ASP3662
Cat. No.: DC11019
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Chemical Structure
1204178-50-6
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Field of application
ASP3662 is a potent, selective, CNS-penetrable and orally active inhibitor of 11β-HSD1 with Ki of 5.3, 2.6 and 23 nM for human, mouse and rat 11β-HSD1, does not inhibit human 11β-HSD2 at 30 uM.
| Cas No.: |
1204178-50-6 |
| Chemical Name: |
4-{5-[2-(4-chloro-2,6-difluorophenoxy)propan-2-yl]-4-methyl-4H-1,2,4-triazol-3-yl}-3-fluorobenzamide |
| Synonyms: |
ASP 3662;ASP-3662 |
| SMILES: |
C(N)(=O)C1=CC=C(C2N(C)C(C(OC3=C(F)C=C(Cl)C=C3F)(C)C)=NN=2)C(F)=C1 |
| Formula: |
C19H16ClF3N4O2 |
| M.Wt: |
424.808 |
| Purity: |
>98% |
| Sotrage: |
2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Description: |
ASP3662 is a potent, selective, CNS-penetrable and orally active inhibitor of 11β-HSD1 with Ki of 5.3, 2.6 and 23 nM for human, mouse and rat 11β-HSD1, does not inhibit human 11β-HSD2 at 30 uM; demonstrates no appreciable binding affinity to or inhibition against 87 off-targets (adenosine receptors, adrenergic receptors, angiotensin receptors, calcium channels, 5-HT receptors etc.); inhibits the in vitro conversion of glucocorticoid from its inactive to active form in the brain and spinal cord; ameliorates mechanical allodynia in spinal nerve ligation (SNL) and streptozotocin-induced diabetic rats and thermal hyperalgesia in chronic constriction nerve injury rats. |
MSDS
COA
| LOT NO. |
DOWNLOAD |
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| 2018-0101 |
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