6 Results for "

VHL-HIF1α

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "VHL-HIF1α" in MCE Product Catalog:

11
11 Cited Publications
Cat. No.: HY-120217
CAS No.: 1448188-62-2
Purity:  99.64%
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

VH032 is a VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. VH032 is a VHL/HIF-1α interaction inhibitor with a Kd[1] .
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Cat. No.: HY-158684
CAS No.: 3049076-98-1
Purity:  99.86%
Research Areas:  

Cancer

YX-02-030 is a VHL-dependent MDM2 PROTAC degrader with a Kd of 35 nM. YX-02-030 recruits the VHL E3 ligase to form a ternary complex, leading to ubiquitination and proteasome-mediated degradation of MDM2. YX-02-030 inhibits MDM2-p53 and VHL-HIF1α binding with IC50 values of 63 and 1350 nM. YX-02-030 activates TAp73, upregulates p53 family target genes and induces apoptosis. YX-02-030 demonstrates on-target efficacy in TNBC xenograft-bearing mice, extending survival without normal cell toxicity [1].
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Cat. No.: HY-136055
CAS No.: 2267282-19-7
Purity:  98.81%
Synonyms: VH032-C5-COOH
(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker conjugate, contains the VH032 VHL-based ligand and a linker to form PROTACs. VH-032 is a selective and potent inhibitor of VHL/HIF-1α interaction with a Kd of 185 nM, has the potential for the study of anemia and ischemic diseases [1].
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Cat. No.: HY-158685
CAS No.: 2360561-90-4
Target:  

MDM-2/p53

Research Areas:  

Cancer

RG7112D is a potent MDM2 inhibitor with IC50s of 11 nM and >10000 nM and for MDM2-p53 and VHL-HIF1α by binding HTRF assay, respectively. RG7112D is coupled by an amide bond to VHL-Amine, resulting in a bi-functional molecule, YX-02-030. YX-02-03, a MDM2-PROTAC, potently inhibits MDM2-p53 binding (HTRF IC50=63nM). RG7112D can stabilize MDM2 protein and increase p53 protein levels [1].
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Cat. No.: HY-138678
CAS No.: 2230826-33-0
Purity:  ≥95.0%
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

(R,S,S)-VH032 is Ligand for E3 Ligase used in the synthesis of PROTACs. VH032 is a VHL ligand and VHL/HIF-1α interaction inhibitor that recruits von Hippel-Lindau (VHL) proteins. (R,S,S)-VH032 synthesizes the tau-targeting small molecule PROTAC C004019 (HY-138669) [1].
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Cat. No.: HY-P5908
Target:  

Inhibitory Antibodies

Research Areas:  

Cardiovascular Disease

DEALA-Hyp-YIPD is an HIF-1α peptide that inhibits VHL/HIF-1α interaction with an IC50 of 0.91 μM and a Kd of 180 nM [1].
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