
CP 316311
CAS No. 175139-41-0
CP 316311 ( —— )
产品货号. M33325 CAS No. 175139-41-0
CP 316311 是一种有效的,选择性的 CRF1 receptor 拮抗剂,IC50 值为 6.8 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥3786 | 有现货 |
![]() ![]() |
5MG | ¥4304 | 有现货 |
![]() ![]() |
10MG | ¥5515 | 有现货 |
![]() ![]() |
25MG | ¥7257 | 有现货 |
![]() ![]() |
50MG | ¥9853 | 有现货 |
![]() ![]() |
100MG | ¥12852 | 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CP 316311
-
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CP 316311 是一种有效的,选择性的 CRF1 receptor 拮抗剂,IC50 值为 6.8 nM。
-
产品描述CP 316311 is a potent and selective CRF1 receptor antagonist with an IC50 value of 6.8 nM.
-
体外实验CP 316311 fully antagonizes CRF-stimulated adenylate cyclase activity in rat cortex and at human CRF1 receptors endogenously expressed in IMR32 cells with apparent Ki values of 7.6 and 8.5 nM, respectively.
-
体内实验CP 316311 (3.2 mg/kg) inhibits 125I-oCRF binding by >80% in rats. CP 316311 significantly attenuates activation of the hypothalamic?pituitary?adrenal (HPA) axis, with an MED value of 10 mg/kg, p.o. CP 316311 blocks the effects of both the exogenous and endogenous CRF in the CNS. CP 316311 blocks the effects induced by the exogeneous or endogeneous CRF in the brain in rat models.
-
同义词——
-
通路GPCR/G Protein
-
靶点CRF Receptor
-
受体CRFR
-
研究领域——
-
适应症——
化学信息
-
CAS Number175139-41-0
-
分子量327.46
-
分子式C21H29NO2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESN=1C(OC=2C(=CC(=CC2C)C)C)=C(C(OC(CC)CC)=CC1C)C
-
化学全称——
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. Chen YL, et al. Synthesis and SAR of 2-aryloxy-4-alkoxy-pyridines as potent orally active corticotropin-releasing factor 1 receptor antagonists. J Med Chem. 2008 Mar 13;51(5):1377-84.?
产品手册




关联产品
-
CRF (6-33)
Corticotropin-releasing factor binding protein (CRFBP) inhibitor peptide; displaces CRF from CRFBP. Suppresses body weight gain and increases motor activity in obese rats in vivo.
-
Urocortin III, mouse
Mouse UcnIII is expressed predominantly in regions of the brain known to be involved in stress-related behaviours, and its expression in the hypothalamus increases following restraint.
-
4-(2-chloro-4-methox...
4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1A)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine is an enantiomeric counterpart of SSR-125543. SSR-125543 is a potent CRF-R1 antagonist with Ki = 1.0 nM for human CRF-R1.