1. Signaling Pathways
  2. JAK/STAT Signaling
    Stem Cell/Wnt
  3. STAT

STAT

STAT

STAT is a family of cytoplasmic protein that regulates many aspects of growth, survival and differentiation in cells. The transcription factors of this family are activated by Janus kinase and dysregulation of this pathway is frequently observed in primary tumours and leads to increased angiogenesis, enhanced survival of tumours and immunosuppression. Gene knockout studies have provided evidence that STAT proteins are involved in the development and function of the immune system and play a role in maintaining immune tolerance and tumour surveillance. STAT proteins were originally described as latent cytoplasmic transcription factors that require phosphorylation for nuclear retention. The unphosphorylated STAT proteins shuttle between cytosol and the nucleus waiting for its activation signal. Once the activated transcription factor reaches the nucleus, it binds to consensus DNA-recognition motif called gamma-activated sites (GAS) in the promoter region of cytokine-inducible genes and activates transcription of these genes.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-13818
    Stattic
    Inhibitor 99.58%
    Stattic is a potent STAT3 inhibitor and inhibits STAT3 phosphorylation (at Y705 and S727). Stattic inhibits the binding of a high affinity phosphopeptide for the SH2 domain of STAT3. Stattic ameliorates the renal dysfunction in Alport syndrome (AS) mice.
    Stattic
  • HY-B0069
    Fludarabine
    Inhibitor 99.85%
    Fludarabine (NSC 118218) is a DNA synthesis inhibitor and a fluorinated purine analogue with antineoplastic activity in lymphoproliferative malignancies. Fludarabine inhibits the cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal resting or activated lymphocytes.
    Fludarabine
  • HY-12000
    AG490
    Inhibitor 99.86%
    AG490 (Tyrphostin AG490) is a tyrosine kinase inhibitor that inhibits EGFR, Stat-3 and JAK2/3.
    AG490
  • HY-16141
    Cilengitide
    Inhibitor 99.80%
    Cilengitide (EMD 121974) is a potent integrins antagonist with IC50s of 0.61 nM (ανβ3), 8.4 nM (ανβ5) and 14.9 nM (α5β1), respectively. Cilengitide inhibits the binding of ανβ3 and ανβ5 to Vitronectin with IC50s of 4 nM and 79 nM, respectively. Cilengitide inhibits TGF-β/Smad signaling, mediates PD-L1 expression. Cilengitide also induces apoptosis, shows antiangiogenic effect in the research against glioblastoma and other cancers.
    Cilengitide
  • HY-14944
    Homoharringtonine
    Inhibitor 99.96%
    Homoharringtonine (Omacetaxine mepesuccinate;HHT) is a cytotoxic alkaloid with antitumor properties which acts by inhibiting translation elongation.
    Homoharringtonine
  • HY-169179
    AK-1690
    Degrader
    AK-1690 is a potent and selective STAT6 PROTAC degrader. AK-1690 reduces the levels of STAT6 protein in cells (DC50=1 nM) and depletes STAT6 protein in mouse tissues. AK-1690 can be used for the research of cancer. (Pink: ligand for target protein STAT6 (HY-169182); Black: linker (HY-W459522); Blue: ligand for E3 ligase (HY-131318).
    AK-1690
  • HY-120113
    SC-2001
    Inhibitor
    SC-2001 is a compound structurally related to obatoclax that has better antitumor effects than obatoclax in liver cancer cell lines, downregulating Mcl-1 protein levels, inhibiting STAT3 phosphorylation, inducing apoptosis, and enhancing SHP1 expression and activity.
    SC-2001
  • HY-P10201A
    Ac-GpYLPQTV-NH2 acetate
    Inhibitor 99.38%
    Ac-GpYLPQTV-NH2 acetate is a STAT3 inhibitor with an IC50 value of 0.33 μM. Ac-GpYLPQTV-NH2 acetate has antitumor activity.
    Ac-GpYLPQTV-NH2 acetate
  • HY-100614
    AS1517499
    Inhibitor 99.17%
    AS1517499 is a potent and brain-permeable STAT6 phosphorylation inhibitor with an IC50 of 21 nM.
    AS1517499
  • HY-B0497
    Niclosamide
    Inhibitor 99.91%
    Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research. Niclosamide is a STAT3 inhibitor with an IC50 of 0.25 μM in HeLa cells. Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells.
    Niclosamide
  • HY-N0193
    Artesunate
    Inhibitor 99.84%
    Artesunate is an inhibitor of both STAT-3 and exported protein 1 (EXP1).
    Artesunate
  • HY-112288
    C188-9
    Inhibitor 99.90%
    C188-9 (TTI-101) is a STAT3 inhibitor, with a Kd of 4.7 nM. C188-9 inhibits G-CSF-induced STAT3 activation and STAT3-dependent gene expression. C188-9 induces apoptosis in AML cell lines and primary samples and inhibits colony formation by primary AML blasts.
    C188-9
  • HY-107632
    GYY4137
    Inhibitor 98.08%
    GY4137 is a sustained-release H2S donor possessing vasodilatory, antihypertensive, and anti-inflammatory activities. GY4137 can inhibit cell growth, induce apoptosis, and cause cell cycle arrest by blocking the STAT3 pathway, demonstrating potent anticancer activity.
    GYY4137
  • HY-15146
    NSC 74859
    Inhibitor 98.35%
    NSC 74859 (S3I-201) is a selective Stat3 inhibitor with an IC50 of 86 μM.
    NSC 74859
  • HY-N2334
    Glycochenodeoxycholic acid
    Activator 99.25%
    Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a relatively toxic bile salt generated in the liver from chenodeoxycholic acid and glycine. Glycochenodeoxycholic acid inhibits Autophagosome formation and impairs lysosomal function by inhibiting lysosomal proteolysis and increasing lysosomal pH in human normal liver cells, leading to the Apoptosis of human hepatocyte cells. Glycochenodeoxycholic acid induces stemness and chemoresistance via activating STAT3 signaling pathway in hepatocellular carcinoma cells (HCC). Glycochenodeoxycholic acid is promising for research in the field of cholestasis desease, hepatocellular carcinoma and primary sclerosing cholangitis (PSC).
    Glycochenodeoxycholic acid
  • HY-148748
    Butyzamide
    Activator 99.62%
    Butyzamide is an orally active activator of Mpl, a thrombopoietin (TPO) receptor. Butyzamide increases the phosphorylation level of JAK2, STAT3, STAT5 and MAPK. Butyzamide increases the level of human platelets in mouse xenotransplantation assay.
    Butyzamide
  • HY-P1061
    Colivelin
    Activator 99.27%
    Colivelin is a brain penetrant neuroprotective peptide and a potent activator of STAT3, suppresses neuronal death by activating STAT3 in vitro. Colivelin exhibits long-term beneficial effects against neurotoxicity, Aβ deposition, neuronal apoptosis, and synaptic plasticity deficits in neurodegenerative disease. Colivelin has the potential for the treatment of alzheimer's disease and ischemic brain injury
    Colivelin
  • HY-B2163
    Astaxanthin
    Inhibitor ≥98.0%
    Astaxanthin, the red dietary carotenoid, is an orally effective and potent antioxidant. Astaxanthin inhibits NF-κB and down-regulates VEGF in blood glucose. Astaxanthin exerts anti-cancer cell proliferation, increases apoptosis, impairs migration and invasion by activating PPARγ and reducing the expression of STAT3. Astaxanthin also has neuroprotective and anti-inflammatory activity and can be used in studies of cancer, diabetic retinopathy, cardiovascular disease, and in the coloring of animal feed.
    Astaxanthin
  • HY-10074
    TPCA-1
    Inhibitor 99.66%
    TPCA-1 is a potent and selective inhibitor of IKK-2 with IC50 of 17.9 nM. TPCA-1 is an effective inhibitor of STAT3 phosphorylation, DNA binding, and transactivation.
    TPCA-1
  • HY-15312
    WP1066
    Inhibitor 99.77%
    WP1066 is an inhibitor of JAK2 and STAT3, and also shows effect on STAT5 and ERK1/2, without affecting JAK1 and JAK3.
    WP1066
Cat. No. Product Name / Synonyms Application Reactivity

STAT3

STAT5

STAT6

STAT1

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STAT Degraders, Inhibitors & Activators
Product NameSTAT3STAT5STAT6STAT1Purity    
Stattic
STAT3
   99.58%
AG490
Stat-3
   99.86%
Cilengitide
STAT3 ([3])
   99.80%
Homoharringtonine
STAT3
   99.96%
Ac-GpYLPQTV-NH2 acetate
STAT3, IC50: 0.33 μM
   99.38%
AS1517499  
STAT6, IC50: 21 nM
 99.17%
Niclosamide
STAT3, IC50: 0.25 μM (in HeLa cells)
   99.91%
Artesunate
Stat-3
   99.84%
C188-9
STAT3, Kd: 4.7 nM
   99.90%
GYY4137
Stat-3
   98.08%
NSC 74859
STAT3, IC50: 86 μM
   98.35%
Butyzamide
STAT3
STAT5
  99.62%
Colivelin
STAT3
   99.27%
Astaxanthin
STAT3
   ≥98.0%
TPCA-1
STAT3
   99.66%
WP1066
STAT3
   99.77%
Scutellarin
STAT3
   99.04%
Napabucasin
STAT3
   99.94%
Cryptotanshinone
STAT3, IC50: 4.6 μM
   98.80%
STAT5-IN-1 
STAT5β, IC50: 47 μM
  98.35%
Pimozide
STAT3
STAT5
  99.91%
Colivelin TFA
STAT3
   99.52%
SD-36
STAT3, Kd: 50 nM
   99.73%
Diosgenin
STAT3
   99.35%
Saikosaponin D
STAT3
   98.76%
AC-4-130 
STAT5
  99.93%
Cucurbitacin I
STAT3
   99.44%
AS2863619 
STAT5
  99.94%
Morusin
STAT3
   99.94%
SH-4-54
STAT3, Kd: 300 nM
STAT5, Kd: 464 nM
  99.45%
Alantolactone
STAT3
   99.94%
BP-1-102
STAT3, IC50: 6.8 μM
   99.52%
SI-109
STAT3, Ki: 9 nM
   99.91%
Nifuroxazide
STAT3
   99.90%
SC-43
p-STAT3
   99.02%
YM-341619  
STAT6, IC50: 0.70 nM
 99.06%
STAT3-IN-1
Stat-3, IC50: 1.82 μM (in HT29 cells)
Stat-3, IC50: 2.14 μM (in MDA-MB 231 cells)
   
AK-2292 
STAT5, DC50: 0.10 μM
  99.73%
AS1810722  
STAT6, IC50: 1.9 nM
 98.14%
Erasin
STAT3, IC50: 9.7 μM
  
STAT1, IC50: 24 μM
NSC-370284
STAT3
STAT5
  
1-Stearoyl-sn-glycero-3-phosphocholine
p-STAT3
   99.53%
Peramivir
STAT3
   99.32%
Atractylenolide II
p-STAT3
   99.94%
Stafia-1 
STAT5a, Ki: 10.9 μM
STAT5a, IC50: 22.2 μM
  99.37%
Brevilin A
STAT3, IC50: 10.6 μM
   99.81%
Broussonin E
STAT3
   98.18%
Flubendazole
STAT3
   99.33%
HJC0152
STAT3
   99.76%
STAT3-IN-3
STAT3
   98.40%
HO-3867
STAT3
   99.67%
Perindopril erbumine
STAT3
   99.98%
BD750 
STAT5
  99.10%
Picroside I  
STAT6
 99.55%
LLL12
p-STAT3
   99.45%
GMB-475 
STAT5
  98.98%
STX-0119
STAT3, IC50: 74 μM (STAT3 transcription)
   99.21%
Garcinone D
p-STAT3
   99.88%
Stafib-1 
STAT5b, IC50: 154 nM
  ≥98.0%
OSM-SMI-10B
p-STAT3
   99.28%
IST5-002 
STAT5a, IC50: 1.5 μM
STAT5b, IC50: 3.5 μM
  99.36%
Cenisertib 
STAT5
  99.86%
inS3-54A18
STAT3
   99.53%
STAT3-IN-25
STAT3
   99.36%
Triacetylresveratrol
STAT3
   99.58%
Ginkgolic acid C17:1
STAT3
   99.90%
Mogrol
STAT3
   99.76%
Corylifol A
STAT3, IC50: 0.81 μM
   99.90%
STAT3-IN-12
STAT3
   99.92%
STAT5-IN-2 
STAT5, EC50: 9 μM (in K562 cells)
STAT5, EC50: 5 μM (in KU812 cells )
  99.08%
Ochromycinone
STAT3
   98.29%
Perindopril
STAT3
   98.11%
Reticuline
STAT3
   98.91%
Golotimod hydrochloride
STAT3
   99.79%
Garcinone C
Stat-3
   99.66%
Arnicolide D
STAT3
   99.69%
HODHBt 
STAT5
  99.93%
Protosappanin A
STAT3
   99.98%
LL-K8-22   
STAT1
99.76%
Tetramethylcurcumin
STAT3
   99.91%
Balsalazide
STAT3
   99.34%
STAT3-IN-15
STAT3
   98.99%
YMU1
STAT3
   99.19%
KT-333
STAT3
   
HJC0416 hydrochloride
STAT3
   98.68%
AS2863619 free base 
STAT5
  99.87%
STAT3-IN-17
STAT3
   ≥98.0%
SC99
STAT3
   98.96%
Golotimod
STAT3
   98.04%
PROTAC FLT-3 degrader 1 
STAT5
  99.74%
ASP3026
STAT3
   99.88%
OK2
p-STAT3
   
Equisetin
STAT3
   99.40%
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
p-STAT3
   98.02%
SB02024   
STAT1
99.7%
Balsalazide sodium hydrate
STAT3
   99.61%
WB436B
STAT3
   99.93%
MNK8
STAT3
   99.76%
ENMD-1198
STAT3
   98.87%
UC-514321
STAT3
STAT5
  ≥98.0%
SH5-07
STAT3, IC50: 3.9 μM
   ≥98.0%
Syk-IN-6
STAT3
STAT5
  
SD-1029
STAT3
   
Vanicoside B
STAT3
   99.82%
APTSTAT3-9R
STAT3
   99.55%
Iminostilbene
STAT3
   99.34%
Pimozide-d4
STAT3
STAT5
  ≥98.0%
Galiellalactone
STAT3, IC50: 250-500 nM
   
Biflorin   
STAT1
99.54%
Stafia-1-dipivaloyloxymethyl ester 
STAT5a
  98.31%
Eupalinolide K
STAT3
   99.20%
Eflepedocokin alfa
STAT3
   ≥99.0%
Niclosamide monohydrate
STAT3, IC50: 0.25 μM (in HeLa cells)
   
SD-1008
STAT3
   99.10%
STAT3-IN-8
STAT3
   
KT-333 diammonium
STAT3
   
YSY01A
Stat-3
   
c-Met-IN-24
STAT3, IC50: 4.7 μM
   
STAT3-IN-37
STAT3
   
STAT3 HiBiT degrader 1
STAT3
   
STAT3-IN-38
STAT3, Kd: 45.33 μM
   
STAT3-IN-29
STAT3
   
VEGFR-2/STAT-3-IN-1
STAT3, IC50: 5.63 nM
   
8α-Tigloyloxyhirsutinolide 13-O-acetate
STAT3
   
STAT1/3-IN-1
STAT3
  
STAT1
KT-333 ammonium
STAT3
   
WR-S-462
STAT3, Kd: 58 nM
   
JAK1/STAT3-IN-1
STAT3
   
FLT3-IN-28 
STAT5
  
SD-436
STAT3, IC50: 19 nM
STAT5, IC50: >10 μM
STAT6, IC50: >10 μM
STAT1, IC50: 270 nM
STAT3/AKT-IN-1
Stat-3
   
ROCK2-IN-7
Stat-3
   
Anti-inflammatory agent 92
STAT3
   
STAT3-IN-41
STAT3
   
Golotimod TFA
STAT3
   
HJC0416
STAT3
   
HJC0123
STAT3
   
HAT-SIL-TG-1&AT
STAT3
STAT5
  
7-epi-Isogarcinol
STAT3
   
Cernuumolide J
Stat-3
   
Atractylenolide II (Standard)
p-STAT3
   
Antitumor agent-73
STAT3
   
STAT3-IN-5
p-STAT3, EC50: 170 nM
   
K882
Stat-3
   
STAT3-IN-32
STAT3
   
WB518
STAT3
p-STAT3
   
Hsp110-STAT3 interaction-IN-2
STAT3
   
Ac-GpYLPQTV-NH2
STAT3, IC50: 0.33 μM
   
STAT3-IN-9
STAT3
   
PROTAC STAT3 degrader-2
STAT3, ID50: 3.54 μM
   
Ascochlorin
STAT3
   
Tyk2-IN-22-d3 
STAT5
  
1-Stearoyl-sn-glycero-3-phosphocholine-d35
p-STAT3
   
NW16
STAT3, Kd: 11.0 μM
   
15(R)-Lipoxin A4  
STAT6
 
Furowanin A
STAT3
   
Antitumor agent-195
STAT3, IC50: 0.52 μM
   
STAT3-IN-10
STAT3, IC50: 5.18 μM
   
Balsalazide disodium
STAT3
   
GYY4137 (GMP)
Stat-3
   
CHMFL-48 
STAT5
  
DETD-35
Stat-3
   
STAT3-IN-39
STAT3
   
TM-233
Stat-3
   
BP-1-108 
STAT5, Ki: 8.3 μM
  
PMMB-187
Stat-3, IC50: 1.81 μM