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SB-277011 hydrochloride (Synonyms: SB-277011A hydrochloride)

رقم الكتالوجGC60334

SB-277011 hydrochloride (SB-277011A hydrochloride) هو أحد مضادات مستقبلات الدوبامين D3 (D3R) القوية ، والانتقائية ، والمتوفرة بيولوجيًا ، والتي تخترق الدماغ بقيم Ki تبلغ 10.7 نانومتر و 11.2 نانومتر عند القوارض والبشر D3R ، على التوالي

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SB-277011 hydrochloride التركيب الكيميائي

Cas No.: 215804-67-4

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
95٫00
متوفر
5mg
90٫00
متوفر
10mg
144٫00
متوفر
50mg
450٫00
متوفر
100mg
765٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description of SB-277011 hydrochloride

SB-277011 hydrochloride (SB-277011A hydrochloride) is a potent, selective, orally bioavailable and brain penetrate dopamine D3 receptor (D3R) antagonist with Ki values of 10.7 nM and 11.2 nM at rodent and human D3R, respectively. SB-277011 hydrochloride displays 80- to 100-fold selectivity over other dopamine receptors with pKis of 8.0, 6.0, <5.2, and 5.9 for D3, D2, 5-HT1B, and 5-HT1D receptors, respectively[1][2].

SB-277011 hydrochloride has an excellent pharmacokinetic profile, exhibits oral bioavailability 43%, half-life:2.0 h, plasma clearance 19 mL/min/kg) and to be highly brain-penetrant (brain:blood ratio of 3.6:1), with a clean P450 profile in the rat[1].SB-277011 hydrochloride (SB 277011; 3 mg/kg, p.o.) completely reverses the effects of quinelorane in the nucleus accumbens, but does not reverse the effects of quinelorane in the striatum at 93 mg/kg in rats[1].SB-277011 (intraperitoneal injection; 12.5-25 mg/kg) significantly and dose-dependently reduces intravenous cocaine self-administration under both low fixed-ratio and progressive-ratio reinforcement conditions in rats. When it increases to 50 mg/kg, SB-277011 can significantly inhibit basal and cocaine-enhanced locomotion in rats[2].

[1]. Stemp G, et al. Design and synthesis of trans-N-[4-[2-(6-cyano-1,2,3, 4-tetrahydroisoquinolin-2-yl)ethyl]cyclohexyl]-4-quinolinecarboxamide (SB-277011): A potent and selective dopamine D(3) receptor antagonist with high oral bioavailability and CNS penetration in the rat. J Med Chem. 2000 May 4;43(9):1878-85. [2]. Rui Song, et al. YQA14: A Novel Dopamine D3 Receptor Antagonist That Inhibits Cocaine Self-Administration in Rats and Mice, but Not in D3 Receptor-Knockout Mice. Addict Biol

Chemical Properties of SB-277011 hydrochloride

Cas No. 215804-67-4 SDF
المرادفات SB-277011A hydrochloride
Canonical SMILES O=C(C1=CC=NC2=CC=CC=C21)N[C@@H]3CC[C@H](CC3)CCN4CC5=C(CC4)C=C(C#N)C=C5.[H]Cl
Formula C28H31ClN4O M.Wt 475.02
الذوبان DMSO: 50 mg/mL (105.26 mM); Water: 16.67 mg/mL (35.09 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of SB-277011 hydrochloride

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.1052 mL 10.5259 mL 21.0517 mL
5 mM 0.421 mL 2.1052 mL 4.2103 mL
10 mM 0.2105 mL 1.0526 mL 2.1052 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

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Review for SB-277011 hydrochloride

Average Rating: 5 ★★★★★ (Based on Reviews and 12 reference(s) in Google Scholar.)

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