PF-06282999
- CAS No.1435467-37-0
- Chemical Name:PF-06282999
- CBNumber:CB93145903
- Molecular Formula:C13H12ClN3O3S
- Formula Weight:325.77
- MOL File:1435467-37-0.mol
- Density 1.52±0.1 g/cm3(Predicted)
- storage temp. room temp
- solubility DMSO:30.0(Max Conc. mg/mL);92.1(Max Conc. mM)
- form powder
- pka 6.85±0.40(Predicted)
- color white to beige
- FDA UNII YO3O4Q2NC8
- UNSPSC Code 51111800
- NACRES NA.77
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H302-H315-H319-H335
- Precautionary statements P261-P305+P351+P338
- Brand: Sigma-Aldrich(India)
- Product number: PZ0375
- Product name : PF-06282999
- Purity: ≥98% (HPLC)
- Packaging: 5MG
- Price: ₹10684.28
- Updated: 2022/06/14
- Buy: Buy
PF-06282999 Chemical Properties,Usage,Production
- Uses PF-06282999 is a potent and selective myeloperoxidase inhibitor which is potential useful for the treatment of cardiovascular diseases.
- Biological Activity PF-06282999 is an orally active thiouracil class myeloperoxidase (MPO) suicide substrate (kinact/KI = 11600 M-1s-1) th at targets MPO heme group for mechanism-based irreversible inactivation wtih high selectivity over thyroid peroxidase (TPO kinact/KI <3 M-1s-1) and heme-containing cytochrome P450 (CYP) isoforms (IC50 >100 μM). PF-06282999 effectively inhibits MPO activity in human blood stimulated by LPS ex vivo (IC50 = 1.9 μM) and in blood of LPS-treated cynomolgus monkeys in vivo (5-80 mg/kg p.o. 1hr post LPS i.v.) with good pharmacokinetics and oral availability (100%/86%/75%/76% in mice/rats/dogs/monkeys). PF-06282999 also exhibits weak PXR activating activity (EC50/Emax = 279 μM/9.36-fold vs.0.8 μM/19.6-fold with rifampin).
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in vivo
PF-06282999 is moderately bound to plasma proteins across preclinical species and humans. The blood/plasma ratios for PF-06282999 are 1.1, 1.1, 0.91, 1.2, and 0.94 in mice, rats, dogs, monkeys, and humans, respectively, suggesting that PF-06282999 is equally distributed into plasma and red blood cells[1]. The in vivo pharmacokinetics of PF-06282999 are examined in greater detail in mice, rats, dogs, and monkeys, wherein it is demonstrated to have low CLp in mice (10.1 mL/min/kg), dogs (3.39 mL/min/kg), monkeys (10.3 mL/min/kg) and moderate CLp in rats (41.8 mL/min/kg). The terminal plasma elimination half-lives (t1/2) range from 0.75 to 3.3 h in the four species. Approximately 26-32% of the iv dose of PF-06282999 is excreted in the unchanged form in rat, dog, and monkey urine, wherein it is also shown that it is well distributed with steady state distribution volumes (Vdss) ranging from 0.5-2.1 L/kg in mice, rats, dogs, and monkeys. Following oral administration, PF-06282999 is rapidly (Tmax=0.78-1.70 h) and well absorbed in mice, rats, dogs, and monkeys with oral bioavailability values of 100%, 86%, 75%, and 76%, respectively[2].
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References
[1] Dong JQ, et al. Pharmacokinetics and Disposition of the Thiouracil Derivative PF-06282999, an Orally Bioavailable, Irreversible Inactivator of Myeloperoxidase Enzyme, Across Animals and Humans. Drug Metab Dispos. 2016 Feb;44(2):209-19. DOI:10.1124/dmd.115.067868
[2] Ruggeri RB, et al. Discovery of 2-(6-(5-Chloro-2-methoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamide (PF-06282999): A Highly Selective Mechanism-Based Myeloperoxidase Inhibitor for the Treatment of Cardiovascular Diseases. J Med Chem. 20 DOI:10.1021/acs.jmedchem.5b00963
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- 抑制剂
- 合成有机化合物配体
- 化合物PF06282999,10 MM DMSO 溶液
- 2-(6-(5-氯-2-甲氧基苯基)-4-氧代-2-硫代氧代-3,4-二氢嘧啶-1(2H)-基)乙酰胺
- 化合物PF06282999
- 6-(5-氯-2-甲氧基苯基)-3,4-二氢-4-氧-2-硫代-1(2H)-嘧啶乙酰胺
- 1435467-37-0
- PF-06282999, 10 mM in DMSO
- PF06282999,Glutathione Peroxidase,PF 06282999,PF-06282999,Inhibitor,inhibit
- PF-06282999 >=98% (HPLC)
- 1(2H)-Pyrimidineacetamide, 6-(5-chloro-2-methoxyphenyl)-3,4-dihydro-4-oxo-2-thioxo-
- PF-06282999;PF 06282999;PF06282999
- CS-2543
- 2-(6-(5-chloro-2-methoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamide
- PF-06282999 (Free base)
- PF-06282999