Name: 20-ethyl Prostaglandin E2
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HIT ID:HIT218832662
Cas No:
Common Name:20-ethyl Prostaglandin E2
alias:20-ethyl PGE2
IUPAC:7-[3-hydroxy-2-(3-hydroxydec-1-en-1-yl)-5-oxocyclopentyl]hept-5-enoic acid
IUPAC:7-[3-hydroxy-2-(3-hydroxydec-1-en-1-yl)-5-oxocyclopentyl]hept-5-enoic acid
InChI key:NXMMZTNQIJBMBC-UHFFFAOYSA-N

Molecular Formula:C22H36O5
Molecular Weight:380.525
Hydrogen Bond Donor (HBD):
Hydrogen Bond Acceptor (HBA):
LogP:
SMILES:CCCCCCCC(O)C=CC1C(O)CC(=O)C1CC=CCCCC(O)=O
SMILES:CCCCCCCC(O)C=CC1C(O)CC(=O)C1CC=CCCCC(O)=O

20-Ethyl Prostaglandin E2 (20-ethyl PGE2) is an analog of Prostaglandin E2 (PGE2) characterized by an extended ω-chain due to two additional methylene carbon atoms. Compared to unoprostone, a clinically approved glaucoma medication and the only extensively studied prostaglandin analog sharing this structural modification, 20-ethyl PGE2 maintains the natural 15(S) allylic hydroxyl in its lower side chain, potentially enhancing its effectiveness. Unoprostone, despite being an F-series prostaglandin, exhibits reduced affinity for FP receptors because of its lower side chain modifications (13,14-dihydro-15-keto), which diminishes its medicinal potency. Notably, 20-ethyl PGE2's efficacy relative to unoprostone and its interaction with EP or other prostanoid receptors remains unconfirmed due to the lack of published ligand binding assays. E-type prostaglandins, including 20-ethyl PGE2, are broadly acknowledged for their inflammatory, cytoprotective, and diverse biological activities.

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