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| Cat.No. | Product name | Product Description |
| R2030113 | Imidazole ketone erastin (IKE) | Imidazole ketone erastin (IKE) is a potent, selective, and metabolically stable |
| R2030114 | L-779450 | L-779450 is a potent and selective B-Raf kinase inhibitor with a Kd of 2.4 nM.&n |
| R2030116 | TAK-981;TAK981 | TAK-981 is a first in class and selective inhibitor of the SUMOylation enzymatic |
| R2030117 | AZ505 | AZ505 is a potent and selective SMYD2 inhibitor with IC50 of 0.12 μM. |
| R2030118 | BAY-598 | BAY-598 is selective small molecule inhibitor of SMYD2 with an IC50 of 27 nM. |
| R2030119 | CTEP (RO 4956371; mGluR5 inhibitor) | CTEP (RO 4956371) is a novel, long-acting, orally bioavailable allosteric antago |
| R2030120 | Basimglurant (RG7090; CTEP Derivative) | Basimglurant (RG7090) is a potent, selective and orally available mGlu5 negative |
| R2030121 | D-Luciferin | D-luciferin is the natural substrate of luciferases that catalyze the production |
| R2030124 | LDN-192960 | LDN-192960 is an inhibitor of Haspin and Dual-specificity Tyrosine-regulated Kin |
| R2030125 | Motesanib Diphosphate (AMG-706) VM-2005 | Motesanib Diphosphate (AMG 706 Diphosphate) is a potent ATP-competitive inhibito |
| R2030126 | PTC-209 | PTC-209 is a specific BMI-1 inhibitor with an IC50 of 0.5 μM. |
| R2030127 | SMI-4a | (Z)-SMI-4a is a poten, selective, cell-permeable and ATP-competitive Pim-1 inhib |
| R2030128 | SU-9516 | SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also shows inhibit |
| R2030129 | TDZD-8 (GSK-3β Inhibitor I; NP 01139) | TDZD-8 is an inhibitor of GSK-3β, with an IC50 of 2 μM; TDZD-8 shows less potent |
| R2030130 | UNC-669 | UNC 669 is a potent antagonist of L3MBTL1(IC50=4.2 uM) and L3MBTL3(IC50=3.1 uM). |
| R2030131 | WZ-811 | WZ811 is an orally active, highly potent competitive antagonist of CXCR4. WZ811 |
| R2030132 | Rilpivirine (R278474; TMC278; DB08864) | Rilpivirine (R278474; TMC278) is a type of anti-HIV medicine called a non-nucleo |
| R2030133 | IM-12 | IM-12 is an inhibitor of GSK-3β, with an IC50 of 53 nM, and also enhances Wnt si |
| R2030134 | Losmapimod (GSK-AHAB; GW856553X; SB856553) | Losmapimod is a selective, potent, and orally active p38 MAPK inhibitor with pKi |
| R2030135 | BH3I-1 (BHI1; BH 3I1) | BH3I-1 is a Bcl-2 family antagonist, which inhibits the binding of the Bak BH3 p |
| R2030136 | IQ-1S free acid | IQ-1S free acid is a prospective inhibitor of NF-κB/activating protein 1 (AP-1) |
| R2030137 | IQ 1 | IQ 1 has many functions such as decreasing Wnt-stimulated phosphorylation, maint |
| R2030138 | A804598 | A-804598 is a CNS penetrant, competitive and selective P2X7 receptor antagonist |
| R2030139 | Pifithrin-α hydrobromide (Pifithrin hydrobromide; PFTα hydrobromide) | Pifithrin-α hydrobromide is a p53 inhibitor which blocks its transcriptional act |
| R2030140 | HMN-176 | HMN-176 is a stilbene derivative which inhibits mitosis, interfering with p |
