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2-[(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-14-yl]-2-oxoethyl 2,2-dimethylpropanoate
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ChemBase ID:
179850
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Molecular Formular:
C26H36O6
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Molecular Mass:
444.56044
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Monoisotopic Mass:
444.25118887
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SMILES and InChIs
SMILES:
[C@]12([C@@](C(=O)COC(=O)C(C)(C)C)(CC[C@H]1[C@H]1[C@@H]([C@@]3(C(=CC(=O)C=C3)CC1)C)[C@H](C2)O)O)C
Canonical SMILES:
O=C1C=C[C@]2(C(=C1)CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2([C@H]1CC[C@]2(O)C(=O)COC(=O)C(C)(C)C)C)C
InChI:
InChI=1S/C26H36O6/c1-23(2,3)22(30)32-14-20(29)26(31)11-9-18-17-7-6-15-12-16(27)8-10-24(15,4)21(17)19(28)13-25(18,26)5/h8,10,12,17-19,21,28,31H,6-7,9,11,13-14H2,1-5H3/t17-,18-,19-,21+,24-,25-,26-/m0/s1
InChIKey:
PHEOVVDXTQVHAZ-XDANTLIUSA-N
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Cite this record
CBID:179850 http://www.chembase.cn/molecule-179850.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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2-[(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-14-yl]-2-oxoethyl 2,2-dimethylpropanoate
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IUPAC Traditional name
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2-[(1S,2R,10S,11S,14R,15S,17S)-14,17-dihydroxy-2,15-dimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-14-yl]-2-oxoethyl 2,2-dimethylpropanoate
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Synonyms
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Mecortolon
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Ultracortenol
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Ultracorterenol
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Vecortenol
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Prednisolone trimethylacetate
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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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12.610195
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H Acceptors
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5
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H Donor
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2
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LogD (pH = 5.5)
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3.5136516
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LogD (pH = 7.4)
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3.513649
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Log P
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3.5136518
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Molar Refractivity
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121.3472 cm3
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Polarizability
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47.390816 Å3
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Polar Surface Area
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100.9 Å2
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Rotatable Bonds
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5
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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
- • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 3, 585B, (nmr)
- • Nobile, A. et al., J.A.C.S., 1955, 77, 4184, (biosynth)
- • Herzog, H.L. et al., Science (Washington, D.C.), 1955, 121, 176, (struct)
- • Zicha, L. et al., Arzneim.-Forsch., 1960, 10, 728; 831, (pharmacol, derivs)
- • Herzog, H.L. et al., Tetrahedron, 1962, 18, 581, (synth)
- • Hirschmann, R. et al., J.A.C.S., 1964, 86, 3903, (synth)
- • Toft, P. et al., Can. J. Spectrosc., 1970, 15, 137, (ms)
- • Gambertoglis, J.G. et al., J. Pharmacokinet. Biopharm., 1980, 8, 1, (rev, pharmacol)
- • Jusko, W.J. et al., Ther. Drug Monit., 1980, 2, 169, (rev, pharmacol)
- • Gonzalez, M.D. et al., Org. Magn. Reson., 1984, 22, 586, (cmr)
- • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 6297; 6321; 6941
- • Kirk, D.N. et al., J.C.S. Perkin 2, 1990, 1567, (pmr)
- • Ali, S.L., Anal. Profiles Drug Subst., 1992, 21, 415, (rev)
- • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 737
- • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, AAF625; PMA000; PMA100; SOV100; PLY300
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PATENTS
PATENTS
PubChem Patent
Google Patent