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 |
Home > Products
| Cat.No. | Product name | Product Description |
| R21082381 | broxaldine | Broxaldine (Brobenzoxaldine) is an antigenitor drug. |
| R21082382 | PE859 | PE859 is an effective inhibitor of Tau and Aβ accumulation with IC50 values of 0 |
| R21082383 | A419259 trihydrochloride | A 419259 trihydrochloride is A Src family kinase inhibitor with IC50 values of 9 |
| R21082384 | AN-2718 | AN2718 inhibits fungal growth by inhibiting protein synthesis through OBORT mech |
| R21082385 | Pleconaril;VP 63843;Win 63843 | Pleconaril is a capsid inhibitor that can be used to treat enteroviruses. Plecon |
| R21082386 | TCS OX2 29 | Cts-ox2-29 is a strong and selective OX2 receptor antagonist with an IC50 of 40 |
| R21082387 | PLX8394 | PLX8394 is a potent, selective Raf inhibitor that inhibits BRAFV600E activity wi |
| R21082388 | AG 555 | AG 555 is an EGFR tyrosine kinase inhibitor. |
| R21082389 | BIX02189 | BIX02189 is a potent and selective MEK5 inhibitor with IC50 of 1.5 nM. BIX02189 |
| 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, |
