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2140301-98-8

2140301-98-8 Structure

2140301-98-8 Structure
IdentificationBack Directory
[Name]

PF-04634817 succinate
[CAS]

2140301-98-8
[Synonyms]

PF 4634817 succinate
PF-04634817 succinate
PF 04634817 succinate,PF04634817 succinate
[Molecular Formula]

C29H42F3N5O7
[MDL Number]

MFCD29079008
[MOL File]

2140301-98-8.mol
[Molecular Weight]

629.68
Chemical PropertiesBack Directory
[storage temp. ]

room temp
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[color ]

White to off-white
[InChIKey]

MCRWZBYTLVCCJJ-DKALBXGISA-N
[SMILES]

CO[C@H]1[C@@H](N[C@@H]2CC[C@@](C(N3C[C@@]4([H])N(C5=NC=NC(C(F)(F)F)=C5)C[C@]3([H])C4)=O)(C(C)C)C2)CCOC1
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

PF-0463481 succinate 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 succinate is safe and well-tolerated and has the potential for the study of diabetic nephropathy[3].
[Biological Activity]

Orally availablepotent and selective CCR2/5 receptor antagonist
[in vivo]

PF-04634817 succinate (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)
[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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