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(1S,2S,4S,5S,7R,8R,9S,11S,13S)-8-hydroxy-1-methyl-7-(propan-2-yl)-3,6,10,16-tetraoxaheptacyclo[11.7.0.02,4.02,9.05,7.09,11.014,18]icos-14(18)-en-17-one
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ChemBase ID:
179017
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Molecular Formular:
C20H24O6
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Molecular Mass:
360.40096
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Monoisotopic Mass:
360.15728849
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SMILES and InChIs
SMILES:
C1C2=C([C@H]3[C@](C1)([C@@]14[C@@]5([C@H](C3)O5)[C@@H]([C@@]3([C@H]([C@H]1O4)O3)C(C)C)O)C)COC2=O
Canonical SMILES:
O=C1OCC2=C1CC[C@]1([C@H]2C[C@H]2[C@@]3([C@@]41O[C@@H]4[C@@H]1O[C@@]1([C@H]3O)C(C)C)O2)C
InChI:
InChI=1S/C20H24O6/c1-8(2)18-13(25-18)14-20(26-14)17(3)5-4-9-10(7-23-15(9)21)11(17)6-12-19(20,24-12)16(18)22/h8,11-14,16,22H,4-7H2,1-3H3/t11-,12-,13-,14-,16+,17-,18-,19+,20+/m0/s1
InChIKey:
DFBIRQPKNDILPW-CIVMWXNOSA-N
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Cite this record
CBID:179017 http://www.chembase.cn/molecule-179017.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(1S,2S,4S,5S,7R,8R,9S,11S,13S)-8-hydroxy-1-methyl-7-(propan-2-yl)-3,6,10,16-tetraoxaheptacyclo[11.7.0.02,4.02,9.05,7.09,11.014,18]icos-14(18)-en-17-one
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IUPAC Traditional name
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Synonyms
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(3bS,4aS,5aS,6R,6aR,7aS,7bS,8aS,8bS)-3b,4,4a,6,6a,7a,7b,8b,9,10-Decahydro-6-hydroxy-8b-methyl-6a-(1-methylethyl)-trisoxireno[4b,5:6,7:8a,9]phenanthro[1,2-c]furan-1(3H)-one
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(-)-Triptolide
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NSC 163062
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PG 490
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Triptolid
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Triptolide
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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12.649559
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H Acceptors
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5
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H Donor
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1
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LogD (pH = 5.5)
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1.3276725
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LogD (pH = 7.4)
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1.3276701
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Log P
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1.3276726
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Molar Refractivity
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87.2606 cm3
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Polarizability
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35.78344 Å3
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Polar Surface Area
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84.12 Å2
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Rotatable Bonds
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1
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
TRC
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Hikim, S., et al.: J. Androl., 21, 431 (2000)
- • Chang, W.-T., et al.: J. Biol. Chem., 276, 222 (2000)
- • Kiviharju, T.M., et al.: Clin. Cancer Res., 8, 2666 (2000)
- • Leuenroth, S.J., et al.: Chem. Biol., 12, 1259 (2000)
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PATENTS
PATENTS
PubChem Patent
Google Patent