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Butidrine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Butidrine
Clinical data
Trade namesBetabloc, Butidrate, Recetan
Other namesButedrine; Butydrine; Hydrobutamine; Idrobutamine
Drug classBeta blocker
Identifiers
  • 2-(butan-2-ylamino)-1-(5,6,7,8-tetrahydronaphthalen-2-yl)ethanol
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H25NO
Molar mass247.382 g·mol−1
3D model (JSmol)
  • CCC(C)NCC(C1=CC2=C(CCCC2)C=C1)O
  • InChI=1S/C16H25NO/c1-3-12(2)17-11-16(18)15-9-8-13-6-4-5-7-14(13)10-15/h8-10,12,16-18H,3-7,11H2,1-2H3
  • Key:GVNYSERWAKVROD-UHFFFAOYSA-N

Butidrine (INNTooltip International Nonproprietary Name), sold under the brand namesBetabloc,Butidrate, andRecetan among others, is abeta blocker (orβ-adrenergic receptorantagonist) related topronethalol[1] andpropranolol[2] that was developed in the 1960s.[3][4] It is notcardioselective (i.e., is notselective for theβ1-adrenergic receptor over theβ2-adrenergic receptor).[5] It hasmembrane stabilizing activity but nointrinsic sympathomimetic activity (i.e.,partial agonist activity).[6] Similarly to certain other beta blockers, butidrine additionally possesseslocal anesthetic properties.[7]

References

[edit]
  1. ^Bristol JA (1986).Cardiovascular drugs. John Wiley & Sons, Incorporated. p. 111.ISBN 978-0-471-09228-5.
  2. ^Drug Metabolism Reviews. Marcel Dekker. 1972.
  3. ^Morton IK, Hall JM (6 December 2012).Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 58–.ISBN 978-94-011-4439-1.
  4. ^Elks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 197–.ISBN 978-1-4757-2085-3.
  5. ^Sokabe, Hirofumi (1985). "A new classification of β-adrenoceptor blocking drugs".Trends in Pharmacological Sciences.6:107–109.doi:10.1016/0165-6147(85)90051-3.
  6. ^Fitzgerald JD (1969). "Perspectives in adrenergic beta-receptor blockade".Clin Pharmacol Ther.10 (3):292–306.doi:10.1002/cpt1969103292.PMID 4894830.
  7. ^Charlier R (1971).Antianginal drugs: pathophysiological, haemodynamic, methodological, pharmacological, biochemical and clinical basis for their use in human therapeutics. Springer-Verlag.ISBN 978-3-540-05365-1.


α1
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Antagonists
α2
Agonists
Antagonists
β
Agonists
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Calcium
VDCCsTooltip Voltage-dependent calcium channels
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Activators
Potassium
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IRKsTooltip Inwardly rectifying potassium channel
Blockers
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KCaTooltip Calcium-activated potassium channel
Blockers
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K2PsTooltip Tandem pore domain potassium channel
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Sodium
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ENaCTooltip Epithelial sodium channel
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Chloride
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CFTRTooltip Cystic fibrosis transmembrane conductance regulator
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TRPsTooltip Transient receptor potential channels
LGICsTooltip Ligand gated ion channels
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