Any feedback?
Literature summary for 3.1.26.13 extracted from
- Synthesis of phenacyl derivatives of frangula-emodin and their HIV-1 RNase H activity (2009), Chem. Nat. Compd., 45, 500-502.
No PubMed abstract available
Inhibitors
| Inhibitors | Comment | Organism | Structure |
|---|---|---|---|
| 1,6,8-trihydroxy-3-methylanthraquinone | i.e. frangula-emodin | Human immunodeficiency virus 1 |  |
| 3-[2-(4-bromophenyl)-2-oxoethoxy]-1,8-dihydroxy-6-methylanthracene-9,10-dione | - |
Human immunodeficiency virus 1 | |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Human immunodeficiency virus 1 | - |
- |
- |
IC50 Value
| IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
|---|---|---|---|---|---|
| 0.029 | - |
- |
Human immunodeficiency virus 1 | 3-[2-(4-bromophenyl)-2-oxoethoxy]-1,8-dihydroxy-6-methylanthracene-9,10-dione | |
| 0.075 | - |
- |
Human immunodeficiency virus 1 | 1,6,8-trihydroxy-3-methylanthraquinone | |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
