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Cat.No. Product name Product Description
R2033155 RMC-4550 RMC-4550 is a potent, selective and allosteric inhibitor of SHP2, with an IC50 o
R2033156 G1T38;Lerociclib Lerociclib (G1T38) is a potent and selective inhibitor of CDK4/6, with IC50s of
R2033157 cFMS Receptor Inhibitor II cFMS Receptor Inhibitor II is a CSF1R kinase inhibitor.CSF-1 is a cytokine.
R2033158 MM102 MM-102 (HMTase Inhibitor IX) is a potent WDR5/MLL interaction inhibitor, achieve
R2033159 Pexacerfont Pexacerfont is a selective corticotropin-releasing factor (CRF1) receptor antago
R2033160 BAY-1895344 BAY-1895344 is a potent, orally available and selective ATR inhibitor, with IC50
R2033161 diABZI STING agonist-1 trihydrochloride diABZI STING agonist-1 (trihydrochloride) is a selective stimulator of interfero
R2033162 Bepridil hydrochloride Bepridil hydrochloride (CERM 1978) is a calcium channel blocker, with antiangina
R2033163 Abrocitinib Abrocitinib (PF-04965842) is a potent, orally active and selective JAK1 inhibito
R2033164 MG101 MG-101 is a potent inhibitor of cysteine proteases which inhibits calpain I, cal
R2033165 ME401 P110δ-IN-1 is a potent and selective inhibitor of P110δ extracted from patent WO
R2033166 BI1347 BI-1347 is a potent CDK8 inhibitor extracted from patent WO2017202719A1, product
R2033167 SNAP94847 SNAP 94847 is a novel, high affinity selective melanin-concentrating hormonerece
R2033168 A-485 A-485 is a potent and selective catalytic inhibitor of p300/CBP with IC50s of 9.
R2033169 Edonerpic maleate Edonerpic maleate is a novel neurotrophic agent which can inhibit amyloid-β pept
R2033170 Phorbol Phorbol is a highly toxic diterpene, whose esters have important biological prop
R2033171 JC-1 JC-1 is a fluorescent lipophilic carbocyanine dye used to measure mitochondrial
R2033172 Cintirorgon Cintirorgon (LYC-55716) is a first-in-class, selective and orally bioavailable R
R2033173 CFI-400945 CFI-400945 is an orally active, potent and selective polo-like kinase 4(PLK4) in
R2033174 BMS1166 BMS-1166 is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM.BMS
R2033175 VU0134992 VU0134992 is the first subtype-preferring, orally active and selective Kir4.1 po
R2033176 MKC3946 MKC3946 is a potent and soluble IRE1α inhibitor, used for cancer research.
R2033177 Palovarotene Palovarotene is a nuclear retinoic acid receptor γ (RAR-γ) agonist.
R2033178 CLP-290 CLP290 is an orally available activator of the neuron-specific K+-Cl− cotranspor
R2033179 VCE-004.8 VCE-004.8, a semi-synthetic multitarget cannabinoquinoid, is a specific PPARγ an
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