G0897

Genistin

from Glycine max (soybean), ≥95% (HPLC)

• Synonym(s): 4′,5,7-Trihydroxyisoflavone 7-glucoside, Genistein 7-glucoside, Genistein-7-O-β-D-glucopyranoside, Genistoside, NSC 5112
• Empirical Formula (Hill Notation): C₂₁H₂₀O₁₀
• CAS Number: 529-59-9
• Molecular Weight: 432.38
• Beilstein: 64479
• MDL number: MFCD00016883
• UNSPSC Code: 12352200
• PubChem Substance ID: 24895028
• NACRES: NA.77

Properties

• biological source: Glycine max (soybean)
• Quality Level: 200
• Assay: ≥95% (HPLC)
• solubility: DMSO: 10 mg/mL
• storage temp.: −20°C
• SMILES string: OC[C@H]1O[C@@H](Oc2cc(O)c3C(=O)C(=COc3c2)c4ccc(O)cc4)[C@H](O)[C@@H](O)[C@@H]1O
• InChI: 1S/C21H20O10/c22-7-15-18(26)19(27)20(28)21(31-15)30-11-5-13(24)16-14(6-11)29-8-12(17(16)25)9-1-3-10(23)4-2-9/h1-6,8,15,18-24,26-28H,7H2/t15-,18-,19+,20-,21-/m1/s1
• InChI key: ZCOLJUOHXJRHDI-CMWLGVBASA-N

Description

Application

Genistin has been used for immune reactivity against influenza viruses in vitro and as an internal standard in isoflavones quantification.

Biochem/physiol Actions

Inactive analog of genistein; useful as a negative control for genistein and other tyrosine kinase inhibitors.

Selective inhibitor of mammalian terminal deoxynucleotidyl transferase (TdT), with no measurable effect on mammalian or microbial DNA polymerases.

Features and Benefits

This compound is featured on the Dopamine and Norepinephrine Metabolism and Histamine Synthesis and Metabolism pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves