TAK1-IN-3
CAS No. 494772-87-1
TAK1-IN-3( —— )
Catalog No. M35215 CAS No. 494772-87-1
TAK1-IN-3 is a novel ATP-competitive TAK1 inhibitor for the study of cancer.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 70 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameTAK1-IN-3
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NoteResearch use only, not for human use.
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Brief DescriptionTAK1-IN-3 is a novel ATP-competitive TAK1 inhibitor for the study of cancer.
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DescriptionTAK1-IN-3 is a potent ATP-competitive TAK1 inhibitor.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMAPK/ERK Signaling
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Targetp38 MAPK
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RecptorMAPK
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Research Area——
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Indication——
Chemical Information
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CAS Number494772-87-1
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Formula Weight317.41
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Molecular FormulaC16H19N3O2S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (315.05 mM; Ultrasonic )
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SMILESO=C(N)C=1SC(=CC1N)C=2C=CC(=CC2)CN3CCOCC3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Kamebakaurine
Kamebakaurin has the ability to protect the liver from APAP-induced hepatotoxicity, presumably by both inhibiting the inflammatory response and oxidative stress.
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SSK1
SSK1 is a compound that selectively kills senescent cells and is a precursor for β-galactosidase, which can reduce the inflammatory response of the body. SSK1 can activate the phosphorylation of p38 MAPK and MKK3/MKK6 in senescent cells, and promote mitochondrial DNA damage in senescent cells.
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Iroxanadine
Iroxanadine (BRX-005) is a Novel small molecule MAPK p38 inhibitor that induces phosphorylation of p38 SAPK and induces concentration-dependent relaxation in guinea pig pulmonary artery preparations precontracted with phenylephrine.
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