General
Preferred name
CARBOPROST
Synonyms
15(S)-15-Methyl Prostaglandin F2α ()
15-Methyl-PGF2α ()
CARBOPROST TROMETHAMINE ()
Carboprost (tromethamine) ()
15(S)-15-Methyl Prostaglandin F2¦Á ()
15-Methyl-PGF2¦Á ()
15(S)-15-methyl Prostaglandin F2.alpha. ()
15-methyl-pgf2.alpha. ()
(15s)-15-methyl-pgf2.alpha. ()
U-32,921 ()
15-methylprostaglandin f2.alpha. ()
Hemabate ()
U-32921 ()
Carboprost tromethamine salt ()
Carboprost trometamol ()
U-32,921E ()
Carboprost Trometanol ()
Prostin/15m ()
U-32921E ()
P&D ID
PD013601
CAS
58551-69-2
59286-19-0
35700-23-3
Tags
available
drug
Approved by
FDA
First approval
1979
Drug indication
postpartum hemorrhage
Abortion
Drug Status
approved
Max Phase
4.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Carboprost (15(S)-15-Methyl Prostaglandin F2¦Á) is a metabolically stable synthetic analog of prostaglandin F2¦Á. Carboprost stimulates uterine contractions and induces abortion. Carboprost is used for postpartum hemorrhage due to uterine atony and for the termination of pregnancy in the second trimester[1][2].
PRICE 146
DESCRIPTION Carboprost (15(S)-15-Methyl Prostaglandin F2??) is a synthetic analogue of PGF2?? with oxytocic properties, commonly used to restore uterine tone.
DESCRIPTION Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2¦Á. Carboprost tromethamine can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after delivery[1][2].
DESCRIPTION Carboprost is a synthetic prostaglandin analogue of PGF2α with oxytocic properties. It is a potent uterine stimulant and abortifacient which can be given intramuscularly to induce labor. It can also induce luteolysis and reduces serum progesterone concentrations. (BOC Sciences Bioactive Compounds)
DESCRIPTION Carboprost (15(S)-15-Methyl Prostaglandin F2α) is a synthetic analogue of PGF2α with oxytocic properties, commonly used to restore uterine tone. (TargetMol Bioactive Compound Library)
DESCRIPTION Adrenergic alpha receptor antagonist; antihypertensive (Tocris Bioactive Compound Library)
Compound Sets
16
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Approved Drugs
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NPC Screening Collection
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
External IDs
49
Properties
(calculated by RDKit )
Molecular Weight
368.26
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
4
Rotatable Bonds
12
Ring Count
1
Aromatic Ring Count
0
cLogP
3.43
TPSA
97.99
Fraction CSP3
0.76
Chiral centers
5.0
Largest ring
5.0
QED
0.31
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
prostaglandin F2α
Prostaglandin Receptor
Primary Target
Prostanoid Receptors
MOA
Agonist
Pathway
GPCR/G protein
Immunology/Inflammation
Therapeutic Class
Abortifacient Agents
Source data