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Cochliomycin B

PubChem CID: 52952746

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Compound Synonyms Cochliomycin B, (2E,5S,9R,10S,11E,14S)-10,18-dihydroxy-20-methoxy-7,7,14-trimethyl-6,8,15-trioxatricyclo[15.4.0.05,9]henicosa-1(17),2,11,18,20-pentaen-16-one, (2E,5S,9R,10S,11E,14S)-10,18-dihydroxy-20-methoxy-7,7,14-trimethyl-6,8,15-trioxatricyclo(15.4.0.05,9)henicosa-1(17),2,11,18,20-pentaen-16-one, CHEBI:211229
Topological Polar Surface Area 94.5
Hydrogen Bond Donor Count 2.0
Heavy Atom Count 29.0
Isotope Atom Count 0.0
Molecular Complexity 629.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 4.0
Iupac Name (2E,5S,9R,10S,11E,14S)-10,18-dihydroxy-20-methoxy-7,7,14-trimethyl-6,8,15-trioxatricyclo[15.4.0.05,9]henicosa-1(17),2,11,18,20-pentaen-16-one
Prediction Hob 1.0
Xlogp 3.8
Molecular Formula C22H28O7
Prediction Swissadme 1.0
Inchi Key ZJDKHUDTMNOVOT-PZUGFNCNSA-N
Fcsp3 0.5
Logs -4.61
Rotatable Bond Count 1.0
Logd 3.347
Compound Name Cochliomycin B
Prediction Hob Swissadme 1.0
Exact Mass 404.184
Formal Charge 0.0
Monoisotopic Mass 404.184
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 404.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 4.0
Total Bond Stereocenter Count 2.0
Esol -4.822449248275864
Inchi InChI=1S/C22H28O7/c1-13-7-5-9-16(23)20-18(28-22(2,3)29-20)10-6-8-14-11-15(26-4)12-17(24)19(14)21(25)27-13/h5-6,8-9,11-13,16,18,20,23-24H,7,10H2,1-4H3/b8-6+,9-5+/t13-,16-,18-,20+/m0/s1
Smiles C[C@H]1C/C=C/[C@@H]([C@@H]2[C@H](C/C=C/C3=C(C(=CC(=C3)OC)O)C(=O)O1)OC(O2)(C)C)O
Nring 3.0
Defined Bond Stereocenter Count 2.0

  • 1. Outgoing r'ship FOUND_IN to/from Curcuma Aromatica (Plant) Rel Props:Source_db:cmaup_ingredients
  • 2. Outgoing r'ship FOUND_IN to/from Lilium Lancifolium (Plant) Rel Props:Source_db:cmaup_ingredients