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86401-95-8 molecular structure
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(1S,2R,8S,10S,11S,14R,15S,17S)-14-[2-(acetyloxy)acetyl]-17-hydroxy-2,8,15-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-14-yl propanoate

ChemBase ID: 174128
Molecular Formular: C27H36O7
Molecular Mass: 472.57054
Monoisotopic Mass: 472.24610349
SMILES and InChIs

SMILES:
[C@@H]12[C@@H](C[C@@H](C3=CC(=O)C=C[C@]23C)C)[C@H]2[C@](C[C@@H]1O)([C@](CC2)(C(=O)COC(=O)C)OC(=O)CC)C
Canonical SMILES:
CCC(=O)O[C@@]1(CC[C@@H]2[C@]1(C)C[C@H](O)[C@H]1[C@H]2C[C@@H](C2=CC(=O)C=C[C@]12C)C)C(=O)COC(=O)C
InChI:
InChI=1S/C27H36O7/c1-6-23(32)34-27(22(31)14-33-16(3)28)10-8-19-18-11-15(2)20-12-17(29)7-9-25(20,4)24(18)21(30)13-26(19,27)5/h7,9,12,15,18-19,21,24,30H,6,8,10-11,13-14H2,1-5H3/t15-,18-,19-,21-,24+,25-,26-,27-/m0/s1
InChIKey:
DALKLAYLIPSCQL-YPYQNWSCSA-N

Cite this record

CBID:174128 http://www.chembase.cn/molecule-174128.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(1S,2R,8S,10S,11S,14R,15S,17S)-14-[2-(acetyloxy)acetyl]-17-hydroxy-2,8,15-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-14-yl propanoate
IUPAC Traditional name
advantan
Synonyms
(6α,11β)-21-(Acetyloxy)-11-hydroxy-6-methyl-17-(1-oxopropoxy)pregna-1,4-diene-3,20-dione
Advantan
ZK 91588
6α-Methyl Prednisolone Aceponate
CAS Number
86401-95-8
PubChem SID
164230038
PubChem CID
63019

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC M325725 external link Add to cart
PubChem 63019 external link
Data Source Data ID Price
TRC
M325725 external link Add to cart Please log in.
Data Source Data ID
PubChem 63019 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 14.804081  H Acceptors
H Donor LogD (pH = 5.5) 3.1427958 
LogD (pH = 7.4) 3.1427956  Log P 3.1427958 
Molar Refractivity 125.9718 cm3 Polarizability 49.399937 Å3
Polar Surface Area 106.97 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
MSDS Link
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Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - M325725 external link
Used in treatment of seborrhoeic dermatitis includes topical treatments such as corticosteroids, antifungals, metronidazole and pimecrolimus.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Miyachi, Y., et al.: Br. J. Dermatol., 114, 231 (1986)
  • • Rallis, E., et al.: Drugs Exp. Clin. Res., 30, 191 (1986)
  • • Ozcan, H., et al.: Eur. J. Dermatol., 17, 313 (1986)
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PATENTS

PATENTS

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INTERNET

INTERNET

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