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| Cat.No. | Product name | Product Description |
| R2304283 | NLX-204HCl | NLX-204 is a potent, selective agonist of ERK1/2 phosphorylation-preferring sero |
| R2304284 | Practolol | Practolol is a potent and selective β1-adrenergic receptor antagonist. Practolol |
| R2304285 | Bisindolylmaleimide VIII acetate | Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) is a potent and selective |
| R2304286 | Ro0335 | RO-0335 is a novel and potent diphenylether nonnucleoside reverse transcriptase |
| R2304287 | CITCO | CITCO, an imidazothiazole derivative, is a selective Constitutive androstane rec |
| R2304288 | JNJ-18038683 | JNJ-18038683 is a 5-Hydroxytryptamine Type 7 (5-HT7) receptor antagonist, with p |
| R2304289 | Aumitin | Aumitin is a diaminopyrimidine-based autophagy inhibitor which inhibits mitochon |
| R2304290 | RAD51-IN-1 | RAD51-IN-1, a derivative of B02, is a potent inhibitor of RAD51. RAD51-IN-1 can |
| R2304291 | MRGPRX1 agonist 1 | MRGPRX1 agonist 1 is a highly potent agonist of MRGPRX1 (Mas-related G-protein-c |
| R2304292 | Menin-MLL inhibitor 20 | Menin-MLL inhibitor 20 is an irreversible menin-MLL interaction inhibitor with a |
| R2304293 | SMS1-IN-1 | SMS1-IN-1, compound SAPA 1j, is a novel and the most potent sphingomyelin syntha |
| R2304294 | LMPTP INHIBITOR 1 dihydrochloride | LMPTP INHIBITOR 1 (dihydrochloride) is a selective inhibitor of low molecular we |
| R2304295 | Gemfibrozil 1-O-β-glucuronide | Gemfibrozil 1-O-β-Glucuronide, a metabolite of Gemfibrozil (CI-719; HY-B0258), i |
| R2304296 | SN-38 glucuronide (SN-38G) | SN-38 glucuronide is an inactive metabolite of the cancer drug Irinotecan. Irino |
| R2304297 | PF-06821497 | PF-06821497 is a selective inhibitor of EZH2 with significant tumor growth inhib |
| R2304298 | Dydrogesterone | Dydrogesterone is a potent, orally active progestogen indicated in a wide variet |
| R2304299 | 7-CKA sodium salt | 7-Chlorokynurenic acid sodium salt (7-CKA sodium salt) is a potent and selective |
| R2304300 | AM103 | AM 103 is a potent and selective FLAP inhibitor, with an IC50 value of 4.2 nM. |
| R2304301 | E-7386 | E-7386 is an orally active CBP/beta-catenin modulator. |
| R2304302 | Iptacopan (LNP023) | Iptacopan (LNP023) is a first-in-class, orally bioavailable, highly potent and h |
| R2304303 | VH032 | VH032 is a VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) pro |
| R2304304 | UDP-D-Glucose disodium salt | Uridine 5′-diphosphoglucose disodium salt (UDP-D-Glucose disodium salt) is the p |
| R2304305 | (S)-PF-06873600 | (S)-PF-06873600 is the S enantiomer of PF-06873600 which is an inhibitor of CDK. |
| R2304306 | SB9200;GS-9992;Inarigivir soproxil | Inarigivir soproxil (SB9200) is an agonist of innate immunity and shows potent a |
| R2304307 | Y-27632 | Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II, wi |
