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Cat. No. Product name CAS No.
DCC0994 bim5078

Potent HNF4α antagonist

337506-43-1
DCC0995 Bin-01-07-07

Novel USP28 inhibitor

848205-71-0
DCC0996 Bio-0554019

Novel selective RORgamma inhibitor, selectively inhibiting Th17 differentiation and RORgamma signature gene expression

DCC0997 Bipbipu

Novel heparanase inhibitor

53859-71-5
DCC0998 Biph(2,3',4,5',6)p5

Potent inhibitor of SHIP-2 catalytic activity; Novel inositol polyphosphate surrogate modulating Ca responses in rat hepatocytes

943545-68-4
DCC0999 Biphalin

Potent peptide opioid receptor agonist, alleviating LPS-Induced activation in rat primary microglial cultures in opioid receptor-dependent and receptor-independent manners

83916-01-2
DCC1000 Bis-2-ai Adjuvant-2

Novel adjuvant to repurpose azithromycin for use against Pseudomonas aeruginosa, exhibiting a 1024-fold reduction in the minimum inhibitory concentration of azithromycin in vitro and displays activity in a Galleria mellonella model of infection

DCC1001 Bis-5-methyl-cyclosal-d4tmp

Novel anti-HIV active dimeric prodrug of 2‘,3‘-dideoxy-2‘,3‘-didehydrothymidine monophosphate (d4TMP)

DCC1002 Bisaramil

Class I antiarrhythmic agent with chronotropic, inotropic, dromotropic and coronary vasodilator effects, potently blocking sodium channel

89194-77-4
DCC1003 Bis-cyclosal-d4tmp

Novel anti-HIV active dimeric prodrug of 2‘,3‘-dideoxy-2‘,3‘-didehydrothymidine monophosphate (d4TMP)

DCC1004 Bisdionin F

Selective hAMCase Inhibitor

917877-86-2
DCC1005 Bisindole-pbd

Novel inhibitor of angiogenesis by regulating STAT3 and VEGF in breast cancer cells

DCC1006 Bisleuconothine A

Novel and selective Wnt signaling inhibitor

DCC1007 bis-n-norgliovictin

Novel inhibitor of LPS-induced inflammation in macrophages, improving survival in sepsis

112900-75-1
DCC1008 Bisoctrizole

UV stabilizer

103597-45-1
DCC1009 Bis-salicyl Fumarate

Potent activator of the Neh2-luc reporter

74134-01-3
DCC1010 Bisthianostat

Novel Orally Efficacious Pan-HDAC Inhibitor

1408234-79-6
DCC1011 Bitc-sg

Inactivator of GSTP1>GST P1-1 through the covalent modification of two Cys47 residues per dimer and one Cys101

62959-30-2
DCC1012 Bit-l15

Novel potent antagonist of RORγt function, displaying an increased selectivity for RORγt over RORα and PPARγ compared to the purely orthosteric and allosteric non-PEG-linked parent compounds

DCC1013 Bix-02188me

Potent and selective dual inhibitor of MEK5 and ERK5

334951-92-7
DCC1014 Bjff078

Potent inhibitor of recombinant human and mouse Transglutaminase enzyme activity, mainly TG2 and the close related enzyme TG1

DCC1015 Bjp-06-005-3

Novel potent and selective covalent Pin1 inhibitor

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