U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H38O5
Molecular Weight 394.5448
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of GEMEPROST

SMILES

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

InChI

InChIKey=KYBOHGVERHWSSV-VNIVIJDLSA-N
InChI=1S/C23H38O5/c1-5-6-15-23(2,3)21(26)14-13-18-17(19(24)16-20(18)25)11-9-7-8-10-12-22(27)28-4/h10,12-14,17-18,20-21,25-26H,5-9,11,15-16H2,1-4H3/b12-10+,14-13+/t17-,18-,20-,21-/m1/s1

HIDE SMILES / InChI
Gemeprost is a PGE1 analogue indicated for softening and dilatation of the cervix uteri prior to operative procedures or therapeutic abortion. The drug is marketed under the name Cervagem.

Originator

Sources: www.ncbi.nlm.nih.gov/pubmed/704915

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CERVAGEM

Approved Use

For the softening and dilatation of the cervix uteri prior to transcervical, intrauterine operative procedures in the first trimester of pregnancy. Therapeutic termination of pregnancy in patients in the second trimester of gestation.

Launch Date

1990
PubMed

PubMed

TitleDatePubMed
The use of prostaglandin E1 analogue pessaries in patients having first trimester induced abortions.
1980 Apr
Abortifacient effect and uterine cervix-dilating action of 16, 16-dimethyl trans delta 2 PGE1 methyl ester (ONO 802) in the form of a vaginal suppository (a randomized, double-blind, controlled study in the second trimester of pregnancy).
1982 Sep
The use of 16,16-dimethyl-trans delta 2 prostaglandin E1 methyl ester (gemeprost) vaginal pessaries for the termination of pregnancy in the early second trimester. A comparison with extra-amniotic prostaglandin E2.
1984 Nov
Patents

Patents

Sample Use Guides

One pessary to be inserted into the posterior vaginal fornix three hours before surgery.
Route of Administration: Vaginal
In Vitro Use Guide
Unknown
Name Type Language
GEMEPROST
INN   JAN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
PREGLANDIN
Brand Name English
Methyl (E)-7-[(1R,2R,3R)-3-hydroxy-2-[(E)-(3R)-3-hydroxy-4,4-dimethyl-1-octenyl]-5-oxocyclopentyl]-2-heptenoate
Systematic Name English
GEMEPROST [MART.]
Common Name English
gemeprost [INN]
Common Name English
GEMEPROST [USAN]
Common Name English
Gemeprost [WHO-DD]
Common Name English
GEMEPROST [JAN]
Common Name English
GEMEPROST [MI]
Common Name English
PROSTA-2,13-DIEN-1-OIC ACID, 11,15-DIHYDROXY-16,16-DIMETHYL-9-OXO-, METHYL ESTER, (2E,11.ALPHA.,13E,15R)-
Common Name English
SC-37681
Code English
U-37026
Common Name English
Classification Tree Code System Code
WHO-ATC G02AD03
Created by admin on Fri Dec 15 15:26:12 GMT 2023 , Edited by admin on Fri Dec 15 15:26:12 GMT 2023
WHO-VATC QG02AD03
Created by admin on Fri Dec 15 15:26:12 GMT 2023 , Edited by admin on Fri Dec 15 15:26:12 GMT 2023
NCI_THESAURUS C78568
Created by admin on Fri Dec 15 15:26:12 GMT 2023 , Edited by admin on Fri Dec 15 15:26:12 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
264-775-9
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PRIMARY
MESH
C021182
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USAN
U-5
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RXCUI
12449
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PRIMARY RxNorm
EPA CompTox
DTXSID40895073
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DRUG BANK
DB08964
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ChEMBL
CHEMBL1908315
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INN
4738
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MERCK INDEX
m5691
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PRIMARY Merck Index
CAS
64318-79-2
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FDA UNII
45KZB1FOLS
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PUBCHEM
5282237
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EVMPD
SUB07893MIG
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NCI_THESAURUS
C87382
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DRUG CENTRAL
1284
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SMS_ID
100000084540
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WIKIPEDIA
GEMEPROST
Created by admin on Fri Dec 15 15:26:12 GMT 2023 , Edited by admin on Fri Dec 15 15:26:12 GMT 2023
PRIMARY