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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
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.
2015-02
The quinone methide aurin is a heat shock response inducer that causes proteotoxic stress and Noxa-dependent apoptosis in malignant melanoma cells.
2015-01-16
Exploring the influence of steric, electronic and lipophilic descriptors of 1,3-diarly propenones on their anti-inflammatory activity.
2010
Discovery of selective glucocorticoid receptor modulators by multiplexed reporter screening.
2009-03-24
Gene expression-based screening for inhibitors of PDGFR signaling.
2008
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Differential activation of heme oxygenase-1 by chalcones and rosolic acid in endothelial cells.
2005-02
[Injectable dyes: more than 70 years of therapeutic usage of dyes].
2005
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Characterization of recombinant integrase of human immunodeficiency virus type 1 (isolate Bru).
2003-09
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.
2001-02
Selective inhibitory activity of polyhydroxycarboxylates derived from phenolic compounds against human immunodeficiency virus replication.
1991
Fuchsin acid selectively inhibits human immunodeficiency virus (HIV) replication in vitro.
1988-09-30
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.
1986-04-14
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:38:46 GMT 2025
Edited
by admin
on Mon Mar 31 20:38:46 GMT 2025
Record UNII
85N4AK3JAU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AURIN
MI  
Common Name English
NSC-7805
Preferred 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
AURIN [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m2142
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY Merck Index
MESH
C017037
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
PUBCHEM
5100
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
WIKIPEDIA
AURIN
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
NSC
7805
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
CAS
603-45-2
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID2022387
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
FDA UNII
85N4AK3JAU
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-041-8
Created by admin on Mon Mar 31 20:38:46 GMT 2025 , Edited by admin on Mon Mar 31 20:38:46 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT