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> Main
CHEBI:27565 - 4-aminosalicylic acid
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ChEBI Name
4-aminosalicylic acid
ChEBI ID
CHEBI:27565
Definition
An aminobenzoic acid that is salicylic acid substituted by an amino group at position 4.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:41152, CHEBI:1789, CHEBI:20320
Supplier Information
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Read full article at Wikipedia
Formula
C7H7NO3
Net Charge
0
Average Mass
153.13540
Monoisotopic Mass
153.04259
InChI
InChI=1S/C7H7NO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,8H2,(H,10,11)
InChIKey
WUBBRNOQWQTFEX-UHFFFAOYSA-N
SMILES
Nc1ccc(C(O)=O)c(O)c1
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
antitubercular agent
A substance that kills or slows the growth of
Mycobacterium tuberculosis
and is used in the treatment of tuberculosis.
Application
(s):
antitubercular agent
A substance that kills or slows the growth of
Mycobacterium tuberculosis
and is used in the treatment of tuberculosis.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
4-aminosalicylic acid (
CHEBI:27565
)
has functional parent
salicylic acid (
CHEBI:16914
)
4-aminosalicylic acid (
CHEBI:27565
)
has role
antitubercular agent (
CHEBI:33231
)
4-aminosalicylic acid (
CHEBI:27565
)
is a
aminobenzoic acid (
CHEBI:22495
)
4-aminosalicylic acid (
CHEBI:27565
)
is a
phenols (
CHEBI:33853
)
4-aminosalicylic acid (
CHEBI:27565
)
is conjugate acid of
4-aminosalicylate(1−) (
CHEBI:137598
)
Incoming
4-aminosalicylate(1−) (
CHEBI:137598
)
is conjugate base of
4-aminosalicylic acid (
CHEBI:27565
)
IUPAC Name
4-amino-2-hydroxybenzoic acid
Synonyms
Sources
2-HYDROXY-4-AMINOBENZOIC ACID
PDBeChem
4-Aminosalicylate
KEGG COMPOUND
4-Aminosalicylic acid
KEGG COMPOUND
Aminosalicylic acid
ChemIDplus
p
-aminosalicylic acid
NIST Chemistry WebBook
Para-amino salicylic acid
ChemIDplus
PAS
ChemIDplus
Brand Name
Source
Paser
DrugBank
Manual Xrefs
Databases
2050
DrugCentral
Aminosalicylic_Acid
Wikipedia
BHA
PDBeChem
C02518
KEGG COMPOUND
D00162
KEGG DRUG
DB00233
DrugBank
DE50835
Patent
HMDB0014378
HMDB
LSM-5862
LINCS
US2844625
Patent
US427564
Patent
View more database links
Registry Numbers
Types
Sources
306153
Gmelin Registry Number
Gmelin
473071
Reaxys Registry Number
Reaxys
65-49-6
CAS Registry Number
ChemIDplus
65-49-6
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
11621575
PubMed citation
Europe PMC
1650428
PubMed citation
Europe PMC
23118010
PubMed citation
Europe PMC
24663015
PubMed citation
Europe PMC
25050392
PubMed citation
Europe PMC
25421465
PubMed citation
Europe PMC
25605031
PubMed citation
Europe PMC
25963985
PubMed citation
Europe PMC
26004847
PubMed citation
Europe PMC
26033719
PubMed citation
Europe PMC
26277036
PubMed citation
Europe PMC
26596566
PubMed citation
Europe PMC
26848874
PubMed citation
Europe PMC
27021327
PubMed citation
Europe PMC
27491492
PubMed citation
Europe PMC
27617928
PubMed citation
Europe PMC
27671064
PubMed citation
Europe PMC
28011126
PubMed citation
Europe PMC
28223391
PubMed citation
Europe PMC
28394286
PubMed citation
Europe PMC
28408267
PubMed citation
Europe PMC
28567674
PubMed citation
Europe PMC
28651968
PubMed citation
Europe PMC
28717039
PubMed citation
Europe PMC
28812999
PubMed citation
Europe PMC
Last Modified
17 August 2017
General Comment
2014-05-06
It is found in samples of blood and urine of individuals who have used this drug.