Comparison

Genistin

Manufacturer ChemScene
Category
Type Molecules
Specific against other
Amount 500mg
Item no. CS-4240-500mg
eClass 6.1 32169090
eClass 9.0 32169090
Available
Alternative Names
Genistine; Genistoside; Genistein 7-O-beta-D-glucopyranoside
CAS
529-59-9
Purity
>98%
Formula
C21H20O10
MWt
432.38
Solubility
DMSO : >= 43 mg/mL (99.45 mM)
Clinical Information
No Development Reported
Pathway
Autophagy
Target
Autophagy
Biological Activity
Genistin is the major isoflavonoid of soybeans and soy products. In Vitro: Genistin is the major isoflavonoid of soybeans and soy products. Genistin shows a dose-dependent superoxide scavenging effect and exhibits major effect at 200 uM, corresponding in activity to 0.08 U/mg protein superoxide dismutase (SOD). Results demonstrate that Genistin exhibits a significantly (P<0.01) and a dose-dependent inhibitory effect on the human cancer cell examined, and at higher concentration (100 uM), the cell viability is 59%. Genistin also induces a significant and dose-dependent increase in ROS formation when compare with the untreated control[1]. In Vivo: Myocardial infarct is markedly diminished by pretreatment with Genistin, particularly at the high dose. After 1?h of reperfusion, preconditioning with Genistin at dosages of 20 to 60?mg/kg significantly attenuats the release of lactate dehydrogenase (LDH), creatine kinase (CK) in a dose-dependent manner compare with the I/R group. Results show that the level of malondialdehyde (MDA) is decreased and the activities of superoxide dismutase (SOD) and catalase (CAT) are increased as well as an increased glutathione (GSH) level in a dose-dependent manner by Genistin treatment in I/R. Pretreatment with Genistin (20, 40 and 60?mg/kg) also prevents the expression of P2X7, p-IkappaBalpha, and p-NF-kappaB p65 compare with the model group[2].

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 500mg
Available: In stock
available

Delivery expected until 6/6/2024 

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