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Home > Products
| Cat.No. | Product name | Product Description |
| R0011181 | Butyzamide | Butyzamide is an effective and oral Mpl activator. It is a novel non-peptide-bas |
| R0011182 | Selatinib | Selatinib is an orally active and potent dual inhibitor of EGFR and ErbB2 with a |
| R0011183 | PI4KIIIbeta-IN-10 | PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ (IC50 of 3.6 nM). |
| R0011184 | ADT-OH | ADT-OH is a hydrogen sulfide-releasing donor. ADT-OH induces apoptosis and inhib |
| R0011185 | Ruboxistaurin hydrochloride | Ruboxistaurin (LY333531) hydrochloride is an orally active, selective PKC beta i |
| R0011186 | 浅蓝菌素 | Cerulenin, a potent, natural inhibitor of fatty acid synthase (FASN), is an epox |
| 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 |
| R0011207 | Lurasidone Hydrochloride | Lurasidone (Hydrochloride) (SM-13496 (Hydrochloride)) 是 dopamine D2 和 5-HT7 的拮抗剂 |
