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1228111-63-4

1228111-63-4 Structure

1228111-63-4 Structure
IdentificationBack Directory
[Name]

PF-4634817
[CAS]

1228111-63-4
[Synonyms]

PF-4634817
PF-04634817
D-erythro-Pentitol, 1,5-anhydro-2,3-dideoxy-4-O-methyl-3-[[(1R,3S)-3-(1-methylethyl)-3-[[(1S,4S)-5-[6-(trifluoromethyl)-4-pyrimidinyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]carbonyl]cyclopentyl]amino]-
[Molecular Formula]

C25H36F3N5O3
[MDL Number]

MFCD27987915
[MOL File]

1228111-63-4.mol
[Molecular Weight]

511.58
Chemical PropertiesBack Directory
[Boiling point ]

630.3±55.0 °C(Predicted)
[density ]

1.30±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 50 mg/mL (97.74 mM)
[form ]

Solid
[pka]

8.62±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

PF-0463481 is a potent and orally active dual CCR2/CCR5 antagonist with comparable human and rodent CCR2 potency (rat IC50=20.8 nM), and displays 10-20 fold less rodent CCR5 potency (rat IC50=470 nM). PF-0463481 is safe and well-tolerated and has the potential for the study of diabetic nephropathy[3].
[in vivo]

PF-04634817 (oral administration; 30 mg/kg; once daily; 31 days intervention (weeks 2-15 after Streptozotocin)) intervention at the onset of diabetes (week 2) has no impact on the fasting blood glucose levels in diabetic Nos3-/- 221 mice. The development of diabetes results in a marked increase in the levels of glycated haemoglobin (HbA1c) in Nos3-/- mice. Early intervention with PF-04634817 induces an additional increase in glycated hemoglobin (HbA1c) levels[1].

Animal Model:Nos3-/- mice on the C57BL/6 background[1]
Dosage:30 mg/kg
Administration:Oral administration; once daily; 31 days intervention (weeks 2-15 after Streptozotocin)
Result:Had no impact on the fasting blood glucose levels, but induced an additional increase in HbA1c levels.
[IC 50]

Rat CCR2: 20.8 nM (IC50); CCR5: 470 nM (IC50)
[storage]

Store at -20°C
[References]

[1] Tesch GH, et al. Combined inhibition of CCR2 and ACE provides added protection against progression of diabetic nephropathy in?Nos3-deficient mice.Am J Physiol Renal Physiol.?2019 Dec 1;317(6):F1439-F1449. DOI:10.1152/ajprenal.00340.2019
[2] Gale JD, et al. A CCR2/5 Inhibitor, PF-04634817, Is Inferior to Monthly Ranibizumab in the Treatment of Diabetic Macular Edema. Invest Ophthalmol Vis Sci. 2018 May 1;59(6):2659-2669. DOI:10.1167/iovs.17-22731
[3] Gale JD, et al. Effect of PF-04634817, an Oral CCR2/5 Chemokine Receptor Antagonist, on Albuminuria in Adults with Overt Diabetic Nephropathy. Kidney Int Rep. 2018 Aug 3;3(6):1316-1327. DOI:10.1016/j.ekir.2018.07.010
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1013101-36-4 1301214-47-0 1037589-69-7

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