Carboprost
{{Short description|Chemical compound}}
{{Infobox drug
| Verifiedfields = changed
| verifiedrevid = 460018936
| IUPAC_name = (5Z,9α,11α,13E,15S)-9,11,15-trihydroxy-15- methylprosta-5,13-dien-1-oic acid
| image = Carboprost.svg
| pronounce =
| tradename = Hemabate
| Drugs.com = {{drugs.com|CONS|carboprost}}
| MedlinePlus = a600042
| licence_CA =
| licence_EU =
| DailyMedID =
| licence_US =
| pregnancy_AU = D
| pregnancy_AU_comment =
| pregnancy_category =
| routes_of_administration = Intramuscular
| class =
| ATCvet =
| ATC_prefix = G02
| ATC_suffix = AD04
| ATC_supplemental =
| legal_AU = S4
| legal_BR =
| legal_BR_comment =
| legal_CA =
| legal_CA_comment =
| legal_DE =
| legal_DE_comment =
| legal_NZ =
| legal_NZ_comment =
| legal_UK =
| legal_UK_comment =
| legal_US =
| legal_US_comment =
| legal_EU =
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| legal_UN =
| legal_UN_comment =
| legal_status = Rx-only
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| index2_label = tromethamine
| CAS_number_Ref = {{cascite|correct|CAS}}
| CAS_number = 35700-23-3
| CAS_number2_Ref = {{cascite|correct|CAS}}
| CAS_number2 = 58551-69-2
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 7B5032XT6O
| UNII2_Ref = {{fdacite|correct|FDA}}
| UNII2 = U4526F86FJ
| PubChem = 5281075
| DrugBank_Ref = {{drugbankcite|changed|drugbank}}
| DrugBank = DB00429
| ChEBI = 3403
| KEGG = D02343
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 4444532
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 1237122
| C=21 | H=36 | O=5
| smiles = O=C(O)CCC/C=C/C[C@H]1[C@@H](O)C[C@@H](O)[C@@H]1/C=C/[C@](O)(C)CCCCC
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C21H36O5/c1-3-4-9-13-21(2,26)14-12-17-16(18(22)15-19(17)23)10-7-5-6-8-11-20(24)25/h5,7,12,14,16-19,22-23,26H,3-4,6,8-11,13,15H2,1-2H3,(H,24,25)/b7-5-,14-12+/t16-,17-,18+,19-,21+/m1/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = DLJKPYFALUEJCK-IIELGFQLSA-N
|drug_name=|alt=|caption=|type=|pregnancy_US=}}
Carboprost (INN, trade names for the tromethamine salts Hemabate, Tham) is a synthetic prostaglandin analogue of PGF2α (specifically, it is 15-methyl-PGF2α) with oxytocic properties.
Carboprost's main use is to reduce postpartum bleeding during the obstetrical emergency of postpartum hemorrhage.
Indication
Carboprost is used in postpartum hemorrhage caused by uterine atony not controlled by other methods. One study has shown that carboprost tromethamine is more effective than oxytocin in preventing postpartum hemorrhage in high-risk patients undergoing cesarean delivery.{{cite journal | vauthors = Bai J, Sun Q, Zhai H | title = A comparison of oxytocin and carboprost tromethamine in the prevention of postpartum hemorrhage in high-risk patients undergoing cesarean delivery | journal = Experimental and Therapeutic Medicine | volume = 7 | issue = 1 | pages = 46–50 | date = January 2014 | pmid = 24348762 | pmc = 3861477 | doi = 10.3892/etm.2013.1379 }}
Carboprost was the first drug widely used for medication abortions. It is still sometimes used for second trimester abortions, but has generally been supplanted by the mifepristone/misoprostol combination.Hemabate [Package Insert]. New York, NY: Pharmacia and Upjohn Company; 2014."Carboprost" - Drug fact sheet, Mayo Clinic. Last updated: July 01, 2024
https://www.mayoclinic.org/drugs-supplements/carboprost-intramuscular-route/proper-use/drg-20067975Vukelić J. Second trimester pregnancy termination in primigravidas by double application of dinoprostone gel and intramuscular administration of carboprost tromethamine. Med Pregl. 2001 Jan-Feb;54(1-2):11-6. English, Croatian. PMID: 11436877.Bygdeman, M., & Gemzell-Danielsson, K. (2008). An Historical Overview of Second Trimester Abortion Methods. Reproductive Health Matters, 16(sup31), 196–204. https://doi.org/10.1016/S0968-8080(08)31385-8Schwallie PC, Lamborn KR. Induction of abortion by intramuscular administration of (15S)-15-methyl PGF2 alpha. An overview of 815 cases. J Reprod Med. 1979 Dec;23(6):289-93. PMID: 392084.Bhaskar A, Dimov V, Baliga S, Kinra G, Hingorani V, Laumas KR. Plasma levels of 15 (S) 15-methyl-PGF 2 alpha-methyl ester following vaginal administration for induction of abortion in women. Contraception. 1979 Nov;20(5):519-31. doi: 10.1016/0010-7824(79)90057-x. PMID: 527343.
Contraindication
Precautions
- asthma
- anemia
- jaundice
- diabetes mellitus
- seizure disorders
- past uterine surgery
Adverse effects
- diarrhea (most common, may be sudden in onset)
- flushing or hot flashes
- fever
- chills
- nausea/vomiting
Storage and availability
Synthesis
A significant deactivating metabolic transformation of natural prostaglandins is enzymatic oxidation of the C-15 hydroxyl to the corresponding ketone. This is prevented, with retention of activity, by methylation to give the C-15 tertiary carbinol series.
File:Carboprost synthesis.svg|inventor1-last=Gordon|inventor1-first=Leonard|inventor2-last=Pike|inventor2-first=John Edward|inventor3-last=Schneider|inventor3-first=William Paul}} G. L. Bundy, {{US patent|3728382}} (1973 to Upjohn).]]
This molecular feature is readily introduced at the stage of the Corey lactone (1) by reaction with methyl Grignard reagent or trimethylaluminium. The resulting mixture of tertiary carbinols (2) is transformed to oxytocic carboprost (3) by standard transformations, including separation of diastereomers, so that the final product is the C-15 analogue. This diastereomer is reputably freeer of prostaglandin side effects than the C-15 (S) isomer.
References
{{reflist}}
Further reading
{{refbegin}}
- {{cite journal | vauthors = Indman PD | title = Use of carboprost to facilitate hysteroscopic resection of submucous myomas | journal = The Journal of the American Association of Gynecologic Laparoscopists | volume = 11 | issue = 1 | pages = 68–72 | date = February 2004 | pmid = 15104835 | doi = 10.1016/S1074-3804(05)60014-X }}
- {{cite journal | vauthors = Vukelić J | title = Second trimester pregnancy termination in primigravidas by double application of dinoprostone gel and intramuscular administration of carboprost tromethamine | journal = Medicinski Pregled | volume = 54 | issue = 1–2 | pages = 11–6 | year = 2001 | pmid = 11436877 }}
- {{cite journal | vauthors = Ippoliti C, Przepiorka D, Mehra R, Neumann J, Wood J, Claxton D, Gajewski J, Khouri I, van Besien K, Andersson B | display-authors = 6 | title = Intravesicular carboprost for the treatment of hemorrhagic cystitis after marrow transplantation | journal = Urology | volume = 46 | issue = 6 | pages = 811–5 | date = December 1995 | pmid = 7502421 | doi = 10.1016/S0090-4295(99)80349-5 }}
{{refend}}
External links
- {{MeshName|Carboprost}}
{{Prostaglandins}}
{{Oxytocics}}
{{Obstetric drugs}}
{{Prostanoidergics}}