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 |
| R2053403 | PF-3758309 hydrochloride | PF-3758309 hydrochloride is a potent, orally available, and reversible ATP-compe |
| R2053404 | GSK621 | GSK621 is a specific and potent AMPK activator. |
| R2053405 | JNK Inhibitor VIII (TCS JNK 6o) | JNK Inhibitor VIII (TCS JNK 6o) is a c-Jun N-terminal kinases (JNK-1, -2, and -3 |
| R2053406 | laninamivir | Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with I |
| R2053407 | Tyk2-IN-8 | Tyk2-IN-8 (compound 10) is a selective TYK2 inhibitor, which binds to TYK2 catal |
| R2053408 | AC1903 | It was found that AC1903 inhibited the activity of TRPC5, and the small molecule |
| R2053385 | GMB-475;GMB475 | GMB-475 is a degrader of BCR-ABL1 tyrosine kinase based on PROTAC, overcoming BC |
| R2053409 | BAY-1816032 | BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimid |
| R2053410 | SBI-797812 | SBI-797812 is structurally similar to active-site directed NAMPT inhibitors and |
| R2053411 | Beraprost sodium;15K99VDU5F | Beraprost sodium, a prostacyclin analog, is a stable and orally active prodrug o |
| R2053412 | Beraprost sodium;15K99VDU5F | Beraprost sodium, a prostacyclin analog, is a stable and orally active prodrug o |
| R2053413 | Tas6417 | TAS6417 is an EGFR inhibitor and an efficacious drug candidate for patients with |
| R2053415 | Beta-d-N4-hydroxycytidine (NHC);EIDD1931 | Beta-d-N4-hydroxycytidine (NHC) is a very potent anti-VEEV (venezuelan equine en |
| R2061701 | GSK2795039 | GSK2795039 is a NADPH oxidase 2 (NOX2) inhibitor with a mean pIC50 of |
| R2053416 | WZ8040 | WZ8040 is an irreversible mutated EGFR T790M inhibitor and inhibits EGFR phospho |
| R2053417 | Prostaglandin E1 (PGE1) | Prostaglandin E1 (PGE1) is a potent vasodilator and activates the prostaglandin |
| R2053418 | Oxamflatin (Metacept-3) | Oxamflatin (Metacept-3) is a potent HDAC inhibitor with an IC50 of 15.7 nM. |
| R2053419 | Dapansutrile(OLT1177) | Dapansutrile is a potent, selective and orally active inhibitor of NLRP3 inflamm |
| R2053420 | MN58b | MN58b is a selective choline kinase α (CHKα) inhibitor, and results in inhibitio |
| R2053421 | VLX600 | VLX600 induces the expression of genes associated with hypoxia, glycolysis, and |
| R2053422 | Tenovin-6 Hydrochloride | Tenovin-6 Hydrochloride is an inhibitor of SIRT1 and SIRT2, slightly inhibits HD |
| R2053423 | VCMMAF | MC-Val-Cit-PAB-MMAF is a drug-linker conjugate for ADC with antitumor activity b |
| R2053424 | Dolastatin 10 | Dolastatin 10 (DLS 10) is a potent antimitotic peptide, isolated from the marine |
| R2053425 | Fmoc-Val-Cit-PAB-MMAE | Fmoc-Val-Cit-PAB-MMAE consists the ADCs linker (Fmoc-Val-Cit-PAB) and potent tub |
| R2053426 | MC-MMAF | McMMAF is a protective group-conjugated MMAF. MMAF is a potent tubulin polymeriz |
