Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38111 |
Dimethyl-W84 (dibromide)
Dimethyl-W84 (dibromide) |
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Dimethyl-W84 is a selective allosteric modulator of the M2 muscarinic acetylcholine receptor. It hinders the dissociation of the orthosteric antagonist N-methylscopolamine from the M2 receptor with an EC50 value of 3 nM. | |||
T23524 |
W-84 dibromide
HDMPPA |
AChR | Neuroscience |
W-84 dibromide (HDMPPA) 是 M2胆碱受体的强变构调节剂,是一种非竞争性毒蕈碱乙酰胆碱受体拮抗剂,具有变构效应。它联合阿托品时,可有效地防止有机磷中毒。它阻碍 [3H]N-甲基东莨菪碱解离,能稳定胆碱能拮抗剂-受体复合物。 | |||
T15454 |
GW843682X
GW843682 |
VEGFR; PLK; CDK; PDGFR; Aurora Kinase | Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors |
GW843682X (GW843682) 是 PLK1 和 PLK3 的特异性和 ATP 竞争性抑制剂,IC50 分别为 2.2 nM 和 9.1 nM。 | |||
T6527 |
GW842166X
2-(2,4-二氯苯基氨基)-4-三氟甲基嘧啶-5-羧酸[(四氢吡喃-4-基)甲基]酰胺 |
Cannabinoid Receptor | GPCR/G Protein |
GW842166X 是一种选择性 cannabinoid receptor 2 激活剂,IC50=63 nM。 | |||
T69571 | SEW84 | ||
SEW84 是 Aha1 刺激的 Hsp90(ASH) ATP 酶活性的抑制剂。SEW84 抑制 Aha1 刺激的 Hsp90(ASH) 活性,IC50值为 0.3 μM。SEW84 可用于蛋白质沉积疾病的研究。 | |||
T27517 |
GW848687X
GW-848687X,GW 848687X |
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GW848687X, a potent and selective prostaglandin EP1 receptor antagonist, is used for the treatment of inflammatory pain. | |||
T27516 | GW844520 | ||
GW844520 is a potent and selective inhibitor of the cytochrome bc1 complex of mitochondrial electron transport in P. falciparum. | |||
T36574 |
GW841819X
GW841819X |
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GW841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomains. GW841819X was a single enantiomer but of undefined chirality at the 4-position of the benzodiazepine ring3. GW841819X and JQ1 were recently discovered that bind to the acetyl-lysine binding pocket of BET bromodomains with Kd ranges from 50 to 370 nM [1]. GW841819X bounded to both the individual BD1 and BD2 domains with affinities of 46 and 52.5 nM, respectively. GW841819X-Brd3 interaction was estimated to be around 70... |