STAT
As proteínas STAT são componentes críticos da via de sinalização JAK/STAT, que transmite sinais extracelulares de citocinas e fatores de crescimento para o núcleo da célula, influenciando a expressão gênica. As proteínas STAT estão envolvidas na regulação de respostas imunológicas, crescimento celular, diferenciação e sobrevivência. A desregulação da sinalização STAT está implicada em várias doenças, incluindo câncer, distúrbios autoimunes e inflamação crônica. Na CymitQuimica, oferecemos uma ampla gama de moduladores da via STAT para apoiar sua pesquisa em transdução de sinal, imunologia e desenvolvimento terapêutico.
Foram encontrados 99 produtos de "STAT"
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Fludarabine
CAS:Fludarabine (Fludarabinum) is a fluorinated purine analog, an inhibitor of nucleic acid synthesis and an inhibitor of STAT1 activation.
Fórmula:C10H12FN5O4Pureza:99.65% - 99.89%Cor e Forma:White SolidPeso molecular:285.23Nifuroxazide
CAS:Nifuroxazide (Diarlidan), an oral nitrofuran antidiarrheal, blocks STAT1/3/5 activation.Fórmula:C12H9N3O5Pureza:99.79% - 99.95%Cor e Forma:Yellow SolidPeso molecular:275.22L002
CAS:L002 is a potent inhibitor of acetyltransferase p300 with an IC50 of 1.98 μM, blocking histone and p53 acetylation, and may treat cardiac hypertrophy.Fórmula:C15H15NO5SPureza:98.59%Cor e Forma:SolidPeso molecular:321.35Niclosamide olamine
CAS:Niclosamide olamine (Niclosamide Ethanolamine salt) is an Repellent, Insect Attractant and Chemosterilant.
Fórmula:C15H15Cl2N3O5Pureza:99.89%Cor e Forma:Bright Yellow Crystalline Physical Description Yellow Solid Insoluble In Water (Ntp 1992)Peso molecular:388.20Diosgenin
CAS:Diosgenin (Nitogenin) is a spirostan found in DIOSCOREA and other plants.Fórmula:C27H42O3Pureza:99.87%Cor e Forma:Flaky Or Needle CrystalPeso molecular:414.62STAT3-IN-1
CAS:STAT3-IN-1 selective and orally active inhibitor of STAT3(in HT29 and MDA-MB 231 cells, with IC50 values of 1.82 μM and 2.14 μM , respectively), induces tumorFórmula:C28H29NO6Pureza:95.89% - 95.89%Cor e Forma:SolidPeso molecular:475.53Ref: TM-T13009
1mg60,00€2mg88,00€5mg131,00€10mg192,00€25mg349,00€50mg523,00€100mg753,00€500mg1.549,00€1mL*10mM (DMSO)137,00€UC-514321
CAS:UC-514321 directly targets STAT3/5 and represses TET1 expression.Fórmula:C26H35NO5Pureza:98.50%Cor e Forma:SolidPeso molecular:441.56Ref: TM-T13950
1mg74,00€5mg160,00€10mg250,00€25mg502,00€50mg753,00€100mg1.130,00€200mg1.549,00€1mL*10mM (DMSO)170,00€Garcinone C
CAS:Garcinone C, a xanthone from Garcinia oblongifolia, is anti-inflammatory, promotes healing, and may fight some cancers.Fórmula:C23H26O7Pureza:99.13% - 99.92%Cor e Forma:SolidPeso molecular:414.45Niclosamide
CAS:Niclosamide (Niclocide)(BAY2353) is used to treat most tapeworm infections by inhibiting DNA replication.Fórmula:C13H8Cl2N2O4Pureza:98.47% - 99.1%Cor e Forma:Pale Yellow Crystals SolidPeso molecular:327.12Artesunate
CAS:Artesunate (WR-256283) is part of the artemisinin group of drugs that treat malaria.Fórmula:C19H28O8Pureza:97.67% - 99.9%Cor e Forma:White Crystalline PowderPeso molecular:384.42CMD178
CMD178 is an important polypeptide that consistently reduces the expression of Foxp3 and STAT5 by inhibiting the IL-2/s IL-2Rα signaling pathway.Fórmula:C46H59N9O7Pureza:98%Cor e Forma:SolidPeso molecular:850.03Ac-GpYLPQTV-NH2 acetate
Ac-GpYLPQTV-NH2 acetate is a STAT3 inhibitor with an IC50 value of 0.33 μM. It also exhibits antitumor properties.Fórmula:C38H60N9O14P·xC2H4O2Cor e Forma:SolidPeso molecular:897.91 (free base)JAK-STAT Compound Library
A unique collection of 252 JAK/STAT signaling targeted compounds for high throughput and high content screening;
Cor e Forma:Odour SolidAnticancer agent 259
Anticanceragent 259 (Compound 3g) is a telmisartan-based cell death regulator that disrupts the STAT5 signaling pathway, thereby increasing the sensitivity of resistant cells to imatinib, with an SC50 of 1.5 μM.Fórmula:C30H26N2O2Cor e Forma:SolidPeso molecular:446.54STAT3-IN-37
CAS:STAT3-IN-37 (Compound 101) is an inhibitor of STAT3, with an IC50 of 15 nM as measured by DNA-HTRF assay and 2 nM as determined through human whole blood SOCS3 qPCR assay.Fórmula:C23H25Cl2N5O2Cor e Forma:SolidPeso molecular:474.38STX-0119
CAS:STX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 μM.
Fórmula:C22H14N4O3Pureza:99.61%Cor e Forma:SolidPeso molecular:382.37STAT3-IN-23
CAS:STAT3-IN-23 (PY*LKTK) acts as a potent inhibitor of STAT3 [1].Fórmula:C36H61N8O12PCor e Forma:SolidPeso molecular:828.89STAT5-IN-3
STAT5-IN-3 (Compound 14a) is a STAT5 inhibitor with anticancer properties. It works by blocking the tyrosine phosphorylation of STAT5A/5B at the Y694/699 sites, significantly reducing the expression of the STAT5B protein. This leads to the inhibition of downstream gene transcription, thereby preventing the proliferation and survival of leukemia cells. Additionally, STAT5-IN-3 has significant potential in overcoming chemotherapy resistance.Fórmula:C25H27N5OCor e Forma:SolidPeso molecular:413.51STAT3-IN-31
STAT3-IN-31 (compound K2071), derived from STATtic, acts as an inhibitor of both STAT3 and mitotic processes. This compound interrupts mitotic progression and impacts the formation of the mitotic spindle. Additionally, STAT3-IN-31 hampers migration in glioblastoma cells, suppresses cellular proliferation within tumor spheroids, induces senescence in glioblastoma, and inhibits the growth of Temozolomide-resistant cells while reducing the secretion of the pro-inflammatory cytokine monocyte chemoattractant protein (MCP-1).Fórmula:C16H15NO3SCor e Forma:SolidPeso molecular:301.36STAT3-IN-34
STAT3-IN-34 (Compound 15E) acts as a STAT3 inhibitor, blocking both the nuclear translocation and the transcriptional regulator activity of STAT3. It effectively inhibits HaCaT cell proliferation with an IC50 value of 0.008 μM. Additionally, STAT3-IN-34 reduces IL-17A expression and mitigates Imiquimod-induced psoriasis in mouse models.Fórmula:C19H16N2O4SCor e Forma:SolidPeso molecular:368.41MNK8
CAS:MNK8 is a potent STAT3 inhibitor, impairs DNA binding, and inhibits liver cancer cell growth.Fórmula:C15H12N2O2Pureza:99.74%Cor e Forma:SolidPeso molecular:252.27STAT4-IN-1
STAT4-IN-1 is a STAT4 inhibitor with a Ki of 0.35 μM. It holds promise for research into autoimmune diseases, including inflammatory bowel disease, multiple sclerosis, rheumatoid arthritis, and diabetes.Cor e Forma:Odour SolidNeocucurbitacin A
CAS:Neocucurbitacin A (compound 7), a STAT3 inhibitor extracted from the pericarp of Aquilaria crassna, serves as a potential agent for anticancer research [1].
Fórmula:C31H42O8Pureza:98%Cor e Forma:SolidPeso molecular:542.66STAT3-IN-41
STAT3-IN-41 (Compound 16) is a prodrug of compound 1. It gradually releases compound 1, which inhibits the STAT3 signaling pathway. STAT3-IN-41 exhibits antitumor activity against lung cancer, hepatocellular carcinoma, and pancreatic cancer.Fórmula:C22H30F3NO7Cor e Forma:SolidPeso molecular:477.471Eflepedocokin alfa
CAS:Eflepedocokin alfa is a recombinant IL-22/IgG2-Fc protein, potentially protecting cells and enhancing immune function and tissue repair.Cor e Forma:LiquidSTAT3-IN-39
CAS:STAT3-IN-39 (compound 10K) is an orally active inhibitor of STAT3, demonstrating effective inhibition of STAT3 phosphorylation with an IC50 of 0.47 μM in NIH-3T3 cells. It hinders TGF-β1-induced fibrotic responses and prevents epithelial-mesenchymal transition in A549 cells. STAT3-IN-39 is applicable for research related to idiopathic pulmonary fibrosis.Fórmula:C20H17F3N2O3SCor e Forma:SolidPeso molecular:422.42(R)-Lisofylline
CAS:(R)-Lisofylline ((R)-Lisophylline) is an inhibitor of lysophosphatidic acid acyltransferase (IC50 = 0.6 µM).Fórmula:C13H20N4O3Pureza:99.50% - 99.85%Cor e Forma:SolidPeso molecular:280.32Balsalazide
CAS:Balsalazide (Balsalazido) is an anti-inflammatory compound used in the treatment of Inflammatory Bowel Disease.Fórmula:C17H15N3O6Pureza:99.31%Cor e Forma:Yellow To Orange Crystalline PowderPeso molecular:357.32Stafib-1
CAS:Stafib-1 is a selective inhibitor of STAT5β targeting SH2 domain with an IC50 of 154 nM and a Ki of 44 nM.Fórmula:C26H24N2O11P2Pureza:97.18%Cor e Forma:SolidPeso molecular:602.42SC-43
CAS:SC-43 is a potent and orally active agonist of SHP-1 (PTPN6).Fórmula:C21H13ClF3N3O2Pureza:98.44%Cor e Forma:SolidPeso molecular:431.8SH-4-54
CAS:SH-4-54 is a most potent, small molecule, nonphosphorylated STAT3 inhibitor.Fórmula:C29H27F5N2O5SPureza:98% - 99.12%Cor e Forma:SolidPeso molecular:610.59Ref: TM-T6669
1mg48,00€2mg63,00€5mg90,00€10mg152,00€25mg295,00€50mg475,00€100mg692,00€1mL*10mM (DMSO)128,00€SC99
CAS:SC99 inhibits JAK2-STAT3, reducing STAT3 genes, platelet activity, and has anti-myeloma, anti-thrombotic effects.Fórmula:C15H8Cl2FN3OPureza:99.56%Cor e Forma:SolidPeso molecular:336.15Ref: TM-T8719
1mg43,00€5mg87,00€10mg133,00€25mg227,00€50mg344,00€100mg429,00€200mg597,00€1mL*10mM (DMSO)94,00€Pimozide
CAS:Pimozide: antipsychotic that blocks type 2 dopamine, alpha-adrenergic, and 5-HT2 receptors, reducing tics and delusions.Fórmula:C28H29F2N3OPureza:99.63% - >99.99%Cor e Forma:SolidPeso molecular:461.55WP1066
CAS:WP1066 is a inhibitor of JAK2 (IC50: 2.30 μM) and STAT3 (IC50: 2.43 μM) in HEL cells; shows activity to JAK2, STAT3/5, and ERK1/2, not JAK1 and JAK3.Fórmula:C17H14BrN3OPureza:98.92% - 99.73%Cor e Forma:SolidPeso molecular:356.22Cucurbitacin I
CAS:Cucurbitacin I (JSI-124), a natural compound, is a selective inhibitor of JAK2/STAT3 with anti-cancer activity.
Fórmula:C30H42O7Pureza:96.69% - 99.8%Cor e Forma:SolidPeso molecular:514.65RSVA405
CAS:RSVA405 is an AMPK activator (EC50 = 1 μM), and is STAT3 inhibitorFórmula:C17H20N4O2Pureza:99.30%Cor e Forma:SolidPeso molecular:312.37Cryptotanshinone
CAS:Cryptotanshinone: STAT3 inhibitor, IC50 4.6 μM; blocks STAT3 Tyr705 phosphorylation, minor effect on Ser727, no impact on STAT1/5.Fórmula:C19H20O3Pureza:97.94% - ≥95%Cor e Forma:Orange Needle CrystalPeso molecular:296.36Scutellarin
CAS:Scutellarin from Scutellaria inhibits RANKL in osteoclasts and STAT3/Girdin/Akt in HCC cells.Fórmula:C21H18O12Pureza:97.12% - 99.75%Cor e Forma:SolidPeso molecular:462.36Brevilin A
CAS:Brevilin A, a sesquiterpene from Centipeda minima, hinders JAK and blocks STAT3 (IC50=10.6μM), inducing apoptosis and autophagy in cancer cells.Fórmula:C20H26O5Pureza:99.97% - >99.99%Cor e Forma:SolidPeso molecular:346.42Ref: TM-T4672
1mg90,00€5mg203,00€10mg350,00€25mg578,00€50mg797,00€100mg1.071,00€500mg2.187,00€1mL*10mM (DMSO)224,00€AS2863619
CAS:AS2863619 is an oral inhibitor of cyclin-dependent kinase(CDK8) and CDK19. Inhibition of CDK8/19 enhances STAT5 activation.Cost-effective and quality-assured.Fórmula:C16H14Cl2N8OPureza:>99.99%Cor e Forma:SolidPeso molecular:405.24Ref: TM-T8378
1mg131,00€2mg180,00€5mg274,00€10mg432,00€25mg715,00€50mg1.008,00€100mg1.359,00€1mL*10mM (DMSO)303,00€Atranorin
CAS:Atranorin has antinociceptive, anti-inflammatory, can be pro-oxidant or antioxidant, and protects cells from H(2)O(2)-induced oxidative stress.Fórmula:C19H18O8Pureza:98.76% - 99.57%Cor e Forma:SolidPeso molecular:374.34CMD178 TFA
CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.Fórmula:C48H60F3N9O9Pureza:>99.99%Cor e Forma:SolidPeso molecular:964.05Ref: TM-TP1433
1mg46,00€5mg92,00€10mg152,00€25mg249,00€50mg358,00€100mg538,00€200mg763,00€1mL*10mM (DMSO)167,00€HO-3867
CAS:HO-3867, an analog of curcumin, is a sspecific STAT3 inhibitor.Fórmula:C28H30F2N2O2Pureza:91.18% - 99.21%Cor e Forma:SolidPeso molecular:464.55S3I-201
CAS:S3I-201 (S3I-201) is a selective Stat3 inhibitor (IC50: 86±33 μM) and low effect towards STAT1/5.Fórmula:C16H15NO7SPureza:97.83%Cor e Forma:SolidPeso molecular:365.36Morusin
CAS:Morusin shows anti-tumor, antioxidant, and anti-inflammatory properties by inhibiting STAT3, NFκB, and inducing apoptosis.Fórmula:C25H24O6Pureza:98.68% - 99.8%Cor e Forma:SolidPeso molecular:420.45STAT5-IN-1
CAS:STAT5-IN-1 (STAT5 Inhibitor) is a cell-permeable inhibitor which suppresses Stat5 via binding to the SH2 domain.Fórmula:C16H11N3O3Pureza:99.44% - ≥95%Cor e Forma:SolidPeso molecular:293.28Napabucasin
CAS:Napabucasin (BBI608) is an orally available Stat3 and Y cell stemness inhibitor.Fórmula:C14H8O4Pureza:98.43% - 99.85%Cor e Forma:SolidPeso molecular:240.21Arnicolide D
CAS:Arnicolide D is a sesquiterpene lactone.Fórmula:C19H24O5Pureza:96.66% - 99.93%Cor e Forma:SolidPeso molecular:332.39HJC0152 hydrochloride
CAS:HJC0152 hydrochloride (HJC0152) is a signal transducer and activator of transcription 3 (STAT3) inhibitor.Fórmula:C15H14Cl3N3O4Pureza:99.01% - 99.06%Cor e Forma:SolidPeso molecular:406.64Nitidine chloride
CAS:1.Fórmula:C21H18ClNO4Pureza:96.59% - 99.55%Cor e Forma:SolidPeso molecular:383.82RO8191
CAS:RO8191 (CDM-3008) (CDM-3008) is an agonist of interferon (IFN) receptor.Fórmula:C14H5F6N5OPureza:98% - 98.85%Cor e Forma:SolidPeso molecular:373.21Ref: TM-T22142
1mg43,00€2mg55,00€5mg93,00€10mg137,00€25mg254,00€50mg380,00€100mg573,00€500mg1.189,00€Balsalazide disodium dihydrate
CAS:Balsalazide sodium hydrate treats mild-to-moderate ulcerative colitis; higher doses enhance remission maintenance; it's safe and effective.Fórmula:C17H17N3Na2O8Pureza:98.95% - 99.49%Cor e Forma:Yellow To Orange Crystalline PowderPeso molecular:437.31BP-1-102
CAS:BP-1-102 is an orally active, effective and specific STAT3 inhibitor.Fórmula:C29H27F5N2O6SPureza:99.25% - 99.44%Cor e Forma:SolidPeso molecular:626.59Ref: TM-T3708
1mg37,00€2mg49,00€5mg79,00€10mg113,00€25mg200,00€50mg334,00€100mg495,00€1mL*10mM (DMSO)99,00€ML116
CAS:ML116 is a potent and selective STAT3 inhibitor.Fórmula:C18H19N3SPureza:99.49%Cor e Forma:SolidPeso molecular:309.43Picroside I
CAS:Picroside I (6'-Cinnamoylcatalpol), a hepatoprotective agent, is reported to be antimicrobial and used against hepatitis B.Fórmula:C24H28O11Pureza:99.70% - 99.93%Cor e Forma:SolidPeso molecular:492.47SH5-07
CAS:SH5-07 is a hydroxamic acid-based Stat3 inhibitor (IC50: 3.9 μM).Fórmula:C29H28F5N3O5SPureza:95.54%Cor e Forma:SolidPeso molecular:625.61Ref: TM-TQ0052
1mg37,00€5mg80,00€10mg117,00€25mg197,00€50mg294,00€100mg425,00€200mg602,00€1mL*10mM (DMSO)99,00€FLLL32
CAS:FLLL32 is an effective JAK2/STAT3 inhibitor (IC50 of <5 μM).Fórmula:C28H32O6Pureza:97% - 97.90%Cor e Forma:SolidPeso molecular:464.55Ref: TM-T6838
2mg46,00€5mg66,00€10mg93,00€25mg124,00€50mg197,00€100mg350,00€500mg840,00€1mL*10mM (DMSO)72,00€2-(1,8-naphthyridin-2-yl)phenol
CAS:2-NP is a STAT1 enhancer.Fórmula:C14H10N2OPureza:99.33% - 99.82%Cor e Forma:SolidPeso molecular:222.24Ref: TM-T2168
5mg60,00€10mg96,00€25mg187,00€50mg298,00€100mg469,00€200mg682,00€500mg1.035,00€1mL*10mM (DMSO)66,00€TPCA-1
CAS:TPCA-1 (TPCA1) is an effective and specific IKK-2 inhibitor (IC50: 17.9 nM); shows >22-fold selectivity over IKK-1 and >550-fold selectivity over others kinasesFórmula:C12H10FN3O2SPureza:95.03% - 97.86%Cor e Forma:SolidPeso molecular:279.29Saikosaponin D
CAS:Saikosaponin D is a novel SERCA inhibitor by inhibiting NF-κB and STAT3 signaling to protect against acetaminophen-induced hepatotoxicity.Fórmula:C42H68O13Pureza:98.34% - 99.73%Cor e Forma:White PowderPeso molecular:780.98Protosappanin A
CAS:Protosappanin A combats brain inflammation, suppresses rat heart transplant rejection, fights MRSA, and inhibits HIV with a 12.6 uM IC50.
Fórmula:C15H12O5Pureza:99.42% - 99.82%Cor e Forma:SolidPeso molecular:272.25AS1517499
CAS:AS1517499 is a blood-brain barrier permeable inhibitor of STAT6 phosphorylation (IC50= 21 nM). High-Quality, Low-Cost!Fórmula:C20H20ClN5O2Pureza:98.27% - 99.3%Cor e Forma:SolidPeso molecular:397.86Ref: TM-T4476
1mg38,00€2mg50,00€5mg84,00€10mg113,00€25mg205,00€50mg313,00€100mg439,00€1mL*10mM (DMSO)93,00€BD750
CAS:BD750 is an effective immunosuppressant and a JAK3/STAT5 inhibitor, inhibits IL-2-induced JAK3/STAT5-dependent T cell proliferation(IC50 of 1.5 μM and 1.1 μM inFórmula:C14H13N3OSPureza:99.02%Cor e Forma:SolidPeso molecular:271.34Astaxanthin
CAS:Astaxanthin, a keto-carotenoid and xanthophyll, offers antioxidant benefits, present in red aquatic species, and used as a colorant in animal feed.
Fórmula:C40H52O4Pureza:95.1% - 99.79%Cor e Forma:Needles From Acetone/Light Petroleum SolidPeso molecular:596.84AS1810722
CAS:AS1810722, a fused bicyclic pyrimidine derivative, is an orally active and potent inhibitor of STAT6, demonstrating an IC50 of 1.9 nM.Fórmula:C25H25F2N7OPureza:99.13%Cor e Forma:SolidPeso molecular:477.511-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
CAS:SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib.Fórmula:C21H13ClF3N3O2Pureza:99.41%Cor e Forma:SolidPeso molecular:431.8Ref: TM-T22424
1mg42,00€2mg55,00€5mg88,00€10mg127,00€25mg264,00€50mg432,00€100mg622,00€200mg873,00€1mL*10mM (DMSO)99,00€Atractylenolide I
CAS:Atractylenolide-I reduces inflammation, improves sepsis, liver, and kidney function, and enhances EOC cell sensitivity to paclitaxel.Fórmula:C15H18O2Pureza:97.55% - 99.92%Cor e Forma:SolidPeso molecular:230.30C188-9
CAS:C188-9 (TTI-101) is a Stat3 inhibitor with an IC50 of 4-7 μM.Fórmula:C27H21NO5SPureza:98.07% - >99.99%Cor e Forma:SolidPeso molecular:471.52Ref: TM-T4650
1g1.839,00€1mg46,00€2mg59,00€5mg87,00€10mg123,00€25mg250,00€50mg398,00€100mg593,00€500mg1.264,00€1mL*10mM (DMSO)96,00€Casticin
CAS:Casticin combats vascular inflammation by blocking ROS-NF-κB and could lead in prostate cancer treatment.Fórmula:C19H18O8Pureza:99.37% - ≥95%Cor e Forma:SolidPeso molecular:374.34Ref: TM-T6S0071
2mg35,00€5mg52,00€10mg88,00€25mg160,00€50mg235,00€100mg354,00€200mg520,00€1mL*10mM (DMSO)86,00€Ref: TM-T4S0145
1mg51,00€5mg96,00€10mg153,00€25mg249,00€50mg369,00€100mg545,00€500mg1.130,00€1mL*10mM (DMSO)145,00€AG490
CAS:AG490 inhibits EGFR (0.1 μM IC50), 135x > selective than ErbB2, blocks JAK2, spares Lyn, Lck, Syk, Btk, Src.Fórmula:C17H14N2O3Pureza:98.6% - 99.85%Cor e Forma:Yellow SolidPeso molecular:294.3Alantolactone
CAS:Alantolactone is a selective inhibitor of STAT3 that induces cancer-associated apoptosis and has antitumor activity.Cost-effective and quality-assured.Fórmula:C15H20O2Pureza:99.02% - 99.66%Cor e Forma:Crystalline PowderPeso molecular:232.32Angoline
CAS:Angoline hydrochloride: IL6/STAT3 inhibitor, IC50: 11.56 μM, blocks STAT3 phosphorylation and cancer cell growth.
Fórmula:C22H21NO5Pureza:99.43% - 99.96%Cor e Forma:SolidPeso molecular:379.41Mogrol
CAS:Mogrol, a biometabolite of mogrosides, functions by inhibiting the ERK1/2 and STAT3 pathways, diminishing CREB activation, and activating AMPK signaling.Fórmula:C30H52O4Pureza:99.85% - 99.90%Cor e Forma:SolidPeso molecular:476.73Colivelin
CAS:Colivelin is a neuroprotective peptide and activator of STAT3. Colivelin is a hybrid peptide synthesized to enhance the neuroprotective effects of humanin (HN).Fórmula:C119H206N32O35Pureza:96.56%Cor e Forma:SolidPeso molecular:2645.1Garcinone D
CAS:Garcinone D is cytotoxic to CEM-SS cells (IC50=3.2 µg/ml), inhibits aromatase and p65 activation (IC50=3.2 µM).
Fórmula:C24H28O7Pureza:99.94%Cor e Forma:SolidPeso molecular:428.47Triacetylresveratrol
CAS:Triacetylresveratrol (Acetyl-trans-resveratrol) has anti-cancer activity, it inhibits the phosphorylation of STAT3 and NFκB in pancreatic cancer cells.
Fórmula:C20H18O6Pureza:99.81%Cor e Forma:Off White PowderPeso molecular:354.35Stafia-1
CAS:Stafia-1 is a potent STAT5a inhibitor ( IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.Fórmula:C24H27O10PPureza:98.08%Cor e Forma:SolidPeso molecular:506.44Ref: TM-T9339
1mg86,00€5mg187,00€10mg309,00€25mg525,00€50mg757,00€100mg1.035,00€500mg2.110,00€1mL*10mM (DMSO)217,00€Ochromycinone
CAS:Ochromycinone (STA 21) is a selective STAT3 inhibitor.Fórmula:C19H14O4Pureza:99.21%Cor e Forma:SolidPeso molecular:306.31Ref: TM-T6995
1mg97,00€5mg137,00€10mg227,00€25mg469,00€50mg825,00€100mg1.111,00€1mL*10mM (DMSO)150,00€Panaxadiol
CAS:Panaxadiol (20(R)-Panaxadiol) is a novel antitumor agent extracted from the Chinese medical herb Panax ginseng.Fórmula:C30H52O3Pureza:98% - 99.9%Cor e Forma:SolidPeso molecular:460.73Tetramethylcurcumin
CAS:Tetramethylcurcumin is a novel curcumin analog, is an effective inhibitors of STAT3 phosphorylation, DNA binding activity, and transactivation in vitro.it alsoFórmula:C25H28O6Pureza:97.69% - 99.94%Cor e Forma:SolidPeso molecular:424.49Stattic
CAS:Stattic (STAT3 Inhibitor V) is a STAT3 inhibitor (IC50=5.1 μM) that selectively inhibits STAT3 activation, dimerization, and nuclear translocation.Fórmula:C8H5NO4SPureza:98.32% - 99.76%Cor e Forma:SolidPeso molecular:211.19Ref: TM-T6308
5mg35,00€10mg51,00€25mg85,00€50mg124,00€100mg187,00€200mg279,00€500mg465,00€1mL*10mM (DMSO)55,00€Homoharringtonine
CAS:Homoharringtonine (HHT) is an alkaloid combatting myeloid cancers and potentially some myelodysplastic syndromes, may treat leukemia and resistant NSC-LC.Fórmula:C29H39NO9Pureza:98.21% - 99.91%Cor e Forma:Off-White CrystPeso molecular:545.62inS3-54-A26
CAS:inS3-54-A26 is an inhibitor of the DNA-binding domain of STAT3. inS3-54-A26 suppresses tumor growth, metastasis and the gene expression of STAT3.Fórmula:C25H19ClN2O2Pureza:99.57%Cor e Forma:SolidPeso molecular:414.88Ref: TM-T27613
1mg115,00€2mg172,00€5mg255,00€10mg375,00€25mg562,00€50mg787,00€100mg1.074,00€500mgA consultarMMPP
CAS:MMPP is a VEGFR2 inhibitor with anti-inflammatory activity, inhibits STAT3 , inhibits angiogenesis, and can be used to alleviate myocardial injury.Fórmula:C17H18O3Pureza:99.31% - 99.83%Cor e Forma:SolidPeso molecular:270.32Antitumor agent-73
CAS:Antitumor Agent-73, derived from Diosgenin, blocks STAT3 and activates Pdia3, showing strong cancer cell line efficacy.Fórmula:C50H82BrO4PPureza:98%Cor e Forma:SolidPeso molecular:858.06inS3-54A18
CAS:inS3-54A18 is an effective inhibitor of STAT3. inS3-54A18 has anticancer effects.Fórmula:C23H16ClNO2Pureza:99.68%Cor e Forma:SolidPeso molecular:373.83Ref: TM-T15582
2mg42,00€5mg65,00€10mg93,00€25mg160,00€50mg226,00€100mg320,00€200mg452,00€1mL*10mM (DMSO)71,00€Stafib-2
CAS:Stafib-2 is a potent and selective inhibitor of the transcription factor STAT5b.Stafib-2 inhibits STAT5b and STAT5a with IC50 values of 82 nM and 1.7 μM,
Fórmula:C28H26N2O12P2Pureza:98.48%Cor e Forma:SolidPeso molecular:644.46ML115
CAS:ML115 is a potent and selective activator of transcription 3 (STAT3), with abn EC50 of 2.0 nM, and is inactive against the related STAT1 and NFκB anti-targets.Fórmula:C15H15ClN2O4Pureza:99.97%Cor e Forma:SolidPeso molecular:322.74Ref: TM-T35544
1mg95,00€5mg227,00€10mg359,00€25mg630,00€50mg882,00€100mg1.188,00€200mg1.596,00€500mg2.357,00€1mL*10mM (DMSO)251,00€STAT3-IN-20
CAS:STAT3-IN-20 (Compound 40), with an IC50 of 0.65 μM, is a selective inhibitor targeting the SH2 domain of STAT3, thereby impeding its phosphorylation, nuclearFórmula:C30H27F4N7SPureza:98%Cor e Forma:SolidPeso molecular:593.64STAT6-IN-3
CAS:STAT6-IN-3 (Compound 18a) serves as an inhibitor of STAT6 with an IC50 value of 44 nM, specifically targeting the Src Homology 2 (SH2) domain.Fórmula:C32H35IN3O7PPureza:98%Cor e Forma:SolidPeso molecular:731.51STAT3-IN-B9
CAS:STAT3-IN-B9 (B9) is an inhibitor of abnormal STAT3 activation and inhibits the proliferation of tumor cells including MDA-MB-468, MDA-MB-231, and DU145.Fórmula:C20H13NO5SPureza:98.19%Cor e Forma:SolidPeso molecular:379.39Ref: TM-T28865
1mg115,00€2mg162,00€5mg249,00€10mg369,00€25mg562,00€50mg787,00€100mg1.054,00€200mg1.406,00€1mL*10mM (DMSO)269,00€STAT6-IN-2
CAS:STAT6-IN-2(R)-84 is a STAT6 inhibitor that inhibits the secretion of eotaxin-3 and the tyrosine phosphorylation of STAT6.Fórmula:C28H31N5O2Pureza:99.67%Cor e Forma:SolidPeso molecular:469.58STAT3-IN-35
CAS:STAT3-IN-35 is a STAT3 inhibitor that binds to the SH2 domain. This compound inhibits the phosphorylation of STAT3 and exhibits antiproliferative activity in triple-negative breast cancer (TNBC) cell lines. Additionally, STAT3-IN-35 has demonstrated toxicity and potent antitumor activity in TNBC xenograft models.Fórmula:C21H23NO4Cor e Forma:SolidPeso molecular:353.41STAT3-IN-8
CAS:"STAT3-IN-8 (compound H172) is a potent inhibitor of STAT3 with potential applications in cancer research [1]."Fórmula:C19H7F7N2O3Pureza:98%Cor e Forma:SolidPeso molecular:444.26WZ-2-033
CAS:WZ-2-033 is a potent STAT3 inhibitor. It inhibits proliferation, colony survival, migration, and invasion of MDA-MB-231, HCC70, and MDA-MB231-4175 cells, with IC50 values of 0.7, 1.3, and 1.3 μM respectively.Fórmula:C25H18F3N3O4SCor e Forma:SolidPeso molecular:513.49PMMB-187
CAS:PMMB-187, a selective STAT3 inhibitor, exhibits an IC50 of 1.81 μM in MDA-MB-231 cells. This compound induces apoptosis in MDA-MB-231 cells by inhibiting STAT3 transcriptional activity and nuclear translocation, reducing mitochondrial membrane potential, increasing reactive oxygen species (ROS) production, and upregulating the expression of apoptosis-related proteins. PMMB-187 is useful for research in the field of cancer.Fórmula:C27H23BrN2O6S2Cor e Forma:SolidPeso molecular:615.52
