RECHEM
Welcome to our website!|Hot Line: 86-21-31433387|E-mail: sales@rechemscience.com
Products Category
Contact Us
| Tel: | +86-21-31433387 |
| +86-15618786686 | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | sales@rechemscience.com |
| Cat.No. | Product name | Product Description |
| R21082390 | Eniporide | Eniporide is a The Na(+)/H(+) exchange inhibitor. |
| R21082391 | HA-1100 | Hydroxyfasudil is a ROCK inhibitor that can inhibit the activity of ROCK1 and RO |
| R21082392 | ZINC00881524 (ROCK inhibitor) | ZINC00881524 is an inhibitor of ROCK. |
| R21082393 | PST2744 | Istaroxime(PST-2744) inhibited Na+/K+ ATPase (Na+/K+ ATPase) with IC50 of 0.43μM |
| R21082394 | JNJ-46778212 | JNJ-46778212 is an effective mGlu5 allosteric modulator (EC50: 260 nM). |
| R21082395 | GPR40 agonist 4 | FAA1 Agonist-1 is a potent free fatty acid receptor 1 (FFA1/GPR40) agonist with |
| R21082396 | Bafetinib | Bafetinib is a Lyn/ BCR-ABL tyrosine kinase inhibitor with antitumor activity. |
| R21082397 | DDP38003 | Dp-38003 dihydrochloride is a novel oral active inhibitor of KDM1A/LSD1, with an |
| R21082398 | IPI3063 | Ipi-3063 is a potent selective PI3K P110 δ inhibitor with an IC50 of 2.5±1.2 nM. |
| R21082399 | ML355 | ML355 is a highly efficient and selective 12-LOx inhibitor with IC50 value of 0. |
| R21082400 | Saquinavir mesylate | Saquinavir mesylate is an HIV protease inhibitor used in retrovirus therapy. |
| R21082401 | NVP-BAG956 | Nvp-bag956 is an ATP-competitive PI3K inhibitor, inhibiting PI3Kδ, PI3Kα, PI3Kγ |
| R21082402 | （-）-MK 801 maleate | (-)-MK 801 Maleate is an enantiomer of (+) -Mk-801, which is a highly selective, |
| R21082403 | CHF5074; CSP-1103;Itanapraced | Itanapraced (CHF5074) is A new type of γ-secretase modulator, which reduces Aβ42 |
| R21082404 | PJ34 | PJ34 is a potent and specific PARPl/2 inhibitor with IC50 of 110 nM and 86 nM, r |
| R21082405 | EHT5372 | EHT 5372 is a potent inhibitor of DYRK with IC50 values of 0.22 nM and 0.28 nM, |
| R21082406 | RRx-001 | Rrx-001 is a potent inhibitor of glucose 6-phosphate dehydrogenase (G6PD). Rrx- |
| R21082407 | FTBMT | FTBMT is a selective GPR52 agonist with an EC50 of 75 nM. Antipsychotic and cog |
| R21082408 | AST2818;Alflutinib | Alflutinib (AST-2818, ASK120067) is a third-generation EGFR mutant selective tyr |
| R21082409 | PD 168077 MALEATE | Pd-168077 maleate is a selective dopamine D4 receptor agonist with a Ki value of |
| R21082410 | PIH | Pyridoxal isonicotinoyl hydrazine (PIH) is a lipophilic ferric chelating agent e |
| R21082411 | SR0987 | SR0987 is an agonist of RORγ T with an EC50 value of 800 nM. |
| R21082412 | C-176 | C-176 is a potent covalent inhibitor of interferon gene - stimulating receptor ( |
| R21082413 | GSK805 | GSK805 is a potent RORγ T inhibitor. |
| R21082414 | Bobcat339 (Bobcat 339) | Bobcat339 (Bobcat339) is a novel cytosine-based TET enzyme inhibitor with IC50 o |
