>>Signaling Pathways>> GPCR/G protein>> CCR>>BX 471

BX 471 (Synonyms: ZK-811752)

Catalog No.GC14519

BX 471(ZK-811752)은 Ki가 1nM인 경구 활성, 강력하고 선택적인 비펩타이드성 CCR1 길항제이며 CCR2, CCR5 및 CXCR4에 비해 CCR1에 대해 250배 선택성을 나타냅니다.

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BX 471 Chemical Structure

Cas No.: 217645-70-0

Size 가격 재고 수량
10mg
US$134.00
재고 있음
50mg
US$573.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

Ki: 1 nM to 5.5 nM

The CC chemokine receptor-1 (CCR1) is a prime therapeutic target for treating autoimmune diseases. BX 471 is a potent, selective, and orally active antagonist of the CC Chemokine Receptor-1.

In vitro: Competition binding studies revealed that BX 471 was able to displace the CCR1 ligands macrophage inflammatory protein-1a, RANTES, and monocyte chemotactic protein-3 with high affinity. BX 471 was a potent functional antagonist based on its ability to inhibit plenty of CCR1-mediated effects. BX 471 also demonstrated a greater than 10,000-fold selectivity for CCR1 compared with 28 G-protein-coupled receptors [1].

In vivo: Pharmacokinetic studies demonstrated that BX 471 was orally active with a 60% bioavailability in dogs. Furthermore, in a rat experimental allergic encephalomyelitis model of multiple sclerosis, BX 471 effectively reduces disease [1].

Clinical trial: Up to now, BX 471 is still in the preclinical development stage.

Reference:
[1] Liang M, Mallari C, Rosser M, Ng HP, May K, Monahan S, Bauman JG, Islam I, Ghannam A, Buckman B, Shaw K, Wei GP, Xu W, Zhao Z, Ho E, Shen J, Oanh H, Subramanyam B, Vergona R, Taub D, Dunning L, Harvey S, Snider RM, Hesselgesser J, Morrissey MM, Perez HD.  Identification and characterization of a potent, selective, and orally active antagonist of the CC chemokine receptor-1. J Biol Chem. 2000 Jun 23;275(25):19000-8.

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