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Cat. No. Product Name Information
PC-73312

FQI2

LSF inhibitor

Factor quinolinone inhibitor 2 (FQI2) is a small molecule inhibitor of transcription factor LSF, inhibits LSF DNA-binding activity both in vitro and in cells (IC50=0.71 uM).
PC-73176

PPA904

Photosensitizer

PPA-904 is a specific phenothiazine photosensitizer in photodynamic therapy (PDT) research, especially topical application for cutaneous leishmaniasis in vivo.
PC-73160

ALC-0315

Vaccine adjuvant

ALC-0315 is a synthetic ionizable amino lipid that has been used in combination with other lipids in the formation of lipid nanoparticles, has attracted attention as a component of the SARS-CoV-2 vaccine.
PC-73146

FR 901463

FR 901463 is an anti-tumor agent isolated from the fermentation broth of Pseudomonas sp. No. 2663.
PC-72761

UbV SP.3

STAMBP inhibitor

UbV SP.3 is potent, selective inhibitor of STAMBP isopeptidase activity with KD/IC50 of 60/9.8 nM, with significant preferential binding to STAMBP over STAMBPL1 (250 -fold selectivity).
PC-72760

UbV SP.1

STAMBP inhibitor

UbV SP.1 is potent, selective inhibitor of STAMBP isopeptidase activity with KD of 0.05/0.18 uM for STAMBP/STAMBPL1, respectively.
PC-72756

TTFB

ZAC antagonist

TTFB (ZAC antagonist TTFB) is a selective antagonist (negative allosteric modulator) of Zinc-Activated Channel (ZAC) with IC50 of 3 uM.
PC-72459

JumOCA peptide Tat

OCA-B peptide inhibitor

JumOCA peptide Tat is a a peptide corresponding to the OCA-B N terminus, as C-terminal fusions to the HIV trans-activator of transcription (Tat) protein for membrane permeability.
PC-72131

BD442618

GPR52 agonist

BD442618 (BD 442618) is a potent small-molecule GPR52 agonist.
PC-72016

CNI103

Calcineurin-NFAT inhibitor

CNI103 (CNI-103) is a highly potent, cell-permeable, metabolically stable peptidyl inhibitor of Calcineurin-NFAT interaction wioth KD 16 nM and IC50 of 220 nM.
PC-35763

5-Formyl-2-pyrimidinecarbonitrile

5-Formyl-2-pyrimidinecarbonitrile is a chemical intermidate..
PC-60921

Ethyl 3,4-dihydroxybenzoate

A prolyl 4-hydroxylase inhibitor and the collagen synthesis inhibitor, selectively reduces procollagen production in fibroblast cultures..

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