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Referencia número: HY-121770

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Rutarin

Revisión del cliente

Based on 1 Customer Validation

Rutarin is a Coumarin (HY-N0709) derivative with antimalarial and antifungal activities. Rutarin inhibits Plasmodium falciparum with an IC₅₀ of 88 μg/mL. Rutarin also inhibits Coniophora cerebella.

Para uso exclusivo en investigación. No vendemos a pacientes.

Pureza: 99.84%
No. CAS: 20320-81-4
Fòrmula: C₂₀H₂₄O₁₀
Peso molecular:424.40

Almacenamiento:

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Rutarin Chemical Structure

No. CAS: 20320-81-4

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Use of MCE Products

Fluorescent Dye

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

Actividad biológica
- Descripciòn
- In Vitro
Chemical Information
Pureza y Documentación
Referencias
Calculators
Help & FAQs
Classifications
Bioz

Actividad biológica

Descripciòn

Ver todos los productos específicos de isoformas Parasite :

In Vitro

Rutarin completely inhibited Coniophora cerebella at a concentration of 40 μg/disc^[3].

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

Chemical Information

No. CAS 20320-81-4
Appearance Solid
Peso molecular 424.40
Fòrmula C₂₀H₂₄O₁₀
Color White to off-white
SMILES

O=C1C=CC2=CC3=C(C(OC4C(O)C(O)C(O)C(O4)CO)=C2O1)OC(C3)C(O)(C)C
Structure Classification
- Phenylpropanoids
- Coumarins
Initial Source
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Pureza y Documentación

Select Batch:

Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

Ficha de datos (273 KB)
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 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]. Banerji A, et al. Prenylated compounds from Atalantia racemosa: isolation and synthesis of two pyranoflavones. Phytochemistry, 1988, 27(11):3637-3640.

[2]. Lacroix D, et al. Structure and in vitro antiparasitic activity of constituents of Citropsis articulata root bark. J Nat Prod. 2011 Oct 28;74(10):2286-9. [Content Brief]

[3]. Wolters B, et al. Antimicrobial substances in callus cultures of Ruta graveolens. Planta Med. 1981 Oct;43(2):166-74. [Content Brief]

Calculators

Calculadora de molaridad

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

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculadora de dilución

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.

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MOQ

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100 mg

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Actividad biológica
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- In Vitro
Chemical Information
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Referencias

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Rutarin

Ver todos los productos específicos de isoformas Parasite

Actividad biológica

Chemical Information

Pureza y Documentación

Referencias

Calculators

Help & FAQs

Rutarin Related Classifications

HY-121770 Related Classifications