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Cat.No. Product name Product Description
R11333 8-hydroxy-5-[1-hydroxy-2-[2-(4-methoxyphenyl)propan-2-ylamino]ethyl]-1H-quinolin-2-one N/A
R11334 Brequinar (Synonyms: DUP785; NSC 368390) Brequinar (DUP785) is a potent inhibitor of dihydroorotate dehydrogenase, with p
R11335 Brequinar sodium Brequinar Sodium is the sodium salt form of Brequinar. Brequinar inhibits the en
R11336 TRIMIPRAMINE N/A
R11337 Metiamide Metiamide (SK&F 92058) is a histamine H2-receptor antagonist developed from
R11338 Tasosartan (Synonyms: WAY-ANA 756) Tasosartan is a long-acting angiotensin II (AngII) receptor 
R11339 Alvameline tartrate N/A
R11340 PNU-282987 PNU-282987 is a selective α7 nicotinic acetylcholine receptor(α7 nAChR) agonist
R11341 Pd 173212 N/A
R11342 JTC 801;JTC-801;JTC801 JTC-801 is a selective opioid receptor-like1 (ORL1) receptor antagonist, binding
R11343 Loxiglumide (CR-1505) Loxiglumide is a cholecystokinin (CCK-1) receptor antagonist.
R11344 methyl 4-[[[4-[[[4-[[(tert-butyloxy)carbonyl]amino]-1-methyl-pyrrol-2-yl]carbonyl]amino]-1-methyl-pyrrol-2-yl]carbonyl]amino]-1-methyl-pyrrole-2-carboxylic acid N/A
R11345 XEN445 XEN445 is a potent and selective EL inhibitor(IC50=0.237 uM), that showed good A
R11348 AZD4721 Vimnerixin (AZD4721) 是酸性 CXC 趋化因子受体 2 (CXCR2) 的有效且具有口服活性的拮抗剂。Vimnerixin 具有研究炎症性疾
R11349 LRRK2-IN-1 LRRK2-IN-1 is a potent and selective LRRK2 inhibitor with IC50&nb
R11350 SB-332235 N/A
R11352 (S)-4-ETHYL-4-HYDROXY-7,8-DIHYDRO-1H-PYRANO[3,4-F]INDOLIZINE-3,6,10(4H)-TRIONE N/A
R11353 3-AMINO-4,5-DIHYDRONAPHTHO[1,2-B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER N/A
R11354 Alvameline N/A
R11355 Tolvaptan N/A
R11356 Nutlin (3a) (Synonyms: Nutlin-3a chiral) Nutlin 3a 是 Nutlin-3 的活性异构体,为一种鼠双微体 2 (MDM2) 抑制剂,抑制 MDM2-p53 相互作用,且稳定 p53 蛋白,因此诱
R11357 Tirabrutinib hydrochloride;ONO-4059 hydrochloride; GS-4059 hydrochloride Tirabrutinib (ONO-4059) hydrochloride is a selective and novel inhibitor of BTK
R11359 ACTB-1003 N/A
R11360 Dubermatinib (Synonyms: TP-0903) Dubermatinib (TP-0903) is a potent and selective Axl receptor tyrosin
R11361 ML281 ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM. ML281 showed
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