(S,R,S)-AHPC-PEG2-NH2
CAS No. 2010159-60-9
(S,R,S)-AHPC-PEG2-NH2( VH032-PEG2-NH2 | VHL Ligand-Linker Conjugates 3 | E3 ligase Ligand-Linker Conjugates 6 Free Base )
Catalog No. M26953 CAS No. 2010159-60-9
(S,R,S)-AHPC-PEG2-NH2 (VH032-PEG2-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker 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 Name(S,R,S)-AHPC-PEG2-NH2
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NoteResearch use only, not for human use.
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Brief Description(S,R,S)-AHPC-PEG2-NH2 (VH032-PEG2-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker used in the synthesis of PROTACs.
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Description(S,R,S)-AHPC-PEG2-NH2 (VH032-PEG2-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker 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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SynonymsVH032-PEG2-NH2 | VHL Ligand-Linker Conjugates 3 | E3 ligase Ligand-Linker Conjugates 6 Free Base
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PathwayOthers
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TargetOther Targets
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Recptorσ1
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Research Area——
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Indication——
Chemical Information
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CAS Number2010159-60-9
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Formula Weight575.72
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Molecular FormulaC28H41N5O6S
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C([C@H]1N(C([C@@H](NC(COCCOCCN)=O)C(C)(C)C)=O)C[C@H](O)C1)NCC2=CC=C(C3=C(C)N=CS3)C=C2
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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.Lan Y, et al. Synthesis and biological evaluation of novel sigma-1 receptor antagonists based on pyrimidine scaffold as agents for treating neuropathic pain. J Med Chem. 2014 Dec 26;57(24):10404-23.
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