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Boc-11-aminoundecanoic acid
CAS No. 10436-25-6
Boc-11-aminoundecanoic acid( —— )
Catalog No. M26913 CAS No. 10436-25-6
Boc-11-aminoundecanoic acid is an Alkyl/ether-based PROTAC linker can be used in the synthesis of MS432.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 27 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBoc-11-aminoundecanoic acid
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NoteResearch use only, not for human use.
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Brief DescriptionBoc-11-aminoundecanoic acid is an Alkyl/ether-based PROTAC linker can be used in the synthesis of MS432.
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DescriptionBoc-11-aminoundecanoic acid is an Alkyl/ether-based PROTAC linker can be used in the synthesis of MS432.(In Vitro):MS432 is a first-in-class and highly selective PD0325901-based VHL-recruiting PROTAC degrader for MEK1 and MEK2. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
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In VitroMS432 is a first-in-class and highly selective PD0325901-based VHL-recruiting?PROTAC?degrader for?MEK1?and?MEK2.PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein.PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorFungal| Human Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number10436-25-6
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Formula Weight301.427
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Molecular FormulaC16H31NO4
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(C)(C)OC(=O)NCCCCCCCCCCC(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
1.Mu W, et al. Production of 4-hydroxyphenyllactic acid by Lactobacillus sp. SK007 fermentation. J Biosci Bioeng. 2010 Apr;109(4):369-71.
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