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TargetSignal transducer and activator of transcription 1-alpha/beta
LigandBDBM50190101
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1591093 (CHEMBL3829061)
IC50>50000±n/a nM
Citation LaPorte, MGWang, ZColombo, RGarzan, APeshkov, VALiang, MJohnston, PASchurdak, MESen, MCamarco, DPHua, YPollock, NILazo, JSGrandis, JRWipf, PHuryn, DM Optimization of pyrazole-containing 1,2,4-triazolo-[3,4-b]thiadiazines, a new class of STAT3 pathway inhibitors. Bioorg Med Chem Lett26:3581-5 (2016) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Signal transducer and activator of transcription 1-alpha/beta
Name:Signal transducer and activator of transcription 1-alpha/beta
Synonyms:STAT1 | STAT1_HUMAN | Signal transducer and activator of transcription 1-alpha/beta | Transcription Factor STAT1 | Transcription factor ISGF-3 components p91/p84 | signal transducer and activator of transcription 1 isoform alpha
Type:Cytosolic Transcription Factor
Mol. Mass.:87327.69
Organism:Homo sapiens (Human)
Description:Stat1 was expressed in sf9 cells from a baculovirus encoding the recombinant proteins. Stat1 dimer binds to DNA.
Residue:750
Sequence:
MSQWYELQQLDSKFLEQVHQLYDDSFPMEIRQYLAQWLEKQDWEHAANDVSFATIRFHDL
LSQLDDQYSRFSLENNFLLQHNIRKSKRNLQDNFQEDPIQMSMIIYSCLKEERKILENAQ
RFNQAQSGNIQSTVMLDKQKELDSKVRNVKDKVMCIEHEIKSLEDLQDEYDFKCKTLQNR
EHETNGVAKSDQKQEQLLLKKMYLMLDNKRKEVVHKIIELLNVTELTQNALINDELVEWK
RRQQSACIGGPPNACLDQLQNWFTIVAESLQQVRQQLKKLEELEQKYTYEHDPITKNKQV
LWDRTFSLFQQLIQSSFVVERQPCMPTHPQRPLVLKTGVQFTVKLRLLVKLQELNYNLKV
KVLFDKDVNERNTVKGFRKFNILGTHTKVMNMEESTNGSLAAEFRHLQLKEQKNAGTRTN
EGPLIVTEELHSLSFETQLCQPGLVIDLETTSLPVVVISNVSQLPSGWASILWYNMLVAE
PRNLSFFLTPPCARWAQLSEVLSWQFSSVTKRGLNVDQLNMLGEKLLGPNASPDGLIPWT
RFCKENINDKNFPFWLWIESILELIKKHLLPLWNDGCIMGFISKERERALLKDQQPGTFL
LRFSESSREGAITFTWVERSQNGGEPDFHAVEPYTKKELSAVTFPDIIRNYKVMAAENIP
ENPLKYLYPNIDKDHAFGKYYSRPKEAPEPMELDGPKGTGYIKTELISVSEVHPSRLQTT
DNLLPMSPEEFDEVSRIVGSVEFDSMMNTV
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  Blast E-value cutoff:
BDBM50190101
n/a
NameBDBM50190101
Synonyms:CHEMBL3827334 | US11111253, Compound 27
TypeSmall organic molecule
Emp. Form.C20H20Cl2N6S
Mol. Mass.447.384
SMILESCC(C)CC1Sc2nnc(-c3[nH]nc4CCCc34)n2N=C1c1ccc(Cl)c(Cl)c1 |c:22|
Structure
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