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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8O2
Molecular Weight 124.1372
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ORCINOL

SMILES

CC1=CC(O)=CC(O)=C1

InChI

InChIKey=OIPPWFOQEKKFEE-UHFFFAOYSA-N
InChI=1S/C7H8O2/c1-5-2-6(8)4-7(9)3-5/h2-4,8-9H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Direct chemical analysis of glycoconjugates for carbohydrates.
2001 May
Epinephrine analogues.
2001 Nov
[Studies on chemical constituents of Umbilicaria esculenta (Miyoshi) minks].
2001 Sep
The toxicity and fate of phenolic pollutants in the contaminated soils associated with the oil-shale industry.
2002
O-methyltransferases involved in the biosynthesis of volatile phenolic derivatives in rose petals.
2002 Aug
Identification of clinically relevant Trichosporon species.
2003 Feb
Glucuronuria in the koala.
2003 Jun
Single side strapping: a new approach to fine tuning the anion recognition properties of calix[4]pyrroles.
2003 Jun 18
Systematics of the anamorphic basidiomycetous yeast genus Trichosporon Behrend with the description of five novel species: Trichosporon vadense, T. smithiae, T. dehoogii, T. scarabaeorum and T. gamsii.
2004 May
Total synthesis of alternariol.
2005 Apr 15
Unusual pseudosubstrate specificity of a novel 3,5-dimethoxyphenol O-methyltransferase cloned from Ruta graveolens L.
2005 Aug 1
Intracellular glycosylphosphatidylinositols accumulate on endosomes: toxicity of alpha-toxin to Leishmania major.
2005 Mar
Role of petal-specific orcinol O-methyltransferases in the evolution of rose scent.
2006 Jan
Biochemical and morphological changes in endothelial cells in response to hypoxic interstitial edema.
2006 Jan 13
Cloning of novel laccase isozyme genes from Trametes sp. AH28-2 and analyses of their differential expression.
2006 Jul
Comparison of transcripts in Phalaenopsis bellina and Phalaenopsis equestris (Orchidaceae) flowers to deduce monoterpene biosynthesis pathway.
2006 Jul 13
A thioredoxin of Sinorhizobium meliloti CE52G is required for melanin production and symbiotic nitrogen fixation.
2007 Aug
Physicochemical and surface-active properties of biosurfactant produced using molasses by a Pseudomonas aeruginosa mutant.
2007 Jan
Beta-orcinol metabolites from the lichen Hypotrachyna revoluta.
2007 May 12
[Chemical constituents from herb of Pholidota cantonensis].
2008 Jul
Evaluation of Antiasthmatic Activity of Curculigo orchioides Gaertn. Rhizomes.
2008 Jul-Aug
A sialylation study of mouse brain gangliosides by MALDI a-TOF and o-TOF mass spectrometry.
2008 Jun
SAM levels, gene expression of SAM synthetase, methionine synthase and ACC oxidase, and ethylene emission from N. suaveolens flowers.
2009 Jul
Glycolipid-Dependent, Protease Sensitive Internalization of Pseudomonas aeruginosa Into Cultured Human Respiratory Epithelial Cells.
2010 Dec 13
Cytotoxicity on human cancer cells of ophidiacerebrosides isolated from the African starfish Narcissia canariensis.
2010 Dec 22
Flavonoid profiling and transcriptome analysis reveals new gene-metabolite correlations in tubers of Solanum tuberosum L.
2010 Feb
Acid loads induced by the detoxification of plant secondary metabolites do not limit feeding by common brushtail possums (Trichosurus vulpecula).
2010 Feb
Bioflocculant exopolysaccharide production by Azotobacter indicus using flower extract of Madhuca latifolia L.
2010 Oct
Mice doubly-deficient in lysosomal hexosaminidase A and neuraminidase 4 show epileptic crises and rapid neuronal loss.
2010 Sep 16
Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol.
2014 May 25
Patents
Name Type Language
ORCINOL
MI  
Systematic Name English
3,5-DIHYDROXYTOLUENE
Systematic Name English
ORCINOL [MI]
Common Name English
NSC-12441
Code English
Code System Code Type Description
FDA UNII
534PMB3438
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
WIKIPEDIA
ORCINOL
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-984-2
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
CHEBI
16536
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
CAS
504-15-4
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
NSC
12441
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
MESH
C005282
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
MERCK INDEX
m8229
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID2060123
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
PUBCHEM
10436
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY