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インゲノール 3-アンゲラート (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "インゲノール 3-アンゲラート" in Japanese language version.

refsWebsite
Global rank Japanese rank
8doi.org
2nd place
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7nih.gov
4th place
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1sigmaaldrich.com
924th place
2,158th place
1leo-pharma.com
low place
low place
1drugs.com
399th place
1,603rd place

doi.org

  • Hohmann1, J.; Evanics, F.; Berta, L.; Bartók, T. (2000). “Diterpenoids from Euphorbia peplus”. Planta Med. 66 (3): 291-294. doi:10.1055/s-2000-8568. PMID 10821064. 
  • Kedei N, Lundberg DJ, Toth A, Welburn P, Garfield SH, Blumberg PM (2004). “Characterization of the interaction of ingenol 3-angelate with protein kinase C”. Cancer Res. 64 (9): 3243-3255. doi:10.1158/0008-5472.CAN-03-3403. PMID 15126366. 
  • Benhadji KA, Serova M, Ghoul A, Cvitkovic E, Le Tourneau C, Ogbourne SM, Lokiec F, Calvo F, Hammel P, Faivre S, Raymond E (2008). “Antiproliferative activity of PEP005, a novel ingenol angelate that modulates PKC functions, alone and in combination with cytotoxic agents in human colon cancer cells”. Br. J. Cancer 99 (11): 1808-1815. doi:10.1038/sj.bjc.6604642. PMC 2600681. PMID 19034280. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600681/. 
  • Sirg, B.; Schmidt, R.; Hecker E. (1987). “Structure/activity relationships of polyfunctional diterpenes of the ingenane type. I. Tumor-promoting activity of homologous, aliphatic 3-esters of ingenol and of Δ7.8-isoingenol-3-tetradecanoate”. Carcinogenesis 8 (1): 1-4. doi:10.1093/carcin/8.1.1. 
  • Adolf W, Chanai S, Hecker E (1983). “3-O-angeloylingenol, the toxic and skin irritant factor from latex of Euphorbia antiquorum L. (Euphorbiaceae) and from a derived Thai purgative and anthelmintic (vermifuge) drug”. ScienceAsia 9: 81-88. doi:10.2306/scienceasia1513-1874.1983.09.081. 
  • Zechmeister, K.; Brandl, F.; Hoppe, W.; Hecker, E.; Opferkuch, H. J.; Adolf, W. (1970). “Structure determination of the new tetracyclic diterpene ingenol-triacetate with triple product methods”. Tetrahedron Lett. 11 (47): 4075-4078. doi:10.1016/S0040-4039(01)98669-1. 
  • Hecker, E. (1977). “New toxic, irritant and cocarcinogenic diterpene esters from Euphorbiaceae and from Thymelaeaceae”. Pure Appl. Chem. 49 (9): 1423-1431. doi:10.1351/pac197749091423. 
  • Winkler, J. D.; Rouse, M. B.; Greaney, M. F.; Harrison, S. J.; Jeon, Y. T. (2002). “The first total synthesis of (±)-ingenol”. J. Am. Chem. Soc. 124 (33): 9726-9728. doi:10.1021/ja026600a. PMID 12175229. 

drugs.com

leo-pharma.com

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hohmann1, J.; Evanics, F.; Berta, L.; Bartók, T. (2000). “Diterpenoids from Euphorbia peplus”. Planta Med. 66 (3): 291-294. doi:10.1055/s-2000-8568. PMID 10821064. 
  • Grossberg AL, Gaspari AA (2011). “Topical antineoplastic agents in the treatment of mucocutaneous diseases”. Curr. Probl. Dermatol. 40: 71-82. PMID 21325841. 
  • Kedei N, Lundberg DJ, Toth A, Welburn P, Garfield SH, Blumberg PM (2004). “Characterization of the interaction of ingenol 3-angelate with protein kinase C”. Cancer Res. 64 (9): 3243-3255. doi:10.1158/0008-5472.CAN-03-3403. PMID 15126366. 
  • Benhadji KA, Serova M, Ghoul A, Cvitkovic E, Le Tourneau C, Ogbourne SM, Lokiec F, Calvo F, Hammel P, Faivre S, Raymond E (2008). “Antiproliferative activity of PEP005, a novel ingenol angelate that modulates PKC functions, alone and in combination with cytotoxic agents in human colon cancer cells”. Br. J. Cancer 99 (11): 1808-1815. doi:10.1038/sj.bjc.6604642. PMC 2600681. PMID 19034280. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600681/. 
  • Winkler, J. D.; Rouse, M. B.; Greaney, M. F.; Harrison, S. J.; Jeon, Y. T. (2002). “The first total synthesis of (±)-ingenol”. J. Am. Chem. Soc. 124 (33): 9726-9728. doi:10.1021/ja026600a. PMID 12175229. 

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

sigmaaldrich.com