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:ABT 702 dihydrochloride;5-(3-BroMophenyl)-7-[6-(4-Morpholinyl)-3-pyrido[2,3-d]byriMidin-4-aMinedihydrochloride CAS:214697-26-4 Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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Company Name: |
EMMX Biotechnology LLC
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Tel: |
888-539-0666 |
Email: |
info@emmx.com |
Products Intro: |
Product Name:ABT 702 dihydrochloride CAS:214697-26-4 Purity:98% HPLC Package:5mg;10mg;25mg;50mg;100mg;250mg;500mg;1g
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| 4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE Basic information |
Product Name: | 4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE | Synonyms: | 5-(3-BROMOPHENYL)-7-[6-(4-MORPHOLINYL-PYRIDIN-3-YL)-3-PYRIDO[2,3-D]PYRIMIDIN-4-AMINE] DIHYDROCHLORIDE;4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE;ABT 702 DIHYDROCHLORIDE;5-(3-Bromophenyl)-7-[6-(4-morpholinyl)-3-pyridinyl]-pyrido[2,3-d]pyrimidin-4-amine;4-Amino-5-(3-bromophenyl)-7-(6-morpholinopyridin-3-yl)pyrido[2,3-d]pyrimidine;5-(3-Bromophenyl)-7-[6-(4-morpholinyl)-3-pyrido[2,3-d]byrimidin-4-aminedihydrochloride;5-(3-broMophenyl)-7-(6-Morpholinopyridin-3-yl)pyrido[2,3-d]pyriMidin-4-aMine;Adenosine Kinase Inhibitor | CAS: | 214697-26-4 | MF: | C22H19BrN6O | MW: | 463.33 | EINECS: | | Product Categories: | Adenosine receptor | Mol File: | 214697-26-4.mol | |
| 4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE Chemical Properties |
Melting point | 227-245 °C(lit.) | storage temp. | Desiccate at RT | solubility | DMSO: 24 mg/mL |
| 4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE Usage And Synthesis |
Uses | ABT 702 Dihydrochloride is employed in the assay for quantitative high-?throughput screening of anti-?hepatitis C virus compounds. | Biological Activity | Potent non-nucleoside adenosine kinase inhibitor (IC 50 = 1.7 nM), selective over other sites of adenosine interaction (A 1 , A 2A and A 3 receptors, adenosine transporter and adenosine deaminase). Displays oral activity in animal models of pain and inflammation. |
| 4-AMINO-5-(3-BROMOPHENYL)-7-(6-MORPHOLINO-PYRIDIN-3-YL)PYRIDO[2,3-D]PYRIMIDINE DIHYDROCHLORIDE Preparation Products And Raw materials |
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