Isoflavonoids
Selleck Chemical LLC 3-hydroxy Puerarin S3260-1mg
3 -hydroxy Puerarin is an isoflavone isolated from Puerariae Lobatae Radix
Cayman Chemical Necrostatin-1 Inactive Contro
A synthetic dipeptide with immunomodulatory properties on both innate and adaptive immune responses in in vitro studies
Cayman Chemical PHGDH-InactIve 10mg
A potential metabolite produced during metabolism of AB-CHMINACA in vivo intended for forensic and research applications
Selleck Chemical LLC Genistin (Genistoside) S2301-50mg
Genistin (Genistoside Genistine Genistein 7-glucoside Genistein glucoside) is an isoflavone found in a number of dietary plants like soy and kudzu Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of Estrogen Receptor (ER ) signaling pathway
Selleck Chemical LLC Daidzin S2289-50mg
Daidzin (Daidzoside Daidzein 7-O-glucoside Daidzein 7-glucoside) a natural organic compound in the class of phytochemicals known as isoflavones is a potent and selective inhibitor of human mitochondrial aldehyde dehydrogenase and inhibits ALDH-I selectively (Ki 20 nM) at least 500 times less effective against ALDH- the cytosolic isozyme (Ki 10 M)
AdipoGen Genistein
Chemical. CAS 446-72-0. Formula C15H10O5. MW 270.2. Synthetic. Cell-permeable, reversible, substrate competitive tyrosine kinase inhibitor including EGFR phosphorylation, implicated in almost all cell growth and proliferation signal cascades. Inhibitor of mammalian DNA topoisomerase II. Anticancer agent, inducing cell cycle arrest and apoptosis. Antiangiogenic agent, down-regulates the transcription of genes involved in controlling angiogenesis. Binds estrogen receptor beta. Can increase the rate of growth of some ER expressing breast cancers. Potent alpha-glucosidase inhibitor. Anthelmintic. Anti-diabetic. Activates nuclear receptors, oestrogen receptors and peroxisome proliferator-activated receptors all PPAR isoforms and it inhibits various enzyme activities. Inhibitor of GLUT4-mediated glucose uptake in 3T3-L1 adipocytes. Stimulator of autophagy vacuolization. Antioxidant. TRAIL sensitizer. Acts as an agonist at the GPR30 receptor.
AdipoGen Genistein
Chemical. CAS 446-72-0. Formula C15H10O5. MW 270.24. Genistein is an isoflavonoid phytoestrogen that has been found in soybeans and has kinase inhibitory, anticancer, pro-cancer and hepatoprotective properties. It is a cell-permeable, reversible, substrate competitive tyrosine kinase inhibitor including EGFR phosphorylation, implicated in almost all cell growth and proliferation signal cascades. Genistein inhibits proliferation and induces cell cycle arrest and apoptosis in a variety of cancer cells. It is antiangiogenic agent, down-regulates the transcription of genes involved in controlling angiogenesis. On a molecular level it also inhibits mammalian DNA topoisomerase II and DNA methyltransferase, and binds to estrogen receptor beta. Genistein has also antidiabetic, anti-inflammatory, antimicrobial and antioxidant properties.
Sigma Aldrich Fine Chemicals Biosciences Genistein synthetic 98 HPL5MG
Genistein is an isoflavonoid present among Leguminosae family of plants. It is structurally similar to estrogen (estradiol-17).
TARGETMOL CHEMICALS INC Formononetin 500MG
Also available in 1 mL, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Formononetin (Flavosil) is an O-methylated isoflavone and a phytoestrogen from the root of Astragalus membranaceus. Purity 99.38%
Cayman Chemical 3-hydroxy PuerarIn 10mg
A multi-kinase inhibitor has been used as an affinity ligand for proteomics-based kinome analyses of cancer cells
Cayman Chemical 3-hydroxy PuerarIn 25mg
A multi-kinase inhibitor has been used as an affinity ligand for proteomics-based kinome analyses of cancer cells
Sigma Aldrich Fine Chemicals Biosciences Genistein synthtic 98 HPL100MG
Genistein is an isoflavonoid present among Leguminosae family of plants. It is structurally similar to estrogen (estradiol-17).
Selleck Chemical LLC Genistein 100mg 446-72-0
Genistein, a phytoestrogen found in soy products, is a highly specific inhibitor of protein tyrosine kinase (PTK) which blocks the mitogenic effect mediated by EGF on NIH-3T3 cells with IC50 of 12?M or by insulin with IC50 of 19 ?M. *For Research & Development use only. Product is not intended for drug, household, or human consumption.