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| Cat.No. | Product name | Product Description |
| R2032591 | PD184352;CI-1040 | CI-1040 (PD 184352) is an orally active, highly specific, small-molecule inhibit |
| R2032592 | INCB39110 | Itacitinib adipate is an orally bioavailable and selective JAK1 inhibitor which |
| R2032593 | SH-4-54 | SH-4-54 is a most potent, small molecule, nonphosphorylated STAT inhibitor, with |
| R2032594 | UNC0638 | UNC0638 selectively inhibits G9a and GLP histone methyltransferase activity with |
| R2032595 | ZSTK-474;ZSTK474 | ZSTK474 is an ATP-competitive pan-class I PI3K inhibitor with IC50s of16 nM, 44 |
| R2032596 | UNBS-5162;UNBS5162 | UNBS5162 is a pan-antagonist of CXCL chemokine expression, with anti-tumor activ |
| R2032597 | FTI-277 hydrochloride | FTI-277 hydrochloride is an inhibitor of farnesyl transferase (FTase); a highly |
| R2032598 | LY2090314 | LY2090314 is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 |
| R2032599 | ReModelin | Remodelin hydrobromide is a novel potent and selective inhibitor of the acetyl-t |
| R2032600 | Ro48-8071 | Ro 48-8071 fumarate is an inhibitor of OSC (Oxidosqualene cyclase) with IC50 of |
| R2032601 | SR1078 | SR1078 is an agonist of retinoic acid receptor-related orphan receptor α/γ (RORα |
| R2032602 | JNJ1661010 | JNJ-1661010 (Takeda-25) a potent and selective fatty acid amide hydrolase (FAAH) |
| R2032603 | SAR405838(MI-773) | SAR405838 is a highly potent and selective MDM2 inhibitor, binds to MDM2 with Ki |
| R2032604 | 4E1RCat | 4E1RCat is an inhibitor of cap-dependent translation, and inhibits eIF4E:eIF4GI |
| R2032605 | Salirasib | Salirasib is a Ras inhibitor that inhibits specifically both oncogenically activ |
| R2032606 | WEHI539 | WEHI-539 is a selective inhibitor of Bcl-XL with an IC50 of 1.1 nM. |
| R2032607 | GSK1324726A(I-BET726) | GSK1324726A is a novel, potent, and selective inhibitor of BET proteins with hig |
| R2032608 | GSK-LSD1 2HCl | GSK-LSD1 2HCl is an irreversible, and selective LSD1 inhibitor with IC50 of 16 n |
| R2032609 | Afuresertib(GSK2110183) | GSK2110183 analog 1 is the structural analogue of GSK2110183. |
| R2032610 | ORG27569 | Org 27569 is a potent CB1 receptor allosteric modulator, which increases agonist |
| R2032611 | NVP-231 | NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=12±2 nM) that |
| R2032612 | b-AP15;NSC 687852) | b-AP15 is a specific inhibitor of the deubiquitinating enzymes UCHL5 and Usp14. |
| R2032613 | AZ5104 | AZ-5104 is an active, demethylated metabolite of AZD 9291.AZ-5104 is an EGFR inh |
| R2032614 | Cathepsin S inhibitor | LY 3000328 is a potent and selective Cathepsin S (Cat S) inhibitor with IC50s of |
| R2032615 | GSK1014802(CNV1014802) | Raxatrigine (GSK-1014802) is a novel small molecule state-dependent sodium chann |
