m-PEG16-alcohol
CAS No. 133604-58-7
m-PEG16-alcohol( —— )
Catalog No. M26970 CAS No. 133604-58-7
m-PEG16-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product Namem-PEG16-alcohol
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NoteResearch use only, not for human use.
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Brief Descriptionm-PEG16-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
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Descriptionm-PEG16-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.(In Vitro):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 VitroPROTACs 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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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number133604-58-7
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Formula Weight736.89
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Molecular FormulaC33H68O17
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Purity>98% (HPLC)
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Solubility——
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SMILESCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
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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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Zearalenone
Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs cattle and sheep with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts.
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Tetradecanedioic aci...
Tetradecanedioic acid is a C14 dicarboxylic acid.
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Silybin B
Silybin B is an effective inhibitor of raloxifene 4 '- and 6-glucosalylation, an effective anti-fibrinogenic and anti-oligomeric component of Silymarin, with free radical scavenging activity of 1, 1-diphenyl-2-pyridinyl hydrazine (DPPH), and a protective effect against cisplatin-induced neurotoxicity by alleviating DNA damage and apoptosis.
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