ESUBERAPROST SODIUM

Investigational

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C24H29O5.Na
Molecular Weight	420.4738
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 6
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[Na+].CC#CC[C@H](C)[C@H](O)\C=C\[C@H]1[C@H](O)C[C@@H]2OC3=C(CCCC([O-])=O)C=CC=C3[C@H]12

InChI

InChIKey=YTCZZXIRLARSET-ZTWNIFTGSA-M

InChI=1S/C24H30O5.Na/c1-3-4-7-15(2)19(25)13-12-17-20(26)14-21-23(17)18-10-5-8-16(24(18)29-21)9-6-11-22(27)28;/h5,8,10,12-13,15,17,19-21,23,25-26H,6-7,9,11,14H2,1-2H3,(H,27,28);/q;+1/p-1/b13-12+;/t15-,17-,19+,20+,21-,23-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	C24H29O5
Molecular Weight	397.4841
Charge	-1
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	6 / 6
E/Z Centers	1
Optical Activity	UNSPECIFIED

Molecular Formula	Na
Molecular Weight	22.98976928
Charge	1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://adisinsight.springer.com/drugs/800040766 | https://pulmonaryhypertensionnews.com/2019/04/11/united-therapeutics-ends-clinical-development-of-esuberaprost-as-add-on-therapy-for-pah/

Esuberaprost (314d) is an active enantiomer of beraprost, a prostacyclin analog. The pharmacologic action of esuberaprost is mediated by specifically binding to PGI2 receptors in smooth muscle cells (the blood vessel’s endothelium) and platelets. Upon binding, the compound widened blood vessels, preventing the formation of blood clots, and lowering blood pressure in the lungs. As a result, it was expected to improve the symptoms of pulmonary arterial hypertension. United Therapeutics announced it has ended its Phase 3 BEAT trial testing esuberaprost as an add-on therapy to its product Tyvaso (inhaled treprostinil) for clinically symptomatic patients with pulmonary arterial hypertension (PAH). According to a company press release, the study failed to reach its main endpoint of delaying the time to first clinical worsening events.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Prostacyclin receptor 9 Target ID: P43119 Gene ID: 5739.0 Gene Symbol: PTGIR Target Organism: Homo sapiens (Human) Sources: https://www.covance.com/content/dam/covance/assetLibrary/posters/PatelACCP16-BPS-314d-MR-Warfarin.pdf	Binding Agent 1076

PubMed

Title	Date	PubMed
Pharmacokinetics and platelet antiaggregating effects of beraprost, an oral stable prostacyclin analogue, in healthy volunteers.	1993-11	7506323
Specific binding of the new stable epoprostenol analogue beraprost sodium to prostacyclin receptors on human and rat platelets.	1989-04	2665758

Sample Use Guides

In Vivo Use Guide

Phase III study: 15 μg tablets for oral, 1 or 2 tablets four times daily (QID) administration

Route of Administration: Oral

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:36:40 GMT 2025` Edited by `admin` on `Mon Mar 31 21:36:40 GMT 2025`
Record UNII	6C8TLD4Q9K
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ESUBERAPROST SODIUM

Official Name

English

APS 314D

Preferred Name

English

BERAPROST SODIUM 314D

Common Name

English

ESUBERAPROST SODIUM [USAN]

Common Name

English

APS-314D

Code

English

GP-1681

Code

English

Esuberaprost sodium [WHO-DD]

Common Name

English

(+)-SODIUM 4-((1R,2R,3AS,8BS)-2-HYDROXY-1-((1E,3S,4S)-3-HYDROXY-4-METHYL-OCT-1-EN-6-YN-1-YL)-2,3,3A,8B-TETRAHYDRO-1H-CYCLOPENTA(B)(1)BENZOFURAN-5-YL)BUTANOATE

Systematic Name

English

BPS-314D

Code

English

GP1681

Code

English

BERAPROST SODIUM, (+)-

Common Name

English

1H-CYCLOPENTA(B)BENZOFURAN-5-BUTANOIC ACID, 2,3,3A,8B-TETRAHYDRO-2-HYDROXY-1-((1E,3S,4S)-3-HYDROXY-4-METHYL-1-OCTEN-6-YN-1-YL)-, SODIUM SALT (1:1), (1R,2R,3AS,8BS)-

Common Name

English

Classification Tree Code System Code

FDA ORPHAN DRUG

355711