Protein Purification
Apexbio Technology LLC HCV protease inhibitor,potent and selective. Boceprevir 10mg. 394730-60-0. MFCD22208555
HCV protease inhibitor,potent and selective. Boceprevir 10mg. 394730-60-0. MFCD22208555
Echelon Biosciences Research Labs PPlases Substare, fluorogenic - 10 mg, CAS#: 142997-31-7
PPlases Substare, fluorogenic - 10mg , Succinyl-Ala-Leu-Pro-Phe-AMC Category/Application: Enzyme Substrates This item is non returnable
Echelon Biosciences Research Labs Granulocyte Elastase Substrate, human - 10 mg,
Granulocyte Elastase Substrate, human - 10mg , Glp-Pro-Val-pNA Category/Application: Enzyme Substrates This item is non returnable
Selleck Chemical LLC AZD7762 5mg 860352-01-8
AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-free assay. It is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck. Phase 1. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC AT7519 25mg 844442-38-2
AT7519 is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM. It is less potent to CDK3 and little active to CDK7. AT7519 also inhibits GSK3? with IC50 of 89 nM. AT7519 induces apoptosis. Phase 2. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC HY-111507 10mg Medchemexpress, PDGFRα kinase inhibitor 1 CAS:2209053-93-8 Purity:>98%
Medchemexpress, HY-111507 10mg PDGFRα kinase inhibitor 1 CAS:2209053-93-8 PDGFRα kinase inhibitor 1 is a highly selective type II PDGFRα kinase inhibitor with IC50s of 132 nM and 6115 nM for PDGFRα and PDGFRβ, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-112373 1mg Medchemexpress, Aurora Kinase Inhibitor 3 CAS:879127-16-9 Purity:>98%
Medchemexpress, HY-112373 1mg Aurora Kinase Inhibitor 3 CAS:879127-16-9 Aurora Kinase Inhibitor 3 is a strong and selective Aurora A kinase inhibitor with an IC50 of 42 nM, and weakly inhibits EGFR with an IC50>10 μM. Aurora Kinase Inhibitor 3 has a binding mode with the cyclopropanecarboxylic acid moiety directed towards the solvent exposed region of the ATP-binding pocket, and several induced structural changes in the active-site compared with other published AIK structures. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Invivogen Escherichia coli outer membrane vesicles (OMVs), 100 ug
Outer membrane vesicles (OMVs) are small, non-replicative, immunogenic spherical bodies secreted by both commensal and pathogenic Gram-negative bacteria such as E. coli. OMVs contain components of the parent bacterium such as DNA, RNA, peptidoglycan, protein, toxins, and lipopolysaccharides (LPS), which act as pathogen-associated molecular patterns (PAMPs).
Medchemexpress LLC KRAS G12D INHIBITOR 18 5MG
MedChemExpress | KRAS G12D inhibitor 18 | 10 mg | HY-156819 -5mg | 2922732-54-3 |Purity: 98.80% | 2922732-54-3 | MW: 1168.44
Echelon Biosciences Research Labs SS14 Tumor Inhibitor Analog - 0.5 mg,
SS14 Tumor Inhibitor Analog - 0.5mg , D-Nal-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2 Category/Application: Neuropeptides Hormones This item is non returnable
Cayman Chemical GPX4 InhIbItr 17 10mg
A GPX4 inhibitor and ferroptosis inducer; inhibits GPX4 activity by 49.16% at 1 µM; increases the production of ROS and levels of MDA in OS-RC-2 cells 0.5 µM; induces ferroptosis in HT-1080 cells (IC50s = 0.007 and 1.486 µM, in the absence and presence of ferrostatin-1, respectively); reduces tumor volume and intratumoral GPX4 levels in an OS-RC-2 mouse xenograft model 20 mg/kg
Cayman Chemical ProstaglndIn E2 InhIbItr 3 5mg
An mPGES-1 inhibitor (IC50 = 0.2 µM); selective for mPGES-1 over COX-1, COX-2, 5-LO, and sEH in cell-free assays at 10 µM; inhibits IL-1β-induced production of PGE2 in A549 cells and LPS-induced IL-6 and PGE2 production in J774A.1 macrophages at 10 and 1 µM, respectively; inhibits the formation of 5-LO products, including LTB4 and 5-H(p)ETE, induced by A23187 alone or with arachidonic acid and A23187 (IC50s = 4.9 and 5.2 µM, respectively); prevents leukocyte infiltration into the peritoneal fluid in a mouse model of zymosan-induced peritonitis at 10 mg/kg
Medchemexpress LLC IDH1 inhibitor 1 | 2234285-81-3 | 100.0% | 450.39 g/mol | C20H18F4N6O2 | 5 MG
IDH1 inhibitor 1 is a small-molecule research compound that selectively inhibits mutant isocitrate dehydrogenase 1 (IDH1), reducing the oncometabolite 2-hydroxyglutarate and showing activity in preclinical cancer models. It is reported to be orally bioavailable and brain-penetrant, and is provided for laboratory research use.
- Selective inhibitor of mutant IDH1 enzymes.
- Reduces 2-hydroxyglutarate (2-HG) production in cell and animal models.
- Orally bioavailable with reported brain penetration.
- High reported purity suitable for research applications.
- Available in small-mass packages for preclinical studies.
Apexbio Technology LLC PRO INHIB COCKT EDTA-FREE 1ML
PRO INHIB COCKT EDTA-FREE 1ML APEXBIO TECHNOLOGIES
AG Scientific Inc Protease Inhib Cocktail VIII
Protease Inhibitor Cocktail VIII is a specially formulated mixture of three protease inhibitors with selective specificity for the inhibition of cysteine proteases, including calpains, cathepsins and papain. Each vial contains: 1.56 mM ALLN 500uM Antipain 1.5 mM E-64 Preparation: Supplied as a liquid in 1 mL DMSO. Add to water, aqueous buffer or directly to extraction media.