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Cat. No.: HY-N21670

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Aristolochic acid IIIa 6-O-β-D-glucoside

Aristolochic acid IIIa 6-O-β-D-glucoside is an aristolochic acid monoglycoside and a nitrophenanthrene derivative that is found in the roots of Aristolochia cinnabarina.

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

CAS No.: 157196-45-7
Formula: C₂₂H₁₉NO₁₂
Molecular Weight:489.39

Storage:

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

Aristolochic acid IIIa 6-O-β-D-glucoside Chemical Structure

CAS No.: 157196-45-7

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

Biological Activity
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- In Vitro
Chemical Information
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Biological Activity

Description

Aristolochic acid IIIa 6-O-β-D-glucoside is an aristolochic acid monoglycoside and a nitrophenanthrene derivative that is found in the roots of Aristolochia cinnabarina^[1]^[2]^[3]^[4]^[5].

All Endogenous Metabolite Isoforms :

In Vitro

The new compound isolated from Aristolochia cinnabarina roots is aristolochic acid IIIa-6-O-β-D-glucoside, a β-D-glucopyranoside of aristolochic acid IIIa, as established by UV, IR, FAB-MS, HRFAB-MS, ¹H NMR and ¹³C NMR analysis^[3].

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

Chemical Information

CAS No. 157196-45-7
Molecular Weight 489.39
Formula C₂₂H₁₉NO₁₂
SMILES

OC[C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1OC2=CC=C3C(C4=C5C(OCO5)=CC(C(O)=O)=C4C([N+]([O-])=O)=C3)=C2
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]. Nachtergael A, et al. In vitro genotoxicity tests point to an unexpected and harmful effect of a Magnolia and Aristolochia association. Journal of ethnopharmacology. 2015 Nov 04;174:178-86.

[2]. Michl J, et al. Medicinally Used Asarum Species: High-Resolution LC-MS Analysis of Aristolochic Acid Analogs and Toxicity Screening in HK-2 Cells. Frontiers in pharmacology. 2017;8:215.

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

[4]. Giang PM, et al. Review on NMR spectroscopic data and recent analytical methods of aristolochic acids and derivatives in Aristolochia herbs. Natural products and bioprospecting. 2025 Jun 24;15(1):41.

[5]. Achenbach H, et al. 6-O-beta-D-glucoside of aristolochic acid IIIa and other components from the roots of Aristolochia baetica. Planta Med. 1997 Dec;63(6):579.

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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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Aristolochic acid IIIa 6-O-β-D-glucoside

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Biological Activity
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Aristolochic acid IIIa 6-O-β-D-glucoside

All Endogenous Metabolite Isoforms

Biological Activity

Description

In Vitro

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

Aristolochic acid IIIa 6-O-β-D-glucoside Related Classifications

HY-N21670 Related Classifications

Bioz

Keywords

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