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Cat.No. Product name Product Description
R2033104 1358099-18-9 C25-140, a first-in-class, fairly selective TRAF6-Ubc13 inhibitor, directly bind
R2033105 ACY775 ACY-775 is a potent and selective inhibitor of the of histone deacetylase 6 (HDA
R2033106 Adavivint(SM04690;Lorecivivint) Adavivint (SM04690; Lorecivivint) is a potent and selective inhibitor of canonic
R2033107 AR231453 AR 231453 is a potent, selective and orally available GPR119 agonist.
R2033108 Asapiprant Asapiprant is a potent and selective DP1 receptor antagonist with a Ki of 0.44 n
R2033109 AVN492 AVN-492 is a very specific and highly-selective antagonist with picomolar affini
R2033110 AZ304 AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits wild t
R2033111 AZD1390 AZD1390 is a potent, highly selective, orally bioavailable, brain-penetrant ATM
R2033112 AZD5069 AZD-5069 is a potent CXCR2 chemokine receptor antagonist, used for caner treatme
R2033113 BIBF1202 BIBF 1202 is the carboxylate metabolite of BIBF 1120 which inhibits VEGFR2 kinas
R2033114 Desidustat Desidustat is an inhibitor of HIF hydroxylase extracted from patent WO 201410281
R2033115 GNE-6776 GNE-6776 is a selective USP7 inhibitor.
R2033116 GSK3179106 GSK3179106 is a potent and selective RET kinase inhibitor with an IC50 of 0.4 nM
R2033117 Imepitoin Imepitoin (AWD 131-138) is a new low-affinity partial benzodiazepine receptor ag
R2033118 JAK3-IN-6 JAK3-IN-6 is a potent, selective irreversible Janus Associated Kinase 3 (JAK3) i
R2033119 LY-2940094 tartrate LY-2940094 is a potent, selective and orally available nociceptin receptor (NOP
R2033120 LY-2940094;LY2940094 LY-2940094 is a potent, selective and orally available nociceptin receptor (NOP
R2033121 LY3023414 LY3023414 potently and selectively inhibits class I PI3K isoforms, DNA-PK, and m
R2033122 Nec-1s Necrostatin 2 racemate (Nec-1S), the Nec-1 stable, is a potent and specific RIPK
R2033123 Nucleozin Nucleozin targets influenza A nucleoprotein (NP), a multifunctional, RNA-binding
R2033124 PF-5274857 PF-5274857 is a potent and selective Smoothened (Smo) antagonist, inhibits Hedge
R2033125 SRI-011381 SRI-011381 hydrochloride is an oral bioavailabile TGF-beta signaling agonist, ex
R2033127 Tinostamustine;EDO-S101 EDO-S101 is a pan HDAC inhibitor; inhibits HDAC1, HDAC2 and HDAC3 with IC50 valu
R2033128 Gefitinib-based PROTAC 3 Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a VHL ligand vi
R2033129 β-Lapachone β-Lapachone (ARQ-501;NSC-26326) is a naturally occurring O-naphthoquinone, acts
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