找到约 9 条 “OT-R antagonist 1” 相关结果 (用时 0.141 秒)

目录号 产品名称 中文名称 靶点
M29995 OT-R antagonist 1 OT-R antagonist 1 Oxytocin Receptor
Oxytocin receptor antagonist 1
OT-R antagonist 1是一种新型有效的选择性非肽类OT-R拮抗剂, 抑制催产素诱发的细胞内Ca2+活动(IC50=8nM)。
M8700 PCS1055 dihydrochloride PCS1055 dihydrochloride Others
PCS1055 is a potent and selective muscarinic M4 acetylcholine receptor competitive antagonist that exhibits >100-fold selectivity over M1-, M3-, and M5-receptors and 30-fold selectivity at the M2 receptor.
M8856 WAY-100135 dihydrochloride WAY-100135 dihydrochloride 5-HT Receptor
WAY-100135 dihydrochloride is a potent, selective 5-HT1A receptor antagonist (IC50 = 15 nM).
M20515 Emedastine Emedastine Histamine Receptor
Emedastine is a potent, high affinity histamine H1-receptor-selective antagonist with Ki of 1.3 ±0.1 nM for H1-receptors while considerably weaker at H2- (K1 = 49,067 ± 11,113 nM) and H3-receptors (Ki = 12,430 ± 1,282 nM).
M20620 ONO-7300243 ONO-7300243 Others
ONO 7300243, ONO7300243
ONO-7300243 is a novel, potent LPA1(Lysophosphatidic Acid Receptor) antagonist with an IC50 of 160 nM.
M20627 A2AR antagonist 1 A2AR antagonist 1 Adenosine Receptor
A2AR antagonist 1 is a potent A2AR (Adenosine A2A Receptor) antagonist with Ki values of 4 nM and 264 nM for A2AR and A1R, respectively.
M20977 BAY 2416964 BAY 2416964 Aryl hydrocarbon Receptor
BAY 2416964 (compound 192) is a potent and orally active antagonist of aryl hydrocarbon receptor (AhR) with IC50 of 341 nM. BAY 2416964 has the potential in the treatment of solid tumors.
M27999 TASP0376377  TASP0376377  Prostaglandin Receptor
TASP0376377 is a potent and selective CRTH2 antagonist (IC50: 13 nM). TASP0376377 has binding affinity for CRTH2 (IC50: 19 nM).
M58144 Recombinant Human IL-1R1 (HEK293, C-6His) 重组人IL-1R1 蛋白 (HEK293, C-6His) Cytokines and Growth Factors
Interleukin-1 Receptor Type 1; IL-1R-1
Interleukin 1 receptor, type I (IL-1R1) is an interleukin receptor that belongs to the interleukin-1 receptor family. IL-1R1 is an important mediator involved in many cytokine induced immune and inflammatory responses. It binds to interleukin-1 associates with the corecptor IL1RAP to form the high affinity interleukin-1 receptor complex which mediates interleukin-1-dependent activation of NF-kappa-B, MAPK and other pathways. Recombinant IL1 receptor Type I is a potent antagonist of IL1 action.








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