| Assay ID | Title | Year | Journal | Article |
|---|
| AID21992 | Water solubility (solubility in mol/L) | 1981 | Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
| Methylangelicins: new potential agents for the photochemotherapy of psoriasis. Structure-activity study on the dark and photochemical interactions with DNA. |
| AID24948 | Water solubility of the compound | 1981 | Journal of medicinal chemistry, Feb, Volume: 24, Issue:2
| New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin. |
| AID129598 | Compound was evaluated for its ability to inhibit RNA synthesis in Ehrlich ascites tumor cells by irradiation (365 nM), | 1981 | Journal of medicinal chemistry, Feb, Volume: 24, Issue:2
| New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin. |
| AID68591 | Compound was evaluated for the inhibition of RNA synthesis in Ehrlich Ascites tumor cells by irradiation (365 nm) at 1.9 x 10 e-5M | 1981 | Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
| Methylangelicins: new potential agents for the photochemotherapy of psoriasis. Structure-activity study on the dark and photochemical interactions with DNA. |
| AID68590 | Compound was evaluated for the inhibition of DNA synthesis in Ehrlich Ascites tumor cells by irradiation (365 nm) at 1.9 x 10 e-5M | 1981 | Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
| Methylangelicins: new potential agents for the photochemotherapy of psoriasis. Structure-activity study on the dark and photochemical interactions with DNA. |
| AID1239151 | Selectivity ratio of Ki for human microsomal CYP1A1 to Ki for human microsomal CYP1A2 | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID129600 | compound was evaluated for its ability to inhibit DNA synthesis in Ehrlich ascites tumor cells by irradiation (365 nM) | 1981 | Journal of medicinal chemistry, Feb, Volume: 24, Issue:2
| New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin. |
| AID1239152 | Selectivity ratio of Ki for human microsomal CYP1B1 to Ki for human microsomal CYP1A2 | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID1239149 | Inhibition of human microsomal CYP1A2-dependent methoxyresorufin-O-demethylase activity by spectrofluorimetric analysis in presence of NADPH regenerating solution | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID1239150 | Inhibition of human microsomal CYP1B1-dependent ethoxyresorufin-O-deethylase activity by spectrofluorimetric analysis in presence of NADPH regenerating solution | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID1239159 | Time-dependent inhibition of human microsomal CYP1A2-dependent methoxyresorufin-O-demethylase activity by spectrofluorimetric analysis in presence of NADPH regenerating solution | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID220349 | Compound was evaluated for association constant in the calf thymus DNA | 1981 | Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
| Methylangelicins: new potential agents for the photochemotherapy of psoriasis. Structure-activity study on the dark and photochemical interactions with DNA. |
| AID467954 | Antiproliferative activity against mouse EAC cells assessed as ratio of ID50 of compound to ID50 of 8-methoxypsoralen | 2009 | European journal of medicinal chemistry, Nov, Volume: 44, Issue:11
| Scoring function for DNA-drug docking of anticancer and antiparasitic compounds based on spectral moments of 2D lattice graphs for molecular dynamics trajectories. |
| AID1239148 | Inhibition of human microsomal CYP1A1-dependent ethoxyresorufin-O-deethylase activity by spectrofluorimetric analysis in presence of NADPH regenerating solution | 2015 | Journal of medicinal chemistry, Aug-27, Volume: 58, Issue:16
| A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2. |
| AID22152 | Specific radioactivity of the compound. | 1981 | Journal of medicinal chemistry, Feb, Volume: 24, Issue:2
| New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin. |
| AID220352 | Compound was evaluated for rate constant in the calf thymus DNA | 1981 | Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
| Methylangelicins: new potential agents for the photochemotherapy of psoriasis. Structure-activity study on the dark and photochemical interactions with DNA. |
| AID54464 | The compound was tested for its ability to bind to calf thymus DNA | 1981 | Journal of medicinal chemistry, Feb, Volume: 24, Issue:2
| New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |