RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
Home > Products
| Cat.No. | Product name | Product Description |
| R2032654 | AVN944 | AVN-944(VX-944) is a selective, noncompetitive inhibitor of the enzyme directed |
| R2032655 | AZD2461 | AZD-2461 is a potent PARP inhibitor, with IC50s of 5 nM, 2 nM and 200 nM for PAR |
| R2032656 | AZD-5597 | AZD-5597 is potent CDK inhibitor with in vitro anti-proliferative effects agains |
| R2032657 | BET bromodomain inhibitor | BET bromodomain inhibitor is a potent BET inhibitor extracted from patent WO/201 |
| R2032658 | B-Raf inhibitor | A Tyrosine kinase inhibitor. |
| R2032659 | BRD7552 | BRD7552 is an inducer of transcription factor PDX1, which increases insulin expr |
| R2032660 | CAY10415;MSDC0160(Mitoglitazone) | MSDC 0160 (Mitoglitazone) is a mitochondrial target of thiazolidinediones (mTOT) |
| R2032661 | CEP28122 | CEP-28122 is a highly potent and selective orally active ALK inhibitor with IC50 |
| R2032662 | CEP-37440 | CEP-37440 is a novel potent and selective Dual FAK/ALK inhibitor with IC50 s of |
| R2032663 | E-64 | E-64 (Proteinase inhibitor E 64) is a potent irreversible inhibitor against gene |
| R2032664 | EPZ011989 | EPZ011989 is a potent, selective orally bioavailable EZH2 inhibitor with Ki < |
| R2032665 | Givinostat hydrochloride monohydrate(ITF2357) | Givinostat hydrochloride monohydrate (ITF-2357 hydrochloride monohydrate) is a H |
| R2032666 | HA130 | HA130 is a selective autotaxin (ATX) inhibitor with an IC50 of 28 nM. |
| R2032667 | LY3009120 | LY3009120 is a pan RAF inhibitor which inhibits BRAFV600E, BRAFWT and CRAFWT wit |
| R2032668 | MK-5108(VX-689) | MK-5108 is a highly potent and specific inhibitor of Aurora A kinase with an IC5 |
| R2032669 | ORY-1001 dihydrochloride(RG-6016) | ORY-1001 (RG-6016) 2HCl is an orally active and selective lysine-specific demeth |
| R2032670 | PCI-27483 | PCI-27483 is a FVIIa/tissue factor inhibitor, with antitumour effects. |
| R2032671 | PD123319 | PD 123319 (ditrifluoroacetate) is a potent, selective AT2 angiotensin II recepto |
| R2032672 | PHA767491 | PHA-767491 is a dual Cdc7/Cdk9 inhibitor, with IC50s of 10 nM and 34 nM, respect |
| R2032673 | Pyroxamide | Pyroxamide is a potent inhibitor of histone deacetylase 1 (HDAC1) with an ID50 o |
| R2032674 | SB-399885 | SB399885 is a potent, selective, brain penetrant and orally active 5-HT6 recepto |
| R2032675 | SB-590885 | SB-590885 is a potent B-Raf inhibitor with Ki of 0.16 nM, and has 11-fold greate |
| R2032676 | Volasertib(BI6727) | Volasertib is a highly potent Polo-like kinase 1 (PLK1) inhibitor with an IC50 o |
| R2032677 | VX-11e | VX-11e is a potent, selective, and orally bioavailable inhibitor of ERK with Ki |
| R2032678 | AMG337 | AMG-337 is a potent and highly selective small molecule ATP-competitive MET kina |
