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Cimiracemoside G

PubChem CID: 21606552

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Compound Synonyms Cimiracemoside G, Cimiracemoside G, (-)-, UNII-Q8C7XHA46F, Q8C7XHA46F, 289632-43-5, alpha-L-Arabinopyranoside, (3beta,12beta,16beta,22R,23R,24R)-12-(acetyloxy)-16,23:22,25-diepoxy-23,24-dihydroxy-9,19-cyclolanost-7-en-3-yl, Q27287112, .ALPHA.-L-ARABINOPYRANOSIDE, (3.BETA.,12.BETA.,16.BETA.,22R,23R,24R)-12-(ACETYLOXY)-16,23:22,25-DIEPOXY-23,24-DIHYDROXY-9,19-CYCLOLANOST-7-EN-3-YL
Topological Polar Surface Area 164.0
Hydrogen Bond Donor Count 5.0
Heavy Atom Count 48.0
Isotope Atom Count 0.0
Molecular Complexity 1410.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 17.0
Iupac Name [(1S,5R,7S,10R,12S,14R,15R,16R,17S,18R,21R,22R,24S)-21,22-dihydroxy-1,6,6,15,17,20,20-heptamethyl-7-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-19,23-dioxaheptacyclo[13.10.0.02,12.05,10.010,12.016,24.018,22]pentacos-2-en-14-yl] acetate
Prediction Hob 0.0
Xlogp 2.2
Molecular Formula C37H56O11
Prediction Swissadme 0.0
Inchi Key IHMRHYCBRKQAFU-LVQFCLPFSA-N
Fcsp3 0.918918918918919
Logs -3.155
Rotatable Bond Count 4.0
Logd 2.549
Compound Name Cimiracemoside G
Prediction Hob Swissadme 0.0
Exact Mass 676.382
Formal Charge 0.0
Monoisotopic Mass 676.382
Hydrogen Bond Acceptor Count 11.0
Molecular Weight 676.8
Covalent Unit Count 1.0
Total Atom Stereocenter Count 17.0
Total Bond Stereocenter Count 0.0
Esol -5.126932800000001
Inchi InChI=1S/C37H56O11/c1-17-25-20(47-37(43)28(17)48-32(5,6)30(37)42)13-33(7)22-10-9-21-31(3,4)23(46-29-27(41)26(40)19(39)15-44-29)11-12-35(21)16-36(22,35)14-24(34(25,33)8)45-18(2)38/h10,17,19-21,23-30,39-43H,9,11-16H2,1-8H3/t17-,19-,20-,21-,23-,24+,25-,26-,27+,28+,29-,30+,33-,34+,35+,36-,37-/m0/s1
Smiles C[C@H]1[C@H]2[C@H](C[C@@]3([C@@]2([C@@H](C[C@]45C3=CC[C@@H]6[C@]4(C5)CC[C@@H](C6(C)C)O[C@H]7[C@@H]([C@H]([C@H](CO7)O)O)O)OC(=O)C)C)C)O[C@]8([C@@H]1OC([C@H]8O)(C)C)O
Nring 7.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Actaea Racemosa (Plant) Rel Props:Source_db:cmaup_ingredients