Substance

ID:431

Names and Identifiers
IUPAC Traditional name
azelaic acid
Synonyms
Azelaic AcidNonanedioic acidLepargylic acidAnchoic acidAzalaic AcidAzelainic acidn-Nonanedioic acidHeptanedicarboxylic acid
IUPAC name
nonanedioic acid
Brand Name
Emery's L-110Emerox 1110AzelexEmerox 1144FinaceaFinevinSkinoren
Registration numbers
PubChem CID
CAS Number
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
1.7
Solubility
2400 mg/L (20 oC)
Molecule Details
Drug Groups
approved
Description
Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley. It is a natural substance that is produced by Malassezia furfur (also known as Pityrosporum ovale), a yeast that lives on normal skin. It is effective against a number of skin conditions, such as mild to moderate acne, when applied topically in a cream formulation of 20%. It works in part by stopping the growth of skin bacteria that cause acne, and by keeping skin pores clear. Azelaic acid's antimicrobial action may be attributable to inhibition of microbial cellular protein synthesis.
Indication
For the topical treatment of mild-to-moderate inflammatory acne vulgaris.
Pharmacology
Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley. It is a natural substance that is produced by Malassezia furfur (also known as Pityrosporum ovale), a yeast that lives on normal skin. It is effective against a number of skin conditions, such as mild to moderate acne, when applied topically in a cream formulation of 20%. It works in part by stopping the growth of skin bacteria that cause acne, and by keeping skin pores clear. Azelaic acid's antimicrobial action may be attributable to inhibition of microbial cellular protein synthesis.
Toxicity
Oral LD50 in rat: >5 g/kg
Affected Organisms
Various aerobic and anaerobic microorganisms
Biotransformation
Mainly excreted unchanged in the urine but undergoes some b-oxidation to shorter chain dicarboxylic acids.
Absorption
Approximately 4% of the topically applied azelaic acid is systemically absorbed.
Half Life
The observed half-lives in healthy subjects are approximately 45 minutes after oral dosing and 12 hours after topical dosing, indicating percutaneous absorption rate-limited kinetics.
Elimination
Azelaic acid is mainly excreted unchanged in the urine, but undergoes some ?-oxidation to shorter chain dicarboxylic acids.
External Links
Molecular Spectra
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References
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