Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

illimaquinone

Known as: 2,5-Cyclohexadiene-1,4-dione, 3-((decahydro-1,2,4a-trimethyl-5-methylene-1-naphthalenyl)methyl)-2-hydroxy-5-methoxy-, (1R-(1alpha,2beta,4abeta,8aalpha))- 
 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Quinones

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A New Sesquiterpenoid Aminoquinone from an Indonesian Marine Sponge
Sponges are a well-known bioresource for bioactive compounds. In this study, antibacterial activity-guided fractionation of the… Expand
2012
2012
Illimaquinone, aSelective Inhibitor oftheRNaseH Activity ofHumanImmunodeficiency VirusType1 Reverse Transcriptase
We studied theeffect ofthenatural marine substance mimaquinone onthecatalytic activities ofreverse transcriptase… Expand
2011
2011
Fluoren-9-ylidene Hydrazine Inhibitors of HIV-1 Ribonuclease H
Screening a library of 5,292 hydrazone/hydrazine compounds for inhibition of HIV reverse transcriptase-associated ribonuclease H… Expand
  • figure 2
  • figure 3
  • figure 4
  • figure 5
  • figure 7
2006
2006
Short partially double-stranded oligodeoxynucleotide induces reverse transcriptase/RNase H-mediated cleavage of HIV RNA and contributes to abrogation of infectivity of virions.
We describe a novel mechanism of viral RNA eradication by an oligodeoxynucleotide A (ODN A) directly in HIV virions. The ODN A… Expand
  • figure 2
  • figure 3
  • figure 4
  • figure 5
  • figure 6
Review
2000
Review
2000
Current lead natural products for the chemotherapy of human immunodeficiency virus (HIV) infection
  • E. De Clercq
  • Medicinal research reviews
  • 2000
    • Corpus ID: 41451102
A large variety of natural products have been described as anti‐HIV agents, and for a portion thereof the target of interaction… Expand
Highly Cited
2000
Highly Cited
2000
Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica.
From the stem-bark of Juglans mandshurica, two new naphthalenyl glucopyranosides, 1,4,8-trihydroxynaphthalene 1-O-[alpha-L… Expand
  • table 1
  • figure 1
  • table 2
  • figure 2
  • table 3
1997
1997
ANTIPROLIFERATIVE EFFECT OF ILLIMAQUINONE ON LEISHMANIA MEXICANA
Illimaquinone, a sponge metabolite that disrupts the Golgi complex in mammalian cells, stopped proliferation and induced… Expand
1994
1994
Dactyltronic acids from the sponge Dactylospongia elegans.
Two new cytotoxic tetronic acid derivatives with a rearranged drimane skeleton [1a and 1b], were isolated from the sponge… Expand
Highly Cited
1993
Highly Cited
1993
The interaction of illimaquinone, a selective inhibitor of the RNase H activity, with the reverse transcriptases of human immunodeficiency and murine leukemia retroviruses.
  • S. Loya, A. Hizi
  • The Journal of biological chemistry
  • 1993
    • Corpus ID: 23294505
Illimaquinone, a natural marine product, was shown by us to inhibit preferentially the ribonuclease H (RNase H) activity of the… Expand
Highly Cited
1990
Highly Cited
1990
Illimaquinone, a selective inhibitor of the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase.
We studied the effect of the natural marine substance illimaquinone on the catalytic activities of reverse transcriptase from… Expand
  • figure 1
  • table 1
  • figure 2
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE