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Biotin-PEG2-CH2CH2N3
CAS No. 945633-30-7
Biotin-PEG2-CH2CH2N3( —— )
Catalog No. M26904 CAS No. 945633-30-7
Biotin-PEG2-CH2CH2N3 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 119 | Get Quote |
|
| 100MG | 194 | Get Quote |
|
| 200MG | 293 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameBiotin-PEG2-CH2CH2N3
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NoteResearch use only, not for human use.
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Brief DescriptionBiotin-PEG2-CH2CH2N3 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
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DescriptionBiotin-PEG2-CH2CH2N3 is a PEG-based PROTAC linker that 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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RecptorNav1.8 channel| Reactive Oxygen Species
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Research Area——
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Indication——
Chemical Information
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CAS Number945633-30-7
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Formula Weight400.5
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Molecular FormulaC16H28N6O4S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (249.69 mM)
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SMILES[H][C@]12CS[C@@H](CCCCC(=O)NCCOCCOCCN=[N+]=[N-])[C@@]1([H])NC(=O)N2
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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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Kaempferol-3-O-(2-O-...
Kaempferol-3-O-(2''-O-β-D-glucopyl)-β-D-rutinoside is a naturally occurring glycoside present in the seeds of Camellia oleifera.
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CRSP-1
Endogenous central calcitonin (CT) receptor agonist that stimulates cAMP formation at a potency 350-fold greater than CT (ED50 values are 0.2 and 71 nM respectively). Displays no activity at calcitonin-gene related peptide (CGRP) and adrenomedullin receptors. Inhibits formation of multinuclear osteoclasts with similar efficacy to CT in vitro. Suppresses food intake and increases body temperature in free-feeding rats, and significantly decreases plasma calcium levels in vivo.
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Fmoc-Lys-OH hydrochl...
Fmoc-Lys-OH hydrochloride is a alkyl-chain-based PROTAC linker. Fmoc-Lys-OH hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
