PROTOANEMONIN

Details

Stereochemistry	ACHIRAL
Molecular Formula	C5H4O2
Molecular Weight	96.0841
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C=C1OC(=O)C=C1

InChI

InChIKey=RNYZJZKPGHQTJR-UHFFFAOYSA-N

InChI=1S/C5H4O2/c1-4-2-3-5(6)7-4/h2-3H,1H2

HIDE SMILES / InChI

Molecular Formula	C5H4O2
Molecular Weight	96.0841
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
The refined X-ray structure of muconate lactonizing enzyme from Pseudomonas putida PRS2000 at 1.85 A resolution.	1995 Dec 15	7500361
From xenobiotic to antibiotic, formation of protoanemonin from 4-chlorocatechol by enzymes of the 3-oxoadipate pathway.	1995 Dec 8	7493952
Detoxification of protoanemonin by dienelactone hydrolase.	1998 Jan	9440530
[Poisonous and less poisonous plants. 52].	2001 Aug	14584174
Polychlorinated biphenyl-degrading microbial communities in soils and sediments.	2002 Jun	12057677
Radiation-activated nuclease activity of o,o'-Diphenyleneiodonium cations (DPI): a reductively initiated chain reaction involving the C1' chemistry.	2003 Apr	12643799
Chemical composition of anther volatiles in Ranunculaceae: genera-specific profiles in Anemone, Aquilegia, Caltha, Pulsatilla, Ranunculus, and Trollius species.	2004 Dec	21652345
The release of 5-methylene-2-furanone from irradiated DNA catalyzed by cationic polyamines and divalent metal cations.	2005 Jan	15606311
25 years of natural product R&D with New South Wales agriculture.	2005 Oct 31	18007515
2-Deoxyribonolactone lesions in X-ray-irradiated DNA: quantitative determination by catalytic 5-methylene-2-furanone release.	2005 Sep 26	16136620
DNA strand damage product analysis provides evidence that the tumor cell-specific cytotoxin tirapazamine produces hydroxyl radical and acts as a surrogate for O(2).	2007 Oct 24	17900117
Pseudomonas aeruginosa strain RW41 mineralizes 4-chlorobenzenesulfonate, the major polar by-product from DDT manufacturing.	2008 Jun	18331335
DNA cleavage and binding selectivity of a heterodinuclear Pt-Cu(3-Clip-Phen) complex.	2008 May	18270754
Salt stress-induced alterations in the root proteome of barley genotypes with contrasting response towards salinity.	2009	19671579
Novel metal-binding site of Pseudomonas reinekei MT1 trans-dienelactone hydrolase.	2009 Dec 25	19895788
Irritant contact dermatitis from plants.	2009 Mar-Apr	19426612
Interleukin-6 and Cyclooxygenase-2 downregulation by fatty-acid fractions of Ranunculus constantinopolitanus.	2009 Nov 16	19917107
Edaphic and Phytochemical Factors as Predictors of Equine Grass Sickness Cases in the UK.	2010	21833167
The biological and metabolic fates of endogenous DNA damage products.	2010 Dec 16	21209721
Antifungal 3,5-disubstituted furanones: From 5-acyloxymethyl to 5-alkylidene derivatives.	2010 Mar 1	20153653
Proteome analysis of soybean leaves, hypocotyls and roots under salt stress.	2010 Mar 29	20350314
Quantification of the 2-deoxyribonolactone and nucleoside 5'-aldehyde products of 2-deoxyribose oxidation in DNA and cells by isotope-dilution gas chromatography mass spectrometry: differential effects of gamma-radiation and Fe2+-EDTA.	2010 May 5	20377226
Factors affecting the yields of C1' and C5' oxidation products in radiation-damaged DNA: the indirect effect.	2010 Nov	20954863
Consortia modulation of the stress response: proteomic analysis of single strain versus mixed culture.	2010 Sep	20406297
Ranunculin.	2010 Sep 4	21587499

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:38:28 UTC 2023` Edited by `admin` on `Fri Dec 15 18:38:28 UTC 2023`
Record UNII	66FQZ1A5SO
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PROTOANEMONIN

Common Name

English

5-METHYLENE-2(5H)-FURANONE

Systematic Name

English

PROTOANEMONIN [MI]

Common Name

English

5-METHYLENE-2,5-DIHYDROFURAN-2-ONE

Systematic Name

English

2(5H)-FURANONE, 5-METHYLENE-

Systematic Name

English

ISOMYCIN

Brand Name

English

2,4-PENTADIEN-4-OLIDE

Common Name

English

Code System Code Type Description

FDA UNII

66FQZ1A5SO