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Home > Products
| Cat.No. | Product name | Product Description |
| R21042827 | Pidotimod | Pidotimod is an immunostimulant. It is a synthetic dipeptide with immunomodulato |
| R21042828 | Riluzole | Riluzole is an anticonvulsant and belongs to a use-dependent family of sodium ch |
| R21042829 | vericiguat | Vericiguat (BAY1021189) is a potent, orally active, soluble guanylate cyclase st |
| R21042830 | CA-4948 | NA |
| R21042831 | Eribulin mesylate | Eribulin mesylate is an anticancer agent targeting microtubules for the treatmen |
| R21042832 | ACT-389949 | ACT-389949 is a pioneering, highly effective and selective formyl peptide recept |
| R21042833 | PK-10571 | |
| R21042834 | PXS-55505 2HCl | |
| R21042835 | GSK620 | |
| R21042836 | Tanespimycin (17-AAG; NSC330507; CP 127374) | 17-AAG is an effective inhibitor of Hsp90 with an IC50 of 5 nM. The binding affi |
| R21042837 | Alvespimycin (hydrochloride);17-DMAG HCl | Alvespimycin Hydrochloride is a potent inhibitor of HSP90 with an EC50 of 62±29 |
| R21042838 | Rhosin hydrochloride | Rhosin hydrochloride is a specific inhibitor of Rho, and the KD value of binding |
| R21042839 | MK-8719 | MK-8719 is a highly effective and selective O-GlcNacase (OGA) inhibitor (Hoga Ki |
| R21042841 | BMS-P5 | BMS-P5 is a novel Peptidylarginine Deiminase 4 (PAD4) inhibitor that blocks del |
| R21042842 | U18666A | U18666A, a cell permeable drug, is an inhibitor of cholesterol synthesis and tra |
| R21042843 | Luzindole | Luzindole (N-0774) is a selective melatonin receptor antagonist.Luzindole prefer |
| R21042844 | Elexacaftor | CFTR Corrector 1 (Compound 1) is a compound modulator of the transmembrane condu |
| R21042845 | YKL-05-099 | YKL-05-099 is a salt-induced kinase (SIK) probe.The IC50 value of SIK2 inhibitio |
| R21042846 | DTHIB | |
| R21042847 | LSZ102 | LSZ-102 is a potent, orally biopotent, selective estrogen receptor depressant wi |
| R21042848 | Calcein-AM | Calcein-AM is a permeable fluorescent dye used to measure cell viability. |
| R21042849 | AZD-4205 | AZD-4205 is a selective JAK1 inhibitor with an IC50 value of 73 nM and a weak in |
| R21042850 | AZD9977 | AZD9977 is a novel, first-rate, selective and oral glucocorticoid receptor (MR) |
| R21042851 | AZD 5718 | AZD5718 (AZD-5718, AZD5718) is a novel and effective inhibitor of 5-lipoxygenase |
| R21071201 | AST5902 trimesylate | AST5902 is the active metabolite of Alflutinib. |
