Cresols
Chem-Impex International, Inc. 4-Methyl-3-nitrophenol | 2042-14-0 | MFCD00007244 | 100G
4-Methyl-3-nitrophenol, 2042-14-0, MFCD00007244, 100G
Chem-Impex International, Inc. 4-Methyl-3-nitrophenol | 2042-14-0 | MFCD00007244 | 250G
4-Methyl-3-nitrophenol, 2042-14-0, MFCD00007244, 250G
eMolecules 2-Ethyl-6-methylphenol | 1687-64-5 | MFCD00962292 | 1g
Apollo Scientific | 2-Ethyl-6-methylphenol | 1g | 562429630 | OR0472 | | 1687-64-5 | MFCD00962292 | 136.194 | C9H12O
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LRRK2-IN-1 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. LRRK2-IN-1 is an effective and selective LRRK2 inhibitor. purity: 98%
Sigma Organic Chemistry Synperonic(R) F 108 | 250G | 2594628 | MFCD00082049 |
Synperonic(R) F 108 | 250G | 2594628 | MFCD00082049 |
P 22077 1247819-59-5 10mM (in 1mL DMSO)
P 22077 (CAS 1247819-59-5) is a small molecule inhibitor targeting ubiquitin-specific protease 7 (USP7 also known as HAUSP) and to a lesser extent deubiquitinase USP4 USP7 modulates the stability of several regulatory proteins including p53 impacting apoptosis pathways in cancer biology P 22077 demonstrates potent USP7 inhibition with IC values of 8 6 nM in singleplex and 7 8 nM in multiplex in vitro assays and shows minimal activity against related enzymes DEN1 and SENP2core Cellular studies suggest that P 22077-mediated USP7 inhibition destabilizes Tip60 attenuating p53-dependent apoptosis The compound is currently utilized in preclinical research investigating the role of deubiquitination in tumorigenesis
Ambeed 4 6 Acryloyloxy hexyl oxy phe
4-((6-(Acryloyloxy)hexyl)oxy)phenyl 4-((6-(acryloyloxy)hexyl)oxy)benzoate, 151464-39-0, 95%
![MAP kinase fragment [Multiple species] 1mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000093073.png-250.jpg)
MAP kinase fragment [Multiple species] 1mg
MAP kinase fragment is a peptide fragment targeting MAP kinases It is designed to facilitate investigations of cell signaling regulation and enzyme-substrate specificity thereby elucidating kinase activities associated with disease pathways MAP kinase fragment exerts its biological activity primarily through participation in phosphorylation cascades that regulate transcription factors and modulatory proteins Based on these properties MAP kinase fragment holds research potential in studies of cancer and inflammatory disorders
Cayman Chemical p-Cresol sulfatepotasIM500mg
A p75NTR ligand completely inhibits NGF binding to p75NTR in PC12 cells at 100 M binds to NGF dimers (Kd 1 M) to induce a conformational change that prevents NGF binding to p75NTR or TrkA inhibits NGF-induced death of SK-N-MC cells and inhibits autophosphorylation of TrkA in PC12 cells reverses NGF-induced decreases inBcatenin mRNA expression in and migration of SKOV3 and OVCAR-3 ovarian cancer cells