Substance

ID:118

Aminosalicylic Acid

Names and Identifiers
IUPAC Traditional name
aminosalicylic acid
IUPAC name
4-amino-2-hydroxybenzoic acid
Synonyms
4-aminosalicylic acidP-Aminosalicylic AcidPara-Amino Salicylic AcidAminosalicylate Sodium4-ASAPASPara-aminosalicylic acidAPASPASKAminosalicylic AcidAmino-PAS
Brand Name
ApacilDeapasilHellipidylNeopasalatePamisylParasalPropasaPAS-CPara-PasParasalindonPasaraPasaPasdiumPasmedPasnodiaPasolacSanipriol-4AminoparFerrosanOsacylPamacylParamycinKyselina P-AminosalicylovaParasalicilRezipasAminoxEntepasGabbropasPasalonPascorbicPasemPaserSanipirol-4
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
1.6
Solubility
1690 mg/L
Molecule Details
Drug Groups
approved
Description
An antitubercular agent often administered in association with isoniazid. The sodium salt of the drug is better tolerated than the free acid. [PubChem]
Indication
For the treatment of tuberculosis
Pharmacology
Aminosalicylic acid is an anti-mycobacterial agent used with other anti-tuberculosis drugs (most often isoniazid) for the treatment of all forms of active tuberculosis due to susceptible strains of tubercle bacilli. The two major considerations in the clinical pharmacology of aminosalicylic acid are the prompt production of a toxic inactive metabolite under acid conditions and the short serum half life of one hour for the free drug. Aminosalicylic acid is bacteriostatic against Mycobacterium tuberculosis (prevents the multiplying of bacteria without destroying them). It also inhibits the onset of bacterial resistance to streptomycin and isoniazid.
Toxicity
LD50=4 gm/kg (orally in mice); LD50=3650 mg/kg (orally in rabbits)
Affected Organisms
Mycobacteria
Biotransformation
Hepatic.
Protein Binding
50-60%
External Links
Molecular Spectra
No Data Available
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References
No Data Available
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