EP2受体拮抗剂2 T67946
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
5 mg | 615273-95-5 | ¥995.00 | 询底价 |
500 mg | 615273-95-5 | ¥13,900.00 | 询底价 |
1 mg | 615273-95-5 | ¥428.00 | 询底价 |
10 mg | 615273-95-5 | ¥1,660.00 | 询底价 |
100 mg | 615273-95-5 | ¥6,980.00 | 询底价 |
1 mL | 615273-95-5 | ¥1,130.00 | 询底价 |
25 mg | 615273-95-5 | ¥3,360.00 | 询底价 |
50 mg | 615273-95-5 | ¥4,900.00 | 询底价 |
Product Introduction
Bioactivity
英文名: EP2 receptor antagonist-2
描述: EP2 receptor antagonist-2 (CID891729)为EP2受体拮抗剂,能够抑制PGE2诱导的EP2受体激活,并阻断由N-甲基-D-天冬氨酸(NMDA)引起的乳酸脱氢酶(LDH)释放。
体内活性: SB 209670 (3 mg kg-1, i.v. bolus + 100 micrograms kg-1, i.v. infusion commencing 15 min prior to LPS ; rats) significantly augmented the hypotension as well as the vascular hyporeactivity to NA caused by endotoxaemia.[5] SB 209670 (3 mg kg-1, i.v. bolus given 15 min prior to LPS ; LPS-rats) resulted in a reduction in 6 h-survival from 71% (control) to 30% and 13%, respectively.[5] SB 209670 (3 mg kg-1, i.v. bolus 15 min prior to LPS ; rats) significantly augmented the serum levels of creatinine, bilirubin, GPT and GOT caused by endotoxin.[5] SB 209670 (3 mg kg-1, i.v. bolus ; rats) significantly augmented the metabolic acidosis caused by LPS.[5]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 112.5 mg/mL (363.7 mM)
相关产品: 15-keto-Prostaglandin E2 | MRE-269 | Seratrodast | DG-041 | Sideritoflavone | Ramatroban | CAY10471 Racemate | AZD1981 | GW627368 | Carboprost tromethamine
相关库: Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | GPCR Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途