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Results for "

(s,s,s)-ahpc hydrochloride

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    12
    TargetMol | Inhibitors_Agonists
  • PROTAC Products
    12
    TargetMol | PROTAC
(S,S,S)-AHPC hydrochloride
(S,S,S)-VH032-NH2 hydrochloride
T138772115897-23-7
(S,S,S)-AHPC hydrochloride ((S,S,S)-VH032-NH2 hydrochloride) is a VHL amino building block and ligand used as a negative control for (S,R,S)-AHPC. It is based on VH032 and is employed in the recruitment of the VHL protein.
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(S,R,S)-AHPC hydrochloride
VHL Ligand 1 hydrochloride, ULM-1, Protein degrader 1 hydrochloride
T42071448189-80-7
(S,R,S)-AHPC hydrochloride (Protein degrader 1 hydrochloride) is a building block in the synthesis of proteolysis-targeting chimera technologies (PROTACs).
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(S,R,S)-AHPC-Me hydrochloride
VHL ligand 2 hydrochloride, E3 ligase Ligand 1
T136711948273-03-7
(S,R,S)-AHPC-Me hydrochloride (VHL ligand 2 hydrochloride) is utilized in the synthesis of ARV-771, a potent BET protein degrader. It selectively degrades BET protein in castration-resistant cells with a DC50 <1 nM. Recognized as VHL ligand 2 hydrochloride, it serves as the VHL ligand from (S,R,S)-AHPC for recruiting von Hippel-Lindau (VHL) protein.
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(S,R,S)-AHPC-PEG2-NH2 hydrochloride
VH032-PEG2-NH2 hydrochloride, VHL Ligand-Linker Conjugates 3 hydrochloride, E3 ligase Ligand-Linker Conjugates 6
T179242097973-72-1
(S,R,S)-AHPC-PEG2-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 6) is a synthesized E3 ligase ligand-linker conjugate that includes the (S,R,S)-AHPC based VHL ligand and a 2-unit PEG linker used in the synthesis of PROTAC.
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(S,R,S)-AHPC-C4-NH2 hydrochloride
VH032-C4-NH2 hydrochloride, E3 ligase Ligand-Linker Conjugates 28, VHL Ligand-Linker Conjugates 13
T186402245697-83-8
(S,R,S)-AHPC-C4-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 28) is a synthesized E3 ligase ligand-linker conjugate comprising the (S,R,S)-AHPC-based VHL ligand and a linker.
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(S,R,S)-AHPC-PEG4-NH2 hydrochloride
E3 ligase Ligand-Linker Conjugates 7, VH032-PEG4-NH2 hydrochloride, VHL Ligand-Linker Conjugates 4 hydrochloride
T151902064292-52-8
(S, R, S)-AHPC-PEG4-NH2 hydrochloride is a chemically synthesized conjugate consisting of an E3 ligase ligand-linker, incorporating the VHL ligand based on (S, R, S)-AHPC, and a 4-unit PEG linker, which are specifically designed for use in PROTAC technology.
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(S,R,S)-AHPC-PEG3-NH2 hydrochloride
VHL Ligand-Linker Conjugates 1 hydrochloride, VHL Ligand-Linker Conjugates 1 HCl, VH032-PEG3-NH2 hydrochloride, E3 ligase Ligand-Linker Conjugates 5
T179222097971-11-2
(S,R,S)-AHPC-PEG3-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 5) is an E3 ligase ligand-linker conjugate that integrates the (S,R,S)-AHPC-based VHL ligand with a 3-unit PEG linker.
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(S,R,S)-AHPC-Me-C10-NH2 hydrochloride
T18669L2471970-07-5
(S,R,S)-AHPC-Me-C10-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate incorporating a VHL ligand and a linker.
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(S,R,S)-AHPC-C6-NH2 hydrochloride
(S,R,S)-AHPC-C6-NH2 hydrochloride,VH032-C6-NH2 hydrochloride
T398982360522-76-3
(S, R, S)-AHPC-C6-NH2 hydrochloride (also known as VH032-C6-NH2 hydrochloride) is a synthetic E3 ligase ligand-linker conjugate. It combines the VH032-based VHL ligand with a linker designed for AKT PROTAC degrader applications.
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(S,R,S)-AHPC-C8-NH2 hydrochloride
(S,R,S)-AHPC-C8-NH2 hydrochloride,VH032-C8-NH2 hydrochloride
T399312376139-49-8
'(S,R,S)-AHPC-C8-NH2 (VH032-C8-NH2) hydrochloride is a synthetic E3 ligase ligand-linker conjugate, consisting of the VH032-based VHL ligand and a linker for use in PROTAC technology.'
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(S,R,S)-AHPC-C3-NH2 hydrochloride
VH032-C3-NH2 hydrochloride
T853342940858-65-9
(S,R,S)-AHPC-C3-NH2 hydrochloride (VH032-C3-NH2 hydrochloride) is an E3 ligase ligand-linker coupler that can be used for the synthesis of PROTAC compounds.
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(S,R,S)-AHPC-CO-C9-NH2 hydrochloride
(S,R,S)-AHPC-C9-NH2 hydrochloride
T853662376139-50-1
(S,R,S)-AHPC-CO-C9-NH2 (hydrochloride) serves as a von Hippel-Lindau (VHL) amino building block essential for the synthesis of E3 ligase ligands, which are necessary for the development of PROTACs.'
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