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Quinagolide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Quinagolide" in English language version.

refsWebsite
Global rank English rank
5doi.org
2nd place
2nd place
5nih.gov
4th place
4th place
1semanticscholar.org
11th place
8th place
1books.google.com
3rd place
3rd place
1espacenet.com
800th place
676th place
1thieme.com
low place
low place

books.google.com

doi.org

  • Di Sarno A, Landi ML, Marzullo P, Di Somma C, Pivonello R, Cerbone G, et al. (July 2000). "The effect of quinagolide and cabergoline, two selective dopamine receptor type 2 agonists, in the treatment of prolactinomas". Clinical Endocrinology. 53 (1): 53–60. doi:10.1046/j.1365-2265.2000.01016.x. PMID 10931080. S2CID 31677949.{{cite journal}}: CS1 maint: overridden setting (link)
  • Nordmann R, Petcher TJ (March 1985). "Octahydrobenzo[g]quinolines: potent dopamine agonists which show the relationship between ergolines and apomorphine". Journal of Medicinal Chemistry. 28 (3): 367–375. doi:10.1021/jm00381a017. PMID 3973904.
  • Bänziger M, Cercus J, Stampfer W, Sunay U (2000). "Practical and Large-Scale Synthesis of rac-(3 S,4a R,10a R)- 6-Methoxy-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline-3-carboxylic Acid Methyl Ester". Organic Process Research & Development. 4 (6): 460–466. doi:10.1021/op0000531.
  • Comparini LM, Menichetti A, Favero L, Di Pietro S, Badalassi F, Ryberg P, et al. (August 2023). "Development of an asymmetric formal synthesis of (-)-quinagolide via enzymatic resolution and stereoselective iminium ion reduction". Organic & Biomolecular Chemistry. 21 (31): 6389–6396. doi:10.1039/D3OB00946G. PMID 37492953.
  • Chavan SP, Kadam AL, Kawale SA (May 2019). "Total Synthesis of (±)-Quinagolide: A Potent D2 Receptor Agonist for the Treatment of Hyperprolactinemia". ACS Omega. 4 (5): 8231–8238. doi:10.1021/acsomega.9b00903. PMC 6648496. PMID 31459911.

espacenet.com

worldwide.espacenet.com

  • EP patent 0077754, Nordmann R, Petcher TJ, "Novel pharmaceutically active 1,2,3,4,4a,5,10,10a-octahydrobenzo(g)quinoline derivatives", issued 1983-04-27, assigned to Sandoz 

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Di Sarno A, Landi ML, Marzullo P, Di Somma C, Pivonello R, Cerbone G, et al. (July 2000). "The effect of quinagolide and cabergoline, two selective dopamine receptor type 2 agonists, in the treatment of prolactinomas". Clinical Endocrinology. 53 (1): 53–60. doi:10.1046/j.1365-2265.2000.01016.x. PMID 10931080. S2CID 31677949.{{cite journal}}: CS1 maint: overridden setting (link)
  • Nordmann R, Petcher TJ (March 1985). "Octahydrobenzo[g]quinolines: potent dopamine agonists which show the relationship between ergolines and apomorphine". Journal of Medicinal Chemistry. 28 (3): 367–375. doi:10.1021/jm00381a017. PMID 3973904.
  • Comparini LM, Menichetti A, Favero L, Di Pietro S, Badalassi F, Ryberg P, et al. (August 2023). "Development of an asymmetric formal synthesis of (-)-quinagolide via enzymatic resolution and stereoselective iminium ion reduction". Organic & Biomolecular Chemistry. 21 (31): 6389–6396. doi:10.1039/D3OB00946G. PMID 37492953.
  • Chavan SP, Kadam AL, Kawale SA (May 2019). "Total Synthesis of (±)-Quinagolide: A Potent D2 Receptor Agonist for the Treatment of Hyperprolactinemia". ACS Omega. 4 (5): 8231–8238. doi:10.1021/acsomega.9b00903. PMC 6648496. PMID 31459911.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

  • Di Sarno A, Landi ML, Marzullo P, Di Somma C, Pivonello R, Cerbone G, et al. (July 2000). "The effect of quinagolide and cabergoline, two selective dopamine receptor type 2 agonists, in the treatment of prolactinomas". Clinical Endocrinology. 53 (1): 53–60. doi:10.1046/j.1365-2265.2000.01016.x. PMID 10931080. S2CID 31677949.{{cite journal}}: CS1 maint: overridden setting (link)

thieme.com

pharmaceutical-substances.thieme.com