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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
86 Results for "
ADH
" in MedChemExpress (MCE) Product Catalog:
Products (86)
86 Results for "ADH" in MCE Product Catalog:
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11 Cited Publications
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7 Cited Publications
Cat. No.: HY-B1811
CAS No.: 11000-17-2
Synonyms: Arginine vasopressin; Antidiuretic hormone
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3 Cited Publications
Synonyms: (Z)-LeukADHerin-1 choline
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ADH-503 ((Z)-Leukadherin-1 choline) is an orally active and allosteric CD11b agonist. ADH-503 leads to the repolarization of tumor-associated macrophages, reduction in the number of tumor-infiltrating immunosuppressive myeloid cells, and enhances dendritic cell responses .
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Sorbitol dehydrogenase-IN-1 is a potent and orally active sorbitol dehydrogenase inhibitor with IC50 s of 4, 5 nM for rat and human, respectively.
Sorbitol Dehydrogenase (SDH) is an enzyme that belongs to the zinc-containing alcohol dehydrogenase (ADH) family.
ADH and ALDH are enzymes that work together to metabolize alcohol .
ADH-6 TFA is a tripyridylamide compound. ADH-6 abrogates self-assembly of the aggregation-nucleating subdomain of mutant p53 DBD. ADH-6 TFA targets and dissociates mutant p53 aggregates in human cancer cells, which restores p53's transcriptional activity, leading to cell cycle arrest and apoptosis. ADH-6 TFA has the potential for the research of cancer diseases .
Cat. No.: HY-164690A
CAS No.: 2600354-60-5
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Nicotinamide-guanine dinucleotide sodium, a NAD sodium (HY-B0445A) analog, is an oxidized forms of nicotinamide guanine dinucleotide. Nicotinamide-guanine dinucleotide sodium serves as coenzymes for alcohol dehydrogenase (ADH) in vitro .
Cat. No.: HY-177303
CAS No.: 717104-43-3
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AXT-914 is a Calcium-sensing receptor (CaSR) inhibitor. AXT-914 has antiviral activity against the coronavirus HCoV 229E and SARS-CoV2. AXT914 reduces cytosolic calcium signalling activity of CaSR mutations. AXT-914 can be used for Bartter syndrome type 5 and autosomal dominant hypocalcemia (ADH) and coronavirus infections research .
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Triterpenes Terpenoids Astragalus oleifolius DC. Sedum sarmentosum Bunge Crassulaceae Extract Plants Compositae Extract Disease Research Fields Inflammation/Immunology
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Alcohol dehydrogenase, yeast is an alcohol dehydrogenase derived from yeast. Alcohol dehydrogenase is a class of oxidoreductases that catalyze the reversible oxidation of alcohols to aldehydes or ketones, with the concomitant reduction of NAD + or NADP +. Alcohol dehydrogenase represents a large family of enzymes, which can be subdivided into at least three distinct enzyme superfamilies: medium-chain dehydrogenase/reductase (MDR), short-chain dehydrogenase/reductase, and iron-activated alcohol dehydrogenase (ADH) .
Cat. No.: HY-145785
CAS No.: 2227429-65-2
ADH-6 is a tripyridylamide compound. ADH-6 abrogates self-assembly of the aggregation-nucleating subdomain of mutant p53 DBD. ADH-6 targets and dissociates mutant p53 aggregates in human cancer cells, which restores p53's transcriptional activity, leading to cell cycle arrest and apoptosis. ADH-6 has the potential for the research of cancer diseases[1].
Cat. No.: HY-RS00370
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ADH5 Human Pre-designed siRNA Set A contains three designed siRNAs for ADH5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-P0049A
CAS No.: 75499-44-4
Synonyms: Arg8-vasopressin diacetate; AVP diacetate; ADH
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Trimethylacetaldehyde (Pivalic aldehyde; Pivalaldehyde) is an inhibitor of E. coli betaine aldehyde dehydrogenase (ALDH) with a Ki of 4.5 mM. Trimethylacetaldehyde serves as a substrate for Drosophila melanogaster alcohol dehydrogenase (AdhS), undergoing oxidation and disproportionation reactions with the release of NADH, and also forms an inactive binary enzyme-aldehyde complex via a compulsory ordered reaction mechanism .
Cat. No.: HY-122297A
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Cat. No.: HY-33914
CAS No.: 25222-43-9
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Methoxyflurane (DA-759) is a volatile anesthetic and nephrotoxic agent. Methoxyflurane undergoes defluorination to generate inorganic fluoride and oxalic acid, leading to polyuric renal insufficiency, proximal tubular necrosis, mitochondrial swelling, and ADH-resistant polyuria. Methoxyflurane inhibits Na +/K + ATPase sodium transport. Methoxyflurane is used in research on neurological diseases and kidney diseases .
Cat. No.: HY-169025
CAS No.: 2711712-81-9
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ADH-353 can inhibit Aβ fibrillation and reduce Aβ-induced cytotoxicity in SH-SY5Y and N2a cells. ADH-353 can be used in Alzheimer's disease-related research .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
