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Cat. No.: HY-N9806

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3',3'''-Biapigenin

Name: 3',3'''-Biapigenin
Brand: MedChemExpress
SKU: HY-N9806
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1 Cited Publications

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Based on 1 publication(s) in Google Scholar

3',3'''-Biapigenin is a naturally occurring C-C linked biflavone composed of two apigenin units connected through a B-ring-B-ring linkage.

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CAS No.: 151455-26-4
Formule: C₃₀H₁₈O₁₀
Masse moléculaire:538.46

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Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (277 KB)

3',3'''-Biapigenin Chemical Structure

CAS No.: 151455-26-4

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Activité biologique
- Description
- In Vitro
Chemical Information
Publications (1)
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
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Activité biologique

Description

3',3'''-Biapigenin is a naturally occurring C-C linked biflavone composed of two apigenin units connected through a B-ring-B-ring linkage^[1].

In Vitro

3',3'''-Biapigenin can be prepared via Suzuki‑Miyaura coupling of boronic acids as the key reaction, followed by Claisen‑Schmidt condensation, cyclization, and deprotection reactions^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS No. 151455-26-4
Masse moléculaire 538.46
Formule C₃₀H₁₈O₁₀
SMILES

O=C1C=C(C2=CC(C3=CC(C(OC4=C5C(O)=CC(O)=C4)=CC5=O)=CC=C3O)=C(O)C=C2)OC6=C1C(O)=CC(O)=C6
Structure Classification
- Flavonoids
Initial Source
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Publications (1)

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Sci Rep

Discovery of natural apigenin analogues as lysine-specific demethylase 1 inhibitors against tumoral testicular germ cells. [Abstract]

2026 Mar 2;16(1):8917. PMID: 41772063

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (277 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[1]. Duan J, et al. Synthesis of biflavonoid frameworks using Suzuki-Miyaura coupling with boronic acids. Agriculture and Natural Resources, 2026, 60(4).

Calculators

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Keywords

3',3'''-Biapigenin

1 Cited Publications

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Activité biologique
- Description
- In Vitro
Chemical Information
Publications (1)
Pureté et documentation
Références

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3',3'''-Biapigenin

Publications Citing Use of MedChemExpress (MCE) 3',3'''-Biapigenin