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1151650-25-7

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1151650-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1151650-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,1,6,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1151650-25:
(9*1)+(8*1)+(7*5)+(6*1)+(5*6)+(4*5)+(3*0)+(2*2)+(1*5)=117
117 % 10 = 7
So 1151650-25-7 is a valid CAS Registry Number.

1151650-25-7Downstream Products

1151650-25-7Relevant articles and documents

Inhibition of Calcium Dependent Protein Kinase 1 (CDPK1) by Pyrazolopyrimidine Analogs Decreases Establishment and Reoccurrence of Central Nervous System Disease by Toxoplasma gondii

Rutaganira, Florentine U.,Barks, Jennifer,Dhason, Mary Savari,Wang, Qiuling,Lopez, Michael S.,Long, Shaojun,Radke, Joshua B.,Jones, Nathaniel G.,Maddirala, Amarendar R.,Janetka, James W.,El Bakkouri, Majida,Hui, Raymond,Shokat, Kevan M.,Sibley, L. David

, p. 9976 - 9989 (2018/01/11)

Calcium dependent protein kinase 1 (CDPK1) is an essential enzyme in the opportunistic pathogen Toxoplasma gondii. CDPK1 controls multiple processes that are critical to the intracellular replicative cycle of T. gondii including secretion of adhesins, motility, invasion, and egress. Remarkably, CDPK1 contains a small glycine gatekeeper residue in the ATP binding pocket making it sensitive to ATP-competitive inhibitors with bulky substituents that complement this expanded binding pocket. Here we explored structure-activity relationships of a series of pyrazolopyrimidine inhibitors of CDPK1 with the goal of increasing selectivity over host enzymes, improving antiparasite potency, and improving metabolic stability. The resulting lead compound 24 exhibited excellent enzyme inhibition and selectivity for CDPK1 and potently inhibited parasite growth in vitro. Compound 24 was also effective at treating acute toxoplasmosis in the mouse, reducing dissemination to the central nervous system, and decreasing reactivation of chronic infection in severely immunocompromised mice. These findings provide proof of concept for the development of small molecule inhibitors of CDPK1 for treatment of CNS toxoplasmosis.

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