

K-7174 dihydrochloride
CAS No. 191089-60-8
K-7174 dihydrochloride( —— )
Catalog No. M12994 CAS No. 191089-60-8
A selctive small molecule inhibitor of the transcription factor GATA-binding protein 2 (GATA2).
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
50MG | 412 | In Stock |
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Biological Information
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Product NameK-7174 dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionA selctive small molecule inhibitor of the transcription factor GATA-binding protein 2 (GATA2).
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DescriptionA selctive small molecule inhibitor of the transcription factor GATA-binding protein 2 (GATA2); suppresses the expression of AR, including ARVs, in 22Rv1 cells, exertes potent anticancer activity against GATA2+/AR+ PC cell lines in vitro; induces transcriptional repression of class I histone deacetylases (HDAC1, -2, and -3) via caspase-8-dependent degradation of Sp1; significantly decreases HAMP expression, also upregulates CEBPB.(In Vitro):K-7174 dihydrochloride (10 μM; 1 h) inhibits the adhesion by VCAM-1 and its ligand.K-7174 dihydrochloride (1-30 μM; 1 h) dose-dependently suppresses the VCAM-1 expression with an IC50 value of 14 μM.K-7174 dihydrochloride (1-30 μM; 1 h) dose-dependently suppresses the induction of VCAM-1 mRNA by TNFα with an IC50 value of 9 μM.K-7174 dihydrochloride (10-20 μM; 24 h) dose-dependently rescues Epo production by Hep3B cells.K-7174 dihydrochloride (2.5-30 μM; 24 h) inhibits the binding activity of GATA.K-7174 dihydrochloride (0-25 μM; 72 h) inhibits MM cells growth and induces cell apoptosis.(In Vivo):K-7174 dihydrochloride (30 mg/kg; i.p. once daily for 9 days) reverses the decreasing of hemoglobin concentrations and reticulocyte counts by IL-1β or TNF-α.K-7174 dihydrochloride (75 mg/kg; i.p. once daily for 14 days) inhibits the tumor growth in vivo.K-7174 dihydrochloride (50 mg/kg; p.o. once daily for 14 days) inhibits the tumor growth in vivo and shows a better effect than intraperitoneal injection.
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In VitroK-7174 dihydrochloride (10 μM; 1 h) inhibits the adhesion by VCAM-1 and its ligand.K-7174 dihydrochloride (1-30 μM; 1 h) dose-dependently suppresses the VCAM-1 expression with an IC50 value of 14 μM.K-7174 dihydrochloride (1-30 μM; 1 h) dose-dependently suppresses the induction of VCAM-1 mRNA by TNFα with an IC50 value of 9 μM.K-7174 dihydrochloride (10-20 μM; 24 h) dose-dependently rescues Epo production by Hep3B cells.K-7174 dihydrochloride (2.5-30 μM; 24 h) inhibits the binding activity of GATA.K-7174 dihydrochloride (0-25 μM; 72 h) inhibits MM cells growth and induces cell apoptosis. Cell Viability Assay Cell Line:KMS12-BM, U266, and RPMI8226 cell lines Concentration:0-25 μM Incubation Time:72 h Result:Inhibited MM cells growth.Apoptosis Analysis Cell Line:KMS12-BM, U266, and RPMI8226 cell lines Concentration:10 μM Incubation Time:48 h Result:Significantly increased apoptosis of MM cells with the increasing percentage of annexin-V-positive cells.
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In VivoK-7174 dihydrochloride (30 mg/kg; i.p. once daily for 9 days) reverses the decreasing of hemoglobin concentrations and reticulocyte counts by IL-1β or TNF-α.K-7174 dihydrochloride (75 mg/kg; i.p. once daily for 14 days) inhibits the tumor growth in vivo.K-7174 dihydrochloride (50 mg/kg; p.o. once daily for 14 days) inhibits the tumor growth in vivo and shows a better effect than intraperitoneal injection. Animal Model:ICR mice with IL-β or TNF-α injection Dosage:30 mg/kg Administration:Intraperitoneal injection; 30 mg/kg once daily for 9 days Result:Increased erythropoietin (Epo) production, reticulocyte counts, and hemoglobin (Hb) concentrations.Animal Model:NOD/SCID mice with murine xenograft Dosage:75 mg/kg Administration:Intraperitoneal injection; once daily for 14 days Result:Significantly decreased tumor volume, but showed a significant body weight reduction after 10 days.Animal Model:NOD/SCID mice with murine xenograft Dosage:50 mg/kg Administration:Oral gavage; once daily for 14 daysResult:Showed an anti-myeloma activity. Porved oral administration is more effective than intraperitoneal injection.
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Synonyms——
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PathwayNuclear Receptor/Transcription Factor
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TargetGATA Binding Protein
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RecptorGATA Binding Protein
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number191089-60-8
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Formula Weight641.6659
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Molecular FormulaC33H50Cl2N2O6
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Purity>98% (HPLC)
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SolubilityH2O: 15 mg/mL
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SMILESCOC1=CC(=CC(=C1OC)OC)C=CCCCN2CCCN(CC2)CCCC=CC3=CC(=C(C(=C3)OC)OC)OC.Cl.Cl
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Chemical Name1H-1,4-Diazepine, hexahydro-1,4-bis[(4E)-5-(3,4,5-trimethoxyphenyl)-4-penten-1-yl]-, hydrochloride (1:2)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. He B, et al. Proc Natl Acad Sci U S A. 2014 Dec 23;111(51):18261-6.
2. Kikuchi J, et al. J Biol Chem. 2013 Aug 30;288(35):25593-602.
3. Fujiwara T, et al. PLoS One. 2013 Sep 27;8(9):e75568.
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