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Cat. No.: HY-N21669

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2-Hydroxy-8-methoxycepharanone A

2-Hydroxy-8-methoxycepharanone A is a tetraoxygenated aristolactam alkaloid that is found in Aristolochia cinnabarina.

For research use only. We do not sell to patients.

CAS No.: 157196-46-8
Formula: C₁₇H₁₁NO₅
Molecular Weight:309.28

Storage:

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

2-Hydroxy-8-methoxycepharanone A Chemical Structure

CAS No.: 157196-46-8

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Use of MCE Products

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

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
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Biological Activity

Description

2-Hydroxy-8-methoxycepharanone A is a tetraoxygenated aristolactam alkaloid that is found in Aristolochia cinnabarina^[1]^[2]^[3]^[4].

All Endogenous Metabolite Isoforms :

In Vitro

2-Hydroxy-8-methoxycepharanone A is a C-2 substituted aristolactam isolated from Aristolochia cinnabarina^[1].
2-Hydroxy-8-methoxycepharanone A is a novel aristolactam isolated from the roots of Aristolochia cinnabarina, characterized by a phenolic hydroxyl group at the C-2 position and a methoxy group at the C-8 position^[2].

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

Chemical Information

CAS No. 157196-46-8
Molecular Weight 309.28
Formula C₁₇H₁₁NO₅
SMILES

O=C1NC=2C=C3C(OC)=CC=CC3=C4C=5OCOC5C(O)=C1C24
Structure Classification
- Alkaloids
- Indole Alkaloids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. Kuo PC,et al. Chemical Constituents and Pharmacology of the Aristolochia ( mădōu ling) species. J Tradit Complement Med. 2012 Oct;2(4):249-66.

[2]. Li H, et al. Eleven aristolochic acid derivatives from Aristolochia cinnabarina. Phytochemistry. 1994 Sep;37(1):237-9.

[3]. Kumar V, et al. Naturally occurring aristolactams, aristolochic acids and dioxoaporphines and their biological activities. Natural product reports. 2003 Dec;20(6):565-83. [Content Brief]

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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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