ((1S,2S,5S,6S,7S,8R,9R,12R)-5,12-diacetyloxy-6-(acetyloxymethyl)-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo(7.2.1.01,6)dodecan-8-yl) pyridine-3-carboxylate, [(1S,2S,5S,6S,7S,8R,9R,12R)-5,12-diacetyloxy-6-(acetyloxymethyl)-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] pyridine-3-carboxylate, CHEMBL2335696
Topological Polar Surface Area 187.0
Hydrogen Bond Donor Count 1.0
Heavy Atom Count 46.0
Isotope Atom Count 0.0
Molecular Complexity 1240.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name [(1S,2S,5S,6S,7S,8R,9R,12R)-5,12-diacetyloxy-6-(acetyloxymethyl)-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] pyridine-3-carboxylate
Prediction Hob 0.0
Xlogp 1.6
Molecular Formula C32H37NO13
Prediction Swissadme 0.0
Inchi Key KXWAUJOSCJAHAC-OWFKIMCMSA-N
Fcsp3 0.5625
Logs -3.652
Rotatable Bond Count 13.0
Logd 1.537
Compound Name Triptersinin G
Prediction Hob Swissadme 0.0
Exact Mass 643.226
Formal Charge 0.0
Monoisotopic Mass 643.226
Hydrogen Bond Acceptor Count 14.0
Molecular Weight 643.6
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Esol -4.144936921739131
Inchi InChI=1S/C32H37NO13/c1-17(34)41-16-31-22(42-18(2)35)9-11-30(6,39)32(31)25(43-19(3)36)23(29(4,5)46-32)24(44-27(37)20-8-7-12-33-14-20)26(31)45-28(38)21-10-13-40-15-21/h7-8,10,12-15,22-26,39H,9,11,16H2,1-6H3/t22-,23+,24+,25+,26+,30-,31-,32-/m0/s1
Smiles CC(=O)OC[C@@]12[C@H](CC[C@]([C@@]13[C@@H]([C@@H]([C@H]([C@H]2OC(=O)C4=COC=C4)OC(=O)C5=CN=CC=C5)C(O3)(C)C)OC(=O)C)(C)O)OC(=O)C
Nring 5.0
Defined Bond Stereocenter Count 0.0