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1107-99-9 molecular structure
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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

ChemBase ID: 179850
Molecular Formular: C26H36O6
Molecular Mass: 444.56044
Monoisotopic Mass: 444.25118887
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

Cite this record

CBID:179850 http://www.chembase.cn/molecule-179850.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
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
IUPAC Traditional name
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
Synonyms
Mecortolon
Ultracortenol
Ultracorterenol
Vecortenol
Prednisolone trimethylacetate
CAS Number
1107-99-9
PubChem SID
164235760
PubChem CID
10095005

DATA SOURCES

DATA SOURCES

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Data Source Data ID Price
InterBioScreen
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Data Source Data ID
PubChem 10095005 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 12.610195  H Acceptors
H Donor LogD (pH = 5.5) 3.5136516 
LogD (pH = 7.4) 3.513649  Log P 3.5136518 
Molar Refractivity 121.3472 cm3 Polarizability 47.390816 Å3
Polar Surface Area 100.9 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Pharmacology Properties Product Information Bioassay(PubChem)
Mechanism of Action
ACTH antagonist expand Show data source
ACTH secretion inhibitor expand Show data source
Adrenocortical steroid expand Show data source
Calcium mobilizer expand Show data source
Gluconeogenesis promoter expand Show data source
Glycogen deposition inhibitor expand Show data source
Phosphorus mobilizer. expand Show data source
Application(s)
Antiallergic agent expand Show data source
Antiinflammatory expand Show data source
Immunosuppressive expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle 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

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INTERNET

INTERNET

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