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Found 193 with Last Name = 'kelland' and Initial = 'lr'
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108806(3,6,8,11,13-pentamethyl-8H-quino[4,3,2-kl]acridin-...)
Affinity DataIC50:  250nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108803(3,11-dichloro-6,8,13-trimethyl-8H-quino[4,3,2-kl]a...)
Affinity DataIC50:  250nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108802(3,11-difluoro-6,8,13-trimethyl-8H-quino[4,3,2-kl]a...)
Affinity DataIC50:  330nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108805(8,13-Dimethyl-8H-8-aza-13-azonia-dibenzo[a,de]anth...)
Affinity DataIC50:  380nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108801(6,8,13-trimethyl-8H-quino[4,3,2-kl]acridin-13-ium;...)
Affinity DataIC50:  760nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068324(3-Dimethylamino-N-[5-(3-dimethylamino-propionylami...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080842(3,6-Bis[3-(4-methylpiperidino)propionamido]acridin...)
Affinity DataIC50:  1.35E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50082524(2,6-Bis(3-pyrrolidinopropionamido)anthracene-9,10-...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibitory activity against Telomerase evaluated by TRAP Assay studies.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068304(CHEMBL343445 | N-[9,10-Dioxo-6-(3-pyrrolidin-1-yl-...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068320(2,7-Bis[3-(pyrrolidino)propionamido]anthraquinone ...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50108804(8,13-Diethyl-6-methyl-8H-8-aza-13-azonia-dibenzo[a...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of telomerase activity using TRAP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068330(CHEMBL144848 | N-[9,10-Dioxo-5-(3-piperidin-1-yl-p...)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080848(3-(2-Methyl-piperidin-1-yl)-N-{6-[3-(2-methyl-pipe...)
Affinity DataIC50:  2.60E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068303(1,5-BIS[3-(DIETHYLAMINO)PROPIONAMIDO]ANTHRACENE-9,...)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080837(3-(2-Ethyl-piperidin-1-yl)-N-{6-[3-(2-ethyl-piperi...)
Affinity DataIC50:  2.70E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080847(3,6-Bis(3-piperidinopropionamido)acridine | 3-Pipe...)
Affinity DataIC50:  2.80E+3nMAssay Description:Inhibitory activity against Telomerase evaluated by TRAP Assay studies.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080847(3,6-Bis(3-piperidinopropionamido)acridine | 3-Pipe...)
Affinity DataIC50:  2.80E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068321(2,7-Bis[3-(piperidino)propionamido]anthraquinone |...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068321(2,7-Bis[3-(piperidino)propionamido]anthraquinone |...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibitory activity against telomeraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080840(3,6-Bis[3-(azepan-1-yl)propionamido]acridine | 3,6...)
Affinity DataIC50:  3.10E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080840(3,6-Bis[3-(azepan-1-yl)propionamido]acridine | 3,6...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibitory activity against Telomerase evaluated by TRAP Assay studies.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068328(CHEMBL144303 | N-[9,10-Dioxo-4-(3-(N,N-diethyl-N-m...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50005750(3-Diethylamino-N-[6-(3-diethylamino-propionylamino...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068332(CHEMBL144386 | N-[9,10-Dioxo-8-(3-piperidin-1-yl-p...)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068311(3-Dimethylamino-N-[6-(3-dimethylamino-propionylami...)
Affinity DataIC50:  4.10E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080850(3-[2-(2-Hydroxy-ethyl)-piperidin-1-yl]-N-(6-{3-[2-...)
Affinity DataIC50:  4.10E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068315(3-Diethylamino-N-[8-(3-diethylamino-propionylamino...)
Affinity DataIC50:  4.20E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068312(2,7-Bis[3-(diethylamino)propionamido]anthraquinone...)
Affinity DataIC50:  4.30E+3nMAssay Description:Inhibitory activity against telomeraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068312(2,7-Bis[3-(diethylamino)propionamido]anthraquinone...)
Affinity DataIC50:  4.30E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068335(CHEMBL422120 | N-[9,10-Dioxo-8-(3-(N,N,N-trimethyl...)
Affinity DataIC50:  4.40E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080839(3-(3-Methyl-piperidin-1-yl)-N-{6-[3-(3-methyl-pipe...)
Affinity DataIC50:  4.40E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50005746(CHEMBL109382 | CHEMBL33618 | N-[9,10-Dioxo-6-(3-pi...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibition of telomerase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50082532(2,6-Bis(3-piperidinopropionamido)anthracene-9,10-d...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibitory activity against Telomerase evaluated by TRAP Assay studies.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50005746(CHEMBL109382 | CHEMBL33618 | N-[9,10-Dioxo-6-(3-pi...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068336(2,7-Bis[3-(dimethylamino)propionamido]anthraquinon...)
Affinity DataIC50:  4.70E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068336(2,7-Bis[3-(dimethylamino)propionamido]anthraquinon...)
Affinity DataIC50:  4.70E+3nMAssay Description:Inhibitory activity against telomeraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068313(CHEMBL143452 | N-[9,10-Dioxo-4-(3-(N-methylpyrroli...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080849(3,6-Bis(3-pyrrolidinopropionamido)acridine | 3-PYR...)
Affinity DataIC50:  5.20E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080849(3,6-Bis(3-pyrrolidinopropionamido)acridine | 3-PYR...)
Affinity DataIC50:  5.20E+3nMAssay Description:Inhibitory activity against Telomerase evaluated by TRAP Assay studies.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080841(3-(2-Hydroxymethyl-piperidin-1-yl)-N-{6-[3-(2-hydr...)
Affinity DataIC50:  5.40E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080844(3-Diethylamino-N-[6-(3-diethylamino-propionylamino...)
Affinity DataIC50:  5.80E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068323(3-Dimethylamino-N-[8-(3-dimethylamino-propionylami...)
Affinity DataIC50:  6.40E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50066349(3-Trimethylammonium-N-[4-(3-dimethylammonium-propi...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068318(CHEMBL145311 | N-[9,10-Dioxo-8-(3-(N,N-diethyl-N-m...)
Affinity DataIC50:  7.50E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068308(CHEMBL14832 | CHEMBL90901 | N-[9,10-Dioxo-7-(3-(N-...)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068308(CHEMBL14832 | CHEMBL90901 | N-[9,10-Dioxo-7-(3-(N-...)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibitory activity against telomeraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068337(CHEMBL343238 | N-[9,10-Dioxo-8-(3-(N-methylpiperid...)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50080845(3-(4-Hydroxy-piperidin-1-yl)-N-{6-[3-(4-hydroxy-pi...)
Affinity DataIC50:  8.00E+3nMAssay Description:Ability to inhibit human telomerase in a modified cell-free TRAP assay using extracts from A2780 cell lineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50079139(3-(2-Hydroxymethyl-piperidin-1-yl)-N-{7-[3-(2-hydr...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibitory activity against telomeraseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
University Of Nottingham

Curated by ChEMBL
LigandPNGBDBM50068322(CHEMBL144219 | N-[9,10-Dioxo-8-(3-(N-methylpyrroli...)
Affinity DataIC50:  8.20E+3nMAssay Description:Inhibitory activity of telomerase was measured using the TRAP assay.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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