| Assay ID | Title | Year | Journal | Article |
|---|
| AID102623 | Percent of inhibitory activity against proliferation of MCF-7 cells in presence of 10e-6 M concentration of [3H]estradiol (E2). | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID103600 | Agonistic activity in MCF-7 cell proliferation. | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID102435 | Effective dose for [3H]- estradiol against proliferation of MCF-7 cells | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID164970 | The percent stimulation or inhibition of protein kinase C III activity was determined for phosphatidylserine (PS) and diolein(PS+DO) in the presence of [Ca2+] | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID42279 | Inhibition of proliferation of BT-20 cells in presence of 10e-5 TPE concentration; nm = not measuable | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID102603 | Inhibition of proliferation of MCF-7 cells versus 0.1 nM [3H]- estradiol; nm = not measuable | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID71133 | Relative binding affinity against estrogen receptor in calf uterus cytosol using [3H]E2 as radioligand, incubated at 2 hours at 0 degree Centigrade. | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID71134 | Relative binding affinity against estrogen receptor in calf uterus cytosol using [3H]E2 as radioligand, incubated at 5 hours at 25 degree Centigrade. | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID103754 | Cytostatic activity against MCF-7 cell proliferation. | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID164971 | Percent stimulation or inhibition of protein kinase C III activity for phosphatidylserine (PS) in the presence of [Ca2+]. | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID102449 | Inhibition of proliferation of MCF-7 cells in presence of 10e-6 M concentration of [3H]- estradiol (E2); nm = not measuable | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID71132 | Relative binding affinity was measured on calf uterus estrogen receptor after 5 hr at 25C. | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID42280 | Percent of inhibitory activity against proliferation of BT-20 cells in presence of TPE at 10e-5 M concentration. | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID102768 | Percent of effective dose for [3H]estradiol against proliferation of MCF-7 cells. | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID102624 | Percent of inhibitory activity versus 0.1 nm [3H]estradiol against proliferation of MCF-7 cells. | 1989 | Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
| Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth. |
| AID164972 | Percent stimulation or inhibition of protein kinase C III activity for protamine sulfate in the presence of EGTA. | 1992 | Journal of medicinal chemistry, Feb-07, Volume: 35, Issue:3
| Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation. |
| AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
| AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
| AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
| AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | | | |
| AID1745845 | Primary qHTS for Inhibitors of ATXN expression | | | |
| AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
| AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
| AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
| AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
| AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
| Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
| AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1
| High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |