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CP-105696

Catalog No. T15002 CAS 158081-99-3

Synonyms: Pfizer 105696

CP-105696 is a potent and selective leukotriene B4 (LTB4) receptor antagonist for the study of allograft rejection.

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CP-105696, CAS 158081-99-3

Pack Size	Availability	Price/USD
5 mg	In stock	$ 128.00
10 mg	In stock	$ 215.00
1 mL * 10 mM (in DMSO)	In stock	$ 146.00

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Purity: 99.78%

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Description	CP-105696 is a potent and selective leukotriene B4 (LTB4) receptor antagonist for the study of allograft rejection.
Targets&IC50	LTB4:8.42±0.26 nM
In vitro	CP-105696 is a structurally novel, selective, and potent LTB4 receptor antagonist. In vitro, it inhibits [3H]LTB4 (0.3 nM) binding to high-affinity LTB4 receptors on human neutrophils with an IC50 value of 8.42±0.26 nM. Scatchard analyses of [3H]LTB4 binding to these high-affinity receptors indicate that CP-105696 acts as a noncompetitive antagonist.In a noncompetitive manner, CP-105696 inhibits human neutrophil chemotaxis mediated by LTB4 (5 nM) with an IC50 value of 5.0±2.0 nM. Scatchard analyses of [3H]LTB4 binding to low-affinity receptors on neutrophils indicate that CP-105696 acts as a competitive antagonist at this receptor. Furthermore, CP-105696 competitively inhibits LTB4-mediated CD11b upregulation on human neutrophils (pA2=8.03±0.19).At 10 μM, CP-105696 does not inhibit either human neutrophil chemotaxis or CD11b upregulation mediated through alternate G-protein coupled chemotactic factor receptors (i.e., C5a, IL-8, PAF). In isolated human monocytes, CP-105696 inhibits LTB4 (5 nM)-mediated Ca2+ mobilization with an IC50 value of 940±70 nM[2].
In vivo	At a dose of 50 mg/kg/day (for 28 days), B10.BR (H2k) allografts transplanted into C57Bl/6 (H2b) recipients show significant protection, as evidenced by the mean survival time compared to control grafts (27±20 days [n=10] vs. 12±6 days [n=14]; P=0.0146). Utilizing an induction protocol (day -1 to day 3), CP-105696 at 100 mg/kg/day significantly prolongs allograft survival (33±23 days [n=9]; P=0.0026), while CP-105696 at 10 mg/kg/day does not (18±16 days [n=8]; P=0.1433). Syngeneic grafts exhibit indefinite survival (n=11).Immunohistological evaluation of allografts at rejection reveals a mononuclear cell infiltrate primarily composed of CD3+ and CD11b+ (Mac-1+) cells, which are infrequent in syngeneic grafts. Allografts from mice treated with CP-105696 at 50 or 100 mg/kg/day demonstrate a selective reduction in β2-integrin (Mac-1) expression on monocytes/macrophages, as indicated by CD11b staining density compared with allograft controls[1].

Synonyms	Pfizer 105696
Molecular Weight	428.52
Formula	C28H28O4
CAS No.	158081-99-3

Storage

store at low temperature

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 80 mg/mL (186.69 mM), Sonication is recommended.

References and Literature

1. Weringer EJ, et al. Antagonizing leukotriene B4 receptors delays cardiac allograft rejection in mice. Transplantation. 1999 Mar 27;67(6):808-15. 2. Showell HJ, et al. The in vitro and in vivo pharmacologic activity of the potent and selective leukotriene B4 receptor antagonist CP-105696. J Pharmacol Exp Ther. 1995 Apr;273(1):176-84.

Related compound libraries

This product is contained In the following compound libraries：

Immunology/Inflammation Compound Library

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Keywords

CP-105696 158081-99-3 Immunology/Inflammation LTR CP 105696 CP105696 Pfizer 105696 inhibitor inhibit

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