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Heterocyclic Ureas: Inhibitors of Acyl-CoA:Cholesterol O-Acyltransferase as Hypocholesterolemic Agents
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.251.1.73openalex-snapshot
Landmark article Oct 15, 1932. Regional ileitis. A pathological and clinical entity. By Burril B. Crohn, Leon Ginzburg, and Gordon D. Oppenheimer
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A convenient and general synthesis of 2‐amino‐1,3,4‐thiadiazoles. Dehydration of acylthiosemicarbazides with methanesulfonic acid
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Subacute Toxicity of a Novel Inhibitor of Acyl-CoA: Cholesterol Acyltransferase in Beagle Dogs
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Cloning and structure-function of the H2 histamine receptor
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Substituted N,N′-diphenyl ureas as potent inhibitors of acyl-CoA:Cholesterol acyltransferase (ACAT)
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122nd National ACS Meeting
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The Reaction of Ketones with Halogens and Thiourea1
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TcO(PnAO-1-(2-nitroimidazole)) [BMS-181321], a new technetium-containing nitroimidazole complex for imaging hypoxia: synthesis, characterization, and xanthine oxidase-catalyzed reduction
inferredcites →https://doi.org/10.1021/jm00037a016openalex-snapshot
Inhibitors of Acyl-CoA:Cholesterol Acyltransferase (ACAT). 7. Development of a Series of Substituted N-Phenyl-N'-[(1-phenylcyclopentyl)methyl]ureas with Enhanced Hypocholesterolemic Activity
inferredcites →https://doi.org/10.1021/jm00038a010openalex-snapshot
Inhibitors of Acyl-CoA:Cholesterol O-Acyl Transferase (ACAT) as Hypocholesterolemic Agents. 8. Incorporation of Amide or Amine Functionalities into a Series of Disubstituted Ureas and Carbamates. Effects on ACAT Inhibition in vitro and Efficacy in vivo
inferredcites →https://doi.org/10.1021/jm00063a016openalex-snapshot
Inhibitors of acyl-CoA:cholesterol acyltransferase (ACAT). 2. Modification of fatty acid anilide ACAT inhibitors: bioisosteric replacement of the amide bond
inferredcites →https://doi.org/10.1021/jm00072a014openalex-snapshot
Inhibitors of acyl-CoA:cholesterol acyltransferase. 5. Identification and structure-activity relationships of novel .beta.-keto amides as hypocholesterolemic agents
inferredcites →https://doi.org/10.1021/jm00074a011openalex-snapshot
Inhibitors of acyl-CoA:cholesterol acyltransferase. 4. A novel series of urea ACAT inhibitors as potential hypocholesterolemic agents
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Cholesterol is required for secretion of very-low-density lipoprotein by rat liver
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Studies on Acetylenic Compounds. XLIV. Synthesis of 3-Aminoisoxazoles and 3-Hydroxyisoxazoles (3-Isoxazolones)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/chin.199707147openalex-snapshot
ChemInform Abstract: Heterocyclic Ureas: Inhibitors of Acyl‐CoA:Cholesterol O‐ Acyltransferase (ACAT) as Hypocholesterolemic Agents.
inferred← citeshttps://doi.org/10.1002/hc.20489openalex-snapshot
A new convenient way to synthesize 1,3,4‐thiadiazol‐2‐yl urea derivatives under microwave irradiation
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Structure–activity relationships of 2-aminothiazoles effective against Mycobacterium tuberculosis
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.12.012openalex-snapshot
Synthesis, characterization and in vitro antibacterial activity of thiourea and urea derivatives of steroids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.12.029openalex-snapshot
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A tandem and tunable Pd catalyzed C–N coupling of heteroarenols with ureas via C–OH bond activation
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Multicomponent synthesis of allomaltol containing 2-aminooxazoles and acid-catalyzed recyclization into substituted furo[3,2-b]pyrans
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Aminoisoxazoles: Preparations and Utility in the Synthesis of Condensed Systems
inferred← citeshttps://doi.org/10.1016/s0968-0896(97)10009-8openalex-snapshot
Inhibitors of acyl-CoA: cholesterol O-acyltransferase (ACAT). Part 1: Identification and structure-activity relationships of a novel series of substituted N-alkyl-N-biphenylylmethyl-N′-arylureas
inferred← citeshttps://doi.org/10.1016/s1359-6446(97)01123-9openalex-snapshot
ACAT inhibitors: evolution from cholesterol-absorption inhibitors to antiatherosclerotic agents
inferred← citeshttps://doi.org/10.1021/np500542xopenalex-snapshot
Isolation and Total Syntheses of Cytotoxic Cryptolactones A 1 , A 2 , B 1 , and B 2 : α,β-Unsaturated δ-Lactones from a Cryptomyzus sp. Aphid
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