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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H32O6
Molecular Weight 368.4645
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of PROSTAGLANDIN G2

SMILES

CCCCC[C@H](OO)\C=C\[C@H]1[C@H]2C[C@H](OO2)[C@@H]1C\C=C/CCCC(O)=O

InChI

InChIKey=SGUKUZOVHSFKPH-YNNPMVKQSA-N
InChI=1S/C20H32O6/c1-2-3-6-9-15(24-23)12-13-17-16(18-14-19(17)26-25-18)10-7-4-5-8-11-20(21)22/h4,7,12-13,15-19,23H,2-3,5-6,8-11,14H2,1H3,(H,21,22)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H32O6
Molecular Weight 368.4645
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 2
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P29476
Gene ID: 24598.0
Gene Symbol: Nos1
Target Organism: Rattus norvegicus (Rat)
0.5 µM [EC50]
PubMed

PubMed

TitleDatePubMed
The cyclooxygenase hydroperoxide product PGG(2) activates synaptic nitric oxide synthase: a possible antioxidant response to membrane lipid peroxidation.
2001 Aug 17
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:15:55 GMT 2023
Edited
by admin
on Sat Dec 16 18:15:55 GMT 2023
Record UNII
AZ87DUD2Y8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROSTAGLANDIN G2
Common Name English
(5Z,9.ALPHA.,11.ALPHA.,13E,15S)-9,11-EPIDIOXY-15-HYDROPEROXYPROSTA-5,13-DIEN-1-OIC ACID
Systematic Name English
PGG2
Common Name English
ENDOPEROXIDE G2
Common Name English
(5Z)-7-((1R,4S,5R,6R)-6-((1E,3S)-3-HYDROPEROXY-1-OCTEN-1-YL)-2,3-DIOXABICYCLO(2.2.1)HEPT-5-YL)-5-HEPTENOIC ACID
Systematic Name English
Code System Code Type Description
CHEBI
27647
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
PUBCHEM
5280883
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID00866229
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
CAS
51982-36-6
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
CHEBI
82629
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
WIKIPEDIA
Prostaglandin G2
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
FDA UNII
AZ87DUD2Y8
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
DRUG BANK
DB03866
Created by admin on Sat Dec 16 18:15:55 GMT 2023 , Edited by admin on Sat Dec 16 18:15:55 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE ACTIVE
METABOLITE ACTIVE -> PARENT