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Home > Products
| Cat.No. | Product name | Product Description |
| R12020 | INCB057643 | INCB-057643 is a novel, orally bioavailable BET inhibitor. |
| R12021 | MIK665 | N/A |
| R12022 | GTS-21 | N/A |
| R12023 | MMAD (Synonyms: Demethyldolastatin 10; Monomethylauristatin D; Monomethyl Dolastatin 10) | MMAD is a potent tubulin inhibitor, is a toxin payload in antibody drug conjugat |
| R12024 | VcMMAE (Synonyms: mc-vc-PAB-MMAE) | VcMMAE (mc-vc-PAB-MMAE) is a drug-linker conjugate for ADC with potent antitumor |
| R12025 | MMAF (Synonyms: Monomethylauristatin F) | MMAF (Monomethylauristatin F) is a potent tubulin polymerization inhibitor and i |
| R12026 | Mc-MMAE (Synonyms: Maleimidocaproyl-monomethylauristatin E) | Mc-MMAE is a protective group (maleimidocaproyl)-conjugated monomethyl auristati |
| R12027 | Mc-Val-Cit-PABC-PNP | Mc-Val-Cit-PABC-PNP is a cathepsin cleavable ADC linker used in the sy |
| R12028 | SMCC-DM1 (Synonyms: DM1-SMCC) | SMCC-DM1 (DM1-SMCC) is a drug-linker conjugate composed of a potent microtubule- |
| R12029 | Fmoc-Val-Cit-PAB | Fmoc-Val-Cit-PAB is a cleavable linker for antibody-drug-conjugation (ADC). |
| R12030 | Fmoc-val-cit-pab-pnp | Fmoc-Val-Cit-PAB-PNP is a cleavable peptide linker, is a linker for antibody-dru |
| R12031 | Val-Cit-PAB | Val-cit-PAB-OH is a cleavable ADC linker. |
| R12032 | Auristatin E | Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor |
| R12033 | NDMM | N/A |
| R12035 | CGP 52432 | N/A |
| R12001 | 4-AMINO-3-FURAZANECARBOXAMIDOXIME | N/A |
| R181129 | NBD-Glucose | 2-NBDG is a fluorescent indicator for direct glucose uptake measurement and also |
| R181130 | SB225002 | SB225002, a potent, selective and non-peptide CXCR2 antagonist, inhibits 125I-IL |
| R181131 | Cutamesine dihydrochloride (Synonyms: SA4503 dihydrochloride; AGY94806 dihydrochloride) | Cutamesine dihydrochloride (SA4503 dihydrochloride; AGY94806 dihydrochloride) is |
| R181132 | Cutamesine (SA4503; AGY-94806) | Cutamesine (SA4503; AGY-94806) is a selective sigma 1 receptor(σ1R) agonist; hig |
| R181133 | Golvatinib (E7050) | Golvatinib (E-7050) is a potent dual inhibitor of both c-Met and VEGFR2 kinases |
| R181134 | GI254023X (Synonyms: GI4023; SRI028594) | GI254023X is a potent MMP9 and ADAM10 inhibitor with IC50s of 2.5 and 5.3 nM, re |
| R181135 | CUDC101 | CUDC-101 is a potent inhibitor of HDAC, EGFR, and HER2 with IC50s of 4.4, 2.4, a |
| R181137 | O-304 | O-304 is a first-in-class, orally available pan-AMPK activator, which increases |
| R181138 | LAU159 | LAU159 is a functionally selective positive modulator of α1β3 GABA(A) receptor w |
