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Home > Products
| Cat.No. | Product name | Product Description |
| R2032429 | KN-93 Phosphate | KN-93 Phosphate is a potent and specific inhibitor of Ca2+/calmodulin-dependent |
| R2032430 | KOBE0065 | Kobe0065 is a novel and effective inhibitor of Ras-Raf interaction, competitivel |
| R2032431 | KPT185 | KPT-185 is an orally bioavailable and selective inhibitor of CRM1 and displays p |
| R2032432 | KPT-276 | KPT-276, analog of KPT-185, is an orally bioavailable selective inhibitors of nu |
| R2032433 | KW2478 | KW-2478 is an inhibitor of Hsp90α, with an IC50 of 3.8 nM, and has antitumor act |
| R2032434 | KX1-004 | KX1-004 is a potent small molecule inhibitor of Src-PTK as a potential protectiv |
| R2032435 | LB42708 | LB42708 is an orally active farnesyltransferase (FTase) inhibitor with IC50 of 0 |
| R2032436 | LCL161 | LCL161 is a IAP inhibitor which inhibits XIAP in HEK293 cell and cIAP1 in MDA-MB |
| R2032437 | LDN-212854 | LDN-212854 is a novel BMP inhibitor that exhibits substantially greater selectiv |
| R2032438 | LDN-57444 | LDN-57444 is a reversible, competitive and site-directed inhibitor of ubiquitin |
| R2032439 | LED209 | LED209 is a potent small molecule inhibitor of bacterial receptor QseC, is a pot |
| R2032440 | LMK-235 | LMK-235 is a potent and selective HDAC4/5 inhibitor, inhibits HDAC5, HDAC4, HDAC |
| R2032441 | LXR623 | LXR-623 is a brain-penetrant partial LXRα and full LXRβ agonist, with IC50s of 2 |
| R2032442 | LY2109761 | LY2109761 is an orally active, selective TGF-β receptor type I/II inhibitor with |
| R2032443 | LY2811376 | LY2811376 is the first orally available non-peptidic β-secretase (BACE1) inhibit |
| R2032444 | LY2979165 | LY2979165 is a mGlu2 agonist, which is a novel potent agent that is used as anti |
| R2032445 | LY303511 | LY303511 is a structural analogue of LY294002.LY303511 does not inhibit PI3K.LY3 |
| R2032446 | LY404039 | LY404039 is an inhibitor for mGluR1(Ki=149 nM) and mGluR2(Ki= 92 nM), which can |
| R2032447 | MAY-262611 | WAY-262611 is a wingless β-Catenin agonist that increases bone formation rate wi |
| R2032448 | MBX-2982 | MBX-2982 is a selective, orally-available G protein-coupled receptor 119 (GPR119 |
| R2032449 | MGCD265 analog | MGCD-265-analog (structurally related to MGCD-265) is an orally bioavailable mul |
| R2032450 | MI-2 | Menin-MLL inhibitor MI-2 is a Menin-MLL interaction inhibitor with IC50 of 446±2 |
| R2032451 | MI-3 | MI-3 (Menin-MLL inhibitor 3) is a potent and high affinity menin-MLL inhibitor w |
| R2032452 | MK6096;Filorexant(MK-6096) | Filorexant (MK-6096) is an orally bioavailable potent and selective reversible a |
| R2032453 | MK-8776(SCH900776) | SCH900776 S-isomer is the S-isomer of SCH900776.SCH900776 is a potent, selective |
