Netupitant
CAS No. 290297-26-6
Netupitant ( AGE94200 | AGE 94200 | Ro 67-3189 | Netupitant )
产品货号. M18372 CAS No. 290297-26-6
Netupitant 是一种特异性神经激肽 1 (NK1) 受体拮抗剂 (Ki: 0.95 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥407 | 有现货 |
|
| 10MG | ¥493 | 有现货 |
|
| 25MG | ¥909 | 有现货 |
|
| 50MG | ¥1479 | 有现货 |
|
| 100MG | ¥2295 | 有现货 |
|
| 200MG | ¥3375 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Netupitant
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Netupitant 是一种特异性神经激肽 1 (NK1) 受体拮抗剂 (Ki: 0.95 nM)。
-
产品描述Netupitant is a selective neurokinin 1 (NK1) receptor antagonist with potential antiemetic activity. Netupitant competitively binds to and blocks the activity of the human substance P/NK1 receptors in the central nervous system (CNS), thereby inhibiting NK1-receptor binding of the endogenous tachykinin neuropeptide substance P (SP), which may result in the prevention of chemotherapy-induced nausea and vomiting (CINV).(In Vitro):Netupitant (CID-6451149) binds with high affinity the human NK1 receptor (pKi=9.0) with more than 1000 fold selectivity over the NK2 and NK3 (pKi=5.8 for both sites).Netupitant (1, 10, 100 nM) concentration-dependently antagonizes the stimulatory effects of substance P (SP) showing insurmountable antagonism (pKB=8.87) in CHO NK1 cells.(In Vivo):Netupitant (CID-6451149; 1-10 mg/kg; ip) dose-dependently inhibits SP-elicited the typical scratching, biting and licking response in mice. In gerbils, foot tapping behavior evoked by the intracerebroventricular injection of a NK1 agonist is dose-dependently counteracted by Netupitant given intraperitoneally (ID50 1.5mg/kg) or orally (ID50 0.5mg/kg).Netupitant (0.1-3 mg/kg; i.v.) produces a concentration-dependent inhibition (mean pKB=9.24) of the responses to SP-methylester (SP-OMe) in the detrusor muscle. Netupitant decreases the frequency of reflex bladder contractions.
-
体外实验Netupitant (CID-6451149) binds with high affinity the human NK1 receptor (pKi=9.0) with more than 1000 fold selectivity over the NK2 and NK3 (pKi=5.8 for both sites). Netupitant (1, 10, 100 nM) concentration-dependently antagonizes the stimulatory effects of substance P (SP) showing insurmountable antagonism (pKB=8.87) in CHO NK1 cells.
-
体内实验Netupitant (CID-6451149; 1-10 mg/kg; ip) dose-dependently inhibits SP-elicited the typical scratching, biting and licking response in mice. In gerbils, foot tapping behavior evoked by the intracerebroventricular injection of a NK1 agonist is dose-dependently counteracted by Netupitant given intraperitoneally (ID50 1.5mg/kg) or orally (ID50 0.5mg/kg). Netupitant (0.1-3 mg/kg; i.v.) produces a concentration-dependent inhibition (mean pKB=9.24) of the responses to SP-methylester (SP-OMe) in the detrusor muscle. Netupitant decreases the frequency of reflex bladder contractions.
-
同义词AGE94200 | AGE 94200 | Ro 67-3189 | Netupitant
-
通路Others
-
靶点Other Targets
-
受体NK1
-
研究领域Neurological Disease
-
适应症——
化学信息
-
CAS Number290297-26-6
-
分子量578.59
-
分子式C30H32F6N4O
-
纯度>98% (HPLC)
-
溶解度DMSO : 23.2 mg/mL; 40.10 mM
-
SMILESCc1ccccc1c1cc(ncc1N(C)C(=O)C(C)(C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F)N1CCN(CC1)C
-
化学全称2-(3,5-bis(trifluoromethyl)phenyl)-N,2-dimethyl-N-(6-(4-methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-yl)propanamide
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Rizzi A,etal.In vitro and in vivo pharmacological characterization of the novel NK? receptor selective antagonist Netupitant.Peptides. 2012 Sep;37(1):86-97.
产品手册
关联产品
-
Biotin-Ahx-ω-Conotox...
Biotin-Ahx-ω-Conotoxin GVIA
-
Diosmetinidin chlori...
Diosmetinidin chloride is a natural product for research related to life sciences.
-
Orexin A (human, rat...
Endogenous agonist at orexin receptors (Ki values are 20 and 38 nM for OX1 and OX2 receptors respectively). Stimulates feeding following central administration and may be involved in the control of sleep-wake cycle and other hypothalamic functions.
021-51111890
购物车()
sales@molnova.cn

