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N-ε-propargyloxycarbonyl-L-lysine hydrochloride
CAS No. 1428330-91-9
N-ε-propargyloxycarbonyl-L-lysine hydrochloride ( H-?L-?Lys(Poc)?-?OH (hydrochloride),N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride )
Catalog No. M22480 CAS No. 1428330-91-9
N-ε-propargyloxycarbonyl-L-lysine hydrochloride is a modified amino acid for cancer therapy development.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 35 | In Stock |
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| 25MG | 56 | In Stock |
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| 50MG | 80 | 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 NameN-ε-propargyloxycarbonyl-L-lysine hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionN-ε-propargyloxycarbonyl-L-lysine hydrochloride is a modified amino acid for cancer therapy development.
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DescriptionN-ε-propargyloxycarbonyl-L-lysine hydrochloride is a modified amino acid for cancer therapy development.
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SynonymsH-?L-?Lys(Poc)?-?OH (hydrochloride),N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride
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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 Number1428330-91-9
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Formula Weight264.71
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Molecular FormulaC10H17ClN2O4
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.N[C@@H](CCCCNC(=O)OCC#C)C(O)=O
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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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BAY524
BAY-524 is an inhibitor of Bub1(IC50 = 450 nM.human Bub1 in the presence of 2 mM ATP).
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Acyl Carrier Protein...
Acyl Carrier Protein (ACP) (65-74) is an active acyl carrier protein (ACP) fragment.Acyl Carrier Protein (ACP) is a component of plastid-located plant fatty acid synthetase. It binds acyl groups covalently via the prosthetic group, 4-phosphopantetheine, during the biosynthesis of fatty acids.
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Bacterial Sortase Su...
Bacterial Substrate III, Abz/DNP TFA is an internally quenched fluorescent peptide substrate. Staphylococcus aureus transpeptidase sortase A (SrtA) reacts with its native substrate Bacterial Sortase Substrate III, Abz/DNP, cleaving it and catalyzing the formation of an amide bond between the carboxyl group of threonine and the amino group of cell-wall crossbridges.
