GBR 12935 (Synonyms:1 - (2 - 乙基)-4 - (3 - 苯丙基)哌嗪, 马来酸盐;1-(2-乙基)-4-(3-苯丙基)哌嗪;1-(2-乙基)-4-(3-苯丙基)哌嗪,马来酸盐;(diphenylmethoxy)gbr - 12935,1 - (2 - 乙基)-4 - (3 - 苯丙基)哌嗪;1-[2-(二苯基甲氧基)乙基]-4-(3-苯丙基)哌嗪)
目录号 : KG12423 CAS No. : 76778-22-8 纯度 : 98%
GBR 12935 is a potent, and selective dopamine reuptake inhibitor.IC50 value: Target: dopamine reuptake inhibitorin vitro: The calculated Kd of [3H]GBR-12935 binding to CYP2D6 was 42.2 nM, indicating that GBR-12935 has a high affinity for CYP2D6. The binding of [3H]GBR-12935 to CYP2D6 was decreased partially by substrates or inhibitors of CYP2D isoforms (quinine, quinidine, propranolol, bufuralol, imipramine, and desipramine). Co-perfusion of 100 microM GBR 12909 or GBR 12935 with either 100 microM sulpiride or raclopride produced a significant reduction in the GBR 12909 or GBR 12935 induced increase in the extracellular levels of dopamine to basal levels. In vitro, GBR 12909 (1-9 nM) dose-dependently inhibited active uptake of [3H]dopamine in homogenates of the nucleus accumbens .in vivo: GBR 12935 elevated locomotion to a greater extent in C57BL/6J mice at the maximally active dose of 10 mg/kg. Locomotor stimulation by GBR 12935 remained consistent in both strains with repeated injections. DBA/2J mice became sensitized to cocaine-induced stereotypy with repeated injections. Cocaine induced no stereotypy in C57BL/6J mice on any test day. No stereotypies were induced by GBR 12935 in either strain on any test day .
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10mg
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50mg
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100mg
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分子式
C28H34N2O
分子量
414.58
CAS号
76778-22-8
中文名称
(diphenylmethoxy)gbr - 12935,1 - (2 - 乙基)-4 - (3 - 苯丙基)哌嗪
储存方式
Store at -20°C
The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2
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