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(22s,25r)-11alpha,16beta,22,26-Tetrahydroxycholest-5-en-3beta-yl beta-d-glucopyranoside

PubChem CID: 53466476

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Compound Synonyms (22s,25r)-11alpha,16beta,22,26-tetrahydroxycholest-5-en-3beta-yl beta-d-glucopyranoside
Topological Polar Surface Area 180.0
Hydrogen Bond Donor Count 8.0
Heavy Atom Count 43.0
Isotope Atom Count 0.0
Molecular Complexity 993.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 17.0
Iupac Name (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,11R,13S,14S,16S,17R)-17-[(2S,3S,6R)-3,7-dihydroxy-6-methylheptan-2-yl]-11,16-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Prediction Hob 0.0
Xlogp 1.5
Molecular Formula C33H56O10
Prediction Swissadme 0.0
Inchi Key IWGAWRNAVDMCGX-HEMASFHRSA-N
Fcsp3 0.9393939393939394
Logs -3.383
Rotatable Bond Count 9.0
Logd 2.444
Compound Name (22s,25r)-11alpha,16beta,22,26-Tetrahydroxycholest-5-en-3beta-yl beta-d-glucopyranoside
Prediction Hob Swissadme 0.0
Exact Mass 612.387
Formal Charge 0.0
Monoisotopic Mass 612.387
Hydrogen Bond Acceptor Count 10.0
Molecular Weight 612.8
Covalent Unit Count 1.0
Total Atom Stereocenter Count 17.0
Total Bond Stereocenter Count 0.0
Esol -3.9966662000000026
Inchi InChI=1S/C33H56O10/c1-16(14-34)5-8-22(36)17(2)26-23(37)12-21-20-7-6-18-11-19(42-31-30(41)29(40)28(39)25(15-35)43-31)9-10-32(18,3)27(20)24(38)13-33(21,26)4/h6,16-17,19-31,34-41H,5,7-15H2,1-4H3/t16-,17-,19+,20+,21+,22+,23+,24-,25-,26+,27-,28-,29+,30-,31-,32+,33+/m1/s1
Smiles C[C@H](CC[C@@H]([C@@H](C)[C@H]1[C@H](C[C@@H]2[C@@]1(C[C@H]([C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)O)C)O)O)CO
Nring 5.0
Defined Bond Stereocenter Count 0.0