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Terbutaline (CID 657301) - Compound BioActivity Data
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BioActivity Outcomes:
Active(15)
 
 
Inactive(921)
 
 
Inconclusive(48)
 
 
Unspecified(15)
 
 
Top Targets:
7TM GPCR Srsx(32)
 
 
 
 
7TM GPCR Srx(27)
 
 
 
Bcl-2 like(12)
 
 
Tryp SPc(12)
 
 
alkPPc(10)
 
 
BioAssay Types:
Screening(581)
 
 
 
 
Confirmatory(309)
 
 
 
 
 
Literature(26)
 
 
 
BioActivity Types:
Potency(228)
 
 
 
 
 
IC50(49)
 
 
 
EC50(13)
 
 
Data download

Chemical Probe    Active    Inactive    Inconclusive    Unspecified   

Total Bioassays: 854    Data Row: 999   Total Pages: 50   Display: Page     
Sort: [Click the result table header to sort]
#SubstanceActivityBioAssayTargetLinks
OutcomeTypeValue [μM]
1
[SID56424025]
IC50 0.0142191Dose responses of compounds that inhibit the Choline Transporter (CHT) - 10 point CRC [AID588401, Type: confirmatory]high affinity choline transporter 1 [Homo sapiens] [gi:11141885]
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2
[SID855787]
Potency 0.0731qHTS assay of beta-arrestin-biased ligands of beta2-adrenergic receptor: Hit Validation with GloSensor [AID588790, Type: confirmatory]beta-2 adrenergic receptor [Homo sapiens] [gi:4501969]
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3
[SID56424025]
IC50 0.084119Dose responses of compounds that inhibit the Choline Transporter (CHT) - 5 point CRC [AID504840, Type: confirmatory]high affinity choline transporter 1 [Homo sapiens] [gi:11141885]
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4
[SID855787]
Potency 1.1582qHTS assay of beta-arrestin-biased ligands of beta2-adrenergic receptor: Hit Validation [AID588463, Type: confirmatory]beta-2 adrenergic receptor [Homo sapiens] [gi:4501969]
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5
[SID56424025]
Primary cell-based screen for identification of compounds that inhibit the Choline Transporter (CHT) [AID488975, Type: screening]high affinity choline transporter 1 [Homo sapiens] [gi:11141885]
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6
[SID56424025]
Confirmatory screen for compounds that inhibit the Choline Transporter (CHT) [AID493221, Type: screening]high affinity choline transporter 1 [Homo sapiens] [gi:11141885]
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7
[SID188124935]
Confirmed inhibitors of the Choline Transporter (CHT) [AID1053196, Type: other]high affinity choline transporter 1 [Homo sapiens] [gi:11141885]
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8
[SID855787]
Allosteric Modulators of D1 Receptors: Secondary Assay 2 [AID647, Type: other]
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9
[SID855787]
Allosteric Modulators of D1 Receptors: Primary Screen [AID641, Type: screening]
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10
[SID855787]
Allosteric Modulators of D1 Receptors: Confirmation Screen [AID642, Type: other]
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11
[SID855787]
Aqueous Solubility from MLSMR Stock Solutions [AID1996, Type: other]
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12
[SID56424025]
HTS to Find Inhibitors of Pathogenic Pemphigus Antibodies [AID588358, Type: screening]
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13
[SID855787]
Discovery of novel allosteric modulators of the M1 muscarinic receptor: Antagonist Primary Screen [AID628, Type: screening]Muscarinic acetylcholine receptor M1 [gi:113121]
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14
[SID56424025]
HTS for Beta-2AR agonists via FAP method, Single Point, Cherry Pick 1 [AID540358, Type: other]beta-2 adrenergic receptor [Homo sapiens] [gi:4501969]
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15
[SID103760630]
Beta-2 adrenergic receptor agonist [AID742548, Type: other]Beta-2 adrenergic receptor [gi:296439450]
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16
[SID103760630]
Partition coefficient (logD7.4) [AID19424, Type: Literature]
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17
[SID56424025]
Potency qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory]acid sphingomyelinase [Homo sapiens] [gi:179095]
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18
[SID8149545]
Assay to identify inhibitors of polyglutamine-induced caspase-3 activation (CASP3) [AID1583, Type: other]
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19
[SID8149545]
Yeast cell-based screen for compounds that suppress polyglutamine aggregation in vivo (75Q-TubU) [AID1593, Type: other]
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20
[SID8149545]
Screen for compounds that correct neuronal dysfunction without cell death as induced by the expression of polyglutamine-expanded, N-terminal huntingtin in C. elegans mechanosensory neurons (HDELENEU) [AID1599, Type: other]
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