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Results for "

vh032

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    115
    TargetMol | Inhibitors_Agonists
  • Dye Reagents
    1
    TargetMol | Dye_Reagents
  • PROTAC Products
    111
    TargetMol | PROTAC
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    TargetMol | Disease_Modeling_Products
  • 1
    TargetMol | Inhibitors_Agonists
VH032
VH-032, VH 032
T291061448188-62-2In house
VH032 commonly used as a precursor to a PROTAC that hijacks VHL as the E3 ubiquitin ligase component.VH032 is a VHL/HIF-1α interaction inhibitor with a KdPROTACs, which can recruit von Hippel-Lindau (VHL) proteins as a ligand of VHL.
  • $40
In Stock
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TargetMol | Citations Cited
VH032 thiol
VHL ligand 6
T186002098836-54-3
VH032 thiol (VHL ligand 6) is a VHL ligand that connects via a linker to the pan-BET inhibitor JQ1 to form a PROTAC[1] compound.
  • $1,980
35 days
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VH032-cyclopropane-F
VHL ligand 3, Phenolic VH101, E3 ligase Ligand 19
T178772306193-99-5
VH032-cyclopropane-F is a VHL ligand based on VH032. It is able to utilize linkers to ligands of target proteins to yield PROTAC molecules such as PROTAC 1. PROTAC 1 is a partial degrader of SMARCA2 and SMARCA4.
  • $35
In Stock
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VH032-PEG5-C6-Cl
HaloPROTAC 2
T179961799506-06-1
VH032-PEG5-C6-Cl (HaloPROTAC 2) is a small molecule that includes the VH032-based VHL ligand and a 5-unit PEG linker, capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
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VH032-thiol-C6-NH2
VHL Ligand-Linker Conjugates 14, E3 ligase Ligand-Linker Conjugates 29
T186022098836-63-4
VH032-thiol-C6-NH2, also known as VHL Ligand-Linker Conjugates 14, is a synthesized compound that functions as an E3 ligase ligand-linker conjugate. This compound combines the VH032 based VHL ligand with a linker commonly utilized in PROTAC technology.
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VH032-OH
VH 032, phenol
T362722244684-42-0
Functionalized von-Hippel-Lindau protein ligand (VHL) for PROTAC research and development; incorporates an E3 ligase ligand with terminal hydroxyl ready for conjugation to a target protein ligand. Part of a range of functionalized tool molecules for PROTAC R&D. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license.
  • $76
5 days
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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).
  • $33
In Stock
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(S,R,S)-AHPC-propargyl
VHL ligand 7, VH032-propargyl
T138762098799-78-9
(S,R,S)-AHPC-propargyl, a VHL ligand, is utilized in click reactions for PROTACs.
  • $83
5 days
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(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.
  • $38
In Stock
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(S,R,S)-AHPC-PEG4-NH2 hydrochloride
VHL Ligand-Linker Conjugates 4 hydrochloride, VH032-PEG4-NH2 hydrochloride, E3 ligase Ligand-Linker Conjugates 7
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.
  • $31
5 days
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(S,R,S)-AHPC-PEG4-NH2
VHL Ligand-Linker Conjugates 4, VH032-PEG4-NH2, E3 ligase Ligand-Linker Conjugates 7 Free Base
T15190L2010159-57-4
(S,R,S)-AHPC-PEG4-NH2 (VHL Ligand-Linker Conjugates 4) is a synthetic E3 ligase ligand-linker conjugate, consisting of a VHL ligand based on (S,R,S)-AHPC combined with a 4-unit PEG linker.
  • $38
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(S,R,S)-AHPC-C10-NH2
VH032-C10-NH2
T178812341796-74-3
(S,R,S)-AHPC-C10-NH2 (VH032-C10-NH2) is a synthesized E3 ligase ligand-linker conjugate, comprising an (S,R,S)-AHPC-based VHL ligand and a linker, designed for BET-targeted PROTAC applications.
  • $51
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(S,R,S)-AHPC-PEG1-OTs
VHL Ligand-Linker Conjugates 2, VH032-PEG1-OTs, E3 ligase Ligand-Linker Conjugates 51
T17905
(S,R,S)-AHPC-PEG1-OTs is a chemically synthesized conjugate serving as a ligase ligand-linker for E3 ligase, incorporating the VHL ligand derived from (S,R,S)-AHPC and a 1-unit PEG linker. This compound is commonly utilized in PROTAC technology.
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(S,R,S)-AHPC-PEG3-N3
VHL Ligand-Linker Conjugates 8, VH032-PEG3-N3, E3 ligase Ligand-Linker Conjugates 12
T179091797406-80-4
(S, R, S)-AHPC-PEG3-N3 (VHL Ligand-Linker Conjugates 8) is a synthesized E3 ligase ligand-linker conjugate. (S, R, S)-AHPC-PEG3-N3 incorporates the (S, R, S)-AHPC based VHL ligand and 3-unit PEG linker used in PROTAC technology.
  • $30
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(S,R,S)-AHPC-PEG2-C4-Cl
VHL Ligand-Linker Conjugates 7, VH032-PEG2-C4-Cl, E3 ligase Ligand-Linker Conjugates 10
T179101835705-57-1
(S,R,S)-AHPC-PEG2-C4-Cl is a small molecule HaloPROTAC, comprising the (S,R,S)-AHPC based VHL ligand and a 2-unit PEG linker, that induces the degradation of GFP-HaloTag7 in cell-based assays[1].
  • $61
5 days
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(S,R,S)-AHPC-C6-PEG3-C4-Cl
VHL Ligand-Linker Conjugates 12, VH032-C6-PEG3-C4-Cl, E3 ligase Ligand-Linker Conjugates 8
T179111835705-55-9
(S,R,S)-AHPC-C6-PEG3-C4-Cl is a small molecule HaloPROTAC incorporating the (S,R,S)-AHPC based VHL ligand and a 3-unit PEG linker, capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
  • $61
5 days
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(S,R,S)-AHPC-PEG2-N3
VHL Ligand-Linker Conjugates 6, VH032-PEG2-N3, E3 ligase Ligand-Linker Conjugates 13
T179132010159-45-0
(S,R,S)-AHPC-PEG2-N3 (VHL Ligand-Linker Conjugates 6) is a synthesized E3 ligase ligand-linker conjugate comprising a (S,R,S)-AHPC-based VHL ligand and a 2-unit PEG linker.
  • $33
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(S,R,S)-AHPC-PEG1-N3
VHL Ligand-Linker Conjugates 9, VH032-PEG1-N3, E3 ligase Ligand-Linker Conjugates 3
T179202101200-09-1
(S,R,S)-AHPC-PEG1-N3 (E3 ligase Ligand-Linker Conjugates 3) is a synthesized E3 ligase ligand-linker conjugate that includes the (S,R,S)-AHPC-based VHL ligand and a 1-unit PEG linker used in PROTAC technology.
  • $33
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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.
  • $39
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(S,R,S)-AHPC-PEG3-NH2
VHL Ligand-Linker Conjugates 1, VH032-PEG3-NH2, E3 ligase Ligand-Linker Conjugates 5 Free Base
T179232010159-56-3
(S,R,S)-AHPC-PEG3-NH2 is a synthetic conjugate composed of the (S,R,S)-AHPC VHL ligand and a 3-unit PEG linker, utilized in PROTAC technology as an E3 ligase ligand-linker.
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(S,R,S)-AHPC-PEG2-NH2 hydrochloride
VHL Ligand-Linker Conjugates 3 hydrochloride, VH032-PEG2-NH2 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.
  • $48
In Stock
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(S,R,S)-AHPC-PEG2-NH2
VHL Ligand-Linker Conjugates 3, VH032-PEG2-NH2, E3 ligase Ligand-Linker Conjugates 6 Free Base
T179252010159-60-9
(S,R,S)-AHPC-PEG2-NH2 (VHL Ligand-Linker Conjugates 3) is a synthesized E3 ligase ligand-linker conjugate, incorporating the (S,R,S)-AHPC based VHL ligand and a 2-unit PEG linker used in PROTAC synthesis.
  • $268
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(S,R,S)-AHPC-PEG6-C4-Cl
VHL Ligand-Linker Conjugates 10, VH032-PEG6-C4-Cl, E3 ligase Ligand-Linker Conjugates 9
T179261835705-59-3
(S,R,S)-AHPC-PEG6-C4-Cl is a small molecule HaloPROTAC comprising the (S,R,S)-AHPC based VHL ligand and a 6-unit PEG linker, capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
  • $61
5 days
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(S,R,S)-AHPC TFA
VHL ligand 1 TFA, VH032-NH2 TFA
T179271631137-51-3
(S,R,S)-AHPC TFA (VHL ligand 1 TFA) (VH032-NH2 TFA) is a VH032-based ligand designed for von Hippel-Lindau (VHL) protein recruitment. This compound can be linked to protein ligands (e.g., BCR-ABL1) using a linker to create PROTACs (e.g., GMB-475), which effectively induce the degradation of BCR-ABL1, demonstrated by an IC50 of 1.11 μM in Ba/F3 cells.
  • $30
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