PROTOANEMONIN

C=C1OC(=O)C=C1

InChIKey=RNYZJZKPGHQTJR-UHFFFAOYSA-N

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

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

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
Radiation-activated nuclease activity of o,o'-Diphenyleneiodonium cations (DPI): a reductively initiated chain reaction involving the C1' chemistry.	2003 Apr	12643799
Phytodermatitis caused by Ceratocephalus falcatus (Ranunculacea).	2005 Sep-Oct	16172054
Antifungal 3,5-disubstituted furanones: From 5-acyloxymethyl to 5-alkylidene derivatives.	2010 Mar 1	20153653

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

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