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| Cat.No. | Product name | Product Description |
| 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 |
| R2202152 | suvn-911 | SUVN-911 is a potent, selective, brain penetrated and orally bioavailable neuron |
| R2202153 | MDR652 | MDR-652 is a highly specific and efficacious transient receptor potential vanill |
| R2202154 | DS-1971a | DS-1971a is a potent, selective, and orally active NaV1.7 inhibitor, with IC50s |
| R2202155 | PK68 | PK68 is a potent and selective type II inhibitor of receptor-interacting kinase |
| R2202156 | Seltorexant | Seltorexant (JNJ-42847922) is an orally active, high-affinity, and selective ore |
| R2202157 | Rineterkib;ERK-IN-1 | Rineterkib (compound B) is an orally active RAF and ERK1/2 inhibitor in the stud |
| R2202158 | Licogliflozin | Licogliflozin is a sodium glucose cotransporter (SGLT1 and SGLT2) inhibitor. |
| R2202159 | LOX-IN-3 dihydrochloride | LOX-IN-3 dihydrochloride is an orally active lysyl oxidase (LOX) inhibitor. LOX- |
| R2202160 | ACH-000143 | ACH-000143 is a potent and orally active melatonin receptor agonist, with EC50 v |
| R2202161 | Nifeviroc | Nifeviroc is an orally active CCR5 antagonist. Nifeviroc is used for the study o |
