NSC19005
CAS No. 5452-87-9
NSC19005( NSC19005 | NSC-19005 | NSC 19005 )
Catalog No. M17535 CAS No. 5452-87-9
NSC19005 is structurally related to Betahistine. NSC19005 is a dimer of Betahistine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 34 | In Stock |
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| 10MG | 56 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameNSC19005
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NoteResearch use only, not for human use.
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Brief DescriptionNSC19005 is structurally related to Betahistine. NSC19005 is a dimer of Betahistine.
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DescriptionNSC19005 is structurally related to Betahistine. NSC19005 is a dimer of Betahistine.
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In VitroBetahistine (0-10 μM) inhibits [125I]iodoproxyfan binding to membranes of CHO (rH3(445)R) and CHO (hH3(445)R) cells with IC50 values of 1.9 μM and 3.3 μM, respectively. Lead to Ki values of 1.4 μM and 2.5 μM, respectively.
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In Vivo——
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SynonymsNSC19005 | NSC-19005 | NSC 19005
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number5452-87-9
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Formula Weight241.34
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Molecular FormulaC15H19N3
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Purity>98% (HPLC)
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Solubility——
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SMILESCN(CCc1ncccc1)CCc1ncccc1
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Chemical NameN-methyl-2-(pyridin-2-yl)-N-(2-(pyridin-2-yl)ethyl)ethan-1-amine
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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FIDAS-5
FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding.?FIDAS-5 has anticancer activities.?FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.FIDAS-5 induces the expression of cell cycle inhibitor, p21WAF1/CIP1. FIDAS-5 (3 μM; 36 h) treatment reduces the levels of both S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) in LS174T cells.FIDAS-5 (3 μM; 7 days; LS174T cells) treatment significantly inhibits the proliferation of LS174T cells.
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Prepro-TRH (178-199)
Prepro-TRH (178-199)
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SHMT-IN-2
SHMT-IN-2 (compound 2) is a specific human SHMT1/2 small molecule inhibitor that acts on SHMT1 (IC50: 13 nM) and SHMT2 (IC50: 66 nM). SHMT-IN-2 inhibits the growth of many human cancer cells and is sensitive to B-cell lymphoma.
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