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| Cat.No. | Product name | Product Description |
| 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. |
| R21082201 | DTP3 | DTP3 is a selective MKK7/GADD45β inhibitor, which inhibits cancer-selective NF-κ |
| R21082202 | MCUi4 | MCU-i4 is a novel negative modulator of the MCU, binding MICU1 and impairing mus |
| R21082203 | Aldoxorubicin (INNO-206) | Aldoxorubicin has effective antitumor activities in various cancer cell lines an |
| R21082204 | XL-092 | JUN04542 is an Axl Mer cMet KDR inhibitor for the treatment of Axl and Mer recep |
| R21082205 | (Z)-4-Hydroxytamoxifen | 4-hydroxytamoxifen is a selective estrogen receptor modulator (SERM). |
| R21082206 | SZL-P1-41 | SZL P1-41 is an Skp2 inhibitor that selectively inhibits Skp2 E3 ligase activity |
| R21082207 | ERD-308 | Erd-308 is a potent proTAC-based estrogen receptor (ER) inhibitor with a DC50 va |
| R21082208 | RO6889678 | RO6889678 is a highly effective inhibitor of HBV capsid formation with favorable |
| R21082209 | CA-4948 | Ca-4948 is a potent, orally active, selective IRAK4 kinase inhibitor with IC50 & |
| R21082210 | HBX19818 | HBX 19818 is a ubiquitin-specific protease (USP7) inhibitor with an IC50 value o |
| R21082211 | Conoidin A | Conoidin A is A cellular permeability inhibitor of toxoplasma gondii peroxidase |
| R21082212 | SRX3207 | SRX3207 is a first-of-its-kind dual inhibitor of Syk/PI3K with oral activity. S |
