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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8N2O2
Molecular Weight 152.1506
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,5-Diaminobenzoic acid

SMILES

NC1=CC(=CC(N)=C1)C(O)=O

InChI

InChIKey=UENRXLSRMCSUSN-UHFFFAOYSA-N
InChI=1S/C7H8N2O2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H,8-9H2,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C7H8N2O2
Molecular Weight 152.1506
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Organic cadmium complexes as proteasome inhibitors and apoptosis inducers in human breast cancer cells.
2013-06
Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities.
2010-10-26
Comparative effects of oleoyl-estrone and a specific beta3-adrenergic agonist (CL316, 243) on the expression of genes involved in energy metabolism of rat white adipose tissue.
2010-02-25
Dendronized polyimides bearing long-chain alkyl groups and their application for vertically aligned nematic liquid crystal displays.
2009-11-19
Three-dimensional metal azide coordination polymers with amino carboxylate coligands: synthesis, structure, and magnetic properties.
2009-06-01
Latent synthesis of electrically conductive surface-silvered polyimide films.
2009-01
Semiquantitative RT-PCR measurement of gene expression in rat tissues including a correction for varying cell size and number.
2007-11-26
Photochemical reactivity of trifluoromethyl aromatic amines: the example of 3,5-diamino-trifluoromethyl-benzene (3,5-DABTF).
2005-09-10
Synthesis of segmented poly(ether urethane)s and poly(ether urethane urea)s incorporating various side-chain or backbone functionalities.
2005
Selective catalysis with peptide dendrimers.
2004-06-30
Reducing the alkali cation adductions of oligonucleotides using sol-gel-assisted laser desorption/ionization mass spectrometry.
2003-08-15
Highly antibacterial active aminoacyl penicillin conjugates with acylated bis-catecholate siderophores based on secondary diamino acids and related compounds.
2002-07-04
A fluorometric assay for the determination of 1-deoxy-D-xylulose 5-phosphate synthase activity.
2001-09-01
Design and synthesis of benzoic acid derivatives as influenza neuraminidase inhibitors using structure-based drug design.
1997-12-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:10:54 GMT 2025
Edited
by admin
on Mon Mar 31 19:10:54 GMT 2025
Record UNII
1609U1093N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,5-DIAMINOBENZOIC ACID [MI]
Preferred Name English
3,5-Diaminobenzoic acid
MI  
Systematic Name English
DIAMINOBENZOIC ACID, 1,5-
Common Name English
Code System Code Type Description
MERCK INDEX
m4250
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY Merck Index
CAS
535-87-5
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-621-0
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY
PUBCHEM
12062
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY
FDA UNII
1609U1093N
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID1044437
Created by admin on Mon Mar 31 19:10:54 GMT 2025 , Edited by admin on Mon Mar 31 19:10:54 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT