Ingenol mebutate (English Wikipedia)

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

refsWebsite

Global rank English rank

10nih.gov

4^th place

8doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

3europa.eu

68^th place

117^th place

3fda.gov

447^th place

338^th place

2drugs.com

399^th place

333^rd place

1skintherapyletter.com

low place

1web.archive.org

1^st place

1rxlist.com

7,927^th place

6,815^th place

1thieme-connect.com

low place

1harvard.edu

18^th place

17^th place

1hres.ca

low place

doi.org

Hohmann J, Evanics F, Berta L, Bartók T (April 2000). "Diterpenoids from Euphorbia peplus". Planta Medica. 66 (3): 291–294. doi:10.1055/s-2000-8568. PMID 10821064. S2CID 260249228.
Liang X, Grue-Sørensen G, Petersen AK, Högberg T (2012). "Semisynthesis of Ingenol 3-Angelate (PEP005): Efficient Stereoconservative Angeloylation of Alcohols" (PDF). Synlett. 23 (18): 2647–2652. doi:10.1055/s-0032-1317415. S2CID 95418968. Retrieved 10 April 2022.
Jørgensen L, McKerrall SJ, Kuttruff CA, Ungeheuer F, Felding J, Baran PS (August 2013). "14-step synthesis of (+)-ingenol from (+)-3-carene". Science. 341 (6148): 878–882. Bibcode:2013Sci...341..878J. doi:10.1126/science.1241606. PMID 23907534. S2CID 26998997.
Freiberger SN, Cheng PF, Iotzova-Weiss G, Neu J, Liu Q, Dziunycz P, et al. (September 2015). "Ingenol Mebutate Signals via PKC/MEK/ERK in Keratinocytes and Induces Interleukin Decoy Receptors IL1R2 and IL13RA2". Molecular Cancer Therapeutics. 14 (9): 2132–2142. doi:10.1158/1535-7163.mct-15-0023-t. PMID 26116359.{{cite journal}}: CS1 maint: overridden setting (link)
Lebwohl M, Swanson N, Anderson LL, Melgaard A, Xu Z, Berman B (March 2012). "Ingenol mebutate gel for actinic keratosis". The New England Journal of Medicine. 366 (11): 1010–1019. doi:10.1056/NEJMoa1111170. PMID 22417254.
Lebwohl M, Shumack S, Stein Gold L, Melgaard A, Larsson T, Tyring SK (June 2013). "Long-term follow-up study of ingenol mebutate gel for the treatment of actinic keratoses". JAMA Dermatology. 149 (6): 666–670. doi:10.1001/jamadermatol.2013.2766. PMID 23553119.
Jiang G, Mendes EA, Kaiser P, Wong DP, Tang Y, Cai I, et al. (July 2015). "Synergistic Reactivation of Latent HIV Expression by Ingenol-3-Angelate, PEP005, Targeted NF-kB Signaling in Combination with JQ1 Induced p-TEFb Activation". PLOS Pathogens. 11 (7): e1005066. doi:10.1371/journal.ppat.1005066. PMC 4520526. PMID 26225771.{{cite journal}}: CS1 maint: overridden setting (link)
Cozzi SJ, Le TT, Ogbourne SM, James C, Suhrbier A (2017). "Tattoo removal with ingenol mebutate". Clinical, Cosmetic and Investigational Dermatology. 10: 205–210. doi:10.2147/ccid.s135716. PMC 5448692. PMID 28579816.

drugs.com

Drugs.com: Picato Side Effects in Detail
"Picato". Drugs.com.

europa.eu

ema.europa.eu

"Picato | European Medicines Agency". Ema.europa.eu. 17 September 2018. Archived from the original on 3 February 2018. Retrieved 10 April 2022.
"Picato : Withdrawal of the marketing authorisation in the European Union" (PDF). Ema.europa.eu. Retrieved 10 April 2022.
"EMA suspends Picato as a precaution while review of skin cancer risk continues". European Medicines Agency. 17 January 2020. Retrieved 10 April 2022.

fda.gov

accessdata.fda.gov

"Drugs@FDA: FDA-Approved Drugs". Accessdata.fda.gov. Retrieved 10 April 2022.
"Picato® Gel label at Drugs@FDA" (PDF). Accessdata.fda.org. Retrieved 10 April 2022.

fda.gov

"Picato (ingenol mebutate) Gel: Drug Safety Communication - FDA Warns of Severe Adverse Events, Requires Label Changes". Food and Drug Administration. 21 August 2015. Retrieved 24 August 2015.

harvard.edu

ui.adsabs.harvard.edu

Jørgensen L, McKerrall SJ, Kuttruff CA, Ungeheuer F, Felding J, Baran PS (August 2013). "14-step synthesis of (+)-ingenol from (+)-3-carene". Science. 341 (6148): 878–882. Bibcode:2013Sci...341..878J. doi:10.1126/science.1241606. PMID 23907534. S2CID 26998997.

hres.ca

hpr-rps.hres.ca

"Summary Safety Review - Picato (ingenol mebutate) - Assessing the Potential Risk of Skin Cancer". Hpr-rps.hres.ca. 23 October 2014. Retrieved 27 October 2020.

nih.gov

pubmed.ncbi.nlm.nih.gov

Fallen RS, Gooderham M (February 2012). "Ingenol mebutate: an introduction". Skin Therapy Letter. 17 (2): 1–3. PMID 22358305.
Hohmann J, Evanics F, Berta L, Bartók T (April 2000). "Diterpenoids from Euphorbia peplus". Planta Medica. 66 (3): 291–294. doi:10.1055/s-2000-8568. PMID 10821064. S2CID 260249228.
Jørgensen L, McKerrall SJ, Kuttruff CA, Ungeheuer F, Felding J, Baran PS (August 2013). "14-step synthesis of (+)-ingenol from (+)-3-carene". Science. 341 (6148): 878–882. Bibcode:2013Sci...341..878J. doi:10.1126/science.1241606. PMID 23907534. S2CID 26998997.
Freiberger SN, Cheng PF, Iotzova-Weiss G, Neu J, Liu Q, Dziunycz P, et al. (September 2015). "Ingenol Mebutate Signals via PKC/MEK/ERK in Keratinocytes and Induces Interleukin Decoy Receptors IL1R2 and IL13RA2". Molecular Cancer Therapeutics. 14 (9): 2132–2142. doi:10.1158/1535-7163.mct-15-0023-t. PMID 26116359.{{cite journal}}: CS1 maint: overridden setting (link)
Lebwohl M, Swanson N, Anderson LL, Melgaard A, Xu Z, Berman B (March 2012). "Ingenol mebutate gel for actinic keratosis". The New England Journal of Medicine. 366 (11): 1010–1019. doi:10.1056/NEJMoa1111170. PMID 22417254.
Lebwohl M, Shumack S, Stein Gold L, Melgaard A, Larsson T, Tyring SK (June 2013). "Long-term follow-up study of ingenol mebutate gel for the treatment of actinic keratoses". JAMA Dermatology. 149 (6): 666–670. doi:10.1001/jamadermatol.2013.2766. PMID 23553119.
Jiang G, Mendes EA, Kaiser P, Wong DP, Tang Y, Cai I, et al. (July 2015). "Synergistic Reactivation of Latent HIV Expression by Ingenol-3-Angelate, PEP005, Targeted NF-kB Signaling in Combination with JQ1 Induced p-TEFb Activation". PLOS Pathogens. 11 (7): e1005066. doi:10.1371/journal.ppat.1005066. PMC 4520526. PMID 26225771.{{cite journal}}: CS1 maint: overridden setting (link)
Cozzi SJ, Le TT, Ogbourne SM, James C, Suhrbier A (2017). "Tattoo removal with ingenol mebutate". Clinical, Cosmetic and Investigational Dermatology. 10: 205–210. doi:10.2147/ccid.s135716. PMC 5448692. PMID 28579816.

ncbi.nlm.nih.gov

Jiang G, Mendes EA, Kaiser P, Wong DP, Tang Y, Cai I, et al. (July 2015). "Synergistic Reactivation of Latent HIV Expression by Ingenol-3-Angelate, PEP005, Targeted NF-kB Signaling in Combination with JQ1 Induced p-TEFb Activation". PLOS Pathogens. 11 (7): e1005066. doi:10.1371/journal.ppat.1005066. PMC 4520526. PMID 26225771.{{cite journal}}: CS1 maint: overridden setting (link)
Cozzi SJ, Le TT, Ogbourne SM, James C, Suhrbier A (2017). "Tattoo removal with ingenol mebutate". Clinical, Cosmetic and Investigational Dermatology. 10: 205–210. doi:10.2147/ccid.s135716. PMC 5448692. PMID 28579816.

rxlist.com

"Picato (Ingenol Mebutate): Side Effects, Interactions, Warning, Dosage & Uses". RxList.com. Retrieved 6 December 2018.

semanticscholar.org

api.semanticscholar.org

Hohmann J, Evanics F, Berta L, Bartók T (April 2000). "Diterpenoids from Euphorbia peplus". Planta Medica. 66 (3): 291–294. doi:10.1055/s-2000-8568. PMID 10821064. S2CID 260249228.
Liang X, Grue-Sørensen G, Petersen AK, Högberg T (2012). "Semisynthesis of Ingenol 3-Angelate (PEP005): Efficient Stereoconservative Angeloylation of Alcohols" (PDF). Synlett. 23 (18): 2647–2652. doi:10.1055/s-0032-1317415. S2CID 95418968. Retrieved 10 April 2022.
Jørgensen L, McKerrall SJ, Kuttruff CA, Ungeheuer F, Felding J, Baran PS (August 2013). "14-step synthesis of (+)-ingenol from (+)-3-carene". Science. 341 (6148): 878–882. Bibcode:2013Sci...341..878J. doi:10.1126/science.1241606. PMID 23907534. S2CID 26998997.

skintherapyletter.com

Fallen RS, Gooderham M (February 2012). "Ingenol mebutate: an introduction". Skin Therapy Letter. 17 (2): 1–3. PMID 22358305.

thieme-connect.com

Liang X, Grue-Sørensen G, Petersen AK, Högberg T (2012). "Semisynthesis of Ingenol 3-Angelate (PEP005): Efficient Stereoconservative Angeloylation of Alcohols" (PDF). Synlett. 23 (18): 2647–2652. doi:10.1055/s-0032-1317415. S2CID 95418968. Retrieved 10 April 2022.

web.archive.org

"Picato | European Medicines Agency". Ema.europa.eu. 17 September 2018. Archived from the original on 3 February 2018. Retrieved 10 April 2022.