26 Results for "

L- wnt3a

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "L- wnt3a" in MCE Product Catalog:

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10
Wnt3a Surrogate Protein, Human (HEK293, Fc)
Wnt3a Surrogate Protein, Human (HEK293, Fc)
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10 Publications Verification
Cat. No.: HY-P70453B
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: wnt3a; wnt Family Member 3a; Wingless-Type MMTV Integration Site Family, Member 3a; Protein wnt-3a
Species:  
Human
Source:  
HEK293
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5
Wnt3a Protein, Mouse (His)
Wnt3a Protein, Mouse (His)
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5 Cited Publications
Cat. No.: HY-P70452
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: wnt3a; wnt Family Member 3a; Wingless-Type MMTV Integration Site Family, Member 3a; Protein wnt-3a
Species:  
Mouse
Source:  
E. coli
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3
Wnt3a Surrogate Protein, Human (HEK293, C-hFc)
Wnt3a Surrogate Protein, Human (HEK293, C-hFc)
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3 Cited Publications
Cat. No.: HY-P70453C
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: wnt3a; wnt Family Member 3a; Wingless-Type MMTV Integration Site Family, Member 3a; Protein wnt-3a
Species:  
Human
Source:  
HEK293
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2
ABC99
ABC99
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2 Cited Publications
Cat. No.: HY-122832
CAS No.: 2331255-53-7
Purity:  98.48%
Target:  

Wnt

Research Areas:  

Cancer

ABC99 is an N-hydroxyhydantoin (NHH) carbamate that selectively inhibits the Wnt-deacylating enzyme NOTUM (IC50=13 nM). ABC99 preserves Wnt3A signaling in the presence of NOTUM .
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2
TFMB-(S)-2-HG
TFMB-(S)-2-HG
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2 Cited Publications
Cat. No.: HY-129079A
CAS No.: 1445703-64-9
Purity:  99.79%
Target:  

DNA Methyltransferase Wnt β-catenin

Research Areas:  

Endocrinology Cancer

TFMB-(S)-2-HG is a potent TET2 inhibitor. TFMB-(S)-2-HG also inhibits the EglN prolyl hydroxylases. TFMB-(S)-2-HG downregulates Wnt3a, β-catenin (intranuclear) protein expression. TFMB-(S)-2-HG inhibits osteogenic differentiation of cells. TFMB-(S)-2-HG has the potential for the research of acute myeloid leukemia (AML) .
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Tizanidine
Tizanidine
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Cat. No.: HY-B0194
CAS No.: 51322-75-9
Target:  

Adrenergic Receptor Apoptosis Akt Wnt β-catenin

Research Areas:  

Neurological Disease Endocrinology Cancer

Tizanidine, a skeletal muscle relaxant, is an orally effective central α2-adrenoceptor agonist (IC50 = 6.9 nmol). Tizanidine primarily exerts muscle relaxation effects by inhibiting the release of excitatory amino acids (glutamate and aspartate) from the presynaptic terminals of spinal cord interneurons. Tizanidine has anti-injury activity and can inhibit gastrointestinal (GI) transport. Tizanidine can inhibit the proliferation, migration, and invasion of lung cancer cells and induce cell apoptosis by upregulating Nischarin and inhibiting the AKT and Wnt3a/β-catenin signaling pathways. Tizanidine can be used to treat spasticity caused by diseases such as multiple sclerosis (MS), stroke, and spinal cord injury (SCI) [3] .
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Tizanidine hydrochloride
Tizanidine hydrochloride
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Cat. No.: HY-B0194A
CAS No.: 64461-82-1
Target:  

Adrenergic Receptor Apoptosis Akt Wnt β-catenin

Research Areas:  

Neurological Disease Endocrinology Cancer

Tizanidine hydrochloride, a skeletal muscle relaxant, is an orally effective central α2-adrenoceptor agonist (IC50 = 6.9 nmol). Tizanidine hydrochloride primarily exerts muscle relaxation effects by inhibiting the release of excitatory amino acids (glutamate and aspartate) from the presynaptic terminals of spinal cord interneurons. Tizanidine hydrochloride has anti-injury activity and can inhibit gastrointestinal (GI) transport. Tizanidine hydrochloride can inhibit the proliferation, migration, and invasion of lung cancer cells and induce cell apoptosis by upregulating Nischarin and inhibiting the AKT and Wnt3a/β-catenin signaling pathways. Tizanidine hydrochloride can be used to treat spasticity caused by diseases such as multiple sclerosis (MS), stroke, and spinal cord injury (SCI) [3] .
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Arjunolic acid
Arjunolic acid
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Cat. No.: HY-N2896
CAS No.: 465-00-9
Category:  

Triterpenes Terpenoids Juglandaceae Extract 500 - Internal Server Error | MedChemExpress

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