跳至內容

N'-異丙基異煙肼

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N'-異丙基異煙肼
臨床資料
商品名英語Drug nomenclatureMarsilid, others
AHFS/Drugs.com國際藥品名稱
ATC碼
藥物動力學數據
生物利用度1
識別資訊
  • N-isopropylisonicotinohydrazide
CAS號54-92-2  checkY
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard英語CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.000.199 編輯維基數據鏈接
化學資訊
化學式C9H13N3O
摩爾質量179.22 g·mol−1
3D模型(JSmol英語JSmol
密度1.084 g/cm3
沸點265.9 °C(510.6 °F)
  • O=C(NNC(C)C)c1ccncc1
  • InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13) checkY
  • Key:NYMGNSNKLVNMIA-UHFFFAOYSA-N checkY

N'-異丙基異煙肼是一種有機化合物,化學式為C9H13N3O,其藥品名為異丙煙肼。它是一種肼類非選擇性的不可逆單胺氧化酶抑制劑[1][2]

毒性

[編輯]

該藥物進行過一系列的毒性測試:

生物體 類別 途徑 劑量 (mg/kg) 文獻
LD50 95 Annals of the New York Academy of Sciences. Vol. 80, Pg. 626, 1959.
TDLo 2.143 /D Acta Neurologia et Psychiatrica Belgica. Vol. 59, Pg. 977, 1959.
LDLo 14 /2W-I Canadian Medical Association Journal. Vol. 78, Pg. 131, 1958.
LD50 640 Annals of the New York Academy of Sciences. Vol. 80, Pg. 626, 1959.
小鼠 LD50 肌內 615 American Review of Tuberculosis. Vol. 65, Pg. 376, 1952.
小鼠 LD50 腹膜內 475 Japanese Journal of Pharmacology. Vol. 13, Pg. 186, 1963.
小鼠 LD50 靜脈內 719 American Review of Tuberculosis. Vol. 65, Pg. 376, 1952.
小鼠 LD50 440 Pharmaceutical Chemistry Journal Vol. 30, Pg. 750, 1996.
小鼠 LD50 皮下 730 American Review of Tuberculosis. Vol. 65, Pg. 376, 1952.
LD50 靜脈內 117 American Review of Tuberculosis. Vol. 65, Pg. 376, 1952.
LD50 125 American Review of Tuberculosis. Vol. 65, Pg. 376, 1952.
LDLo 2000 Huntingdon Research Center Reports. Vol. -, Pg. -, 1972.
大鼠 LD50 皮下 538 Japanese Journal of Pharmacology. Vol. 13, Pg. 186, 1963.
大鼠 LD50 未報道 350 Nature. Vol. 185, Pg. 532, 1960.
大鼠 LD50 365 Journal of Pharmacology and Experimental Therapeutics. Vol. 119, Pg. 444, 1957.
大鼠 LD50 腹膜內 375 Arzneimittel-Forschung. Drug Research. Vol. 20, Pg. 363, 1970.

參考文獻

[編輯]
  1. ^ Maxwell RA, Eckhardt SB. Iproniazid. Drug Discovery. Humana Press. 1990: 143–154. ISBN 9780896031807. 
  2. ^ Fagervall I, Ross SB. Inhibition of monoamine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors. Biochemical Pharmacology. April 1986, 35 (8): 1381–1387. PMID 2870717. doi:10.1016/0006-2952(86)90285-6.