Search results for " 3-Amino-1"

showing 4 items of 4 documents

Ethanol Modulates Corticotropin Releasing Hormone Release From the Rat Hypothalamus: Does Acetaldehyde Play a Role?

2010

BACKGROUND AND METHODS Ethanol (EtOH) activates hypothalamic-pituitary-adrenal (HPA) axis, resulting in adrenocorticotropin hormone, glucocorticoid release, and in modifications of the response of the axis to other stressors. The initial site of EtOH action within the HPA system seems to be the hypothalamus. Thus, to determine the mechanisms responsible for these effects, we investigated: (i) whether EtOH was able to release corticotrophic releasing hormone (CRH) from incubated hypothalamic explants; (ii) whether acetaldehyde (ACD), its first metabolite formed in the brain by catalase activity, might play a role in EtOH activity. To this aim, rat hypothalamic explants were incubated with: (…

Maleendocrine systemmedicine.medical_specialtySettore BIO/14 - FARMACOLOGIACorticotropin-Releasing HormoneHypothalamusMedicine (miscellaneous)AcetaldehydeIn Vitro TechniquesToxicologychemistry.chemical_compoundCorticotropin-releasing hormoneInternal medicinemental disordersmedicineAnimalsRats Wistarreproductive and urinary physiologyEthanolbiologyEthanolAcetaldehydeRatsPsychiatry and Mental healthEndocrinologyMechanism of actionchemistryEthanol Acetaldehyde Hypothalamic CRH Release 3-Amino-124-triazole d-Penicillamine.CatalaseHypothalamusCRHbiology.proteinLiberationmedicine.symptomhormones hormone substitutes and hormone antagonistsGlucocorticoidmedicine.drug
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Susceptibility of Methyl 3-Amino-1H-pyrazole-5-carboxylate to Acylation

2009

Abstract In the search for a new method of synthesis of hybrid peptides with aminopyrazole carboxylic acid, we tried to force selective acylation at the aromatic amino group instead of at the ring nitrogen atom with fairly gentle acylating agents. The acylating agents used were acid anhydrides: acetic anhydride, tert-butyl pyrocarbonate, and 2-(2-methoxyethoxy)ethoxyacetic acid/dicyclohexylcarbodiimide. We succceded in acylation at this amino group with almost none at the ring nitrogen atom. Sometimes, however, acylation in small quantities at the ring nitrogen atom was observed as a by-product. To remove this by-product, imidazole was used. Thus, we were able to obtain the hybrid peptides …

chemistry.chemical_classificationmethyl 3-amino-1H-pyrazole-5-carboxylatearomatic amineCarboxylic acidOrganic ChemistryAromatic aminePyrazoletert-butyloxycarbonylationRing (chemistry)Combinatorial chemistryAcylationchemistry.chemical_compoundAcetic anhydridechemistryacylationOrganic chemistryImidazoleCarboxylate2-(2-methoxyethoxy)ethoxyacetylationacetylationSynthetic Communications
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Gamma-Ray-Induced Structural Transformation of GQDs towards the Improvement of Their Optical Properties, Monitoring of Selected Toxic Compounds, and …

2022

Structural modification of different carbon-based nanomaterials is often necessary to improve their morphology and optical properties, particularly the incorporation of N-atoms in graphene quantum dots (GQDs). Here, a clean, simple, one-step, and eco-friendly method for N-doping of GQDs using gamma irradiation is reported. GQDs were irradiated in the presence of the different ethylenediamine (EDA) amounts (1 g, 5 g, and 10 g) and the highest % of N was detected in the presence of 10 g. N-doped GQDs emitted strong, blue photoluminescence (PL). Photoluminescence quantum yield was increased from 1.45, as obtained for non-irradiated dots, to 7.24% for those irradiated in the presence of 1 g of …

graphene quantum dots3-amino-124-triazolegamma-irradiationGeneral Chemical Engineeringgraphene quantum dots; N-doping; gamma-irradiation; photoluminescence; carbofuran; 3-amino-124-triazole; detection; antibacterial effectsdetectionGeneral Materials Sciencephotoluminescenceantibacterial effectsSettore CHIM/02 - Chimica FisicaN-dopingcarbofuranNanomaterials (Basel, Switzerland)
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CCDC 631805: Experimental Crystal Structure Determination

2008

Related Article: A.Kusakiewicz-Dawid, E.Masiukiewicz, B.Rzeszotarska, I.Dybala, A.E.Koziol, M.A.Broda|2007|Chem.Pharm.Bull.|55|747|doi:10.1248/cpb.55.747

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersEthyl 3-amino-1H-pyrazole-4-carboxylateExperimental 3D Coordinates
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