找到约 26 条 “Cannabinoid” 相关结果 (用时 0.117 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
---|---|---|---|
M2012 | AM1241 | AM1241 | Cannabinoid |
AM1241是一种选择性的cannabinoid CB2 receptor激动剂,Ki为3.4 nM,比作用于CB1受体选择性高82倍。 | |||
M2051 | CP 945598 hydrochloride | CP 945598 hydrochloride | Cannabinoid |
Otenabant HCl; Otenabant hydrochloride | |||
Otenabant (CP-945598) HCl是一种有效的,选择性cannabinoid receptor CB1拮抗剂,Ki为0.7 nM,比作用于人类CB2受体选择性高10,000倍。 | |||
M2461 | BML-190 | BML-190 | Cannabinoid |
IMMA | |||
BML-190是一种选择性的cannabinoid CB2 receptor逆向激动剂,Ki为435 nM,比作用于CB1受体选择性高50倍。 | |||
M2552 | CP 945598 | CP 945598 | Cannabinoid |
Otenabant, CP945598 | |||
Otenabant (CP-945598) HCl是一种有效的,选择性cannabinoid receptor CB1拮抗剂,Ki为0.7 nM,比作用于人类CB2受体选择性高10,000倍。 | |||
M3266 | WIN 55212-2 mesylate | WIN 55212-2 mesylate | Cannabinoid |
(R)-(+)-WIN 55212 | |||
win55212 -2是一种有效的 cannabinoid receptor 激动剂,在人克隆CB1和CB2受体上的Ki分别为62.3和3.3 nM。 | |||
M3282 | GW842166X | GW842166X | Cannabinoid |
GW842166X是一种有效的,高选择性cannabinoid receptor CB2受体激动剂,EC50为63 nM,对CB1受体没有显著的活性。 | |||
M6626 | CP 55,940 | CP 55,940 | Others |
CP 55,940 is a potent, non-selective cannabinoid receptor agonist. | |||
M7325 | Rimonabant Hydrochloride | 盐酸利莫那班 | Cannabinoid |
SR 141716A; SR 151716A | |||
Rimonabant hydrochloride 是一种大麻素受体 (cannabinoid receptor) 拮抗剂,高亲和力地选择性结合到中枢大麻素受体 (CB1),Ki 为 2 nM。 | |||
M7418 | Tocrifluor T1117 | Tocrifluor T1117 | Others |
Tocrifluor T1117 is a fluorescent cannabinoid ligand; fluorescent form of AM 251. | |||
M7821 | GW833972A | GW833972A | Others |
GW833972A is a CB2 cannabinoid receptor agonist with 1000-fold selectivity relative to CB1. | |||
M7970 | NIDA-41020 | NIDA-41020 | Others |
NIDA-41020 is a CB1 cannabinoid receptor antagonist. | |||
M8377 | UCM710 | UCM710 | Others |
UCM710 is a dual inhibitor of fatty acid amide hydrolase (FAAH) and α/β hydrolase domain 6 (ABHD6) the enzymes that hydrolyze endocannabinoids. | |||
M8414 | MJN110 | MJN110 | MAGL |
MJN110 is a potent selective inhibitor of MAGL, the enzyme predominantly responsible for the degradation of the endocannabinoid 2-arachidonoylglycerol (2-AG) with >10,000 selectivity over FAAH. | |||
M8596 | WWL70 | WWL70 | Others |
WWL70 is a selective inhibitor of α/β-hydrolase domain-containing 6 (ABHD6), a serine hydrolase that acts as an alternative hydrolase of the endocannabinoid 2-arachidonoylglycerol (2-AG). | |||
M8725 | SR144528 | SR144528 | Others |
SR144528 is a potent and highly selective cannabinoid CB2 receptor inverse agonist. | |||
M8735 | GAT211 | GAT211 | Others |
GAT211 is a positive allosteric modulator (PAM) of cannabinoid CB1 receptor signaling. | |||
M8749 | GAT228 | GAT228 | Others |
GAT228 is the R-(+)-enantiomer of GAT211, a positive allosteric modulator (PAM) of cannabinoid CB1 receptor signaling that was found to amplify the therapeutic effect of endocannabinoids without the negative side effects of psychoactivity or tolerance. | |||
M8985 | LY2828360 | LY2828360 | Cannabinoid |
LY2828360是一种新型强效,选择性和有效的CB2 cannabinoid激动剂。 | |||
M10652 | Voacamine | 老刺木胺 | Cannabinoid |
Voacamine is an indole alkaloid, exhibits potent cannabinoid CB1 receptor antagonistic activity. Voacamine also inhibits P-glycoprotein (P-gp) action in multidrug-resistant tumor cells. | |||
M10891 | Taranabant | Taranabant | Others |
MK-0364 | |||
Taranabant 是一种有效的选择性的 cannabinoid 1 (CB1) 受体反向激动剂,抑制结合和多种激动剂的功能活性,作用于人 CB1R,Ki 为 0.13 nM。 | |||
M45341 | Ajulemic acid | Ajulemic acid | Cannabinoid |
Lenabasum; IP 751 | |||
Ajulemic acid是一种合成的,可口服的 Δ9-四氢大麻酚代谢类似物,同时也是大麻素受体 (cannabinoid receptor) 激动剂,对 hCB1 和 hCB2 的 Ki 值分别为 5.7 nM,56.1 nM,EC50 值分别为 11.6 nM,13.4 nM。 | |||
M25437 | Noladin ether | Noladin ether | Cannabinoid |
Noladin ether 是一种有效的,选择性的 cannabinoid 1 (CB1) 受体激动剂,Ki 值为 21.2 nM。 | |||
M28030 | AM-6538 | AM-6538 | Cannabinoid |
AM6538 是一种长效、高亲和力、伪不可逆的 cannabinoid (CB) 拮抗剂。AM6538 是利莫那班的结构类似物。AM6538可有效评价大麻素完全和部分激动剂的表观疗效。AM6538 可能在未来需要暂时减少大麻素受体可用性的研究中有用。 | |||
M30122 | Ibipinabant | Ibipinabant | Cannabinoid |
SLV319; BMS-646256 | |||
Ibipinabant (SLV319) 是一种有效,选择性和具有口服活性的大麻素 CB1 受体 (cannabinoid CB1 receptor) 的拮抗剂,Ki 值为 7.8 nM。Ibipinabant 对 CB1 的选择性比对 CB2 (Ki=7943 nM) 的选择性高 1000 倍以上。Ibipinabant 可用于肥胖和糖尿病的研究。 | |||
M30173 | NESS 0327 | NESS 0327 | Cannabinoid |
NESS 0327 是一种大麻素 cannabinoid 拮抗剂,对大麻素 CB1 受体具有高选择性。 | |||
M54860 | Vicasinabin | Vicasinabin | Cannabinoid |
RG7774 | |||
Vicasinabin (RG7774) 是一种 cannabinoid receptor 2 (CB2) 的有效激动剂。 |
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