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| Cat.No. | Product name | Product Description |
| R21102588 | Triptonide | Triptonide (NSC 165677) is a natural product identified in Tripterygium wil |
| R240402001 | Cysteamine S-phosphate sodium | Cysteamine S-phosphate (Cystaphos) sodium can be hydroIyzed to Cysteamine by hum |
| R240402002 | LLY-284 | LLY-284 is the diastereomer of LLY-283 with much less active. LLY-283 is a poten |
| R240402003 | EZM0414 | EZM0414 is a potent, selective, orally bioavailable inhibitor of SETD2 (IC50=18 |
| R240402004 | NSC14355 | 1,3-dimethyl-8-sulfanylidene-7,9-dihydropurine-2,6-dione |
| R240402005 | (S)-3,5-二羟基苯基甘氨酸 | (S)-3,5-DHPG is a weak, but selective group I metabotropic glutamate receptors ( |
| R240402006 | N-乙酰基-4-苯醌亚胺 | NAPQI is the toxic metabolite of Acetaminophen (HY-66005). It is also an inhibit |
| R240402007 | L-天冬氨酸β-异羟肟酸酯 | L-Aspartic acid β-hydroxamate is an aspartic acid derivative. |
| R240402008 | GNE-7883 | GNE-7883 is a pan-TEAD inhibitor with anti-cell proliferation activity. It overc |
| R240402009 | Zotatifin (eFT226) | Zotatifin (eFT226) is a potent, selective, and well-tolerated eIF4A inhibitor. I |
| R240402010 | NSD1 inhibitor BT5 | NSD-IN-2 (compound 151) is a potent and irreversible NSD1 inhibitor. It can be u |
| R240402011 | Asymmetrin | Hadacidin is an inhibitor of AMP synthesis. Hadacidin and hadacidin analogues ha |
| R240402012 | 6-氨基-5,6,7,8-四氢萘-2,3-二醇氢溴酸盐 | ADTN hydrobromide is a long-acting dopamine agonist. It significantly decreases |
| R240402013 | N-去乙酰秋水仙碱 | Trimethylcolchicinic acid methyl ether, Antimitotic agent that intercepts microt |
| R240402014 | icFSP1 | icFSP1 is a potent ferroptosis suppressor protein-1 (FSP1) inhibitor. It does no |
| R240402015 | KSQ-4279 | KSQ-4279 (USP1-IN-1) is a potent, first-in-class, and highly selective USP1 inhi |
| R240402016 | LY3537982 | KRAS G12C inhibitor 19 is a potent inhibitor of KRAS G12C. |
| R240402017 | UM171 | UM171 is a selective agonist of human hematopoietic stem cell self-renewal. It b |
| R240402018 | Filanesib hydrochloride(ARRY-520) | Filanesib (ARRY-520) hydrochloride is a selective and noncompetitive kinesin spi |
| R240402019 | ZEN-3694 | BET-IN-19 (Compound 146) is a BET inhibitor. It inhibits hlL-6 mRNA transcriptio |
| R240402020 | PF-07220060 | PF-07220060 (CDK4/6-IN-6; example A94) is a potent CDK4/CDK6 inhibitor with a Ki |
| R240402021 | Tulmimetostat (CPI-0209) | Tulmimetostat (CPI-0209) is an orally active EZH1/EZH2 inhibitor that targets an |
| R240402022 | Sonrotoclax | Sonrotoclax is a potent, orally active Bcl2 inhibitor. It has effective cell kil |
| R240402023 | Zidesamtinib | Zidesamtinib (NVL-520) is a potent, selective, orally active and brain-penetrant |
| R240402024 | Ro 31-8220 mesylate | Ro 31-8220 is a potent PKC inhibitor, with IC50s of 5, 24, 14, 27, 24 and 23 nM |
