Aristolochic acid

Catalog Number	ACM313677-1
CAS Number	313-67-7
Structure
Synonyms	Aristolochic acid A
IUPAC Name	8-Methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
Molecular Weight	341.27
Molecular Formula	C17H11NO7
Canonical SMILES	COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O
InChI	InChI=1S/C17H11NO7/c1-23-12-4-2-3-8-9(12)5-11(18(21)22)14-10(17(19)20)6-13-16(15(8)14)25-7-24-13/h2-6H,7H2,1H3,(H,19,20)
InChI Key	BBFQZRXNYIEMAW-UHFFFAOYSA-N
Purity	98%+ (HPLC)
Storage	Store in dry, low temperature, sealed, 2-8 °C.
Complexity	550
Exact Mass	341.05355169
Heavy Atom Count	25
Monoisotopic Mass	341.05355169
Topological Polar Surface Area	111Ų

Custom Q&A

What is the melting point of Aristolochic acid?

The melting point of Aristolochic acid is 260 °C.

What is the boiling point of Aristolochic acid estimated to be?

The estimated boiling point of Aristolochic acid is 476.92°C.

In what form does Aristolochic acid exist?

Aristolochic acid exists in the form of a powder.

What is the solubility of Aristolochic acid in DMSO?

Aristolochic acid is soluble in DMSO.

What is the hazard class of Aristolochic acid?

Aristolochic acid belongs to Hazard Class 6.1(b).

What are the safety statements associated with Aristolochic acid?

The safety statements associated with Aristolochic acid include 7-35-45-36/37/39-26-53.

What is the main historical use of Aristolochic acid in Chinese medicine?

Aristolochic acid was used in Chinese medicine to treat kidney and urinary diseases, gout, snakebites, asthma, hiccups, pains, and spasms.

What is the main indication for the toxicity of Aristolochic acid according to the FDA?

Due to the associated kidney problems and urothelial cancers, the FDA has issued warnings regarding consumption of AA-containing supplements.

What is the main brand name of Aristolochic acid?

The main brand name of Aristolochic acid is Acidum aristolchicum.

What is the primary use of Aristolochic acid according to pharmacology?

Aristolochic acid is a potent phospholipase A2 inhibitor and is associated with kidney tumor formation in experimental animal models.

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