10114 Results for "

biolipid function

" in MedChemExpress (MCE) Product Catalog:
Products (10114)

10114 Results for "biolipid function" in MCE Product Catalog:

6
6 Cited Publications
Art. -Nr.: HY-Y0271
CAS. Nr.: 57-13-6
Synonyms: Carbonyl diamide
Urea is a powerful protein denaturant via both direct and indirect mechanisms . A potent emollient and keratolytic agent . Used as a diuretic agent. Blood urea nitrogen (BUN) has been utilized to evaluate renal function . Widely used in fertilizers as a source of nitrogen and is an important raw material for the chemical industry.
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6
6 Cited Publications
Art. -Nr.: HY-103192
CAS. Nr.: 40297-09-4
Reinheit:  99.82%
Synonyms: RMI12330A
Forschungsgebiete:  

Neurological Disease Cancer

MDL12330A (RMI12330A) is an adenylyl cyclases inhibitor. MDL12330A can inhibit KV channels, increases insulin secretion and Ca 2+ levels. MDL12330A accentuates contractions in uterine rings and inhibits cardiac functions. MDL12330A can be used for the research of endocrinology, metabolic and cardiovascular disease .
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6
6 Cited Publications
Art. -Nr.: HY-111793
CAS. Nr.: 1060524-97-1
Reinheit:  98.40%
Target:  

CXCR

Forschungsgebiete:  

Neurological Disease

NUCC-390 is a novel and selective small-molecule CXCR4 receptor agonist. NUCC-390 induces internalization of CXCR4 receptors and acts in an opposite way of AMD3100 (HY-10046) . NUCC-390 promotes nerve recovery of function after neurodegeneration in vivo .
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6
6 Cited Publications
Art. -Nr.: HY-N0502
CAS. Nr.: 88901-36-4
Mogroside V is a the major active constituent of a traditional Chinese medicine Siraitiae Fructus. Mogroside V reduces the intracellular reactive oxygen species (ROS) levels and enhances mitochondrial function. Mogroside V has anti-oxidative, anti-diabetic and anti-carcinogenic effects. Mogroside V can be used for diabetic diseases research .
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6
6 Cited Publications
Art. -Nr.: HY-P2764
CAS. Nr.: 9000-95-7
Target:  

NTPDase

Forschungsgebiete:  

Inflammation/Immunology

Apyrase is an Nucleoside triphosphate diphosphohydrolase (NTPDase). Apyrase can hydrolyze extracellular adenosine triphosphate (ATP) and adenosine diphosphate (ADP). Apyrase can inhibit Stx2 toxin release of enterohemorrhagic Escherichia coli (EHEC) infection and protect the intestinal barrier function. Apyrase can be used for the research of infection and inflammation, such as hemorrhagic colitis .
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6
6 Cited Publications
Art. -Nr.: HY-16969
CAS. Nr.: 1401708-83-5
Synonyms: PNB-0408; N-hexanoic-Try-Ile-(6)-amino hexanoic amide; Hexanoyl-Tyr-Ile-Ahx-NH2
Target:  

c-Met/HGFR

Forschungsgebiete:  

Neurological Disease

Dihexa, an oligopeptide drug, is an orally active and blood-brain barrier-permeable angiotensin IV analog. Dihexa binds to hepatocyte growth factor (HGF) with high affinity (Kd=65 pM) and potentiates its activity at its receptor, c-Met. Dihexa exhibits excellent antidementia activity and improves cognitive function in animal models. Dihexa may have therapeutic potential as a treatment Alzheimer’s disease .
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6
6 Cited Publications
Art. -Nr.: HY-141539A
Reinheit:  99.77%
Forschungsgebiete:  

Cancer

SETDB1-TTD-IN-1 TFA is a potent, selective and endogenous binder competitive ligand of SET domain bifurcated protein 1 tandem tudor domain (SETDB1-TTD) that binds to TTD, with a Kd of 88 nM. SETDB1-TTD-IN-1 TFA increases SETDB1 methyltransferase activity. SETDB1-TTD-IN-1 TFA can be used for the research of biological functions and disease associations of SETDB1-TTD .
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5
5 Cited Publications
Art. -Nr.: HY-P99029
CAS. Nr.: 2169232-81-7
Synonyms: Hu5F9-G4

Target:  

CD47

Forschungsgebiete:  

Cancer

Magrolimab (Hu5F9-G4) is a humanized anti-CD47 antibody. Magrolimab, an IgG4 isotype, lacks ADCC function and exhibits relatively weak ADCP effector function. Magrolimab can be used for the study of malignant bone tumors and breast cancer .
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5
5 Cited Publications
Art. -Nr.: HY-113216
CAS. Nr.: 30315-93-6
Reinheit:  ≥98.0%
Synonyms: NG,NG-Dimethylarginine
Asymmetric dimethylarginine is an endogenous inhibitor of nitric oxide synthase (NOS), and functions as a marker of endothelial dysfunction in a number of pathological states.
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5
5 Cited Publications
Art. -Nr.: HY-145603
CAS. Nr.: 2374124-49-7
Reinheit:  98.19%
Synonyms: VX-121
Target:  

CFTR Chloride Channel

Forschungsgebiete:  

Neurological Disease

Vanzacaftor (VX-121) is an orally active noval corrector of Cystic fibrosis transmembrane conductance regulator (CFTR). Vanzacaftor improves processing and trafficking of CFTR protein as well as increases chloride transport in triple combined with Tezacaftor (HY-15448) and Deutivacaftor. Vanzacaftor-Tezacaftor-Deutivacaftor is safe and well tolerated, improving lung function, respiratory symptoms, and CFTR function with cystic fibrosis, which is promising for research in the field of cystic fibrosis diseases .
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5
5 Cited Publications
Art. -Nr.: HY-B0132
CAS. Nr.: 70458-96-7
Synonyms: MK-0366
Norfloxacin (MK-0366) is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria, which functions by inhibiting DNA gyrase.
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5
5 Cited Publications
Art. -Nr.: HY-14273
CAS. Nr.: 241479-67-4
Reinheit:  99.97%
Synonyms: BAL-4815; RO-0094815
Forschungsgebiete:  

Infection Cancer

Isavuconazole (BAL-4815) is a triazole proagent with antifungal activity against yeasts, molds, and dimorphic fungi. Isavuconazole inhibits ergosterol biosynthesis and results in the disruption of fungal membrane structure and function. Isavuconazole is a moderate inhibitor of CYP3A4.
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5
5 Cited Publications
Art. -Nr.: HY-B0594
CAS. Nr.: 66108-95-0
Target:  

Autophagy Mitophagy

Forschungsgebiete:  

Cancer

Iohexol is a non-ionic, water-soluble contrast agent used as a reference marker for the determination of glomerular filtration rate (GFR) at the level of renal function. Iohexol can be used for contrast in myelography, computerized tomography (cisternography, ventriculography) and MicroCT imaging .
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5
5 Cited Publications
Art. -Nr.: HY-12776
CAS. Nr.: 1426802-50-7
Reinheit:  98.01%
Target:  

ROR

Forschungsgebiete:  

Inflammation/Immunology

GSK805 is an orally active and CNS penetrant RORγt inhibitor. GSK805 inhibits RORγ and Th17 cells differentiation with pIC50 values of 8.4 and >8.2. GSK805 inhibits the function of Th17 cells. GSK805 can be used for the research of immunity .
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5
5 Cited Publications
Art. -Nr.: HY-B0315
CAS. Nr.: 68-19-9
Synonyms: Cyanocobalamin
Vitamin B12 is a vitamin that can pass through the blood-brain barrier. Vitamin B12 plays a key role in the normal functioning of the brain and nervous system, and for the formation of blood. Vitamin B12 is beneficial for many inflammatory diseases and also provides protection in oxidative-stress-associated pathologies .
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5
5 Cited Publications
Art. -Nr.: HY-B0315B
CAS. Nr.: 194937-59-2
Synonyms: Cyanocobalamin hydrate
Vitamin B12 (Cyanocobalamin) hydrate is a vitamin that can pass through the blood-brain barrier. Vitamin B12 plays a key role in the normal functioning of the brain and nervous system, and for the formation of blood. Vitamin B12 hydrate is beneficial for many inflammatory diseases and also provides protection in oxidative-stress-associated pathologies .
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5
5 Cited Publications
Art. -Nr.: HY-113354
CAS. Nr.: 584-85-0
Reinheit:  99.85%
Anserine, a methylated form of Carnosine, is an orally active, natural Histidine-containing dipeptide found in skeletal muscle of vertebrates. Anserine is not cleaved by serum carnosinase and act as biochemical buffers, chelators, antioxidants, and anti-glycation agents. Anserine has blood-brain barrier permeability, and improves memory functions in Alzheimer's disease (AD)-model mice .
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5
5 Cited Publications
Art. -Nr.: HY-13968
CAS. Nr.: 664993-53-7
Reinheit:  99.83%
Target:  

PARP

Forschungsgebiete:  

Cancer

JW 55 is a potent and selective β-catenin signaling pathway inhibitor, which functions via inhibition of the PARP domain of tankyrase 1 and tankyrase 2 (TNKS1/2). JW 55 decreases auto-PARsylation of TNKS1/2 in vitro with IC50s of 1.9 μM and 830 nM respectively.
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5
5 Cited Publications
Art. -Nr.: HY-110117
CAS. Nr.: 213211-10-0
Reinheit:  99.82%
Forschungsgebiete:  

Inflammation/Immunology

BIRT 377 is a potent amd orally bioavailable inhibitor of the interaction between intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1 (LFA-1). BIRT 377 also inhibits the production of IL-2 in vivo. BIRT 377 can be used for researching inflammatory and immune disorders .
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5
5 Cited Publications
Art. -Nr.: HY-B1836
CAS. Nr.: 76144-81-5
Synonyms: MET-88; Quaterin
Meldonium (MET-88) functions as a cardioprotective agent by cpmpetetively inhibiting γ-butyrobetaine hydroxylase (BBOX) and carnitine/organic cation transporter type 2 (OCTN2). Meldonium exhibits IC50 values of 34-62 μM for human recombinant BBOX and an EC50 of 21 μM for human OCTN2. Meldonium is a fatty acid oxidation inhibitor .
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