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CTEP (RO4956371) (Synonyms: RO 4956371; mGluR5 inhibitor)

رقم الكتالوجGC16619

CTEP (RO4956371) (RO 4956371) هو مضاد خيفي جديد طويل المفعول ومتوفر بيولوجيًا عن طريق الفم لمستقبلات mGlu5 مع IC50 من 2.2 نانومتر ، ويظهر انتقائية أكثر من 1000 ضعف على مستقبلات mGlu الأخرى.

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CTEP (RO4956371) التركيب الكيميائي

Cas No.: 871362-31-1

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
107٫00
متوفر
5mg
88٫00
متوفر
10mg
133٫00
متوفر
25mg
286٫00
متوفر
50mg
527٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

CTEP is a potent, long-acting, and orally bioavailable inhibitor of metabotropic glutamate receptor 5 (mGlu5) with IC50 value of 11.4nM [1].

CTEP is a negative allosteric modulator of mGlu5 and has inverse agonist activity. In the in vitro binding assay, CTEP binds to human, mouse and rat mGlu5 with Kd values of 1.7nM, 1.8nM and 1.5 nM, respectively. In HEK293 cells expressing mGlu5, CTEP inhibits quisqualate-induced Ca2+ mobilization and inositol phosphate accumulation with IC50 value of 11.4nM and 6.4nM, respectively. In addition, it shows an IC50 value of 40.1nM in the IP accumulation assay, demonstrating its inverse agonist activity. CTEP is proved to be a highly selective inhibitor of mGlu5. It shows no significant activity against mGlu1, mGlu2, mGlu3, mGlu4, mGlu6, mGlu7 or mGlu8 at concentration up to 10μM [1].

In the in vivo Vogel conflict drinking test, CTEP markedly increases drinking time at doses of 0.3mg/kg. In adult C57BL/6 mice brain, CTEP displaces the mGlu5 antagonist ABP688 in the regions expressing mGlu5 by 50% at dose of 77.5 ng/g [1].

References:
[1] Lindemann L, Jaeschke G, Michalon A, et al. CTEP: a novel, potent, long-acting, and orally bioavailable metabotropic glutamate receptor 5 inhibitor. Journal of Pharmacology and Experimental Therapeutics, 2011, 339(2): 474-486.

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