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 About 8 results found for searched term "C21" (0.14 seconds)

Cat.No.  Name Target
M6257 ONC212 GPR/FFAR
ONC212, a fluorinated-ONC201 analogue, is broadly efficacious across most solid tumors and hematological malignancies in the low nanomolar range and has robust anti-leukemic activity.
M13907 AT2 receptor agonist C21 Angiotensin Receptor
AT2 receptor agonist C21 is a druglike selective angiotensin II AT2 receptor agonist with Ki values of 0.4 nM and >10 µM for the AT2 receptor and AT1 receptor, respectively.
M20982 BNC210 AChR/AChE
H-Ile-Trp-OH, IW-2143
BNC210 (H-Ile-Trp-OH, IW-2143) is a negative allosteric modulator of alpha-7 nicotinic acetylcholine receptor (α7 nAChR).
M25496 DRI-C21045 TNF Receptor
DRI-C21045 is a potent and selective inhibitor of the CD40-CD40L costimulatory protein-protein interaction (PPI) with an IC50 of 0.17 µM. DRI-C21045 shows concentration-dependent inhibition of the activation of NF-κB and B cell proliferation all induced by CD40L with IC50s of 17.1 µM and 4.5 µM, respectively.
M27987 CC214-2  mTOR
CC214-2 is an oral active and selective mTOR kinase inhibitor. CC214-2 targets to both of mTORC1 (pS6) and mTORC2 (pAktS473). CC214-2 induces autophagy, which is a potential target for host-directed therapy (HDT) in tuberculosis. CC214-2 exhibits synergistic bactericidal and sterilizing activity agasinst tuberculosis (TB), and shortens the treatment duration. CC214-2 also inhibits Rapamycin-resistant signaling and the growth of glioblastomas in vitro and in vivo.
M41376 DRI-C21041 TNF Receptor
DRI-C21041 is a CD40/CD40L interaction inhibitor, with an IC50 of 0.31 μM.
M53315 C21 Histone Methyltransferase
C21 is a potent, irreversible, and selective PRMT1 inhibitor with an IC50 of 1.8 μM.
M54819 TC-2153 5-HT Receptor
TC2153
TC-2153 is a selective inhibitor of striatal-enriched protein tyrosine phosphatase (STEP). TC-2153 also inhibits 5-HT2A receptor-mediated signaling.



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