Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H20ClN3O |
| Molecular Weight | 401.888 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C1)C2=CC=C(C=C2)C(=O)NC[C@H](N3C=CN=C3)C4=CC=CC=C4
InChI
InChIKey=FHHNSSGZEIVGMS-QHCPKHFHSA-N
InChI=1S/C24H20ClN3O/c25-22-12-10-19(11-13-22)18-6-8-21(9-7-18)24(29)27-16-23(28-15-14-26-17-28)20-4-2-1-3-5-20/h1-15,17,23H,16H2,(H,27,29)/t23-/m0/s1
| Molecular Formula | C24H20ClN3O |
| Molecular Weight | 401.888 |
| 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: CHEMBL4521 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17240137 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Homology model of 1alpha,25-dihydroxyvitamin D3 24-hydroxylase cytochrome P450 24A1 (CYP24A1): active site architecture and ligand binding. | 2007-04 |
|
| The mechanism of 1,25-dihydroxyvitamin D(3) autoregulation in keratinocytes. | 2002-10-04 |
|
| Selective inhibitors of CYP24: mechanistic tools to explore vitamin D metabolism in human keratinocytes. | 2001-02-17 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:10:08 GMT 2025
by
admin
on
Mon Mar 31 18:10:08 GMT 2025
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| Record UNII |
A53Q3K00XS
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| Record Status |
Validated (UNII)
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| Record Version |
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174262-10-3
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A53Q3K00XS
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10476195
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DTXSID40169802
Created by
admin on Mon Mar 31 18:10:08 GMT 2025 , Edited by admin on Mon Mar 31 18:10:08 GMT 2025
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PRIMARY |