Company Name: |
3B Pharmachem (Wuhan) International Co.,Ltd.
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Tel: |
821-50328103-801 18930552037 |
Email: |
3bsc@sina.com |
Products Intro: |
Product Name:CP 154526;N-Butyl-N-ethyl-2,5-diMethyl-7-(2,4,6-triMethylphenyl)-7H-pyrrolo[2,3-d]pyriMidin-4-aMinehydrochloride CAS:157286-86-7 Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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Company Name: |
LETOPHARM LIMITED
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Tel: |
+86-21-5821 5861 |
Email: |
sales@letopharm.com |
Products Intro: |
Product Name:CP154526 CAS:157286-86-7
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Company Name: |
TargetMol Chemicals Inc.
|
Tel: |
4008200310 |
Email: |
marketing@tsbiochem.com |
Products Intro: |
Product Name:CP 154,526 CAS:157286-86-7 Package:50mg/RMB 16800;100mg/RMB 21500;25mg/RMB 12800
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CP-154,526 manufacturers
- CP 154,526
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- $2380.00 / 50mg
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2024-10-28
- CAS:157286-86-7
- Min. Order:
- Purity:
- Supply Ability: 10g
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| CP-154,526 Basic information |
Product Name: | CP-154,526 | Synonyms: | N-Butyl-N-ethyl-2,5-dimethyl-7-(2,4,6-trimethylphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine;7H-Pyrrolo[2,3-d]pyrimidin-4-amine,N-butyl-N-ethyl-2,5-dimethyl-7-(2,4,6-trimethylphenyl)-;CP-154,526;N-Butyl-N-ethyl-2,5-dimethyl-7-(2,4,6-trimethylphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-aminehydrochloride;CP-154;CP154;CP 154;N-butyl-N-ethyl-2,5-dimethyl-7-(2,4,6-trimethylphenyl)pyrrolo[2,3-d]pyrimidin-4-amine | CAS: | 157286-86-7 | MF: | C23H32N4 | MW: | 364.53 | EINECS: | | Product Categories: | Amines;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Neurochemicals;Pfizer Compounds;Pharmaceuticals | Mol File: | 157286-86-7.mol | |
| CP-154,526 Chemical Properties |
Boiling point | 423.5±45.0 °C(Predicted) | density | 1.06 | storage temp. | Desiccate at +4°C | pka | 6.97±0.30(Predicted) |
| CP-154,526 Usage And Synthesis |
Uses | A selective, non-peptide antagonist of corticotropin releasing factor receptors (CRF1). It blocks CRF-induced adenylate cyclase activation and attenuates activation of the HPA axis by CRF. It displayed anxiolytic-like activity in the rat elevated plus-maze test; brain penetrant. | Biological Activity | Selective, non-peptide CRF 1 receptor antagonist (K i values are 2.7 and > 10000 nM for CRF 1 and CRF 2 receptors respectively). Blocks CRF-induced adenylate cyclase activation (K i = 3.7 nM) and attenuates activation of the HPA axis by CRF. Displays anxiolytic-like activity in the rat elevated plus-maze test; brain penetrant. |
| CP-154,526 Preparation Products And Raw materials |
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