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ingenol

Known as: 1a alpha,2 alpha,5 beta,5a beta,6 beta,beta,9 alpha, 10,10a alpha-octahydro-5,5a,6-trihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-1H-2,8a alpha-methano cyclopenta(a)cyclopropa(e)cyclodecen-11-one 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2014
Highly Cited
2014
HIV infection is not cleared by antiretroviral drugs due to the presence of latently infected cells that are not eliminated with… 
Highly Cited
2011
Highly Cited
2011
A facile synthesis was employed to make a 56π-electron methano-PC(61)BM with a very small 1,2-dihydromethano (CH(2)) group. This… 
Review
2010
Review
2010
The synthesis of cyclonucleosides having a C–C bridge is reviewed. The report contains 54 references <div class=" textboxdefault… 
Highly Cited
2004
Highly Cited
2004
Highly Cited
2000
Highly Cited
2000
CD36, a class B scavenger receptor, is a macrophage receptor for oxidized low density lipoprotein (OxLDL) and may play a critical… 
Highly Cited
1999
Highly Cited
1999
A short and practical process for the isolation of ingenol (1a) from an agricultural commodity (the seeds of Euphorbia lathyris… 
1992
1992
We have examined the ability of ingenol to bind to and activate protein kinase C and to induce similar responses to the phorbol…