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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H30O4
Molecular Weight 334.4498
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of PROSTAGLANDIN A2

SMILES

CCCCC[C@H](O)\C=C\[C@H]1C=CC(=O)[C@@H]1C\C=C/CCCC(O)=O

InChI

InChIKey=MYHXHCUNDDAEOZ-FOSBLDSVSA-N
InChI=1S/C20H30O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h4,7,12-18,21H,2-3,5-6,8-11H2,1H3,(H,23,24)/b7-4-,14-12+/t16-,17-,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H30O4
Molecular Weight 334.4498
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 2
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Prostaglandin A inhibits replication of human immunodeficiency virus during acute infection.
1991 Nov
Inhibition of nuclear factor kappa B by prostaglandin A1: an effect associated with heat shock transcription factor activation.
1997 Jan 21
Prostaglandins stimulate the stress-induced synthesis of hsp27 and alpha B crystallin.
1997 Mar
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:44:38 GMT 2023
Edited
by admin
on Fri Dec 15 19:44:38 GMT 2023
Record UNII
K6VT5BDY9E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROSTAGLANDIN A2
Common Name English
NSC-165561
Code English
(Z)-7-((1R,2S)-2-((E)-(3S)-3-HYDROXYOCT-1-ENYL)-5-OXOCYCLOPENT-3-ENYL)HEPT-5-ENOIC ACID
Systematic Name English
(+)-PROSTAGLANDIN A2
Common Name English
15(S)-HYDROXY-9-OXO-5-CIS-10,13-TRANS-PROSTATRIENOIC ACID
Systematic Name English
DINOPROSTONE IMPURITY D [EP IMPURITY]
Common Name English
PGA2
Common Name English
PROSTA-5,10,13-TRIEN-1-OIC ACID, 15-HYDROXY-9-OXO-, (5Z,13E,15S)-
Systematic Name English
(5Z,13E,15S)-15-HYDROXY-9-OXOPROSTA-5, 10,13-TRIENE-1-OIC ACID
Systematic Name English
MEDULLIN
Brand Name English
DINOPROSTONE IMPURITY, (5Z,13E,15S)-15-HYDROXY-9-OXOPROSTA-5, 10,13-TRIENE-1-OIC ACID- [USP IMPURITY]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID20864388
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
CHEBI
27820
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
NSC
165561
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
CAS
13345-50-1
Created by admin on Fri Dec 15 19:44:38 GMT 2023 , Edited by admin on Fri Dec 15 19:44:38 GMT 2023
PRIMARY
CHEBI
133370
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
MESH
C100008
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
PUBCHEM
5280880
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
FDA UNII
K6VT5BDY9E
Created by admin on Fri Dec 15 19:44:39 GMT 2023 , Edited by admin on Fri Dec 15 19:44:39 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP