Protease Inhibitors

Immunogen 16 amino amino terminus of human DFF40. Application Used as a blocking peptide in immunoblotting applications.

DOCK2-IN-1 (compound 3), a CPYPP ( HY-110100 ) analogue, is an inhibitor of DOCK2 as well ( IC 50 =19.1 μM). DOCK2-IN-1 binds to DOCK2 DHR-2 domain in a reversible manner to inhibits its catalytic activity. DOCK2-IN-1 blocks the activation of both

DOCK2-IN-1 (compound 3), a CPYPP ( HY-110100 ) analogue, is an inhibitor of DOCK2 as well ( IC 50 =19.1 μM). DOCK2-IN-1 binds to DOCK2 DHR-2 domain in a reversible manner to inhibits its catalytic activity. DOCK2-IN-1 blocks the activation of both

Dolastatin 15 is a member of the dolastatin family. Dolastatins are marine natural products isolated from the sea hare|Dolabella auricularia|with a structure related to Dolastin 10. Dolastatin 15 is an anti-neoplastic pseudopeptide that inhibits

DOTA-PEG5-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:SolidIC50&amp: Target:PEGsIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3 ubiquitin ligase and the

DOTA-PEG5-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Appearance:SolidIC50&amp: Target:PEGsIn Vitro:PROTACs contain two different ligands connected by a linker: one is a ligand for an E3 ubiquitin ligase and the

Biochem/physiol Actions dTRIM24, a conjugate of IACS-9571 a TRIM24 bromodomain ligand and VL-269 a VHL E3 ubiquitin ligase ligand, is a selective bifunctional degrader of bromodomain-containing transcriptional regulator TRIM24 (transcriptional

Biochem/physiol Actions dTRIM24, a conjugate of IACS-9571 a TRIM24 bromodomain ligand and VL-269 a VHL E3 ubiquitin ligase ligand, is a selective bifunctional degrader of bromodomain-containing transcriptional regulator TRIM24 (transcriptional

A cell-permeable thiophenylethanone compound that acts a direct, reversible, and selective inhibitor of deubiquitylating enzymes (DUBs) USP7 and USP47 (IC 50 = 8.01 &amp 8.

DUB-IN-3 is a potent deubiquitinase (USP) enzyme inhibitor extracted from reference compound 22c with an IC 50 of 0.56 μM for USP8Form:SolidIC50&amp: Target:IC50: 0.56 μM (USP8).

DUB-IN-3 is a potent deubiquitinase (USP) enzyme inhibitor extracted from reference compound 22c with an IC 50 of 0.56 μM for USP8Form:SolidIC50&amp: Target:IC50: 0.56 μM (USP8).

DUB-IN-3 is a potent deubiquitinase (USP) enzyme inhibitor extracted from reference compound 22c with an IC 50 of 0.56 μM for USP8Form:SolidIC50&amp: Target:IC50: 0.56 μM (USP8).