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Art. -Nr.: HY-119958

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Acamelin

Acamelin is a Benzofuranoquinone compound that acts as a contact sensitizer. It can be isolated from the heartwood of Acacia melanoxylon R. Br., an Australian blackwood. Acamelin induces positive skin reactions and contact allergy in guinea pigs. It is applicable to research related to allergic contact dermatitis.

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CAS. Nr.: 74161-27-6
Formel: C₁₀H₈O₄
Molecular Weight:192.17

Speicherung:

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

Acamelin Chemical Structure

CAS. Nr.: 74161-27-6

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Use of MCE Products

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

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

Beschreibung

In Vivo

Acamelin (1% concentration; epicutaneous; single application) acts as a contact sensitizer in sensitized Pirbright white-strain guinea pigs, eliciting positive skin reactions in all tested animals, with slightly stronger and longer-lasting responses than 2,6-Dimethoxy-1,4-benzoquinone (HY-N1677)^[1].

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

Animal Model:

Pirbright white-strain (female, allergic contact dermatitis model)^[1]
Dosage:

1% concentration
Administration:

epicutaneous; single application
Result:

Elicited ++ skin reaction in 2 of 5 guinea pigs, + reaction in 2, and (+) reaction in 1 at 24 hours post-challenge.
Elicited ++ skin reaction in 2 of 5 guinea pigs, + reaction in 2, and (+) reaction in 1 at 48 hours post-challenge.
Induced slightly stronger and longer-lasting skin reactions than co-isolated 2,6-dimethoxy-1,4-benzoquinone.

Chemical Information

CAS. Nr. 74161-27-6
Appearance Solid
Molecular Weight 192.17
Formel C₁₀H₈O₄
SMILES

O=C(C=C(C1=O)OC)C2=C1OC(C)=C2
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]. Hausen BM, et al. Quinonoid constituents as contact sensitisers in Australian blackwood (Acacia melanoxylon RBR). British journal of industrial medicine. 1981 May;38(2):105-9.

[2]. McKittrick B A, et al. A simple synthesis of the natural benzofuranoquinone, acamelin[J]. Journal of the Chemical Society, Perkin Transactions 1, 1983, 12: 2423-2424.

[3]. Schmalle H W, et al. Acamelin, A new sensitizing furano-quinone from Acacia melanoxylon R. BR[J]. Tetrahedron Letters, 1980, 21(2): 149-152.

[4]. Mann J, et al. Rearrangements of aryl-8-oxabicyclo [3.2. 1] octenones: synthesis of novel biaryls and 1-aryl-3-furylpropanones[J]. Journal of the Chemical Society, Chemical Communications, 1985, 21(21): 1543-1544.

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.

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MOQ

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100 mg

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