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| Cat.No. | Product name | Product Description |
| R0016041 | Benzeneacetic acid, α-[(4-methylbenzoyl)amino]- | Benzeneacetic acid, α-[(4-methylbenzoyl)amino]- |
| R0016042 | Benzeneacetic acid, α-[(3-chlorobenzoyl)amino]- | Benzeneacetic acid, α-[(3-chlorobenzoyl)amino]- |
| R0016043 | 顺-3-碘丙烯酸乙酯 | Ethyl cis-3-Iodoacrylate (stabilized with Copper chip) |
| R0016044 | 3-叔丁硫基-2-氨基吡啶 | 3-(tert-Butylthio)pyridin-2-amine |
| R0016045 | 反式-3-(苄氧基)环丁醇 | trans-3-(Benzyloxy)cyclobutanol |
| R0016046 | cis-cyclobutane-1,3-diol | cis-cyclobutane-1,3-diol |
| R0016047 | 6-氨基螺[3.3]庚烷-2-羧酸甲酯盐酸盐 | Methyl 6-aminospiro[3.3]heptane-2-carboxylate hydrochloride |
| R0016048 | 1-(6,7-二氢-5H-吡咯[2,1-C][1,2,4]三唑-3-甲胺 | 6,7-Dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazole-3-methanamine |
| R0016049 | 3-methylsulfonylbicyclo[1.1.1]pentan-1-amine | 3-methylsulfonylbicyclo[1.1.1]pentan-1-amine |
| R0016050 | 2-(8-乙基-3-(甲氧基甲氧基)萘-1-基)-4,4,5,5-四甲基-1,3,2-二氧硼杂环戊烷 | 2-(8-Ethyl-3-(methoxymethoxy)naphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxabor |
| RH131509 | Pyr6 | Pyr6 is a selective inhibitor of TRPC3 with IC50 of 0.49 uM. |
| RH131512 | PSB-12062(N-(p-Methylphenylsulfonyl)phenoxazine) | PSB-12062 is a potent and selective P2X4 antagonist with an IC50 of 1.38 μM for |
| RH131513 | KKL-35 | KKL-35 is a trans-translation tagging reaction inhibitor with an IC50 of 0.9 µM. |
| RH131514 | N'-(4-(二乙基氨基)-2-羟基亚苄基)异烟酰肼 | RSVA405 is a potent, orally active activator of AMPK, with an EC50 of 1 μM. RSVA |
| RH131515 | N'-[4-(diethylamino)-2-hydroxybenzylidene]isonicotinohydrazide | N'-[4-(diethylamino)-2-hydroxybenzylidene]isonicotinohydrazide |
| RH131517 | 四甲基姜黄素 | Tetramethylcurcumin (FLLL31), derived from curcumin, specifically suppresses the |
| RH131518 | IGS-1.76 | IGS-1.76 efficiently inhibits the human NCS-1/Ric8a complex. IGS-1.76 shows a si |
| RH131519 | Anti-inflammatory agent 34 | Anti-inflammatory agent 34 (Compound IVf) is an orally active anti-inflammatory |
| RH131520 | Benzamide, 4-chloro-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)- | Benzamide, 4-chloro-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)- |
| RH131521 | COH-SR4 | COH-SR4 is an AMPK activator. COH-SR4 shows potent anti-proliferative activities |
| RH131522 | N-((6-甲基吡啶-2-基)羰基)苯甲酰胺 | N-((6-Methylpyridin-2-yl)carbamothioyl)benzamide |
| RH131523 | 4-([1,1'-biphenyl]-4-yl)-N-(6-methylpyridin-2-yl)thiazol-2-amine | 4-([1,1'-biphenyl]-4-yl)-N-(6-methylpyridin-2-yl)thiazol-2-amine |
| RH131524 | 5H-Indolo[2,3-b]quinoxaline, 9-methyl- | 5H-Indolo[2,3-b]quinoxaline, 9-methyl- |
| RH131525 | Propanedinitrile, 2-[(5Z)-5-[[4-(dimethylamino)phenyl]methylene]-4-oxo-2-thiazolidinylidene]- | Propanedinitrile, 2-[(5Z)-5-[[4-(dimethylamino)phenyl]methylene]-4-oxo-2-thiazol |
| RH131526 | 5-LOX-IN-1 | 5-LOX-IN-1 (compound 2b) is an inhibitor of human 5-Lipoxygenase (5-LOX) with an |
