Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H44N2O.2ClH |
Molecular Weight | 461.552 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.[H][C@@]12CC[C@H](N(C)CCCN(C)C)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC=C4C[C@@H](O)CC[C@]34C
InChI
InChIKey=BZFBDUQOBQHBSZ-DLCQERRASA-N
InChI=1S/C25H44N2O.2ClH/c1-24-13-11-19(28)17-18(24)7-8-20-21-9-10-23(25(21,2)14-12-22(20)24)27(5)16-6-15-26(3)4;;/h7,19-23,28H,6,8-17H2,1-5H3;2*1H/t19-,20-,21-,22-,23-,24-,25-;;/m0../s1
Molecular Formula | C25H44N2O |
Molecular Weight | 388.6297 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Azacosterol (Ornitrol, 20,25-diazacholesterol dihydrochloride, SC 12937) is a cholesterol-lowering drug (hypocholesteremic) which was marketed previously but has since been discontinued. Azacosterol is a sterol derivative of cholesterol with two nitrogen atoms replacing two carbon atoms that acts as a hypocholesteremic agent by blocking delta-24-reductase. Azacosterol has the unintended side effect of causing myotonia. It is an avian contraceptive compound, which reduces fertility by inhibiting cholesterol synthesis. Azacosterol is also useful in the control of rodent populations.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12507656
The effect of intraperitoneal administration for 28 days of 10, 20, and 30 mg/kg body weight per day of 20,25-diazacholesterol dihydrochloride on the testis of Parkes (P) strain mice was investigated. Histologically, testes in mice treated with 10 or 20 mg/kg body weight of SC 12937 showed non-uniform degenerative changes in the seminiferous tubules. Testes in mice treated with 30 mg/kg body weight of the drug exhibited a degenerated appearance of germ cells in all seminiferous tubules.
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11377165
The epimeric mixtures 22,25-diazacholesterol (Azacosterol) and 3beta-hydroxy-22,25-diazacholestane were among the most active of phosphatidylinositol phospholipase C (PI-PLC) inhibitors, with IC(50) values of 7.4 and 7.5 uM, respectively.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:07:18 GMT 2023
by
admin
on
Fri Dec 15 15:07:18 GMT 2023
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Record UNII |
B32804UAUQ
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Common Name | English | ||
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29703
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NCI_THESAURUS |
C471
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EPA PESTICIDE CODE |
98101
Created by
admin on Fri Dec 15 15:07:18 GMT 2023 , Edited by admin on Fri Dec 15 15:07:18 GMT 2023
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Code System | Code | Type | Description | ||
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DTXSID8058297
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B32804UAUQ
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1249-84-9
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m1017
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PRIMARY | Merck Index | ||
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11954297
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CHEMBL1615357
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C78049
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |