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Lobatin B

PubChem CID: 6440752

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Compound Synonyms LOBATIN B, 84754-02-9, [(2Z,4R,8S,9S,10R,11R)-10-hydroxy-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 3-methylbutanoate, Butanoic acid, 3-methyl-, (3aS,4S,5R,6R,10Z,11aR)-2,3,3a,4,5,6,7,11a-octahydro-5-hydroxy-6,10-dimethyl-3-methylene-2,7-dioxo-6,9-epoxycyclodeca(b)furan-4-yl ester, ((2Z,4R,8S,9S,10R,11R)-10-hydroxy-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo(9.2.1.04,8)tetradeca-1(13),2-dien-9-yl) 3-methylbutanoate, CHEMBL1172805
Topological Polar Surface Area 99.1
Hydrogen Bond Donor Count 1.0
Heavy Atom Count 27.0
Isotope Atom Count 0.0
Molecular Complexity 775.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name [(2Z,4R,8S,9S,10R,11R)-10-hydroxy-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradeca-1(13),2-dien-9-yl] 3-methylbutanoate
Prediction Hob 1.0
Xlogp 1.5
Molecular Formula C20H24O7
Prediction Swissadme 1.0
Inchi Key JXMKTEYFXIBRKC-BXRXTLJPSA-N
Fcsp3 0.55
Logs -4.079
Rotatable Bond Count 4.0
Logd 1.364
Compound Name Lobatin B
Prediction Hob Swissadme 1.0
Exact Mass 376.152
Formal Charge 0.0
Monoisotopic Mass 376.152
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 376.4
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 1.0
Esol -2.867311000000001
Inchi InChI=1S/C20H24O7/c1-9(2)6-15(22)26-17-16-11(4)19(24)25-13(16)7-10(3)12-8-14(21)20(5,27-12)18(17)23/h7-9,13,16-18,23H,4,6H2,1-3,5H3/b10-7-/t13-,16+,17+,18-,20+/m1/s1
Smiles C/C/1=C/[C@@H]2[C@@H]([C@@H]([C@H]([C@@]3(C(=O)C=C1O3)C)O)OC(=O)CC(C)C)C(=C)C(=O)O2
Nring 3.0
Defined Bond Stereocenter Count 1.0

  • 1. Outgoing r'ship FOUND_IN to/from Neurolaena Lobata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all