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等級
produced by Wacker Chemie AG, Burghausen, Germany
品質等級
化驗
≥99.0% (GC)
bp
218 °C (lit.)
mp
105-108 °C (lit.)
SMILES 字串
Cc1cc(C)[nH]n1
InChI
1S/C5H8N2/c1-4-3-5(2)7-6-4/h3H,1-2H3,(H,6,7)
InChI 密鑰
SDXAWLJRERMRKF-UHFFFAOYSA-N
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訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - STOT RE 2
標靶器官
Liver
儲存類別代碼
13 - Non Combustible Solids
水污染物質分類（WGK）
WGK 3
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Gabriella Cavallini et al.
Autophagy, 3(1), 26-27 (2006-09-12)
Autophagy is a major intracellular degradation/recycling system ubiquitous in eukaryotic cells. It contributes to the turnover of cellular components by delivering portions of the cytoplasm and organelles to lysosomes, where they are digested. Starvation-induced autophagy is required for maintaining an
C Redekopp et al.
Journal of endocrinological investigation, 7(4), 277-281 (1984-08-01)
The inhibitory and stimulatory effects of somatostatin analogues on growth hormone secretion have been studied in the sheep. Plasma immunoreactive growth hormone (GH) was stimulated by the iv administration of the antilipolytic compound 3,5-dimethylpyrazole and was followed by infusion of
Effects of antilipolytic agents on peroxisomal beta-oxidation of fatty acids in rat liver.
T Locci-Cubeddu et al.
Biochemical pharmacology, 32(11), 1807-1809 (1983-06-01)
The regulation of liver protein degradation by aminoacids in vivo. Effects of glutamine and leucine.
E Bergamini et al.
Archives of physiology and biochemistry, 103(4), 512-515 (1995-08-01)
The effects in vivo of the two major in vitro regulatory aminoacids, leucine and glutamine, on liver protein degradation were explored in male young adult Sprague Dawley rats. Protein degradation was stimulated by the injection of the antilipolytic drug 3,5
P Masiello et al.
Metabolism: clinical and experimental, 51(1), 110-114 (2002-01-10)
This study intended to test the hypothesis that intracellular lipolysis in the pancreatic beta cells is implicated in the regulation of insulin secretion stimulated by nutrient secretagogues or cyclic adenosine monophosphate (cAMP) agonists. Indeed, although lipid signaling molecules were repeatedly
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