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| Cat.No. | Product name | Product Description |
| R0011187 | EIPA | EIPA (L593754) is an orally active TRPP3 channel inhibitor with an IC50 of 10.5 |
| R0011188 | GSK-7975A | GSK-7975A is a potent and orally available CRAC channel inhibitor. |
| R0011189 | Dimethylaminomicheliolide HCl | Dimethylaminomicheliolide HCl has potential anti-inflammatory and anti-tumor act |
| R0011190 | malonyl-NAC | malonyl-NAC increases cellular propylation, resulting in reduced endogenous GAPD |
| R0011191 | Aggreceride C | Aggreceride C |
| R0011192 | (S)-2-((S)-2-氨基-3-(1H-咪唑-4-基)丙胺基)丙酸 | h-his-ala-oh |
| R0011193 | Iruplinalkib | Iruplinalkib (WX-0593) is a potent, selective, and orally active inhibitor of AL |
| R0011194 | KI696 | KI696 is a high affinity probe that disrupts the Keap1/NRF2 interaction. KI696 i |
| R0011195 | KI696 isomer | KI696 isomer is the less active isomer of KI696 (HY-101140). KI696 is a high aff |
| R0011197 | NaV1.2/1.6 channel blocker-1 | NaV1.2/1.6 channel blocker-1 is a potent NaV1.2/1.6 channel blocker, with IC50s |
| R0011198 | CTPB | CTPB is a good activator of p300 histone acetyl transferase (HAT) enzyme. |
| R0011199 | JNJ16259685 | JNJ16259685 is a selective antagonist of mGlu1 receptor, and inhibits the synapt |
| R0011200 | IMT1B | IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric in |
| R0011201 | Zilurgisertib fumarate | Zilurgisertib fumarate (INB-000928 fumarate, NBU-928 fumarate), a selective ALK- |
| R0011202 | INCB-000928 | Zilurgisertib (INCB-000928) is a selective and potent ALK 2 inhibitor for the st |
| R0011203 | CCT241533 hydrochloride | CCT241533 hydrochloride is a potent and selective CHK2 inhibitor with an IC50 of |
| R0011204 | BNTA | BNTA, a potent extracellular matrix (ECM) modulator, facilitates cartilage struc |
| R0011205 | PHI-101 | PHI-101 is an orally active FLT3 inhibitor that overcomes resistance to multiple |
| R0012005 | Enpatoran | Enpatoran (M5049) is a potent, orally active and dual TLR7/8 inhibitor with IC50 |
| R0012007 | 2'-去氧-2'-氟-2'-C-甲基胞苷 | PSI-6130 is a potent and selective inhibitor of HCV NS5B polymerase, and inhibit |
| R0012008 | Mericitabine | Mericitabine (RG 7128; R-7128) is a nucleoside inhibitor of the HCV NS5B polymer |
| R0012021 | AZ194 | AZ194 is a first-in-class, orally active inhibitor of CRMP2-Ubc9 interaction and |
| R0012024 | FTO-IN-7 | FTO-IN-7 is an inhibitor of FTO. FTO-IN-7 can be used in study Alzheimer's disea |
| R0012025 | FTO-IN-1 | FTO-IN-1 is a fat mass and obesity-associated enzyme (FTO) inhibitor extracted f |
| R0012026 | NS3623 | NS3623 is an activator of human ether-a-go-go-related gene (hERG1/KV11.1) potass |
