Cannabinoid Receptor(大麻素受体)
The cannabinoid receptor (CB1 and CB2) is a member of G-protein coupled receptor which plays a significant role in physiologic processes such as cognitive and immune functions.
Products for Cannabinoid Receptor
- Cat.No. 产品名称 Information
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GC17116
Hemopressin (rat)
血红蛋白Α1链HEMOPRESSIN(RAT)
Hemopressin (rat) 是一种衍生自血红蛋白 α1 链的九肽,最初是从大鼠脑匀浆中分离出来的。 -
GC13660
JD5037
JD5037 是一种有效的 CB1R 拮抗剂,IC50 为 1.5 nM。
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GC16644
JTE 907
N-(1,3-苯并二氧戊环-5-基甲基)-1,2-二氢-7-甲氧基-2-氧代-8-(戊氧基)-3-喹啉甲酰胺
A selective CB2 receptor inverse agonist -
GC18496
Leelamine (hydrochloride)
脱氢松香胺盐酸盐
An inhibitor of pyruvate dehydrogenase kinase -
GC50273
LEI 101 hydrochloride
Potent and selective CB2 partial agonist; orally biovailable
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GC12538
LH 21
Weak CB1 antagonist
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GC13318
LY 320135
[6-甲氧基-2-(4-甲氧基苯基)苯并[B]呋喃-3-基](4-氰基苯基)甲酮
A selective CB1 receptor antagonist -
GC19231
LY2828360
A selective CB2 receptor agonist
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GC12420
MAFP
Methyl Arachidonyl Fluorophosphonate
An inhibitor of MAGL, FAAH, cPLA2, and iPLA2 -
GC18866
MCHB-1
NMethylcyclohexyl benzimidazole analog 1
A CB2 receptor agonist -
GC91240
Methyl γ-Linolenyl Fluorophosphonate
MγLnFP
一种磷脂酶抑制剂
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GC15788
MJ 15
A potent CB1 receptor antagonist
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GC11453
ML-191
CCG-152883,CID-23612552
An antagonist of GPR55 -
GC14626
MM-22
biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide
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GC71262
Monlunabant
Monlunabant ((S)-MRI-1891)是一种固体分散化合物,也是大麻素CB1受体抑制剂。
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GC70724
MRL-650
MRL-650(CB1反向激动剂1)是CB1受体的高效、口服活性和特异性反向激动剂,CB1和CB2受体的IC50分别为7.5 nM和4100 nM。
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GC14750
N-Arachidonylglycine
N-Arachidonyl Glycine, NAGly
A metabolite of anandamide with analgesic activity -
GC31536
N-Oleoyl glycine
A putative substrate for peptidyl glycine α-
amidating enzyme -
GC18041
NESS 0327
A potent CB1 receptor antagonist
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GC13267
NIDA 41020
A CB1 receptor antagonist
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GC69562
Nimacimab
RYI-018
Nimacimab (RYI-018) 是一种靶向 CB1 受体 的负变构调节单克隆抗体。Nimacimab 可用于代谢性疾病研究。 -
GC17699
O-1821
Cannabidiorcin, Cannabidiorcol, Cannabidiorocol, CBD-C1, CBDO
An analog of O-1918, a selective antagonist of a non-CB1/CB2 receptor -
GC13847
O-1918
1,3-二甲氧基-5-甲基-2-[(1R,6R)-3-甲基-6-(1-甲基乙烯基)-2-环己烯-1-基]苯
A selective antagonist of abnormal cannabidiol-mediated effects -
GC14042
Oleamide
油酸酰胺
An amide of oleic acid and agonist of CB1 receptors -
GC30966
Olivetol
橄榄醇
An Analytical Reference Standard -
GC30504
Olorinab (APD 371)
APD 371
Olorinab (APD 371) (APD 371) 是一种高效、选择性和完全有效的 2 型大麻素受体 (CB2) 激动剂,对 hCB2 的 EC50 为 6.2 nM。
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GC10664
Org 27569
ORG275695-氯-3-乙基-N-[2-[4-(1-哌啶基)苯基]乙基-1H-吲哚-2-甲酰胺
Org 27569 是一种有效的 CB1 受体变构调节剂,可增加激动剂的结合,但阻断激动剂诱导的 CB1 信号传导。 -
GC10843
Otenabant
奥替那班,CP 945598;CP-945598;CP945598
Otenabant 是一种有效的选择性大麻素受体 CB1 拮抗剂,Ki 为 0.7 nM,对人 CB2 受体的选择性高 10,000 倍。 -
GC47866
Palmitoyl Ethanolamide-d5
Palmidrold5, PEA15,15,16,16,16d5
A neuropeptide with diverse biological activities -
GC16548
Palmitoylisopropylamide
PIA
FAAH inhibitor -
GC16171
PF 514273
CB1 receptor antagonist
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GC70955
PGN36
PGN36(化合物18)是一种选择性大麻素CB2受体(CB2R)拮抗剂,Ki为0.09µM。
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GC50387
PM 226
PM 226 是一种选择性大麻素 CB2R 激动剂 (Ki (CB2R)\u003d13 nM; EC50 (CB2R)\u003d39 nM; Ki (CB1R) \u003e40 μM;),在体外和体内具有神经保护特性。
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GC12920
Pregnenolone
孕烯醇酮; 3β-Hydroxy-5-pregnen-20-one
A natural steroid hormone -
GC36963
Pregnenolone monosulfate
3β-Hydroxy-5-pregnen-20-one monosulfate
Pregnenolone monosulfate 是大麻素 CB1 受体的特异性抑制剂。 -
GC44680
Pregnenolone sulfate (sodium salt)
3β-Hydroxy-5-pregnen-20-one monosulfate sodium
Pregnenolone sulfate (sodium salt)是一种孕烯醇酮的神经活性代谢产物,对氨基丁酸A型受体(GABAAR)的IC50值为26±2μmol/L,对不含γ亚基的GABAAR的IC50值为18±3μmol/L。 -
GC65106
Pregnenolone-d4-1
妊娠烯醇酮-D4,3β-Hydroxy-5-pregnen-20-one-d4-1
Pregnenolone-d4-1 (3β-Hydroxy-5-pregnen-20-one-d4-1) 是一种氘代标记的 Pregnenolone。Pregnenolone (3β-Hydroxy-5-pregnen-20-one) 是一种功能强大的神经甾体,是包括甾体酮在内的各种甾体激素的主要前体。Pregnenolone 是大麻素 CB1 受体的信号传导特异性抑制剂,抑制由 CB1 受体介导的四氢大麻酚 (THC) 的作用。Pregnenolone 可以保护大脑免受大麻中毒。Pregnenolone 也是一种 TRPM3 通道激活剂,也可以弱激活 TRPM1 通道。 -
GC50435
PSB CB5
CID-85469571
A GPR18 antagonist -
GC74008
PSB-KK1415
PSB-KK1415是人类孤儿G蛋白偶联受体GPR18的选择性激动剂,EC50为19.1nM。
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GC41087
PSB-SB1202
A CB1 and CB2 receptor agonist
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GC50143
PSNCBAM-1
1-(4-氯苯基)-3-[3-[6-(吡咯烷-1-基)吡啶-2-基]苯基]脲
A CB1 receptor antagonist -
GC14177
R-1 Methanandamide Phosphate
R-1MAP,(R)-(+)-Arachidonyl-1'-Hydroxy-2'-Propylamide Phosphate
A water soluble prodrug AEA analog -
GC13190
R-Palmitoyl-(1-methyl) Ethanolamide
R-1 PMA
A synthetic analog of palmitoyl ethanolamide -
GC17259
Rimonabant
利莫那班; SR141716
A potent and selective CB1 receptor antagonist -
GC16466
Rimonabant hydrochloride
盐酸利莫那班; SR 141716A Hydrochloride
A potent and selective CB1 receptor antagonist -
GC63617
RTICBM-189
RTICBM-189 is a potent, brain-penetrant allosteric modulator of the cannabinoid type-1 (CB1) receptor with a pIC50 of 7.54 in Ca2+ mobilization assay.
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GC66413
RVD-Hpα TFA
RVD-Hpα TFA is the N-terminally extended form of human hemopressin that acts as a selective CB1 receptor agonist. RVD-Hpα TFA increases intracellular Ca2+ levels in cells expressing CB1 receptors in vitro. RVD-Hpα TFA also high affinity CB2 positive allosteric modulator (Ki=50 nM).
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GC13605
S-1 Methanandamide
(S)-(−)-Arachidonyl-1'-Hydroxy-2'-Propylamide
A CB1 receptor ligand -
GC12868
S-2 Methanandamide
(S)-(+)-Arachidonyl-2'-Hydroxy-1'-Propylamide
A potent CB1 receptor agonist -
GC67972
S-777469
S-777469 是一种选择性,具有口服活性的大麻素 2 型受体 (CB2) 激动剂,Ki 为 36 nM。S-777469 以剂量依赖性方式显著抑制化合物 48/80 诱导的小鼠抓挠行为。S-777469 通过 CB2 兴奋抑制瘙痒信号的传递,从而产生止痒作用。