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Art. -Nr.: HY-N21889

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Lansiumamide C

Lansiumamide C is a cinnamamide derivative isolated from the diethyl ether extract of Clausena lansium seeds. Lansiumamide C exhibits antifungal activity against Sclerotinia sclerotiorum. Lansiumamide C can be used in fungi-related research.

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CAS. Nr.: 121817-38-7
Formel: C₁₈H₁₉NO
Molecular Weight:265.35

Speicherung:

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

Lansiumamide C Chemical Structure

CAS. Nr.: 121817-38-7

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Use of MCE Products

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

Biologische Aktivität
- Beschreibung
- In Vitro
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

In Vitro

Fungal InfectionOthers

Fungal Infection

Lansiumamide C (compound 2) (3-5 days) exhibits high antifungal activity against Sclerotinia sclerotiorum with an EC₅₀ of 13.24 μg/mL^[3].

Others

Lansiumamide C is predicted to have a relatively strong binding affinity for the PTGS2 protein in molecular docking analysis^[1].
Lansiumamide C is predicted to target the EGFR protein in molecular docking analysis, although no strong binding affinity was reported for it^[1].
Lansiumamide C is predicted to have a strong binding affinity for the MMP9 protein in molecular docking analysis^[1].

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

Chemical Information

CAS. Nr. 121817-38-7
Molecular Weight 265.35
Formel C₁₈H₁₉NO
SMILES

CN(CCC1=CC=CC=C1)C(/C=C/C2=CC=CC=C2)=O
Structure Classification
- Alkaloids
- Alkaloid Dimers
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

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

Reinheit & Dokumentation

Handling Instructions (2659 KB)

Verweise

[1]. Dewan S, et al. An integrative evaluation of in vitro anti-inflammatory potential, network pharmacology and molecular docking of Girardinia diversifolia (Urticaceae) relevant to rheumatoid arthritis. In Silico Pharmacol. 2026 Sep 6;14(3):232.

[2]. Yang Y, et al. Design and synthesis of novel cinnamamide derivatives-based lansiumamide B as potent fungicidal candidates. Pest management science. 2025 Aug;81(8):4863-4874.

[3]. He Y, et al. Bioassay‑guided isolation of antifungal amides against Sclerotinia sclerotiorum from the seeds of Clausena lansium. Industrial Crops & Products. 2018;121:352‑359.

Calculators

Molaritätsrechner

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

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

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

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MOQ

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100 mg

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