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Curassavioside M2

PubChem CID: 162968266

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Compound Synonyms Curassavioside M2
Topological Polar Surface Area 274.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 84.0
Isotope Atom Count 0.0
Molecular Complexity 2290.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 28.0
Iupac Name [(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14,17-trihydroxy-3-[(2R,4S,5S,6R)-4-hydroxy-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] benzoate
Prediction Hob 0.0
Xlogp 3.4
Molecular Formula C62H94O22
Prediction Swissadme 0.0
Inchi Key AGOSNPVTDFUKSI-WUTQGBJGSA-N
Fcsp3 0.8387096774193549
Logs -4.561
Rotatable Bond Count 18.0
Logd 3.377
Compound Name Curassavioside M2
Prediction Hob Swissadme 0.0
Exact Mass 1190.62
Formal Charge 0.0
Monoisotopic Mass 1190.62
Hydrogen Bond Acceptor Count 22.0
Molecular Weight 1191.4
Covalent Unit Count 1.0
Total Atom Stereocenter Count 28.0
Total Bond Stereocenter Count 0.0
Esol -8.24621154285714
Inchi InChI=1S/C62H94O22/c1-31-52(65)41(70-9)26-48(74-31)82-54-34(4)77-50(28-43(54)72-11)84-56-35(5)78-51(29-44(56)73-12)83-55-33(3)76-49(27-42(55)71-10)81-53-32(2)75-47(25-40(53)64)79-39-19-20-58(7)38(24-39)18-21-61(68)45(58)30-46(80-57(66)37-16-14-13-15-17-37)59(8)60(67,36(6)63)22-23-62(59,61)69/h13-18,31-35,39-56,64-65,67-69H,19-30H2,1-12H3/t31-,32-,33-,34-,35-,39+,40+,41-,42+,43-,44-,45-,46-,47+,48+,49+,50+,51+,52-,53-,54-,55-,56-,58+,59-,60-,61+,62-/m1/s1
Smiles C[C@@H]1[C@H]([C@@H](C[C@@H](O1)O[C@@H]2[C@H](O[C@H](C[C@H]2OC)O[C@@H]3[C@H](O[C@H](C[C@H]3OC)O[C@@H]4[C@H](O[C@H](C[C@@H]4OC)O[C@@H]5[C@H](O[C@H](C[C@@H]5O)O[C@H]6CC[C@@]7([C@H]8C[C@H]([C@@]9([C@@](CC[C@@]9([C@@]8(CC=C7C6)O)O)(C(=O)C)O)C)OC(=O)C1=CC=CC=C1)C)C)C)C)C)OC)O
Nring 10.0
Defined Bond Stereocenter Count 0.0