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Ambap17754-44-8

PubChem CID: 118701294

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Compound Synonyms atractyloside, C09064, Ambap17754-44-8, AC1L9C35
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 272.0
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC23CCC4CCC(CC5CCCCC5)CC4C2CCC1C3
Np Classifier Class Norkaurane diterpenoids
Deep Smiles OC[C@H]O[C@@H]O[C@@H]C[C@@H]C=O)O))C[C@]C6)C)CCC[C@@H]C[C@@]6CC%10))[C@@H]O)C5=C)))))))))))))))[C@@H][C@H][C@@H]6OS=O)=O)[O-]))))OS=O)=O)[O-]))))OC=O)CCC)C.[K+].[K+]
Heavy Atom Count 50.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CC23CCC4CCC(OC5CCCCO5)CC4C2CCC1C3
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 1440.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 11.0
Iupac Name dipotassium, [(2R,3R,4R,5R,6R)-2-[[(1R,5R,7R,9R,13R,15S)-5-carboxy-15-hydroxy-9-methyl-14-methylidene-7-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]oxy]-6-(hydroxymethyl)-3-(3-methylbutanoyloxy)-5-sulfonatooxyoxan-4-yl] sulfate
Prediction Hob 0.0
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Gsk 4 400 Rule False
Molecular Formula C30H44K2O16S2
Scaffold Graph Node Bond Level C=C1CC23CCC4CCC(OC5CCCCO5)CC4C2CCC1C3
Prediction Swissadme 0.0
Inchi Key IUCNQFHEWLYECJ-BDQDKTDDSA-L
Silicos It Class Soluble
Fcsp3 0.8666666666666667
Logs -0.046
Rotatable Bond Count 10.0
Logd -0.024
Synonyms atractyloside
Esol Class Moderately soluble
Functional Groups C=C(C)C, CC(=O)O, CC(=O)OC, CO, COS(=O)(=O)[O-], CO[C@@H](C)OC, [K+]
Compound Name Ambap17754-44-8
Prediction Hob Swissadme 0.0
Exact Mass 802.134
Formal Charge 0.0
Monoisotopic Mass 802.134
Hydrogen Bond Acceptor Count 16.0
Molecular Weight 803.0
Gi Absorption False
Covalent Unit Count 3.0
Total Atom Stereocenter Count 13.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C30H46O16S2.2K/c1-14(2)9-22(32)44-25-24(46-48(39,40)41)23(45-47(36,37)38)20(13-31)43-28(25)42-17-10-18(27(34)35)19-7-8-30-11-16(15(3)26(30)33)5-6-21(30)29(19,4)12-17, , /h14,16-21,23-26,28,31,33H,3,5-13H2,1-2,4H3,(H,34,35)(H,36,37,38)(H,39,40,41), , /q, 2*+1/p-2/t16-,17-,18-,19?,20-,21?,23-,24+,25-,26+,28-,29-,30-, , /m1../s1
Smiles CC(C)CC(=O)O[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1O[C@@H]2C[C@H](C3CC[C@@]45C[C@@H](CCC4[C@@]3(C2)C)C(=C)[C@@H]5O)C(=O)O)CO)OS(=O)(=O)[O-])OS(=O)(=O)[O-].[K+].[K+]
Nring 5.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Diterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Coffea Arabica (Plant) Rel Props:Reference:ISBN:9780387706375
  • 2. Outgoing r'ship FOUND_IN to/from Xanthium Sibiricum (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 3. Outgoing r'ship FOUND_IN to/from Xanthium Strumarium (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all