STAT
STAT Isoform Specific Products
All Product Categories
-
STAT Inhibitors
(655)
View all products
-
STAT Agonists
(7)
View all products
-
STAT Antagonists
(4)
View all products
-
STAT Activators
(61)
View all products
-
STAT Modulators
(20)
View all products
-
STAT Inducers
(2)
View all products
-
STAT Degraders
(25)
View all products
-
STAT Controls
(2)
View all products
-
STAT Ligands
(7)
View all products
-
STAT 관련 제품 (846)
관련 제품 (846)
-
Antibodies (25)
-
STAT Isoform Comparison
- Bromisoval (Standard)
-
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Perindopril-d5
0 ImagesCat. No.: HY-B0130S1Synonyms: S-9490-d5Perindopril-d5 (S-9490-d5) is deuterium labeled Perindopril. Perindopril (S-9490) is an orally available, long-acting angiotensin-converting enzyme (ACE) inhibitor. Perindopril inhibits inflammatory cell influx and intimal thickening, preserving elastin on the inside of the aorta. Perindopril effectively inhibits experimental abdominal aortic aneurysm (AAA) formation in a rat model and reduces pulmonary vasoconstriction in rats with pulmonary hypertension. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Golotimod (Standard)
0 ImagesCat. No.: HY-14743RCAS No.: 229305-39-9Synonyms: SCV 07 (Standard); Gamma-D-glutamyl-L-tryptophan (Standard)Golotimod (Standard) is the analytical standard of Golotimod. This product is intended for research and analytical applications. Golotimod (SCV-07), an immunomodulating peptide with antimicrobial activity, significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function. Golotimod (SCV-07) inhibits STAT3 signaling and modulates the duration and severity of oral mucositis in animal models that received radiation or a combination of radiation and Cisplatin. Golotimod (SCV-07) is also a potential therapeutic for recurrent genital herpes simplex virus type 2 (HSV-2). -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Phlorizin (Standard)
0 ImagesPhlorizin (Floridzin) (Standard) is the analytical standard of Phlorizin. This product is intended for research and analytical applications. Phlorizin is an orally active non-selective sodium-glucose cotransporter (SGLT) inhibitor, with an IC50 of 0.04 μM and a Ki of 39 nM against hSGLT2, and an IC50 of 0.17 μM and a Ki of 0.31 μM against hSGLT1. Phlorizin promotes GLUT4 translocation, inhibits gluconeogenesis and promotes glycogen synthesis by activating the PI3K/Akt/mTOR pathway. Phlorizin reduces DNA damage and apoptosis (apoptosis) by inhibiting the NF-κB inflammatory pathway. Phlorizin induces apoptosis via activating the Caspase pathway by antagonizing the JAK/STAT3 and PCK pathways. Phlorizin also exhibits antibacterial, anti-inflammatory and neuroprotective activities. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
GPA512
0 ImagesCat. No.: HY-123827CAS No.: 1808115-35-6GPA512 is an orally active STAT3 inhibitor and a prodrug of Galiellalactone (HY-125170). GPA512 inhibits the binding of STAT3 to DNA, downregulates STAT3-activated genes, and suppresses tumor growth in prostate cancer xenograft models. GPA512 is rapidly converted to Galiellalactone in plasma. GPA512 can be used in research related to castration-resistant prostate cancer. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Corylifol A (Standard)
0 ImagesCat. No.: HY-N0897RCAS No.: 775351-88-7Synonyms: Corylifol-A (Standard); Corylinin (Standard)Corylifol A (Standard) is the analytical standard of Corylifol A. This product is intended for research and analytical applications. Corylifol A inhibits IL-6-induced STAT3 activation and phosphorylation, with an IC50 of 0.81 μM. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Niclosamide-d3
0 ImagesCat. No.: HY-B0497S2CAS No.: 2665663-60-3Synonyms: BAY2353-d3Niclosamide-d3 (BAY2353-d3) is deuterium labeled Niclosamide. 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. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
STAT3-IN-1 (Standard)
0 ImagesCat. No.: HY-100753RCAS No.: 2059952-75-7STAT3-IN-1 (Standard) is the analytical standard of STAT3-IN-1 (HY-100753). This product is intended for research and analytical applications. STAT3-IN-1 (compound 7d) is an excellent, selective and orally active STAT3 inhibitor, with IC50 values of 1.82 μM and 2.14 μM in HT29 and MDA-MB 231 cells, respectively. STAT3-IN-1 (compound 7d) induces tumor cells apoptosis. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Madindoline A
0 ImagesCat. No.: HY-N14323CAS No.: 184877-64-3Madindoline A is an orally active gp130 antagonist with a KD of 288 μM. Madindoline A inhibits IL-6- and IL-11-induced osteoclastogenesis, suppresses IL-6-stimulated serum amyloid A protein production, inhibits bone resorption and bone loss, and also inhibits IL-6- and IL-11-dependent cell line growth, as well as IL-6-dependent Stat3 tyrosine phosphorylation. Madindoline A is applicable for the research of hormone-dependent postmenopausal osteoporosis. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Iridin (Standard)
0 ImagesIridin (Standard) is the analytical standard of Iridin. This product is intended for research and analytical applications. Iridin is an orally active natural isoflavone. Iridin inhibits the PI3K/AKT and PKM2 signaling pathways, and downregulates the JAK/STAT and NF-κB pathways. Iridin induces Fas-mediated extrinsic apoptosis, G2/M cell cycle arrest, and inhibits cell proliferation. Iridin reduces inflammation, inhibits ROS production, suppresses glycolysis, and also exhibits antioxidant and antidiabetic activities. Iridin can be used in research related to gastric cancer and acute lung injury. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
YLL545
0 ImagesCat. No.: HY-164551CAS No.: 1423126-69-5YLL545 is a type of vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor. YLL545 can inhibit VEGF-induced phosphorylation of VEGFR2 and the activation of downstream signaling factors (like phosphorylated STAT3 and phosphorylated ERK1/2) in human umbilical vein endothelial cells (HUVEC). YLL545 can suppress the proliferation, migration, invasion, and angiogenesis of HUVEC. YLL545 can induce apoptosis in breast cancer mice and inhibit tumor growth. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
AH057
0 ImagesCat. No.: HY-183519CAS No.: 118499-11-9 -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
XZH-5
0 ImagesCat. No.: HY-120376CAS No.: 1360562-98-6 -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Atiprimod hydrochloride
0 ImagesCat. No.: HY-110102CAS No.: 130065-61-1Synonyms: Azaspirane hydrochloride; SKF 106615-12 hydrochloride; SKF 106615Atiprimod (Azaspirane) hydrochloride is a STAT3 inhibitor with antitumor, anti-inflammatory, and anti-angiogenic activities. Atiprimod blocks the signaling pathways of IL-6 and VEGF by inhibiting the phosphorylation of signal transducer and activator of STAT3. Atiprimod blocks the JAK-STAT signaling pathway by inhibiting the phosphorylation of JAK2 and JAK3. Atiprimod also inhibits cell proliferation, induces cell cycle arrest, and induces autophagy and apoptosis. Atiprimod triggers persistent ER stress-mediated apoptosis in breast cancer cells by activating the PERK/eIF2α/ATF4/CHOP axis and inhibiting the nuclear translocation of STAT3/NF-κB. Atiprimod shows great anti-tumor activities in tumor xenograft mouse models. Atiprimod can be used for the study of pituitary adenoma, breast cancer, multiple myeloma and acute myeloid leukemia (AML). -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
AS1517499 (Standard)
0 ImagesCat. No.: HY-100614RCAS No.: 919486-40-1 -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
- HJC0152 free base
-
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
- STAT3 ligand 5
-
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
CDK8-IN-16
0 ImagesCat. No.: HY-171174CAS No.: 1860885-61-5CDK8-IN-16 (Compound 51) is an orally active dual inhibitor for CDK8 and CDK19 wih IC50 of 5.1 nM and 5.6 nM. CDK8-IN-16 inhibits the phospho-STAT1SER727 with an IC50 of 17.9 nM in SW620 cell, inhibits WNT signaling pathway with an IC50 of 7.2 nM in 7dF3 cell. CDK8-IN-16 exhibits good pharmacokinetic characteristics in rat models with an oral bioavailability of 57%. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
BVB808
0 ImagesCat. No.: HY-120604CAS No.: 1414587-22-6Synonyms: NVP_BVB808BVB808 (NVP_BVB808) is a selective JAK2 inhibitor with approximately 10-fold selectivity for JAK2 over other JAK family members (such as JAK1, JAK3 or TYK2) in vitro. BVB808 inhibits the activity of JAK2 and reduces the phosphorylation of STAT5, thereby blocking the JAK2-dependent cell proliferation and survival signaling pathways. BVB808 can be used in cancer research. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Anthraquinone-2-carboxylic acid (Standard)
0 ImagesCat. No.: HY-W031757RCAS No.: 117-78-2Anthraquinone-2-carboxylic acid (Standard) is the analytical standard of Anthraquinone-2-carboxylic acid (HY-W031757). This product is intended for research and analytical applications. Anthraquinone-2-carboxylic acid is an orally active anthraquinone compound and Antibacterial agent. Anthraquinone-2-carboxylic acid can be isolated from Bajitian. Anthraquinone-2-carboxylic acid inhibits the activation of DPP-IV, COX-2, NF-κB and AP-1. Anthraquinone-2-carboxylic acid blocks IAV-induced activation of the RIG-I/STAT1 pathway, alleviates IAV-mediated weight loss, and protects against lethal IAV infection. Anthraquinone-2-carboxylic acid inhibits the growth of various Staphylococcus strains. It possesses potent anti-inflammatory, immunomodulatory, analgesic and antibacterial activities.\n -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.