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Toonaciliatin G

PubChem CID: 23626638

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Compound Synonyms Toonaciliatin G, (1S,2S,3R,4R,7S,8R,10S,12R,14S,15S,17R,19S,20R)-15-(Furan-3-yl)-3,4,8,20-tetrahydroxy-2,7,14,20-tetramethyl-6,11,18-trioxahexacyclo[10.8.0.02,10.03,7.014,19.017,19]icosan-5-one, (1S,2S,3R,4R,7S,8R,10S,12R,14S,15S,17R,19S,20R)-15-(furan-3-yl)-3,4,8,20-tetrahydroxy-2,7,14,20-tetramethyl-6,11,18-trioxahexacyclo(10.8.0.02,10.03,7.014,19.017,19)icosan-5-one, CHEMBL4442271, 948556-30-7
Topological Polar Surface Area 142.0
Hydrogen Bond Donor Count 4.0
Heavy Atom Count 34.0
Isotope Atom Count 0.0
Molecular Complexity 974.0
Database Name cmaup_ingredients;pubchem
Defined Atom Stereocenter Count 13.0
Iupac Name (1S,2S,3R,4R,7S,8R,10S,12R,14S,15S,17R,19S,20R)-15-(furan-3-yl)-3,4,8,20-tetrahydroxy-2,7,14,20-tetramethyl-6,11,18-trioxahexacyclo[10.8.0.02,10.03,7.014,19.017,19]icosan-5-one
Prediction Hob 0.0
Xlogp -0.2
Molecular Formula C25H32O9
Prediction Swissadme 0.0
Inchi Key LJYUJPUTKALHOJ-ATUOXGKOSA-N
Fcsp3 0.8
Logs -4.156
Rotatable Bond Count 1.0
Logd 0.748
Compound Name Toonaciliatin G
Prediction Hob Swissadme 0.0
Exact Mass 476.205
Formal Charge 0.0
Monoisotopic Mass 476.205
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 476.5
Covalent Unit Count 1.0
Total Atom Stereocenter Count 13.0
Total Bond Stereocenter Count 0.0
Esol -2.6986599294117664
Inchi InChI=1S/C25H32O9/c1-20-9-13-17(22(3,29)25(20)16(33-25)7-12(20)11-5-6-31-10-11)21(2)15(32-13)8-14(26)23(4)24(21,30)18(27)19(28)34-23/h5-6,10,12-18,26-27,29-30H,7-9H2,1-4H3/t12-,13+,14+,15-,16+,17+,18-,20-,21+,22+,23-,24-,25+/m0/s1
Smiles C[C@@]12C[C@@H]3[C@H]([C@]4([C@@H](O3)C[C@H]([C@]5([C@@]4([C@H](C(=O)O5)O)O)C)O)C)[C@@]([C@@]16[C@H](O6)C[C@H]2C7=COC=C7)(C)O
Nring 7.0
Defined Bond Stereocenter Count 0.0

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