Aminosalicylic Acid

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Also known as AminosalicylateAminosalicylic acid resin complexGranupasNSC-2083P-aminosalicylic acidPara-aminosalicylic acidParasalPasPaserRezipasParaaminosalicyclic acidSID855553para-aminosalicyclic acidSID29215427SID56422457AminosalycilateACIDE_AMINOSALICYLIQUEAMINOSALICYLATE SODIUMPara amino salicylic acid

Summary

Aminosalicylic Acid (CHEMBL1169) is an approved small-molecule antitubercular agent (ATC J04AA01); indicated across 5 conditions including tuberculosis and pulmonary tuberculosis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J04AA01
  • Indications: 5 conditions
  • Clinical trials: 14
  • Chemistry: 153.14 Da · C7H7NO3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1169
NameAminosalicylic Acid
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID4649
ChEBICHEBI:27565
ATCJ04AA01
Molecular formulaC7H7NO3
Molecular weight153.14
InChIKeyWUBBRNOQWQTFEX-UHFFFAOYSA-N

SMILES: C1=CC(=C(C=C1N)O)C(=O)O

IUPAC name: 4-amino-2-hydroxybenzoic acid

ChEBI definition: An aminobenzoic acid that is salicylic acid substituted by an amino group at position 4.

Pharmacological roles (ChEBI): antitubercular agent.

Also known as: Aminosalicylate, Aminosalicylic acid, Aminosalicylic acid resin complex, Granupas, NSC-2083, P-aminosalicylic acid, Para-aminosalicylic acid, Parasal, Pas, Paser, Rezipas, p-aminosalicylic acid

Parent form; salt/anhydrous children: CHEMBL1200584, CHEMBL1200966, CHEMBL1343453, CHEMBL1378207, CHEMBL2096646, CHEMBL2105983

Patent coverage: 20,894 distinct patent families (51,677 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 51,605 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 3 (assay-derived). Sample: Microtubule-associated protein tau, Lysine-specific demethylase 4E, Tyrosine-protein phosphatase non-receptor type 1.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

1 approved indication. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
tuberculosis4MONDO:0018076MONDO:0018076

3 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
pulmonary tuberculosis3MONDO:0006052EFO:1000049
ulcerative colitis2MONDO:0005101EFO:0000729
Crohn disease2MONDO:0005011EFO:0000384

Clinical trials

Total trials: 14.

Phase distribution

PhaseTrials
Not specified6
PHASE34
PHASE12
PHASE41
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02331823PHASE4UNKNOWNResearch on New Regimens for Retreatment Pulmonary Tuberculosis
NCT06081361PHASE3ACTIVE_NOT_RECRUITINGInnovating Shorter, All- Oral, Precised, Individualized Treatment Regimen for Rifampicin Resistant Tuberculosis:Contezolid, Delamanid and Bedaquiline Cohort
NCT00984568PHASE3TERMINATEDConventional Step-Up Versus Infliximab Monotherapy in Patients With Ulcerative Colitis (P05553)
NCT01320436PHASE3COMPLETEDCurcumin + Aminosalicylic Acid (5ASA) Versus 5ASA Alone in the Treatment of Mild to Moderate Ulcerative Colitis
NCT02683733PHASE3UNKNOWNBio-enhanced Curcumin as an Add-On Treatment in Mild to Moderate Ulcerative Colitis
NCT00417690PHASE2TERMINATEDHigh Dose Oral 4-Aminosalicylic Acid (PASER®) to Control Acute Flares of Mild to Moderate Crohn’s Disease
NCT00069498PHASE1COMPLETEDEffect of an Anti-Inflammatory Drug on Gut Mucosa in HIV Infected Patients
NCT03070405PHASE1UNKNOWNThe Effect of PAS on the Pharmacokinetics of Tenofovir in Healthy Subjects
NCT00000796Not specifiedCOMPLETEDA Prospective Study of Multidrug Resistance and a Pilot Study of the Safety of and Clinical and Microbiologic Response to Levofloxacin in Combination With Other Antimycobacterial Drugs for Treatment of Multidrug-Resistant Pulmonary Tuberculosis (MDRTB) in HIV-Infected Patients.
NCT00905866Not specifiedCOMPLETEDQuality of Life in Patients Undergoing Parathyroidectomy
NCT01875068Not specifiedTERMINATEDA Program of Physician Supervision to Improve the Quality of Patient Referrals From Nurse Practitioners and Physician Assistants
NCT02284087Not specifiedCOMPLETEDPaired Associative Stimulation in Post-stroke Hand Motor Deficits
NCT04499495Not specifiedCOMPLETEDAssessment of 5-Aminosalicylic Acid Prescription Patterns and Treatment Outcomes in Patients With Ulcerative Colitis in Korea
NCT04938284Not specifiedCOMPLETEDCombining PAS to Non-invasive VNS

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

PharmGKB dosing guidelines (1) — CPIC / DPWG genotype-guided dosing for this drug (drug × pharmacogene):

GuidelineSourceGene(s)DosingRecommendation
Annotation of CPIC Guideline for aminosalicylic acid, chloramphenicol,CPICG6PD

PharmGKB also curates 0 clinical and 1 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).