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Referencia número: HY-N2463

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Kushenol E

2 Cited Publications

Revisión del cliente

Based on 2 publication(s) in Google Scholar

Kushenol E is a class of flavonoids isolated from Sophora flavescens and is a non-competitive indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor with an IC₅₀ of 7.7 µM and a K_i of 9.5 µM, has anti-tumor activity.

Para uso exclusivo en investigación. No vendemos a pacientes.

Pureza: 95.32%
No. CAS: 99119-72-9
Fòrmula: C₂₅H₂₈O₆
Peso molecular:424.49

Almacenamiento:

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Kushenol E Chemical Structure

No. CAS: 99119-72-9

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Actividad biológica

Descripciòn

Ver todos los productos específicos de isoformas Indoleamine 2,3-Dioxygenase (IDO) :

Chemical Information

No. CAS 99119-72-9
Appearance Solid
Peso molecular 424.49
Fòrmula C₂₅H₂₈O₆
Color Off-white to light yellow
SMILES

O=C1C[C@@H](C2=CC=C(O)C=C2O)OC3=C(C/C=C(C)\C)C(O)=C(C/C=C(C)\C)C(O)=C13
Structure Classification
- Flavonoids
- Flavonones
- Phenols
- Polyphenols
Initial Source
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Publications (2)

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Phytomedicine

2026 May 25;157:158338.
IET Nanobiotechnol

PLGA-PEG-c(RGDfK)- Kushenol E Micelles With a Therapeutic Potential for Targeting Ovarian Cancer. [Abstract]

2024 Nov 29:2024:7136323. PMID: 39649540

Pureza y Documentación

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Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

Ficha de datos (268 KB)
SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 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)
Instrucciones de manejo (2659 KB)

Referencias

[1]. Kwon M, et al. Inhibitory effects of flavonoids isolated from Sophora flavescens on indoleamine 2,3-dioxygenase 1 activity. J Enzyme Inhib Med Chem. 2019 Dec;34(1):1481-1488. [Content Brief]

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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.

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Kushenol E

2 Cited Publications

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Actividad biológica
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Chemical Information
Publications (2)
Pureza y Documentación
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Kushenol E

Publications Citing Use of MedChemExpress (MCE) Kushenol E

Ver todos los productos específicos de isoformas Indoleamine 2,3-Dioxygenase (IDO)

Actividad biológica

Chemical Information

Publications (2)

Pureza y Documentación

Referencias

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Kushenol E Related Classifications

HY-N2463 Related Classifications