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Home > Products
| Cat.No. | Product name | Product Description |
| R2053534 | Rigosertib sodium (ON-01910 sodium) | Rigosertib sodium (ON-01910 sodium) is a multi-kinase inhibitor and a selective |
| R2053535 | DO-264 | DO-264 is a selective and in vivo-active inhibitor of Abhydrolase Domain Contain |
| R2053536 | PK1-IN-4 (compound 8) | RIPK1-IN-4 (compound 8) is a potent and selective type II kinase inhibitor of re |
| R2053537 | CADD522 | CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA |
| R2053538 | Z433927330 | Z433927330 is a potent and selective inhibitor of Aquaporin-7 (AQP7), less poten |
| R2053539 | Deferiprone | Deferiprone is the only orally active iron-chelating drug to be used therapeutic |
| R2053540 | Deferoxamine mesylate | Deferoxamine mesylate is an iron chelator that binds free iron in a stable compl |
| R2090401 | BI 894999 | BRD4 Inhibitor-10 is a potent BRD4-BD1 inhibitor extracted from patent |
| R2090901 | T-5224 | T-5224 is a transcription factor c-Fos/activator protein (AP)-1 inhibi |
| R2090921 | ML406 | ML406 is a small molecular probe that exerts anti-tb activity by inhibiting Mtbb |
| R2090922 | SR-717 | SR-717 is a non-nucleotide STING agonist with EC50s of 2.1 μM and |
| R2090923 | LY 345899;LY345899 | LY 345899 is a Folate analog and is a methylene tetrahydrofolate dehydrogen |
| R2092301 | 4',5,7-Trimethoxyflavone | 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) t |
| R2092302 | WC5-2 | CAS NO.：922722-84-7 Product Name：WC5-2 Synonyms： EINECS: Molecular Formula：C15H9 |
| R2103541 | BIA;TMBIM6 antagonist-1 | TMBIM6 antagonist-1, a potential TMBIM6 antagonist, prevents TMBIM6 binding to m |
| R2103542 | ML417 | ML417 is a selective and brain penetrant D3 dopamine receptor (D3R) agonist, wit |
| R2103543 | PRI-724 | PRI-724 is a selective inhibitor of the CBP/β-catenin interaction. |
| R2103544 | KGA-2727 | KGA-2727 is a first selective, high-affinity and orally active SGLT1 inhibitor w |
| R2103545 | URB937 | URB 937 is a potent inhibitor of fatty-acid amide hydrolase (FAAH), an intracell |
| R2103546 | GNE-8324 | GNE-8324 is a potent and selective NMDA receptor PAM. |
| R2103547 | BMS986165 | BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor |
| R2103548 | TAS-116 | TAS-116 is an oral bioavailable, ATP-competitive, highly specific HSP90α/HSP90β |
| R2103549 | SAR131675 | SAR131675 is a potent and selective VEGFR3 inhibitor with an IC50 of 23 nM. |
| R2103550 | iFSP1 | iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosi |
| R2103551 | N-[[(1,2,3,5,6,7-hexahydro-s-indacen-4-yl) amino]carbonyl]-1-(1-methylethyl)-1H-Pyrazole-3-sulfonamide | N-[[(1,2,3,5,6,7-hexahydro-s-indacen-4-yl) amino]carbonyl]-1-(1-methylethyl)-1H- |
