Bookmark and Share
selinidin (CID 668081) - Compound BioActivity Data
.
BioActivity Outcomes:
Active(5)
 
 
Inactive(406)
 
 
Inconclusive(3)
 
 
Unspecified(13)
 
 
Top Targets:
7TM GPCR Srx(14)
 
 
7TM GPCR Srsx(12)
 
 
alkPPc(4)
 
 
Peptidase C48(4)
 
 
RasGEF(4)
 
 
BioAssay Types:
Screening(297)
 
 
 
Confirmatory(96)
 
 
 
 
Literature(25)
 
 
 
 
BioActivity Types:
Potency(87)
 
 
 
 
IC50(9)
 
 
 
Data download

Chemical Probe    Active    Inactive    Inconclusive    Unspecified   

Total Bioassays: 387    Data Row: 427   Total Pages: 22   Display: Page     
Sort: [Click the result table header to sort]
#SubstanceActivityBioAssayTargetLinks
OutcomeTypeValue [μM]
1
[SID85149155]
Fluorescence-based biochemical high throughput confirmation assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID651616, Type: screening]fructose-bisphosphate aldolase [Mycobacterium tuberculosis H37Rv] [gi:15607504]
View
2
[SID85149155]
Fluorescence-based biochemical primary high throughput screening assay to identify inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis [AID588726, Type: screening]fructose-bisphosphate aldolase [Mycobacterium tuberculosis H37Rv] [gi:15607504]
View
3
[SID85149155]
Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis: Fluroescence-based biochemical high throughput Glycerophosphate Dehydrogenase-Triosephosphate Isomerase (GDH-TPI) assay to identify assay artifacts [AID652141, Type: screening]
View
4
[SID103600421]
Binding affinity to spinach calmodulin assessed as modification of electrophoretic mobility at 0.033 ug/mL after 1.5 hrs by SDS-PAGE in presence of calcium chloride [AID334851, Type: Literature]Calmodulin [gi:122063217]
View
5
[SID103600421]
Binding affinity to bovine brain calmodulin assessed as modification of electrophoretic mobility at 0.033 ug/mL after 1.5 hrs by SDS-PAGE in presence of calcium chloride [AID334850, Type: Literature]Calmodulin [gi:49037473]
View
6
[SID103600421]
IC50 260Phytotoxicity against Amaranthus hypochondriacus assessed as inhibition of radicle elongation by petri dish bioassay [AID334616, Type: Literature]
View
7
[SID103600421]
IC50 863Phytotoxicity against Echinochloa crus-galli assessed as inhibition of radicle elongation by petri dish bioassay [AID334617, Type: Literature]
View
8
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as growth inhibition at 12 uM after 3 days relative to control [AID334618, Type: Literature]
View
9
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as growth inhibition at 25 uM after 3 days relative to control [AID334619, Type: Literature]
View
10
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as growth inhibition at 50 uM after 3 days relative to control [AID334620, Type: Literature]
View
11
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as growth inhibition at 100 uM after 3 days relative to control [AID334621, Type: Literature]
View
12
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as chlorophyll reduction at 25 uM after 3 days by ultraviolet spectroscopy relative to control [AID334622, Type: Literature]
View
13
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as chlorophyll reduction at 50 uM after 3 days by ultraviolet spectroscopy relative to control [AID334623, Type: Literature]
View
14
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as chlorophyll reduction at 100 uM after 3 days by ultraviolet spectroscopy relative to control [AID334624, Type: Literature]
View
15
[SID103600421]
Phytotoxicity against Lemna paucicostata assessed as chlorophyll reduction at 12 uM after 3 days by ultraviolet spectroscopy relative to control [AID334853, Type: Literature]
View
16
[SID103600421]
Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM [AID977599, Type: Literature]
View
17
[SID103600421]
Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM [AID977602, Type: Literature]
View
18
[SID85149155]
Potency qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory]acid sphingomyelinase [Homo sapiens] [gi:179095]
View
19
[SID85149155]
Potency 31.6228qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1): qHTS [AID588456, Type: confirmatory]thioredoxin reductase [Rattus norvegicus] [gi:8659577]
View
20
[SID85149155]
Potency 89.1251HTS for Inhibitors of HP1-beta Chromodomain Interactions with Methylated Histone Tails [AID540317, Type: confirmatory]chromobox protein homolog 1 [Homo sapiens] [gi:187960037]
View