Name | 2,6-diamino-7-(thiophen-3-ylmethyl)-1,5-dihydropyrrolo[3,2-d]pyrimidin-4-one,hydrochloride |
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Synonyms | ci 972 |
Description | CI 972 anhydrous is a potent, orally active, and competitive inhibitor of purine nucleoside phosphorylase (PNP) (Ki=0.83 μM) under development as a T cell-selective immunosuppressive agent[1][2]. |
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Related Catalog | |
Target |
Ki: 0.83 μM (PNP)[1] |
In Vivo | CI 972 anhydrous (5-150 mg/kg; p.o.) produces dose-dependent elevation of plasma inosine one hour after administration to rats[1]. |
References |
Boiling Point | 602.2ºC at 760mmHg |
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Molecular Formula | C11H12ClN5OS |
Molecular Weight | 297.76400 |
Flash Point | 318ºC |
Exact Mass | 297.04500 |
PSA | 142.55000 |
LogP | 2.38120 |
Vapour Pressure | 1.87E-14mmHg at 25°C |
Hazard Codes | Xi |
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