7 Results for "

FEM1B

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "FEM1B" in MCE Product Catalog:

  • Isoforms Recommended:
1
1 Cited Publications
Cat. No.: HY-W229874
CAS No.: 757192-67-9
EN106 is a potent inhibitor of FEMIB. EN106 is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1. EN106 reduces oxidative stress and rescues high glucose-induced impaired angiogenesis in HUVECs [1] .
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Cat. No.: HY-143348
CAS No.: 2709040-02-6
Purity:  98.74%
Research Areas:  

Others

NJH-2-030 can be used as a covalent recruiter for FEM1B in targeted protein degradation applications.
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Cat. No.: HY-RS04859
Research Areas:  

Others

FEM1B Human Pre-designed siRNA Set A contains three designed siRNAs for FEM1B gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS22506
Research Areas:  

Others

Fem1b Mouse Pre-designed siRNA Set A contains three designed siRNAs for Fem1b gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS29027
Research Areas:  

Others

Fem1b Rat Pre-designed siRNA Set A contains three designed siRNAs for Fem1b gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Cat. No.: HY-168863
Target:  

PROTACs HDAC Apoptosis

Research Areas:  

Neurological Disease Cancer

FF2049 is a selective HDAC1-3 PROTAC degrader (with a DC50 of 257 nM against HDAC1). FF2049 recruits the E3 ligase FEM1B to mediate ubiquitination and proteasomal degradation of HDAC1-3. FF2049 induces cell cycle arrest and Apoptosis in cells. FF2049 can be used in research related to multiple myeloma, acute monocytic leukemia, triple-negative breast cancer and glioblastoma [1].
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Cat. No.: HY-168865
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

E3 ligase Ligand 53 is a FEM1B ligand used to recruit Fem-1 homologue B (FEM1B) proteins. E3 ligase Ligand 53 can be attached to target protein ligands (e.g. HDAC1) via a linker to form PROTAC molecules (e.g. FF2049) [1].
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