CAS NO:394208-27-6 3-Phenylpyrazolo[1,5-a]pyrimidine
CAS NO:394208-27-6 NAME:3-Phenylpyrazolo[1,5-a]pyrimidine MF:C12H9N3 MW:195.22 PURITY:97%+ COA:Available
Categories:
Life Science Chemicals
Pharmaceutical Intermediates
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Product introduction
| PRODUCT NAME | 3-Phenylpyrazolo[1,5-a]pyrimidine |
| CAS NO | 394208-27-6 |
| MF | C12H9N3 |
| MW | 195.22 |
| APPEARANCE | Asked |
| STORAGE | Sealed in dry,Room Temperature |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:394208-27-6 3-Phenylpyrazolo[1,5-a]pyrimidine
3-Phenylpyrazolo[1,5-a]pyrimidine is a nitrogen-containing heterocyclic compound . It has been used as a base to design and synthesize various compounds with potential biological activities
3-Phenylpyrazolo[1,5-a]pyrimidine is a substance that inhibits the replication of viruses. It has a broad spectrum of activity against HIV, herpes simplex virus type 1 (HSV-1), and herpes simplex virus type 2 (HSV-2). The antiviral activity is due to its ability to inhibit viral DNA polymerases and RNA polymerases. 3-Phenylpyrazolo[1,5-a]pyrimidine binds to the active site of these enzymes in a micromolar range. This compound also has factor-1 inhibitor activity, which can be used for the treatment of hepatitis C.

Applications of CAS NO:394208-27-6 3-Phenylpyrazolo[1,5-a]pyrimidine
1)Synthesis and Electrophilic Substitutions
2)Design of Corticotropin-Releasing Factor Receptor Antagonists
3)Antitumor, Antimicrobial, and Antioxidant Activities
4)Crystal Structure and Biological Activity
The crystal structure of a specific derivative of pyrazolo[1,5-a]pyrimidine has been analyzed, revealing its moderate anticancer activity.
5)Synthesis of Glycosylhydrazinyl-Pyrazolo[1,5-c]pyrimidines
New glycosylhydrazinyl-pyrazolo[1,5-c]pyrimidines have been synthesized, showing inhibition of proliferation in certain cancer cells. These compounds could be potential anti-proliferative agents in cancer treatment.
6)Pharmacokinetic Predictions and Anti-inflammatory Evaluation
Pyrazolo[3,4-d]pyrimidine derivatives have been synthesized and evaluated for their cyclooxygenase inhibition and anti-inflammatory activity. Such studies are important for developing new anti-inflammatory drugs.
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