U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C11H10O2
Molecular Weight 174.1959
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 3-PHENYLPROPYNOATE

SMILES

CCOC(=O)C#CC1=CC=CC=C1

InChI

InChIKey=ACJOYTKWHPEIHW-UHFFFAOYSA-N
InChI=1S/C11H10O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C11H10O2
Molecular Weight 174.1959
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Murine epidermal xanthine oxidase activity: correlation with degree of hyperplasia induced by tumor promoters.
1987 Dec 1
Cytokine induction in human epidermal keratinocytes exposed to contact irritants and its relation to chemical-induced inflammation in mouse skin.
1994 Jun
A mechanistic approach to the in vivo anti-inflammatory activity of sesquiterpenoid compounds isolated from Inula viscosa.
2001 Nov
Anti-inflammatory and antioxidant properties of Helichrysum italicum.
2002 Mar
Models of acute inflammation in the ear.
2003
The analgesic, antipyretic and anti-inflammatory activity of Diospyros variegata Kruz.
2003 Apr
Anti-inflammatory activity of (E)-1-(3,4-dimethoxyphenyl) butadiene from Zingiber cassumunar Roxb.
2003 Aug
Anti-inflammatory activity of gel containing novel elastic niosomes entrapped with diclofenac diethylammonium.
2008 Aug 6
Anti-inflammatory, analgesic and wound healing activities of the leaves of Memecylon edule Roxb.
2009 Jan 21
Anti-HIV-1 and anti-inflammatory lupanes from the leaves, twigs, and resin of Garcinia hanburyi.
2010 Mar
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:15:20 GMT 2023
Edited
by admin
on Fri Dec 15 19:15:20 GMT 2023
Record UNII
09CYB3Z9MR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL 3-PHENYLPROPYNOATE
Systematic Name English
NSC-41566
Code English
ETHYL 3-PHENYL-2-PROPYNOATE
Systematic Name English
ETHYL 2-PHENYLACETYLENECARBOXYLATE
Systematic Name English
3-PHENYL-2-PROPYNOIC ACID ETHYL ESTER
Systematic Name English
ETHYL PHENYLPROPIOLATE
Systematic Name English
ETHYL PHENYLACETYLENECARBOXYLATE
Systematic Name English
PROPIOLIC ACID, PHENYL-, ETHYL ESTER
Systematic Name English
ETHYL PHENYLPROPYNOATE
Systematic Name English
ETHYL 3-PHENYLPROPARGYLATE
Common Name English
2-PROPYNOIC ACID, 3-PHENYL-, ETHYL ESTER
Systematic Name English
ETHYL 3-PHENYLPROPIOLATE
Systematic Name English
Code System Code Type Description
PUBCHEM
91516
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY
CAS
2216-94-6
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-703-8
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY
NSC
41566
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID9074858
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY
FDA UNII
09CYB3Z9MR
Created by admin on Fri Dec 15 19:15:20 GMT 2023 , Edited by admin on Fri Dec 15 19:15:20 GMT 2023
PRIMARY