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Home > Products
| Cat.No. | Product name | Product Description |
| R2202126 | AZD9056 hydrochloride | AZD9056 hydrochloride is a selective orally active inhibitor of P2X7 which plays |
| R2202127 | UCB-9260 | UCB-9260, an orally active compound, inhibits TNF signaling by stabilising an as |
| R2202128 | LM22A-4 | LM22A-4 is a specific agonist of tyrosine kinase receptor B, used for neurologic |
| R2202129 | BI-4464 | BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC5 |
| R2204281 | Brusatol | Brusatol (NSC 172924) is a unique inhibitor of the Nrf2 pathway t |
| R2202132 | Besifovir (LB8033) | Besifovir (LB80331), a parent drug converted by LB80380, further metabolizes to |
| R2202133 | Cichoric Acid | Cichoric Acid, a natural product, is reported to be antioxidative. |
| R2202134 | BMS-P5 hydrochloride | BMS-P5 is a specific and orally active peptidylarginine deiminase 4 (PAD4) inhib |
| R2202135 | Letrozole | Letrozole (CGS 20267) is a potent, selective, reversible and orally active non-s |
| R2202136 | Anastrozole | Anastrozole is a potent, highly selective aromatase inhibitor, which inhibits hu |
| R2202137 | Glibenclamide impurity Ⅱ | Glibenclamide (Glyburide) is an orally active ATP-sensitive K+ channel (KATP) in |
| R2202138 | FM-479 | FM-479 is the negative control of FM-381 (HY-102046) and has no activity on JAK3 |
| R2202139 | T56-LIMKi | T56-LIMKi is a selective inhibitor of LIMK2; inhibits the growth of Panc-1 cells |
| R2202140 | INE963 | 4-Piperidinol, 4-(aminomethyl)-1-[5-[2-methoxy-6-(1-methylethyl)-3-pyridinyl]imi |
| R2202141 | JQKD-82 | JQKD82 (JADA82) is a cell-permeable and selective KDM5 inhibitor. JQKD82 increas |
| R2202142 | SKF89976A hydrochloride | SKF89976A hydrochloride is a selective GABA transporter (GAT-1) inhibitor with I |
| R2202143 | Complement factor D-IN-2 | Complement factor D-IN-2 is an inhibitor of complement factor D extracted from p |
| R2202144 | SR1664 | SR1664 is a PPARγ antagonist. SR1664 binds to PPARγ and potently inhibits Cdk5-m |
| R2202145 | Bocidelpar | Bocidelpar is a modulator of peroxisome proliferator-activated receptor del |
| R2202146 | ML339 | ML339 is a potent and selective CXCR6 (IC50 of 140 nM) antagonist that is select |
| R2202147 | SCD1 inhibitor-3 | SCD1 inhibitor-3 is a safe, potent and orally active SCD1 inhibitor. SCD1 inhibi |
| R2202148 | YTX-465 | YTX-465 is a stearoyl-CoA desaturase (Ole1/SCD) inhibitor. YTX-465 inhibits Ole1 |
| R2202149 | BMS-615 | TLR7/8/9-IN-1 is a potent and orally bioavailable small molecule antagonist (IC5 |
| R2202150 | VU6015929 | VU6015929 is a potent, selective and orally active dual discoidin domain re |
| R2202151 | Tavapadon | Tavapadon (PF-06649751) is an orally active and highly selective dopamine D1/D5 |
