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Cat.No. Product name Product Description
RH131542 JP1302 JP1302 is a potent, selective, high affinity antagonist of the α2C-adrenoceptor,
RH131543 JP1302 dihydrochloride JP1302 dihydrochloride is a potent, selective, high affinity antagonist of the α
RH131544 Y11 Y11 inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397 and de
RH131545 3-亚环己基-1,3-二氢-2H-吲哚-2-酮 3-Cyclohexylidene-1,3-dihydro-2H-indol-2-one
RH131546 Raf inhibitor 2 Raf inhibitor 2 is a potent raf kinase (IC50<1.0 μM) inhibitor, compound 32,
RH131547 DC260126 DC260126 is a potent antagonist of GPR40 (FFAR1). DC260126 dose-dependently inhi
RH131548 2,3-Diphenylquinoxaline-6-carboxylic acid 2,3-Diphenylquinoxaline-6-carboxylic acid is used for end-capping in the synthes
RH131549 NLRP3/AIM2-IN-2 NLRP3/aim2-in-2 (compound 8) is a new potent inhibitor with different species-sp
RH131550 CID 60168009 CID 60168009
RH131551 3-苯基-2-硫代-2,3-二氢-4(1H)-喹唑啉酮 3-PHENYL-2-THIOXO-1,2,3,4-TETRAHYDROQUINAZOLIN-4-ONE
RH131552 WAY-313356 WAY-313356
RH131553 1-Cinnamoylpyrrolidine 1-Cinnamoylpyrrolidine (Compound 3), a crude extract prepared from Piper caninum
RH131554 Tyrosinase-IN-2 Tyrosinase-IN-2 (compound 67) is a potent inhibitor of tyrosinase. Tyrosinase is
RH131555 Resorcinolnaphthalein Resorcinolnaphthalein is a specific angiotensin-converting enzyme 2 (ACE2) 
RH131556 4-(N-(1,8-萘酰亚胺))-N-丁酸 Virstatin inhibits the pili system synthesis and prevents A. baumannii biofilm f
RH131557 Hepln-13 Hepln-13 is a potent and orally active Hepsin inhibitor with an IC50 of 0.33 µM.
RH131558 硫酸盐离子载体I sulfate-ionophore i
RH131559 NSC756093 NSC756093
RH131560 M-31850 M-31850 is a potent, selective and competitive β-hexosaminidase (Hex) inhibitor
RH131561 FQ FQ is a tyrosinase inhibitor that effectively inhibits the diphenolase activity
RH131562 Difluorinated Curcumin(3,4-Difluorobenzylidene curcumin) Difluorinated Curcumin (3,4-Difluorobenzylidene curcumin) is a fluorinated curcu
RH131563 Zoldonrasib(RMC-9805; KRAS G12D inhibitor 18) RMC-9805 (KRAS G12D inhibitor 18) is a potent and orally active KRAS G12D inhibi
RH131564 Z-LEED-FMK Z-LEED-FMK is a caspase-13 and caspase-4 inhibitor. Z-LEED-FMK also inhibits cas
RH131565 Z-LEVD-FMK Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor. Z-LEVD-FMK blocks ER stress-
RH131566 Z-LEHD-FMK Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects agai
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