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Parasal sodium, Granupas (previously para-aminosalicylic acid lucane)(aminosalicylic acid)
Granupas, Neopasalate, Parasal, Rezipas (aminosalicylic acid) is a small molecule pharmaceutical. Aminosalicylic acid was first approved as Parasal sodium on 1982-01-01. It is used to treat crohn disease and tuberculosis in the USA. It has been approved in Europe to treat tuberculosis. The pharmaceutical is active against peroxisome proliferator-activated receptor gamma.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
digestive system diseasesD004066
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Aminosalicylate sodium
Tradename
Company
Number
Date
Products
PARASAL SODIUMPanray CorporationN-006811 DISCN1982-01-01
2 products
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Aminosalicylic acid
Tradename
Company
Number
Date
Products
PARASALPanray CorporationN-006811 DISCN1982-01-01
2 products
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Aminosalicylic acid resin complex
Tradename
Company
Number
Date
Products
REZIPASBristol Myers SquibbN-009052 DISCN1982-01-01
1 products
Hide discontinued
Labels
FDA
EMA
No data
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
crohn diseaseEFO_0000384D003424K50
tuberculosisEFO_0000774D014376A15-A19
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
A: Alimentary tract and metabolism drugs
A07: Antidiarrheals, intestinal antiinflammatory/antiinfective agents
A07E: Intestinal antiinflammatory agents
A07EC: Aminosalicylic acid and similar agents
J: Antiinfectives for systemic use
J04: Antimycobacterials
J04A: Drugs for treatment of tuberculosis
J04AA: Aminosalicylic acid and derivatives
J04AA01: 4-aminosalicylic acid
HCPCS
No data
Clinical
Clinical Trials
17 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Ulcerative colitisD003093EFO_0000729K5125118
Hiv infectionsD015658EFO_0000764B201124
Crohn diseaseD003424EFO_0000384K502114
Immune system diseasesD007154D89.911
Acquired immunodeficiency syndromeD000163EFO_0000765B2011
Sexually transmitted diseasesD012749A50-A6411
Lentivirus infectionsD016180EFO_100135711
Inflammatory bowel diseasesD015212EFO_000376711
Pulmonary tuberculosisD014397EFO_1000049A1511
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Fecal microbiota transplantationD000069467111
Indications Phases 2
No data
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients11
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
TuberculosisD014376EFO_0000774A15-A1911
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameAMINOSALICYLIC ACID
INN
Description
4-aminosalicylic acid is an aminobenzoic acid that is salicylic acid substituted by an amino group at position 4. It has a role as an antitubercular agent. It is an aminobenzoic acid and a member of phenols. It is functionally related to a salicylic acid. It is a conjugate acid of a 4-aminosalicylate(1-).
Classification
Small molecule
Drug classanti-inflammatory agents (salicylic acid derivatives)
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Nc1ccc(C(=O)O)c(O)c1
Identifiers
PDB
CAS-ID65-49-6
RxCUI7833
ChEMBL IDCHEMBL1169
ChEBI ID27565
PubChem CID4649
DrugBankDB00233
UNII ID
Target
Agency Approved
PPARG
PPARG
Organism
Homo sapiens
Gene name
PPARG
Gene synonyms
NR1C3
NCBI Gene ID
Protein name
peroxisome proliferator-activated receptor gamma
Protein synonyms
Nuclear receptor subfamily 1 group C member 3, peroxisome proliferator-activated receptor-gamma 5, peroxisome proliferator-activated receptor-gamma splicing, PPAR-gamma
Uniprot ID
Mouse ortholog
Pparg (19016)
peroxisome proliferator-activated receptor gamma (P37238)
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 10,816 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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67,065 adverse events reported
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