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Charantoside Iv

PubChem CID: 23626170

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Compound Synonyms charantoside IV, (2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-(((1R,4S,5S,8R,9R,12S,13S,16S)-5,9,17,17-tetramethyl-8-((2R,4E)-6-methylhepta-4,6-dien-2-yl)-18-oxapentacyclo(10.5.2.01,13.04,12.05,9)nonadec-2-en-16-yl)oxy)oxane-3,4,5-triol, (2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-[[(1R,4S,5S,8R,9R,12S,13S,16S)-5,9,17,17-tetramethyl-8-[(2R,4E)-6-methylhepta-4,6-dien-2-yl]-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-yl]oxy]oxane-3,4,5-triol, CHEMBL409790, 951646-20-1
Topological Polar Surface Area 109.0
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 43.0
Isotope Atom Count 0.0
Molecular Complexity 1150.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 14.0
Iupac Name (2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-[[(1R,4S,5S,8R,9R,12S,13S,16S)-5,9,17,17-tetramethyl-8-[(2R,4E)-6-methylhepta-4,6-dien-2-yl]-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-yl]oxy]oxane-3,4,5-triol
Prediction Hob 0.0
Xlogp 6.3
Molecular Formula C36H56O7
Prediction Swissadme 0.0
Inchi Key QFMGCFIFVIVJLB-LZRINOBGSA-N
Fcsp3 0.8333333333333334
Logs -5.028
Rotatable Bond Count 7.0
Logd 4.307
Compound Name Charantoside Iv
Prediction Hob Swissadme 0.0
Exact Mass 600.403
Formal Charge 0.0
Monoisotopic Mass 600.403
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 600.8
Covalent Unit Count 1.0
Total Atom Stereocenter Count 14.0
Total Bond Stereocenter Count 1.0
Esol -7.0658894
Inchi InChI=1S/C36H56O7/c1-21(2)9-8-10-22(3)23-13-15-34(7)25-14-16-36-26(35(25,20-41-36)18-17-33(23,34)6)11-12-27(32(36,4)5)43-31-30(40)29(39)28(38)24(19-37)42-31/h8-9,14,16,22-31,37-40H,1,10-13,15,17-20H2,2-7H3/b9-8+/t22-,23-,24-,25+,26+,27+,28-,29-,30-,31+,33-,34+,35+,36-/m1/s1
Smiles C[C@H](C/C=C/C(=C)C)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2C=C[C@]5([C@H]3CC[C@@H](C5(C)C)O[C@H]6[C@@H]([C@@H]([C@@H]([C@H](O6)CO)O)O)O)OC4)C)C
Nring 6.0
Defined Bond Stereocenter Count 1.0

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