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Merck

F7001

Sigma-Aldrich

5-Fluorotryptamine hydrochloride

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About This Item

经验公式(希尔记法):
C10H11FN2 · HCl
CAS号:
分子量:
214.67
EC號碼:
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.32

儲存溫度

−20°C

SMILES 字串

Cl.NCCc1c[nH]c2ccc(F)cc12

InChI

1S/C10H11FN2.ClH/c11-8-1-2-10-9(5-8)7(3-4-12)6-13-10;/h1-2,5-6,13H,3-4,12H2;1H

InChI 密鑰

YZAWADGJXKCLTI-UHFFFAOYSA-N

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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J Sastre Toraño et al.
Biomedical chromatography : BMC, 14(5), 306-310 (2000-08-29)
A validated new and precise reversed-phase high-performance liquid chromatographic method for the determination of melatonin in human plasma and cerebrospinal fluid, with 5-fluorotryptamine as internal standard, is described. Liquid-liquid extraction with dichloromethane was performed under alkaline conditions. After evaporation of
E A Tembe et al.
Parasitology, 106 ( Pt 1), 67-73 (1993-01-01)
5-HT is a candidate for the excitatory transmitter at the neuromuscular junction in trematodes including Fasciola hepatica. This study has determined the response of a muscle strip preparation from Fasciola hepatica to 5-HT and a range of agonists that distinguish
P A Mirau et al.
Biochemistry, 21(4), 615-620 (1982-02-16)
Fluorine-19 nuclear magnetic resonance (19F NMR), optical absorption, and fluorescence spectroscopy have been used to study the interaction of 5-fluorotryptamine (5FTA) with polynucleotides as a model for protein--nucleic acid interactions. In the presence of DNA, denatured DNA, poly(A), and poly(A).poly(U)
Thrombin: active-site topography.
L J Berliner et al.
Annals of the New York Academy of Sciences, 485, 80-95 (1986-01-01)
Kiowa S Bower et al.
European journal of pharmacology, 580(3), 291-297 (2007-12-18)
Antagonists, but not agonists, of the 5-HT3 receptor are useful therapeutic agents, and it is possible that partial agonists may also be potentially useful in the clinic. Here we show that 5-fluorotryptamine (5-FT) is a partial agonist at both 5-HT3A

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