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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

Molecular Formula C7H8O2
Molecular Weight 124.1372
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Metabolism of resorcinylic compounds by bacteria: orcinol pathway in Pseudomonas putida.
1976 Mar
Estimation of biodegradation parameters of phenolic compounds on activated sludge by respirometry.
2001 Aug
Direct chemical analysis of glycoconjugates for carbohydrates.
2001 May
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
Single side strapping: a new approach to fine tuning the anion recognition properties of calix[4]pyrroles.
2003 Jun 18
Structures and histamine release inhibitory effects of prenylated orcinol derivatives from Rhododendron dauricum.
2004 Jul
Total synthesis of alternariol.
2005 Apr 15
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
Nutrition rehabilitation of undernourished children utilizing Spiruline and Misola.
2006 Jan 23
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
Ganglioside from eel serum high density lipoprotein (HDL) and its role as a ligand for HDL binding protein.
2007 Aug
Physicochemical and surface-active properties of biosurfactant produced using molasses by a Pseudomonas aeruginosa mutant.
2007 Jan
[Chemical constituents from herb of Pholidota cantonensis].
2008 Jul
Anti-HIV-1 activities of compounds isolated from the medicinal plant Rhus chinensis.
2008 May 8
New insight into the effects of lead modulation on antioxidant defense mechanism and trace element concentration in rat bone.
2009 Mar
Bioactive metabolites produced by Penicillium sp. 1 and sp. 2, two endophytes associated with Alibertia macrophylla (Rubiaceae).
2009 Nov-Dec
Acid loads induced by the detoxification of plant secondary metabolites do not limit feeding by common brushtail possums (Trichosurus vulpecula).
2010 Feb
Identification of orcinol reactive substance in pleural fluid cell lysate--a new parameter for classification of pleural effusion.
2010 May 2
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:51:19 GMT 2023
Edited
by admin
on Fri Dec 15 18:51:19 GMT 2023
Record UNII
534PMB3438
Record Status Validated (UNII)
Record Version
  • Download
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