Cinnamic acids and derivatives
Selleck Chemical LLC Bisdemethoxycurcumin (BDMC) S3938-25mg
Bisdemethoxycurcumin (BDMC) is a natural demethoxy derivative of curcumin and possesses several biological activities such as anti-inflammation and anti-cancer activities
Selleck Chemical LLC p-Coumaric acid ethyl ester
p-Coumaric acid ethyl ester is the ethyl ester of p-Coumaric acid which is a plant metabolite which exhibits antioxidant and anti-inflammatory properties
TARGETMOL CHEMICALS INC DUVELISIB R ENANTIOMER H 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib.
Cayman Chemical CurcumIn-d6 500ug
An internal standard for the quantification of curcumin by GC- or LC-MS
eMolecules 3-(4-Fluorobenzyloxy)-bromobenzene | 845866-52-6 | MFCD06411657 | 1g
Oakwood Chemical | 3-(4-Fluorobenzyloxy)-bromobenzene | 1g | 537680681 | 023248 | | 845866-52-6 | MFCD06411657 | 281.124 | C13H10BrFO
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TARGETMOL CHEMICALS INC TYRPHOSTIN AG 538 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Tyrphostin AG 538 is a chalcone compound an IGF-1 receptor kinase inhibitor (IC₅0 for 400 nM) that is potent cell-permeable reversible and competitive. purity: 99%
Apexbio Technology LLC Tyrphostin AG 1296 146535-11-7 25mg
Tyrphostin AG 1296 (CAS 146535-11-7) is a selective inhibitor of platelet-derived growth factor receptor (PDGFR) kinase via ATP-competitive binding Its inhibitory activity (IC50 0 3 0 5 M) results from inducing conformational changes in the ATP-binding domain of PDGFR blocking receptor autophosphorylation induced by ligand binding In vitro studies demonstrate inhibition of PDGF-stimulated mitogenesis (IC50 1 5 M) and cell proliferation (IC50 3 2 M) using Swiss 3T3 cells without significant effects on EGF receptor signaling at concentrations up to 100 M Tyrphostin AG 1296 serves as a research tool for investigating PDGFR-mediated signaling pathways
Medchemexpress LLC Z-entacapone | 145195-63-7 | 305.29 | C14H15N3O5 | 5 MG
Z-entacapone is the Z-isomer of entacapone and functions as a catechol-O-methyltransferase (COMT) inhibitor supplied for laboratory research use only. The compound is a characterized research reagent with associated documentation to support quality control and safe handling in experimental workflows.
- Research-grade COMT inhibitor for biochemical and pharmacology studies.
- Supplied in small, accurately weighed quantities suitable for assay development.
- Molecular formula C14H15N3O5 and molecular weight 305.29 g/mol.
- Certificate of analysis and documentation available for quality verification.
- Not for human or therapeutic use; for research use only.
Indofine Chemical Ferulic Acid, 99%, 25 Gm
FERULIC ACID 25 GM, Rare Organics & Biochemicals, 4-Hydroxy-3-methoxycinnamic acid, C10H10O4, MW: 194.19, 0.99, 1135-24-6, MFCD00004400