SC75741
CAS No. 913822-46-5
SC75741( SC75741 | SC-75741 | SC 75741 )
Catalog No. M17655 CAS No. 913822-46-5
SC75741 is a potent NF-κB inhibitor with EC50 of 200 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 71 | In Stock |
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| 10MG | 125 | In Stock |
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| 25MG | 222 | In Stock |
|
| 50MG | 430 | In Stock |
|
| 100MG | 620 | In Stock |
|
| 500MG | 1332 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameSC75741
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NoteResearch use only, not for human use.
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Brief DescriptionSC75741 is a potent NF-κB inhibitor with EC50 of 200 nM.
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DescriptionSC75741 is a NF-kappaB inhibitor. SC75741 protects mice against highly pathogenic avian influenza A virus. SC75741 significantly protects mice against infection with highly pathogenic avian influenza A viruses of the H5N1 and H7N7 subtypes. SC75741 efficiently blocks influenza virus propagation and confers a high barrier for development of viral resistance.(In Vitro):SC75741 (5 μM; 24-96 hours) inhibits long-term A549 cells proliferation.SC75741 (1-10 μM; 5.5-65 hours) reduces A549 cells viability in a concentration-dependent manner indicating a cytostatic effect for A549 cells within a time frame of about 50 and 65?hours.SC75741 (5 μM; 24 hours) strongly inhibits cleavage of the effector caspase 3 induced upon H7N7-infection.(In Vivo):SC75741 (intraperitoneal injection; 15?mg/kg; for 2 days) leads to a reduced propagation of the H5N1 virus mRNA by 90% in the lungs of infected mice.The plasma-levels of SC74751 (intravenously of 5 mg/kg and intraperitoneally of 15 mg/kg; for 3.5 and 6 hours) after i.v. administration decreases mono-exponentially and half-life is roughly 40 min. After i.p. administration, elimination of SC75741 seems to be limited by a slow uptake from the peritoneum and a half-life of 55 min is observed.
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In VitroSC75741 (5 μM; 24-96 hours) inhibits long-term A549 cells proliferation.SC75741 (1-10 μM; 5.5-65 hours) reduces A549 cells viability in a concentration-dependent manner indicating a cytostatic effect for A549 cells within a time frame of about 50 and 65?hours.SC75741 (5 μM; 24 hours) strongly inhibits cleavage of the effector caspase 3 induced upon H7N7-infection. Cell Proliferation Assay Cell Line:A549 cells Concentration:5?μM Incubation Time:24, 48, 72 and 96?hours Result:Inhibited long-term cell proliferation Cell Viability Assay Cell Line:A549 cells Concentration:1, 2, 5 or 10?μM Incubation Time:5.5, 29, 50, 65 hours Result:Reduced cells viability in a concentration-dependent manner.Western Blot Analysis Cell Line:MDCK cells Concentration:5?μM Incubation Time:24 hours Result:Inhibited cleavage of the effector caspase 3 induced upon H7N7-infection.
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In VivoSC75741 (intraperitoneal injection; 15?mg/kg; for 2 days) leads to a reduced propagation of the H5N1 virus mRNA by 90% in the lungs of infected mice.The plasma-levels of SC74751 (intravenously of 5 mg/kg and intraperitoneally of 15 mg/kg; for 3.5 and 6 hours) after i.v. administration decreases mono-exponentially and half-life is roughly 40 min. After i.p. administration, elimination of SC75741 seems to be limited by a slow uptake from the peritoneum and a half-life of 55 min is observed. Animal Model:Inbred female C57BL/6 mice at the age of 6-8 weeks Dosage:15?mg/kg Administration:Intraperitoneal injection; for 2 days Result:Reduced the amount of viral mRNA by 90%.Animal Model:Inbred female C57BL/6 mice at the age of 6-8 weeks Dosage:5 mg/kg or 15 mg/kg Administration:Intravenously of 5 mg/kg and intraperitoneally of 15 mg/kg; 3.5 and 6 hours Result:Half-life was roughly 40 min and 55 min for i.v. and i.p. administration, respectively.
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SynonymsSC75741 | SC-75741 | SC 75741
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PathwayCell Cycle/DNA Damage
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TargetGPR
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RecptorNF-κB
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number913822-46-5
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Formula Weight565.67
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Molecular FormulaC29H23N7O2S2
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 125 mg/mL; 220.98 mM
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SMILESO=C(NC1=NC2=CC=C(C=C2N1)C(=O)C1=CC=CC=C1)C1=CSC(=N1)C1CCN(CC1)C1=C2SC=CC2=NC=N1
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Chemical NameN-(6-benzoyl-1H-benzimidazol-2-yl)-2-(1-thieno[3,2-d]pyrimidin-4-yl-4-piperidinyl)-4-thiazolecarboxamide
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. Leban J, et al. Bioorg Med Chem Lett. 2007, 17(21), 5858-5862.
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