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| Cat.No. | Product name | Product Description |
| R21082238 | Desmethoxyyangonin | Desmethoxyyangonin is a reversible inhibitor of MAO-B. |
| R21082239 | MK2-IN-3 | MK2-IN-3 is a potent, cell-permeable inhibitor of mitogen-activated protein kina |
| R21082240 | NS8593 hydrochloride | NS8593 is a potent selective INHIBITOR of SK Channels (small-conductance calcium |
| R21082241 | KL001 | KL001 is a cryptochrome protein (CRY) stabilizer that specifically interacts wit |
| R21082242 | Caroverine HCL | Caroverine HCL is a potent, competitive and reversible antagonist of NMDA and AM |
| R21082243 | BSJ-4-116 | BSJ-4-116 is a highly potent and selective CDK12 degrader (PROTAC) with an IC50 |
| R21082244 | MK-0591 | MK591 (Free ACID) is a FLAP specific inhibitor with IC50 of 1.6 nM. |
| R21082245 | Ertugliflozin L-pyroglutamic acid | Ertugliflozin (PF-04971729) l-pyroglutamic Acid is a potent, selective, and oral |
| R21082246 | obovatol | Obovatol has antioxidant, neuroprotective, antiinflammatory, antithrombotic and |
| R21082247 | Tandospirone | Tandospirone(SM-3997) is a partial agonist of 5-HT1A receptor with a Ki of 27 nM |
| R21082248 | AH 7614 | Ah-7614 is an effective and selective FFA4 antagonist with pIC50 values of 7.1, |
| R21082250 | ZLDI-8 | ZLDI-8 is an inhibitor of Notch activating/cleaving enzyme ADAM-17 and inhibits |
| R21082251 | K-604 dihydrochloride | K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransfe |
| R21082252 | AZD-8529 mesylate | AZD-8529 mesylate is a potent, highly selective and orally bioavailable positive |
| R21082253 | AZD-8529 | Azd-8529 is an effective, highly selective, oral positive regulator of mGluR2 wi |
| R21082254 | ATX inhibitor 1 | ATX inhibitor 1 is effective ATX (IC50=1.23 nM, FS-3; 2.18 nM, bis-PNPP) inhibi |
| R21082255 | KDM5-C70 | KDM5-C70 is an ethyl ester derivative of KDM5-C49. KDM5-C70 is an effective, cel |
| R21082256 | EGFR-IN-8 | EGFR-IN-8 can be a promising candidate for further development to target EGFR TK |
| R21082257 | TCH-165 | TCH-165 is a small molecule modulator of proteasome assembly, resulting in an in |
| R21082258 | KDM5-IN-1 | Kdm5-in-1 is a highly selective and orally active KDM5 inhibitor with an IC50 va |
| R21082259 | Paradol | 6-paradol is a pungent phenolic substance found in ginger and other Zingiberacea |
| R21082260 | Boc-Dap-NE | Boc-Dap-NE used in the synthesis of antibody-drug conjugates (ADCs).It is a clea |
| R21082261 | Z-VAD(OH)-FMK (Caspase Inhibitor VI) | Z-VAD-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor. |
| R21082262 | Z-YVAD-FMK | AA-Z-YVAD-FMK is a Irreversible caspase-1 inhibitor,with anti-inflammatory and a |
| R21082263 | (1R, 3S, 4R)-ent-Entecavir | Entecavir (SQ 34676; BMS 200475) is a selective and effective HBV inhibitor. T |
