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Boeravinone B - ≥97.0%, high purity , CAS No.114567-34-9

  • ≥97%
Item Number
B647406
Grouped product items
SKUSizeAvailabilityPrice Qty
B647406-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$350.90

Phenols Polyphenols Others

Basic Description

Synonymsboeravinone B|114567-34-9|6,9,11-trihydroxy-10-methyl-6H-chromeno[3,4-b]chromen-12-one|6a,12a-Dehydro-6,9,11-trihydroxy-10-methylrotenone|10-Methyl-6,9,11-trihydroxy[1]benzopyrano[3,4-b][1]benzopyran-12(6H)-one|boeravinoneB|CHEMBL376240|SCHEMBL3320676|Boe
Specifications & Purity≥97%
Biochemical and Physiological MechanismsBoeravinone B, a dual inhibitor of NorA bacterial efflux pump of Staphylococcus aureus and human P-Glycoprotein , reduces the biofilm formation and intracellular invasion of bacteria. Boeravinone B act as anti-aging and anti-apoptosis phyto-molecules duri
Storage TempProtected from light,Store at -80°C
Shipped InIce chest + Ice pads
Product Description

Boeravinone B, a dual inhibitor of NorA bacterial efflux pump of Staphylococcus aureus and human P-Glycoprotein , reduces the biofilm formation and intracellular invasion of bacteria. Boeravinone B act as anti-aging and anti-apoptosis phyto-molecules during oxidative stress.

In Vitro

Boeravinone B is also active against a methicillin-resistant S. aureus (MRSA) strain, which showed a fourfold reduction in the ciprofloxacin MIC. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Associated Targets

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCG2 Tchem ATP-binding cassette sub-family G member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 6,9,11-trihydroxy-10-methyl-6H-chromeno[3,4-b]chromen-12-one
INCHI InChI=1S/C17H12O6/c1-7-9(18)6-11-13(14(7)19)15(20)12-8-4-2-3-5-10(8)23-17(21)16(12)22-11/h2-6,17-19,21H,1H3
InChi Key YVVDYYFGAWQOGB-UHFFFAOYSA-N
Canonical SMILES CC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=CC=CC=C4OC3O)O
Isomeric SMILES CC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=CC=CC=C4OC3O)O
Alternate CAS 114567-34-9
PubChem CID 14018348
MeSH Entry Terms 6,9,11-trihydroxy-10-methyl-6a,12a-dehydroretenoid;boeravinone B
Molecular Weight 312.27

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMSO : 50 mg/mL (160.12 mM; Need ultrasonic)

Related Documents

Solution Calculators