Free shipping on all orders over $ 500

BMS CCR2 22 

Cat. No. M30109

All AbMole products are for research use only, cannot be used for human consumption.

BMS CCR2 22  Structure
Size Price Availability Quantity
5mg USD 240  USD240 In stock
10mg USD 380  USD380 In stock
25mg USD 740  USD740 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

BMS CCR2 22 is a potent, specific and high affinity CC-type chemokine receptor 2 (CCR2) antagonist with excellent binding affinity (binding IC50 of 5.1 nM) and potent functional antagonism (calcium flux IC50 of 18 nM and chemotaxis IC50 of 1 nM).

Chemical Information
Molecular Weight 593.66
Formula C28H34F3N5O4S
CAS Number 445479-97-0
Form Solid
Solubility (25°C) DMSO 250 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Tianyue Zhai, et al. Cancer Med. Combination therapy with bevacizumab and a CCR2 inhibitor for human ovarian cancer: An in vivo validation study

[2] Michelle L D'Antoni, et al. J Leukoc Biol. Cenicriviroc inhibits trans-endothelial passage of monocytes and is associated with impaired E-selectin expression

[3] Robert J Cherney, et al. Bioorg Med Chem Lett. Benzimidazoles as benzamide replacements within cyclohexane-based CC chemokine receptor 2 (CCR2) antagonists

[4] Percy H Carter, et al. Bioorg Med Chem Lett. Discovery of an orally-bioavailable CC Chemokine Receptor 2 antagonist derived from an acyclic diaminoalcohol backbone

[5] Simone Kredel, et al. J Biomol Screen. High-content analysis of CCR2 antagonists on human primary monocytes

Related CCR Products
C-021 dihydrochloride

C-021 dihydrochloride is a potent CC chemokine receptor-4 (CCR4) antagonist. C-021 dihydrochloride potently inhibits functional chemotaxis in human and mouse with IC50s of 140 nM and 39 nM, respectively.

C-021

C-021 is a potent CC chemokine receptor-4 (CCR4) antagonist. C-021 potently inhibits functional chemotaxis in human and mouse with IC50s of 140 nM and 39 nM, respectively.

AZD-5672 

AZD-5672 is an orally active, potent, and selective CCR5 antagonist (IC50=0.32 nM).

MLN3126 

MLN3126 is an orally active and potent CCR9 antagonist.

AZD2423 

AZD2423 is a potent, selective, orally bioavailable, and non-competitive CCR2 chemokine receptor negative allosteric modulator.

  Catalog
Abmole Inhibitor Catalog




Keywords: BMS CCR2 22  supplier, CCR, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.