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259674-19-6

中文名称:
259674-19-6
中文同义词:
英文名称:
TRPM8 Antagonist
英文同义词:
TRPM8 Antagonist;TRPM8 ANTAGONIST;259674-19-6;TRPM8 antagonist 2;L-Tryptophan, N,N-bis(phenylmethyl)-, methyl ester;Methyl N,N-dibenzyl-L-tryptophanate
CAS号:
259674-19-6
分子式:
C26H26N2O2
分子量:
398.5
EINECS号:
相关类别:
API
Mol文件:
259674-19-6.mol
沸点 
567.5±50.0 °C(Predicted)
密度 
1.195±0.06 g/cm3(Predicted)
储存条件 
Inert atmosphere,2-8°C
酸度系数(pKa)
17.02±0.30(Predicted)
生物活性
TRPM8 antagonist 2 (TRPM8 Antagonist)是一种有效的 TRPM8 的拮抗剂,IC50值为0.2 nM,可用于神经性疼痛综合征的药理治疗。
靶点
Target Value TRPM8 (Cell-free assay) 0.2 nM
Target
Value
TRPM8 (Cell-free assay)
0.2 nM
体外研究
TRPM8 antagonist 2 (Compound 14) is a potent and selective TRPM8 antagonist, with an IC 50 of 0.2 nM, used in the research of neuropathic pain syndromes. TRPM8 antagonist 2 potently inhibits menthol-induced increase in intracellular Ca 2+ levels in Ca 2+ fluorimetric assays in HEK293 cells stably expressing the rat isoform of TRPM8 channels (IC 50 , 40 nM).
体内研究
TRPM8 antagonist 2 (1, 10, and 30 mg/kg, s.c.) shows a marked, dose-dependent antinociceptive activity, and inhibits wet-dog shakes (WDS)-like cold hypersensitivity in mice by 63% at 30 mg/kg. In addition, TRPM8 antagonist 2 (0.1 and 1 μg, s.c.) attenuates Oxaliplatin (OXP)-induced cold allodynia in mice.
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CAS    号: 259674-19-6
规       格:10g/20g/100g/1kg
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详细介绍
英文名:
TRPM8 Antagonist
外观:
纯度:
请咨询卖家
分子式:
C26H26N2O2
分子量:
398.5
中文名称:
259674-19-6
中文同义词:
英文名称:
TRPM8 Antagonist
英文同义词:
TRPM8 Antagonist;TRPM8 ANTAGONIST;259674-19-6;TRPM8 antagonist 2;L-Tryptophan, N,N-bis(phenylmethyl)-, methyl ester;Methyl N,N-dibenzyl-L-tryptophanate
CAS号:
259674-19-6
分子式:
C26H26N2O2
分子量:
398.5
EINECS号:
相关类别:
API
Mol文件:
259674-19-6.mol
沸点 
567.5±50.0 °C(Predicted)
密度 
1.195±0.06 g/cm3(Predicted)
储存条件 
Inert atmosphere,2-8°C
酸度系数(pKa)
17.02±0.30(Predicted)
生物活性
TRPM8 antagonist 2 (TRPM8 Antagonist)是一种有效的 TRPM8 的拮抗剂,IC50值为0.2 nM,可用于神经性疼痛综合征的药理治疗。
靶点
Target Value TRPM8 (Cell-free assay) 0.2 nM
Target
Value
TRPM8 (Cell-free assay)
0.2 nM
体外研究
TRPM8 antagonist 2 (Compound 14) is a potent and selective TRPM8 antagonist, with an IC 50 of 0.2 nM, used in the research of neuropathic pain syndromes. TRPM8 antagonist 2 potently inhibits menthol-induced increase in intracellular Ca 2+ levels in Ca 2+ fluorimetric assays in HEK293 cells stably expressing the rat isoform of TRPM8 channels (IC 50 , 40 nM).
体内研究
TRPM8 antagonist 2 (1, 10, and 30 mg/kg, s.c.) shows a marked, dose-dependent antinociceptive activity, and inhibits wet-dog shakes (WDS)-like cold hypersensitivity in mice by 63% at 30 mg/kg. In addition, TRPM8 antagonist 2 (0.1 and 1 μg, s.c.) attenuates Oxaliplatin (OXP)-induced cold allodynia in mice.
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