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4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one
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ChemBase ID:
179727
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Molecular Formular:
C23H34O5
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Molecular Mass:
390.51306
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Monoisotopic Mass:
390.24062419
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SMILES and InChIs
SMILES:
[C@@]12([C@@]([C@@H](C3=CC(=O)OC3)CC2)(CC[C@@H]2[C@@]3([C@@](C[C@H](CC3)O)(CC[C@@H]12)O)C)C)O
Canonical SMILES:
O[C@H]1CC[C@]2([C@](C1)(O)CC[C@@H]1[C@@H]2CC[C@]2([C@]1(O)CC[C@@H]2C1=CC(=O)OC1)C)C
InChI:
InChI=1S/C23H34O5/c1-20-7-3-15(24)12-22(20,26)9-5-18-17(20)4-8-21(2)16(6-10-23(18,21)27)14-11-19(25)28-13-14/h11,15-18,24,26-27H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,20+,21+,22-,23-/m0/s1
InChIKey:
QJPCKAJTLHDNCS-FBAXFMHRSA-N
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Cite this record
CBID:179727 http://www.chembase.cn/molecule-179727.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one
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IUPAC Traditional name
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4-[(1S,2R,5S,7S,10R,11S,14R,15R)-5,7,11-trihydroxy-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadecan-14-yl]-2,5-dihydrofuran-2-one
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Synonyms
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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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7.1826363
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H Acceptors
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4
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H Donor
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3
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LogD (pH = 5.5)
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1.826343
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LogD (pH = 7.4)
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1.4129112
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Log P
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1.8352609
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Molar Refractivity
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105.1251 cm3
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Polarizability
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41.84968 Å3
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Polar Surface Area
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86.99 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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REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Speiser, P. et al., Experientia, 1947, 3, 323, (isol)
- • Speiser, P. et al., Helv. Chim. Acta, 1948, 31, 622, (struct)
- • Lichti, H. et al., Helv. Chim. Acta, 1956, 39, 1914, (Ledienoside, Periplogenin digitoxoside)
- • Zelnik, R. et al., Helv. Chim. Acta, 1957, 40, 2110
- • Deghenghi, R. et al., Tet. Lett., 1963, 2045, (synth)
- • Shoji, J. et al., Chem. Pharm. Bull., 1967, 15, 720, (isol)
- • Sauer, H.H. et al., Phytochemistry, 1968, 7, 1543, (biosynth)
- • Kamano, Y. et al., J.C.S. Perkin 1, 1975, 1976, (synth)
- • Pauli, G.F., Planta Med., 1995, 61, 162, (Periplorhamnoside, Periplogenin glucoside, pmr)
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PATENTS
PATENTS
PubChem Patent
Google Patent