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Details

Stereochemistry ACHIRAL
Molecular Formula C19H14O3
Molecular Weight 290.3127
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AURIN

SMILES

OC1=CC=C(C=C1)C(C2=CC=C(O)C=C2)=C3C=CC(=O)C=C3

InChI

InChIKey=FYEHYMARPSSOBO-UHFFFAOYSA-N
InChI=1S/C19H14O3/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15/h1-12,20-21H

HIDE SMILES / InChI

Molecular Formula C19H14O3
Molecular Weight 290.3127
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Aurintricarboxylic acid and Evans Blue represent two different classes of anionic compounds which selectively inhibit the cytopathogenicity of human T-cell lymphotropic virus type III/lymphadenopathy-associated virus.
1986 Apr 14
Fuchsin acid selectively inhibits human immunodeficiency virus (HIV) replication in vitro.
1988 Sep 30
Selective inhibitory activity of polyhydroxycarboxylates derived from phenolic compounds against human immunodeficiency virus replication.
1991
Identification of caspase-3 and caspase-activated deoxyribonuclease in rat blastocysts and their implication in the induction of chromatin degradation (but not nuclear fragmentation) by high glucose.
2001 Feb
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003 Oct
Characterization of recombinant integrase of human immunodeficiency virus type 1 (isolate Bru).
2003 Sep
[Injectable dyes: more than 70 years of therapeutic usage of dyes].
2005
Differential activation of heme oxygenase-1 by chalcones and rosolic acid in endothelial cells.
2005 Feb
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Gene expression-based screening for inhibitors of PDGFR signaling.
2008
Discovery of selective glucocorticoid receptor modulators by multiplexed reporter screening.
2009 Mar 24
Exploring the influence of steric, electronic and lipophilic descriptors of 1,3-diarly propenones on their anti-inflammatory activity.
2010
Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein.
2015 Feb
The quinone methide aurin is a heat shock response inducer that causes proteotoxic stress and Noxa-dependent apoptosis in malignant melanoma cells.
2015 Jan 16
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 00:40:02 GMT 2023
Edited
by admin
on Sat Dec 16 00:40:02 GMT 2023
Record UNII
85N4AK3JAU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AURIN
MI  
Common Name English
2,5-CYCLOHEXADIEN-1-ONE, 4-(BIS(4-HYDROXYPHENYL)METHYLENE)-
Systematic Name English
4-(P,P'-DIHYDROXYBENZHYDRYLIDENE)-2,5-CYCLOHEXADIEN-1-ONE
Common Name English
4,4'-DIHYDROXYFUCHSONE
Common Name English
4-(BIS(P-HYDROXYPHENYL)METHYLENE)CYCLOHEXA-2,5-DIEN-1-ONE
Common Name English
4-(BIS(4-HYDROXYPHENYL)METHYLENE)CYCLOHEXA-2,5-DIEN-1-ONE
Systematic Name English
NSC-7805
Code English
AURIN [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m2142
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY Merck Index
MESH
C017037
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
PUBCHEM
5100
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
WIKIPEDIA
AURIN
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
NSC
7805
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
CAS
603-45-2
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID2022387
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
FDA UNII
85N4AK3JAU
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
ECHA (EC/EINECS)
210-041-8
Created by admin on Sat Dec 16 00:40:02 GMT 2023 , Edited by admin on Sat Dec 16 00:40:02 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT