Tools

JAK/STAT Pathway

JAK-STAT signaling pathway mediates cell-to-cell signaling and is essential for development, cell differentiation and homeostasis in vivo. The JAK-STAT signaling pathway has many evolutionarily conserved functions, including cell proliferation and hematopoiesis.JAK belongs to a family of non-receptor protein tyrosine kinases, approximately 130 kDa, consisting of JAK1, JAK2, JAK3. STATs are potential cytoplasmic transcription factors that are activated upon recruitment to activated receptor complexes. Seven STAT proteins, STAT1-6, have been identified, including STAT5a and STAT5b (encoded by different genes). Mechanistically, the JAK/STAT signaling pathway is relatively simple, with only a few major component members. Various ligands, including cytokines, hormones and growth factors, and their receptors can activate the JAK/STAT pathway. However, the biological consequences of the activation of this pathway are complicated by its interaction with other signaling pathways.
Cat. No. Product name
BP15243 APTSTAT3-9R acetate
APTSTAT3-9R acetate is a selective peptide binding STAT3 with antiproliferative and antitumor activity. APTSTAT3-9R acetate and inhibits STAT3 activation and downstream signaling by specifically blocking STAT3 phosphorylation.
BP15244 AS1517499
AS1517499 is a potent STAT6 inhibitor with IC50 of 21 nM
BP15245 CMD178 TFA
CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.
BP15246 Colivelin
Colivelin is a neuroprotective peptide and activator of STAT3. Colivelin is a hybrid peptide synthesized to enhance the neuroprotective effects of humanin (HN).
BP15247 Corylin
Corylin is a major bioactive compound isolated from Psoralea corylifolia L; it has the activity of antibiotic or anticancer.
BP15248 Eupalinolide I
Eupalinolide I is a natural product from Eupatorium lindleyanum.
BP15249 Golotimod (TFA) (229305-39-9 free base)
Golotimod (TFA), an immunomodulating peptide with antimicrobial activity, significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function.
BP15250 Golotimod hydrochloride (229305-39-9 free base)
Golotimod hydrochloride (SCV 07 hydrochloride), an immunomodulating peptide with antimicrobial activity, significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function.
BP15251 Isocryptotanshinone
Isocryptotanshinone inhibits protein tyrosine phosphatase 1B (PTP1B) activity with 50% inhibitory concentration values of 56.1±6.3 μM, PTP1B acts as a negative regulator of insulin signaling, and selective inhibition of PTP1B has served as a potential drug target for the treatment of type 2 diabetes.
BP15252 Kurarinol
Kurarinol is a potent inhibitor of sortase A, with an IC50 value of 107.7 ± 6.6 μM. Kurarinol has extremely strong tyrosinase inhibitory activity, exerts varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis, is a candidate as skin-whitening agents.
BP15253 ML115
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.
BP15254 Mogrol
Mogrol is a biometabolite of mogrosides. Mogrol acts via inhibition of the ERK1/2 and STAT3 pathways, or reducing CREB activation and activating AMPK signaling.
BP15255 NSC 370284
NSC 370284 is a small molecule that directly binds to and inhibits STAT3/5, significantly and selectively suppresses the viability of AML cells with high level of TET1 expression both in vitro and in vivo.
BP15256 SH5-07
SH5-07 is a hydroxamic acid-based Stat3 inhibitor (IC50: 3.9 μM).
BP15257 SI-109
SI-109 is a potent inhibitor of STAT3 SH2 domain (Ki=9 nM),and with antitumor activity.
BP15258 Stafia-1
Stafia-1 is a potent STAT5a inhibitor (IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.
BP15259 STAT3-IN-3
STAT3-IN-3 is a potent and selective signal transducer inhibitor and transcription 3 (STAT3) activator.
BP15260 STAT3-IN-B9
STAT3-IN-B9 is an inhibitor of abnormal STAT3 activation and inhibits the proliferation of tumor cells including MDA-MB-468, MDA-MB-231, and DU145.
BP15261 STAT5-IN-1
STAT5 Inhibitor is a cell-permeable inhibitor which suppresses Stat5 via binding to the SH2 domain.
BP22553 NSC 74859
NSC 74859 (S3I-201) is a selective Stat3 inhibitor with an IC50 of 86 μM.
APTSTAT3-9R acetate
BP15243
APTSTAT3-9R acetate is a selective peptide binding STAT3 with antiproliferative and antitumor activity. APTSTAT3-9R acetate and inhibits STAT3 activation and downstream signaling by specifically blocking STAT3 phosphorylation.
AS1517499
BP15244
AS1517499 is a potent STAT6 inhibitor with IC50 of 21 nM
CMD178 TFA
BP15245
CMD178 (TFA) is a lead peptide that consistently reduces the expression of Foxp3 and STAT5 induced by IL-2/s IL-2Rα signaling.
Colivelin
BP15246
Colivelin is a neuroprotective peptide and activator of STAT3. Colivelin is a hybrid peptide synthesized to enhance the neuroprotective effects of humanin (HN).
Corylin
BP15247
Corylin is a major bioactive compound isolated from Psoralea corylifolia L; it has the activity of antibiotic or anticancer.
Eupalinolide I
BP15248
Eupalinolide I is a natural product from Eupatorium lindleyanum.
Golotimod (TFA) (229305-39-9 free base)
BP15249
Golotimod (TFA), an immunomodulating peptide with antimicrobial activity, significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function.
Golotimod hydrochloride (229305-39-9 free base)
BP15250
Golotimod hydrochloride (SCV 07 hydrochloride), an immunomodulating peptide with antimicrobial activity, significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function.
Isocryptotanshinone
BP15251
Isocryptotanshinone inhibits protein tyrosine phosphatase 1B (PTP1B) activity with 50% inhibitory concentration values of 56.1±6.3 μM, PTP1B acts as a negative regulator of insulin signaling, and selective inhibition of PTP1B has served as a potential drug target for the treatment of type 2 diabetes.
Kurarinol
BP15252
Kurarinol is a potent inhibitor of sortase A, with an IC50 value of 107.7 ± 6.6 μM. Kurarinol has extremely strong tyrosinase inhibitory activity, exerts varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis, is a candidate as skin-whitening agents.
ML115
BP15253
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.
Mogrol
BP15254
Mogrol is a biometabolite of mogrosides. Mogrol acts via inhibition of the ERK1/2 and STAT3 pathways, or reducing CREB activation and activating AMPK signaling.
NSC 370284
BP15255
NSC 370284 is a small molecule that directly binds to and inhibits STAT3/5, significantly and selectively suppresses the viability of AML cells with high level of TET1 expression both in vitro and in vivo.
SH5-07
BP15256
SH5-07 is a hydroxamic acid-based Stat3 inhibitor (IC50: 3.9 μM).
SI-109
BP15257
SI-109 is a potent inhibitor of STAT3 SH2 domain (Ki=9 nM),and with antitumor activity.
Stafia-1
BP15258
Stafia-1 is a potent STAT5a inhibitor (IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.
STAT3-IN-3
BP15259
STAT3-IN-3 is a potent and selective signal transducer inhibitor and transcription 3 (STAT3) activator.
STAT3-IN-B9
BP15260
STAT3-IN-B9 is an inhibitor of abnormal STAT3 activation and inhibits the proliferation of tumor cells including MDA-MB-468, MDA-MB-231, and DU145.
STAT5-IN-1
BP15261
STAT5 Inhibitor is a cell-permeable inhibitor which suppresses Stat5 via binding to the SH2 domain.
NSC 74859
BP22553
NSC 74859 (S3I-201) is a selective Stat3 inhibitor with an IC50 of 86 μM.