Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C14H13N3.ClH |
Molecular Weight | 259.734 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.N#CC1=CC=C(C=C1)[C@H]2CCCC3=CN=CN23
InChI
InChIKey=UKCVAQGKEOJTSR-PFEQFJNWSA-N
InChI=1S/C14H13N3.ClH/c15-8-11-4-6-12(7-5-11)14-3-1-2-13-9-16-10-17(13)14;/h4-7,9-10,14H,1-3H2;1H/t14-;/m1./s1
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 |
Molecular Formula | C14H13N3 |
Molecular Weight | 223.2731 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P19099 Gene ID: 1585.0 Gene Symbol: CYP11B2 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/20699715 |
3.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22275532
In a preclinical study, (+)-fadrozole was given to rats at a dose of 30 mg/kg.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28759940
(+)-Fadrozole inhibited angiotensin II-stimulated basal aldosterone production in NCI-H295R cells, showing a maximal effect at 10 nmol/l.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:05:37 GMT 2023
by
admin
on
Sat Dec 16 11:05:37 GMT 2023
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Record UNII |
6T3TZF5EG8
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Record Status |
Validated (UNII)
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Record Version |
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PARENT -> SALT/SOLVATE |
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