PROSTAGLANDIN B1

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C20H32O4
Molecular Weight	336.4657
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCCCC[C@H](O)\C=C\C1=C(CCCCCCC(O)=O)C(=O)CC1

InChI

InChIKey=YBHMPNRDOVPQIN-VSOYFRJCSA-N

InChI=1S/C20H32O4/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/h12,14,17,21H,2-11,13,15H2,1H3,(H,23,24)/b14-12+/t17-/m0/s1

HIDE SMILES / InChI

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Solute carrier organic anion transporter family member 2A1 1 Target ID: CHEMBL2073680 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8863817	Inhibitor 8504		71.2 nM [Ki]

PubMed

Title	Date	PubMed
Glucuronidation of oxidized fatty acids and prostaglandins B1 and E2 by human hepatic and recombinant UDP-glucuronosyltransferases.	2004-09	15231852
Inhibition of nuclear factor kappa B by prostaglandin A1: an effect associated with heat shock transcription factor activation.	1997-01-21	9012856
Microdetermination of the prostaglandin B1 in human plasma by gas chromatography/selected ion monitoring using [18O]prostaglandin B1 as an internal standard.	1995-04	7667505
Prostaglandin A inhibits replication of human immunodeficiency virus during acute infection.	1991-11	1940869

Patents

Name

Type

Language

ALPROSTADIL IMPURITY B [EP IMPURITY]

Preferred Name

English

PROSTAGLANDIN B1

Common Name

English

15.ALPHA.-HYDROXY-9-KETOPROSTA-8(12),13-DIENOIC ACID

Systematic Name

English

PROSTA-8(12),13-DIEN-1-OIC ACID, 15-HYDROXY-9-OXO-, (13E,15S)-

Systematic Name

English

PGE1-278

Common Name

English

PROSTAGLANDIN B1 [USP-RS]

Common Name

English

PROSTAGLANDIN E1-278

Common Name

English

7-(2-((1E,3S)-3-HYDROXYOCT-1-ENYL)-5-OXOCYCLOPENT-1-ENYL)HEPTANOIC ACID

Systematic Name

English

PGB1

Common Name

English

15.ALPHA.-HYDROXY-9-OXO-8(12),13E-PROSTADIENOIC ACID

Systematic Name

English

Code System Code Type Description

PUBCHEM

5280388