Assay ID | Title | Year | Journal | Article |
AID277973 | Displacement of [3H]OH-DPAT from rat cortex 5HT1A receptor | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298492 | Displacement of [3H]prazosin from adrenergic alpha1 receptor in rat cerebral cortex | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277983 | Ratio of ED50 for LLR induction to ED50 for normalization in ip dosed rat | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298485 | Displacement of [3H]mesulergine from 5HT2C receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277987 | Activity at human D2 receptor expressed in Xenopus oocytes | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277975 | Displacement of [3H]YM-09151-2 from rat striatum D2 receptor | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277980 | Induction of lower lip retraction in ip dosed rat after 15 min | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298494 | Displacement of [3H]pyrilamine from histaminergic H1 receptor guinea pig cerebellum | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277974 | Displacement of [3H]ketanserin from rat cortex 5HT2A receptor | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277977 | Agonist activity at human 5HT1A receptor in HeLa cells assessed as stimulation of [35S]GTPgammaS binding relative to serotonin | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298486 | Displacement of [3H]LSD from human 5HT6 receptor expressed in HEK293 cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298488 | Displacement of [3H]BLR-43694 from human 5HT3 receptor expressed in HEK293 cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298491 | Displacement of [3H]4-DAMP from human M4 receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277981 | Induction of flat body posture in ip dosed rat after 15 min | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298480 | Displacement of [3H]spiperone from human dopamine D4.4 receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298493 | Displacement of [3H]RX 821002 from adrenergic alpha-2 receptor in rat cerebral cortex | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277979 | Induction of catalepsy in ip dosed rat after 60 min by crossed-leg position test | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298483 | Displacement of [3H]LSD from 5HT2B receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277984 | Ratio of ED50 for catalepsy induction to ED50 for normalization in ip dosed rat | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277985 | Antagonist activity against rat D2 receptor assessed effect on quinelorane-stimulated [35S]GTP-gamma-S binding | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277978 | Normalizing effect on methylphenidate-induced behaviours in ip dosed rat after 30 min | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298478 | Displacement of [3H]spiperone from human dopamine D2 receptor short form expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298482 | Displacement of [3H]ketanserin from human 5HT2A receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298490 | Displacement of [3H]pirenzepine from human M1 receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298487 | Displacement of [3H]LSD from human 5HT7 receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID277976 | Agonist activity at human 5HT1A receptor in HeLa cells assessed as stimulation of [35S]GTP-gamma-S binding | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID277986 | Antagonist activity against rat D2 receptor assessed as [35S]GTPgammaS binding relative to quinelorane | 2007 | Journal of medicinal chemistry, Feb-22, Volume: 50, Issue:4
| Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities. |
AID298481 | Displacement of [3H]8-OH-DPAT from human 5HT1A receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298489 | Displacement of [3H]paraxetine from human 5HT transporter expressed in HEK293 cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID298479 | Displacement of [3H]spiperone from human dopamine D3 receptor expressed in CHO cells | 2007 | Journal of medicinal chemistry, Oct-18, Volume: 50, Issue:21
| Principal component analysis differentiates the receptor binding profiles of three antipsychotic drug candidates from current antipsychotic drugs. |
AID1347159 | Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
| Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1347160 | Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1803435 | Binding Affinity Assay from Article 10.3109/14756366.2013.776556: \\Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones.\\ | 2014 | Journal of enzyme inhibition and medicinal chemistry, Apr, Volume: 29, Issue:2
| Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones. |
AID1803434 | Binding Affinity Assay from Article 10.3109/14756366.2013.776556: \\Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones.\\ | 2014 | Journal of enzyme inhibition and medicinal chemistry, Apr, Volume: 29, Issue:2
| Synthesis and dual D2 and 5-HT1A receptor binding affinities of 5-piperidinyl and 5-piperazinyl-1H-benzo[d]imidazol-2(3H)-ones. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |