1,4-anthraquinone

structure in first source

Networked: 4 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Organic Chemicals: 133
- Hydrocarbons: 1713
  - Cyclic Hydrocarbons: 97
    - Aromatic Hydrocarbons: 291
      - Polycyclic Aromatic Hydrocarbons: 2020
        Anthracenes: 12
        Anthrones: 12
        Anthraquinones: 788
        1,4-anthraquinone: 4
- Quinones: 434
  - Anthraquinones: 788
    - 1,4-anthraquinone: 4
Polycyclic Compounds: 6
- Polycyclic Aromatic Hydrocarbons: 2020
  - Anthracenes: 12
    - Anthrones: 12
      - Anthraquinones: 788
        1,4-anthraquinone: 4

Experts

1.	Hua, Duy H: 3 articles (11/2007 - 02/2004)
2.	Lou, Kaiyan: 3 articles (11/2007 - 02/2004)
3.	Perchellet, Elisabeth M: 3 articles (11/2007 - 02/2004)
4.	Wang, Yang: 3 articles (11/2007 - 02/2004)
5.	Perchellet, Jean-Pierre H: 2 articles (11/2007 - 10/2005)
6.	Betancur-Galvis, Liliana: 1 article (04/2019)
7.	Castro, Mª Ángeles: 1 article (04/2019)
8.	García, Pablo A: 1 article (04/2019)
9.	Miranda-Brand, Yaneth: 1 article (04/2019)
10.	Ochoa, Rodrigo: 1 article (04/2019)

Related Diseases

1.	Dengue (Dengue Fever) 04/02/2019 - "In this study, the anti-herpetic and anti-dengue evaluation of 27 terpenyl-1,4-naphthoquinone (NQ), 1,4-anthraquinone (AQ) and heterocycle-fused quinone (HetQ) derivatives was done in vitro against Human Herpesvirus (HHV) type 1 and 2, and Dengue virus serotype 2 (DENV-2). " 04/02/2019 - "Anti-Herpetic, Anti-Dengue and Antineoplastic Activities of Simple and Heterocycle-Fused Derivatives of Terpenyl-1,4-Naphthoquinone and 1,4-Anthraquinone."
2.	Neoplasms (Cancer) 02/01/2004 - "Synthetic analogs of 1,4-anthraquinone (AQ code number), a compound that mimics the antiproliferative effects of daunorubicin (daunomycin) in the nanomolar range in vitro but has the advantage of blocking nucleoside transport and retaining its efficacy in multidrug-resistant tumor cells, were tested for their ability to induce apoptosis in the HL-60 cell system. " 10/01/2005 - "Since synthetic analogs of 1,4-anthraquinone (AQ code number), such as AQ8, AQ9 and AQ10, can trigger cytochrome c release without caspase activation and retain their ability to induce apoptosis in multidrug-resistant (MDR) tumor cells, fluorescent probes of transmembrane potential have been used to determine whether these anti-tumor compounds might directly target mitochondria in cell and cell-free systems to cause the collapse of mitochondrial membrane potential (/Deltapsim) that is linked to permeability transition pore (PTP) opening. " 11/01/2007 - "Synthetic analogs of 1,4-anthraquinone (AQ code number), which block nucleoside transport, decrease DNA, RNA and protein syntheses, trigger cytochrome c release without caspase activation, induce apoptotic DNA fragmentation and inhibit the proliferation of wild-type and multidrug resistant tumor cells in the nM range in vitro, rapidly cause the collapse of mitochondrial transmembrane potential in cell and cell-free systems. "

Related Drugs and Biologics

1.	terpenyl-1,4-naphthoquinone
2.	quinone (benzoquinone)
3.	Cytochromes c (Cytochrome c)
4.	Caspases
5.	Nucleosides
6.	RNA (Ribonucleic Acid)
7.	Proteins (Proteins, Gene)
8.	Fluorescent Dyes (Fluorescent Probes)
9.	DNA (Deoxyribonucleic Acid)
10.	Daunorubicin (Cerubidine)