推薦產品
SMILES 字串
Cl.CN(C)CCCN1c2ccccc2Sc3ccc(cc13)C(F)(F)F
InChI
1S/C18H19F3N2S.ClH/c1-22(2)10-5-11-23-14-6-3-4-7-16(14)24-17-9-8-13(12-15(17)23)18(19,20)21;/h3-4,6-9,12H,5,10-11H2,1-2H3;1H
InChI 密鑰
FTNWXGFYRHWUKG-UHFFFAOYSA-N
基因資訊
human ... DRD2(1813)
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應用
Triflupromazine hydrochloride has been used for the screening of inhibitors of S. mansoni miracidial transformation5. It has also been used to study its intracellular localization in central nervous system cells using secondary ion mass spectrometry microscopy6.
生化／生理作用
Triflupromazine is a D2 dopamine antagonist and a phenothiazine antipsychotic. It is also a potent tranquilizer7 and can significantly reduce body temperature8.
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
個人防護裝備
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
A study of triflupromazine in dominant-lethal, cytogenetic and host-mediated assays.
V A Ray et al.
Mutation research, 18(3), 301-309 (1973-06-01)
D Jovanović-Mićić et al.
European journal of pharmacology, 272(1), 21-30 (1995-01-05)
Intracerebroventricular injection of dopamine (0.5-4.0 mg) produced dose-dependent and short-lasting emesis (1-8 min) in cats, which was abolished after ablation of the area postrema. Relatively selective alpha 2-adrenoceptor antagonists (yohimbine and idazoxan) and a mixed alpha 1- and alpha 2-adrenoceptor
L L Zhang et al.
Biology of the cell, 74(1), 99-103 (1992-01-01)
The intracellular localization of two neurotropic drugs, flunitrazepam (benzodiazepine) and triflupromazine (phenothiazine), was studied by secondary ion mass spectrometry microscopy (SIMS) in three varieties of cells. The images of the intracellular distributions of the two drugs are easily obtained by
The structure of triflupromazine, a phenothiazine 'tranquilizer' drug molecule.
Phelps, D. W., and Cordes, A. W.
Acta Crystallographica Section B, Structural Crystallography and Crystal Chemistry, 30(12), 2812-2816 (1974)
M Tatsumi et al.
European journal of pharmacology, 368(2-3), 277-283 (1999-04-08)
Using radioligand binding techniques, we determined the equilibrium dissociation constants (K(D)) for 37 neuroleptics and one metabolite of a neuroleptic (haloperidol metabolite) for the human serotonin, norepinephrine, and dopamine transporters with [3H]imipramine, [3H]nisoxetine, and [3H]WIN35428, respectively. Among neuroleptics, the four
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