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Conjugates of Degraded and Oxidized Hydroxyethyl Starch and Sulfonylureas: Synthesis, Characterization, and in Vivo Antidiabetic Activity

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/star.201200065openalex-snapshot

Selective degradation, oxidation, and characterization of hydroxyethyl starch for potential use as a drug carrier

inferredcites →https://doi.org/10.1007/s00018-004-4153-5openalex-snapshot

Targeted polymeric micelles for delivery of poorly soluble drugs

inferredcites →https://doi.org/10.1007/s00232-003-2030-zopenalex-snapshot

Comparative Pharmacology of the Activity of Wild-type and G551D Mutated CFTR Chloride Channel: Effect of the Benzimidazolone Derivative NS004

inferredcites →https://doi.org/10.1007/s00540-012-1430-6openalex-snapshot

Pharmacokinetics and safety of 6 % hydroxyethyl starch 130/0.4 in healthy male volunteers of Japanese ethnicity after single infusion of 500 ml solution

inferredcites →https://doi.org/10.1007/s00706-011-0600-9openalex-snapshot

Synthesis, characterization, and hypoglycemic activity of 3-(arylsulfonyl)spiroimidazolidine-2,4-diones

inferredcites →https://doi.org/10.1007/s11164-014-1814-3openalex-snapshot

Synthesis and in vivo hypoglycemic activity of new imidazolidine-2,4-dione derivatives

inferredcites →https://doi.org/10.1016/0032-3861(92)91123-jopenalex-snapshot

Protective groups in organic synthesis

inferredcites →https://doi.org/10.1016/0223-5234(92)90112-eopenalex-snapshot

Synthesis and aldose reductase inhibitory activity of substituted 2(1H)-benzimidazolone- and oxindole-1-acetic acids

inferredcites →https://doi.org/10.1016/j.bmcl.2012.11.039openalex-snapshot

Dual action spirobicycloimidazolidine-2,4-diones: Antidiabetic agents and inhibitors of aldose reductase-an enzyme involved in diabetic complications

inferredcites →https://doi.org/10.1016/j.progpolymsci.2007.05.008openalex-snapshot

Polymer–drug conjugation, recent achievements and general strategies

inferredcites →https://doi.org/10.1016/s0040-4020(01)80708-0openalex-snapshot

Ambident heterocyclic reactivity: Alkylation of 2-substituted-4-methylbenzimidazoles

inferredcites →https://doi.org/10.1016/s0040-4020(01)81192-3openalex-snapshot

Mimicking of ergot alkaloids and synthetic piperidine drugs by 2,5-substituted piperidines derived from cis and trans ethyl 1-benzyl-6-cyano-3-piperidinecarboxylate.

inferredcites →https://doi.org/10.1016/s0142-9612(00)00193-9openalex-snapshot

Peptide and protein PEGylation

inferredcites →https://doi.org/10.1021/jm00170a009openalex-snapshot

Synthesis of a new class of 2,3-dihydro-2-oxo-1H-benzimidazole-1-carboxylic acid derivatives as highly potent 5-HT3 receptor antagonists

inferredcites →https://doi.org/10.1021/jo00111a014openalex-snapshot

Regiospecific Functionalization of 1,3-Dihydro-2H-benzimidazol-2-one and Structurally Related Cyclic Urea Derivatives

inferredcites →https://doi.org/10.1021/jo00960a013openalex-snapshot

Novel Lossen rearrangements of 3-benzenesulfonyloxy(1H- and 1-methyl)-2,4-quinazolinediones induced by alkoxide ions

inferredcites →https://doi.org/10.1067/mge.2000.109718openalex-snapshot

Polyethylene glycol-induced pancreatitis

inferredcites →https://doi.org/10.1097/00000539-200104000-00011openalex-snapshot

Voluven®, a Lower Substituted Novel Hydroxyethyl Starch (HES 130/0.4), Causes Fewer Effects on Coagulation in Major Orthopedic Surgery than HES 200/0.5

inferredcites →https://doi.org/10.1097/00000539-200209000-00007openalex-snapshot

The Pharmacokinetics and Tolerability of an Intravenous Infusion of the New Hydroxyethyl Starch 130/0.4 (6%, 500 mL) in Mild-to-Severe Renal Impairment

inferredcites →https://doi.org/10.1097/01.anes.0000265422.07864.37openalex-snapshot

Volume Replacement Therapy during Major Orthopedic Surgery Using Voluven® (Hydroxyethyl Starch 130/0.4) or Hetastarch

inferredcites →https://doi.org/10.1152/jn.1994.71.5.1873openalex-snapshot

Opening of large-conductance calcium-activated potassium channels by the substituted benzimidazolone NS004

inferredcites →https://doi.org/10.14233/ajchem.2013.13372openalex-snapshot

Preparation of 2(3H)-Benzimidazolone and its Derivative Under Aqueous Condition As a Potential Agent for Antidiabetic Compounds

inferredcites →https://doi.org/10.1515/znb-2002-0315openalex-snapshot

N-Arylsulfonyl-benzimidazolones as Potential Hypoglycemic Agents

inferredcites →https://doi.org/10.2165/00126839-200405010-00001openalex-snapshot

Volume Efficacy and Reduced Influence on Measures of Coagulation Using Hydroxyethyl Starch 130/0.4 (6%) with an Optimised in???Vivo???Molecular Weight in Orthopaedic Surgery

inferredcites →https://doi.org/10.3390/polym3031076openalex-snapshot

Multimeric, Multifunctional Derivatives of Poly(ethylene glycol)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4637580openalex-extracted

inferred← citeshttps://doi.org/10.1002/ddr.70369openalex-snapshot

Design, Synthesis, and Biological Evaluation of Benzimidazol‐2‐One Hybrids as Potential Anti‐Alzheimer's Disease Agents

inferred← citeshttps://doi.org/10.1007/s10593-017-1999-7openalex-snapshot

Synthesis of 1,3-dihydro-2H-benzimidazol-2-ones (microreview)

inferred← citeshttps://doi.org/10.1007/s11030-018-9851-2openalex-snapshot

Synthesis of new chiral 1,3,4-thiadiazole-based di- and tri-arylsulfonamide residues and evaluation of in vitro anti-HIV activity and cytotoxicity

inferred← citeshttps://doi.org/10.1016/b978-0-12-821437-4.00019-0openalex-snapshot

Biopolymer–drug conjugates as biomaterials

inferred← citeshttps://doi.org/10.1016/j.envres.2024.118760openalex-snapshot

RETRACTED: Environmentally friendly and efficient TBHP-mediated catalytic reaction for the synthesis of substituted benzimidazole-2-ones: In-silico approach to pharmaceutical applications

inferred← citeshttps://doi.org/10.1021/jacs.2c02004openalex-snapshot

Access to Cyclic N -Trifluoromethyl Ureas through Photocatalytic Activation of Carbamoyl Azides

inferred← citeshttps://doi.org/10.1039/d3ra02916fopenalex-snapshot

Design, synthesis, in silico , and in vitro evaluation of benzylbenzimidazolone derivatives as potential drugs on α-glucosidase and glucokinase as pharmacological targets

inferred← citeshttps://doi.org/10.2139/ssrn.4173284openalex-snapshot

Design, Synthesis and Biological Evaluation of Conformationnally-Restricted Analogues of E7010 as Inhibitors of Tubulin Assembly (ITA) and Vascular Disrupting Agents (VDA)

inferred← citeshttps://doi.org/10.25135/acg.oc.41.18.03.069openalex-snapshot

New symmetrical acyclic and alicyclic bisurea derivatives of 4,4'-methylenebis(phenyl isocyanate): Synthesis, characterization, bioactivity and antioxidant activity evaluation and molecular docking studies

inferred← citeshttps://doi.org/10.3390/catal9010028openalex-snapshot

Recent Advances in the Catalytic Synthesis of Imidazolidin-2-ones and Benzimidazolidin-2-ones

inferred← citeshttps://doi.org/10.3390/molecules201119676openalex-snapshot

Design, Synthesis and in Vivo Evaluation of Novel Glycosylated Sulfonylureas as Antihyperglycemic Agents

inferred← citeshttps://doi.org/10.3390/ph18121899openalex-snapshot

Evaluation of Antiproliferative Activity and Molecular Modeling Studies of Some Novel Benzimidazolone-Bridged Hybrid Compounds

inferred← citeshttps://doi.org/10.4314/bajopas.v13i1.9openalex-snapshot

Synthesis and characterizations of water soluble acetaminophen starch conjugate with methylene carbonyl bridge and improved solubility

inferred← citeshttps://doi.org/10.5281/zenodo.154526openalex-snapshot

Acne At The Bottom Of The Main Sequence

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