4 Results for "

PRT062607

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "PRT062607" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-15323
CAS No.: 1370261-97-4
Purity:  98.07%
Synonyms: P505-15 Hydrochloride
Research Areas:  

Cancer

PRT062607 (P505-15) Hydrochloride is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis. PRT062607 Hydrochloride exerts potent antitumor activity in tumor xenograft mouse models .
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5
5 Cited Publications
Cat. No.: HY-15322
CAS No.: 1370261-96-3
Purity:  99.38%
Synonyms: P505-15; PRT-2607; BIIB-057
Target:  

Syk Apoptosis Caspase

Research Areas:  

Inflammation/Immunology Cancer

PRT062607 (P505-15; PRT-2607) is an orally active ATP-competitive Syk inhibitor with an IC50 value of 1 nM, and exhibits at least 80-fold selectivity over other kinases. PRT062607 blocks B cell antigen receptor-mediated activation, Fcε receptor 1-mediated basophil degranulation and microglial phagocytosis, and induces caspase-dependent apoptosis and microglial death. PRT062607 inhibits tumor growth and peripheral nerve injury-induced mechanical allodynia, and prevents neuronal loss. PRT062607 can be used in research related to rheumatoid arthritis, chronic lymphocytic leukemia, non-Hodgkin's lymphoma, neurodegenerative diseases and neuropathic pain .
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5
5 Cited Publications
Cat. No.: HY-15324
CAS No.: 1370261-98-5
Purity:  99.83%
Synonyms: P505-15 acetate; PRT-2607 acetate; BIIB-057 acetate
Research Areas:  

Cancer

PRT062607 (P505-15) acetate is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis. PRT062607 acetate exerts potent antitumor activity in tumor xenograft mouse models . .
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Cat. No.: HY-15322A
CAS No.: 1194954-52-3
Synonyms: (rel)-P505-15; (rel)-PRT-2607; (rel)-BIIB-057
Target:  

Syk Drug Isomer

Research Areas:  

Inflammation/Immunology

(rel)-PRT062607 ((rel)-P505-15) is the relative configuration of PRT062607 (HY-15322). PRT062607 is a highly selective inhibitor of Syk kinase, with an IC50 value of 1-2 nM, and is more than 80 times less potent against Fgr, Lyn, FAK, Pyk2, and Zap70.
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