62 Results for "

apical

" in MedChemExpress (MCE) Product Catalog:
Products (62)

62 Results for "apical" in MCE Product Catalog:

Cat. No.: HY-151883
CAS No.: 2923433-95-6
Purity:  98.28%
Target:  

Apoptosis MDM-2/p53

Research Areas:  

Cancer

APE1-IN-2 (compound AP1) is a Pt(IV) proagent, targeting a critical BER protein, apurinic/apyrimidinic endonuclease 1 (APE1). APE1-IN-2 shows anticancer activity. APE1-IN-2 induces intracellular accumulation of platinum and activates DNA damage response and apoptosis signals .
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Cat. No.: HY-B1363R
CAS No.: 73-48-3
Synonyms: Bendrofluazide (Standard)
Research Areas:  

Cardiovascular Disease

Bendroflumethiazide (Standard) (Bendrofluazide (Standard)) is the analytical standard of Bendroflumethiazide (HY-B1363). This product is intended for research and analytical applications. Bendroflumethiazide (Bendrofluazide) is an orally available diuretic. Bendroflumethiazide inhibits the electroneutral sodium-chloride symporter located in the apical membrane of the early segment of the distal convoluted tubule and can effectively lower blood pressure. Bendroflumethiazide is used in the study of hypertension and edema. Bendroflumethiazide has an antidiuretic effect in diabetes insipidus .
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Cat. No.: HY-B1363S
CAS No.: 1330183-13-5
Synonyms: Bendrofluazide-d5
Bendroflumethiazide-d5 (Bendrofluazide-d5) is the deuterium labeled Bendroflumethiazide (HY-B1363).Bendroflumethiazide (Bendrofluazide) is an orally available diuretic. Bendroflumethiazide inhibits the electroneutral sodium-chloride symporter located in the apical membrane of the early segment of the distal convoluted tubule and can effectively lower blood pressure. Bendroflumethiazide is used in the study of hypertension and edema. Bendroflumethiazide has an antidiuretic effect in diabetes insipidus .
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Cat. No.: HY-E70425
CAS No.: 9030-05-1
Target:  

Glycosyltransferase

Research Areas:  

Metabolic Disease

Sucrose synthase belongs to glycosyltransferases and is a reversible catalyst present in plants, which catalyzes the conversion of sucrose into fructose and UDP-G or ADP-G. Sucrose synthase localizes to the cytoplasm, plasma membrane, cell wall, vacuole and mitochondria of plants. Sucrose synthase regulates sugar metabolism, supports the development of taproots, fruits, seeds and vascular tissues, drives the synthesis of starch, cellulose and callose, and enhances nitrogen fixation capacity. Sucrose synthase mediates signal transduction in plant meristems. Sucrose synthase is associated with plant growth, anaerobic stress tolerance, as well as shoot apical meristem and leaf morphology; overexpression of this enzyme promotes plant growth, increases xylem size, and elevates cellulose and starch contents .
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Cat. No.: HY-NP014
Protein A-PE is a biochemical reagent that can be used as a biological material or organic compound for life science related research .
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Cat. No.: HY-126425
CAS No.: 344359-25-7
Purity:  99.22%
Target:  

Parasite

Research Areas:  

Infection

NCGC00262650 is a potent apical membrane antigen 1-rhoptry neck protein 2 (AMA1-RON2) interaction inhibitor. NCGC00262650 can block entry of merozoites into red blood cells with an IC50 of 9.8 μM .
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Cat. No.: HY-129982
CAS No.: 289037-67-8
Purity:  99.14%
SC-435 is an orally effective apical sodium codependent bile acid transporter (ASBT) inhibitor. SC-435 effectively removes neurotoxic bile acids and ammonia from the blood by inhibiting intestinal ASBT, thereby alleviating liver and brain damage caused by liver failure. SC-435 can alter hepatic cholesterol metabolism and lower plasma low-density lipoprotein-cholesterol concentrations .
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Cat. No.: HY-149442
CAS No.: 1227098-30-7
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

APE1-IN-3 (Compound 1) is a APE1 inhibitor. APE1-IN-3 can be used for the research of cancer .
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Cat. No.: HY-B2217
CAS No.: 1305-62-0
Synonyms: Dihydroxycalcium
Calcium hydroxide (Dihydroxycalcium) is a strongly alkaline inorganic compound that can create a strongly alkaline environment by releasing hydroxide ions. Calcium hydroxide can cause lipid peroxidation of bacterial cell membranes, protein denaturation, and DNA strand breaks. Calcium hydroxide can be used in research on osteoporosis, apical periodontitis, and bacterial infections .
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Cat. No.: HY-15790H
CAS No.: 439087-68-0
Synonyms: (S)-A 3309; (S)-AZD 7806
(S)-Elobixibat is the S enantiomer of Elobixibat (HY-15790). (S)-Elobixibat is an orally effective Apical Sodium-Dependent Bile (IBAT) inhibitor. (S)-Elobixibat decreases LDL cholesterol, increases serum GLP-1, promotes colon motility, and has the potential to study metabolic syndrome. (S)-Elobixibat can be used to study constipation, dyslipidemia, non-alcoholic hepatitis, and liver tumors .
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Cat. No.: HY-19133
CAS No.: 133903-90-9
Synonyms: EF-4040
Target:  

Na+/K+ ATPase Myosin PKA

Research Areas:  

Metabolic Disease

ME-3407 (EF-4040) is a H +-K +-ATPase redistribution disruptor and myosin light chain kinase (MLCK) and protein kinase A inhibitor. ME-3407 blocks gastric acid secretion and aminopyrine accumulation by inhibiting microsomal-to-apical membrane redistribution of H +-K +-ATPase and suppressing MLCK-mediated myosin light chain phosphorylation. ME-3407 is promising for research of peptic ulcer .
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Cat. No.: HY-15131
CAS No.: 550368-41-7
Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

PNRI-299 is a selective AP-1 transcription inhibitor with an IC50 of 20 uM. PNRI-299 is a selective APE/Ref-1 inhibitor. PNRI-299 has no effect on NF-κB transcription or thioredoxin (up to 200 uM). PNRI-299 significantly reduces airway eosinophil infiltration, mucus hypersecretion, edema, and IL-4 levels in a mouse asthma model .
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Cat. No.: HY-P3347
CAS No.: 2891469-81-9
Target:  

Apelin Receptor (APJ)

Research Areas:  

Cardiovascular Disease

NH2-c[X-R-L-S-X]-K-G-P-(D-2Nal) (compound 40), a macrocyclic analogue of Ape13, is a potent APJ agonist (Ki=5.7 nM). NH2-c[X-R-L-S-X]-K-G-P-(D-2Nal) exhibits a favorable Gα12-biased signaling and an increased in vivo half-life .
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Cat. No.: HY-179014
OGG1 activator-1 (Compound 30) is a selective 8-oxoguanine DNA glycosylase-1 (OGG1) activator with an AC50 value of 0.58 μM. OGG1 activator-1 does not activate nor inhibit the key downstream repair enzyme APE1, and shows > 150-fold selectivity for the activation effect on OGG1. OGG1 activator-1 exhibits extremely high metabolic stability and almost no cytotoxicity. OGG1 activator-1 can be used for the study of oxidative stress-related diseases (such as neurodegenerative diseases, fibrotic diseases, cancer, inflammation, etc.) .
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Cat. No.: HY-B2098A
CAS No.: 548-57-2
Target:  

Autophagy Parasite

Research Areas:  

Cancer

Lucanthone hydrochloride is an endonuclease inhibitor of Apurinic endonuclease-1 (APE-1).
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Cat. No.: HY-133795
CAS No.: 5615-06-5
Target:  

DNA/RNA Synthesis

Research Areas:  

Others

Lucanthone N-oxide is the nitrogen oxide of Lucanthone (HY-B2098), an endonuclease inhibitor of Apurinic endonuclease-1 (APE-1) .
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Cat. No.: HY-B2098R
CAS No.: 479-50-5
Research Areas:  

Cancer

Lucanthone (Standard) is the analytical standard of Lucanthone. This product is intended for research and analytical applications. Lucanthone is an endonuclease inhibitor of Apurinic endonuclease-1 (APE-1).
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Cat. No.: HY-P5824
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Anthopleurin-C (APE 2-1) is a cardiotonic polypeptide that shows a powerful positive inotropic effect .
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Cat. No.: HY-N3625
CAS No.: 268214-52-4
Synonyms: Coronalonic acid
Coronalolic acid, extract from the apical bud of Gardenia sootepenesis Hutch, inhibits TNF-α-induced NF-κB activity and NO production .
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Cat. No.: HY-122521
CAS No.: 1154518-97-4
Sootepin D (compound 6), a triterpene from the apical bud of Gardenia sootepensis, inhibits TNF-α-induced NF-κB activity with an IC50 of 8.3μM. Sootepin D has anti-inflammatory activity .
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