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Details

Stereochemistry ACHIRAL
Molecular Formula C14H11N
Molecular Weight 193.2438
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-AMINOANTHRACENE

SMILES

NC1=CC=CC2=CC3=CC=CC=C3C=C12

InChI

InChIKey=YUENFNPLGJCNRB-UHFFFAOYSA-N
InChI=1S/C14H11N/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-9H,15H2

HIDE SMILES / InChI

Molecular Formula C14H11N
Molecular Weight 193.2438
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Doxorubicin toxicity can be ameliorated during antioxidant L-carnitine supplementation.
2011-02-11
Comparison of different cytotoxicity measurements for the in vitro micronucleus assay using L5178Y and TK6 cells in support of OECD draft Test Guideline 487.
2010-10-29
Effect of 1-aminoanthracene (1-AMA) binding on the structure of three lipocalin proteins, the dimeric β lactoglobulin, the dimeric odorant binding protein and the monomeric α1-acid glycoprotein. Fluorescence spectra and lifetimes studies.
2010-09
m-Azipropofol (AziPm) a photoactive analogue of the intravenous general anesthetic propofol.
2010-08-12
Ligand binding turns moth pheromone-binding protein into a pH sensor: effect on the Antheraea polyphemus PBP1 conformation.
2009-11-13
A high-throughput approach for identification of novel general anesthetics.
2009-09-24
Phenylalanine 35 and tyrosine 82 are involved in the uptake and release of ligand by porcine odorant-binding protein.
2009-08
Microbial metabolism of 1-aminoanthracene by Beauveria bassiana.
2008-05-01
Determination of highly soluble L-carnitine in biological samples by reverse phase high performance liquid chromatography with fluorescent derivatization.
2007-08
Dissociation and unfolding of bovine odorant binding protein at acidic pH.
2007-07
Purification, cloning and regulation of a novel acid-lipase-like protein of hamster expressed in lacrimal glands and tears during lactation.
2007-01
Odorant binding protein has the biochemical properties of a scavenger for 4-hydroxy-2-nonenal in mammalian nasal mucosa.
2006-11
Roles of replicative and specialized DNA polymerases in frameshift mutagenesis: mutability of Salmonella typhimurium strains lacking one or all of SOS-inducible DNA polymerases to 26 chemicals.
2005-09-28
Odorant binding initially occurring at the central pocket in bovine odorant-binding protein.
2005-08-12
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
Binding of the volatile general anesthetics halothane and isoflurane to a mammalian beta-barrel protein.
2005-01
Crystal structures of bovine odorant-binding protein in complex with odorant molecules.
2004-10
Unfolding and refolding of porcine odorant binding protein in guanidinium hydrochloride: equilibrium studies at neutral pH.
2003-12-01
In vitro lipolysis by human pancreatic lipase is specifically abolished by its inactive forms.
2003-02-21
Control of domain swapping in bovine odorant-binding protein.
2002-08-01
Identification of a third rat odorant-binding protein (OBP3).
2001-07
Revisiting the specificity of Mamestra brassicae and Antheraea polyphemus pheromone-binding proteins with a fluorescence binding assay.
2001-06-08
Genotoxic potency in Drosophila melanogaster of selected aromatic amines and polycyclic aromatic hydrocarbons as assayed in the DNA repair test.
1993-12
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:44:42 GMT 2025
Edited
by admin
on Mon Mar 31 18:44:42 GMT 2025
Record UNII
8H6056DWN2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-60017
Preferred Name English
1-AMINOANTHRACENE
Systematic Name English
1-ANTHRACYLAMINE
Systematic Name English
AMINOANTHRACENE, 1-
Systematic Name English
1-ANTHRYLAMINE
Systematic Name English
1-ANTHRACENYLAMINE
Systematic Name English
.ALPHA.-AMINOANTHRACENE
Common Name English
1-ANTHRACENAMINE
Systematic Name English
1-ANTHRAMINE
Systematic Name English
Code System Code Type Description
DRUG BANK
DB01976
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID00209859
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
NSC
60017
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-225-8
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
MESH
C049062
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
PUBCHEM
11885
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
FDA UNII
8H6056DWN2
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
CAS
610-49-1
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
WIKIPEDIA
Anthramine
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY
CHEBI
40678
Created by admin on Mon Mar 31 18:44:42 GMT 2025 , Edited by admin on Mon Mar 31 18:44:42 GMT 2025
PRIMARY