11 Results for "

FSGS

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "FSGS" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-112489
CAS No.: 1158383-34-6
Purity:  99.95%
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

FSG67 is a glycerol 3-phosphate acyltransferase (GPAT) inhibitor with an IC50 of 24 μM .
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1
1 Cited Publications
Cat. No.: HY-122051
CAS No.: 831234-13-0
Purity:  99.80%
Target:  

TRP Channel

Research Areas:  

Metabolic Disease

AC1903 is a specific and selective inhibitor of TRPC5 and has podocyte-protective properties. AC1903 does no effects on TRPC4 or TRPC6 currents and shows no off-target effects in kinase profiling assays. AC1903 suppresses severe proteinuria and prevents podocyte loss in focal segmental glomerulosclerosis (FSGS) rat model .
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1
1 Cited Publications
Cat. No.: HY-135470
CAS No.: 13411-16-0
Purity:  98.70%
Synonyms: P-7138
Target:  

Bacterial

Research Areas:  

Infection

Nifurpirinol (P-7138) is a selective prosubstrate of bacterial nitroreductase (NTR). NTR catalyzes the reduction of nifurpirinol to generate cytotoxic metabolites that induce apoptosis in target cells. Nifurpirinol selectively ablates NTR-expressing cells such as pancreatic β cells, osteoblasts, dopaminergic neurons, and podocytes in transgenic zebrafish models. Nifurpirinol can be used in regeneration studies and disease modeling such as focal segmental glomerulosclerosis (FSGS) .
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Cat. No.: HY-132820
CAS No.: 2446816-88-0
Purity:  99.44%
Synonyms: VX-147
Target:  

Apolipoprotein

Research Areas:  

Others

Inaxaplin (VX-147) is an orally active apolipoprotein L1 (APOL1) function inhibitor (WO2020131807, compound 2). Inaxaplin can be used for the research of kidney disease .
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Cat. No.: HY-141885
CAS No.: 2446817-72-5
Purity:  99.85%
Target:  

Apolipoprotein

Research Areas:  

Metabolic Disease

APOL1-IN-1 is a apolipoprotein L1 (APOL1) inhibitor extracted from patent WO2020131807A1 compound 87. APOL1-IN-1 can be used for the research of focal segmental glomerulosclerosis (FSGS) and non-diabetic kidney disease (NDKD) .
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Cat. No.: HY-W744699
CAS No.: 1438-66-0
Synonyms: (+)-Larixol
Larixol is an fMLP inhibitor and also inhibits Src kinase, ERK1/2, p38 and AKT phosphorylation signals in immune regulation. Larixol can interfere with the interaction between the βγ subunit of the fMLP receptor Gi protein and its downstream molecules, thereby inhibiting fMLP-induced respiratory burst. Larixol inhibits fMLP (0.1 μM)-induced superoxide anion production (IC50: 1.98 μM), cathepsin G release (IC50: 2.76 μM), and chemotaxis. Larixol improves neutrophil hyperactivation and reduces inflammation or tissue damage. A series of Larixol derivatives were found to have inhibitory effects on FSGS-related TRPC6 functional mutants .
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Cat. No.: HY-P991666

Target:  

TNF Receptor

Research Areas:  

Inflammation/Immunology

BMS-986090 is a humanized monoclonal antibody antagonist targeting CD40. BMS-986090 is promising for research of autoimmune diseases such as systemic lupus erythematosus (SLE) and focal segmental glomerulosclerosis (FSGS) .
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Cat. No.: HY-RS00226
Research Areas:  

Others

ACTN4 Human Pre-designed siRNA Set A contains three designed siRNAs for ACTN4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-135470R
CAS No.: 13411-16-0
Synonyms: P-7138 (Standard)
Research Areas:  

Infection

Nifurpirinol (P-7138) (Standard) is the analytical standard of Nifurpirinol (HY-135470). This product is intended for research and analytical applications. Nifurpirinol (P-7138) is a selective prosubstrate of bacterial nitroreductase (NTR). NTR catalyzes the reduction of nifurpirinol to generate cytotoxic metabolites that induce apoptosis in target cells. Nifurpirinol selectively ablates NTR-expressing cells such as pancreatic β cells, osteoblasts, dopaminergic neurons, and podocytes in transgenic zebrafish models. Nifurpirinol can be used in regeneration studies and disease modeling such as focal segmental glomerulosclerosis (FSGS) .
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Cat. No.: HY-W745090
CAS No.: 58024-13-8
Isomaltulose monohydrate is a fMLP inhibitor and also inhibits Src kinase, ERK1/2, p38 and AKT phosphorylation signals in immune regulation. Isomaltulose monohydrate can interfere with the interaction between the βγ subunit of the fMLP receptor Gi protein and its downstream molecules, thereby inhibiting fMLP-induced respiratory burst. Isomaltulose monohydrate inhibits fMLP (0.1 μM)-induced superoxide anion production (IC50: 1.98 μM) , cathepsin G release (IC< sub>50: 2.76 μM) and chemotaxis. Isomaltulose monohydrate can improve excessive activation of neutrophils and reduce inflammation or tissue damage. A series of derivatives of Isomaltulose monohydrate are found to have inhibitory effects on FSGS-related TRPC6 functional mutants .
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Cat. No.: HY-P701113
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ACTININ-4; FSGS; FSGS1
Species:  
Source:  
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