T2891
色胺
≥99%, crystalline
别名:
β-吲哚基乙胺, 3-(2-氨乙基)吲哚
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关于此项目
经验公式（希尔记法）:
C10H12N2
化学文摘社编号:
分子量:
160.22
EC Number:
200-510-5
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
125513
assay
≥99%
form
crystalline
color
white
bp
137 °C/0.15 mmHg (lit.)
mp
113-116 °C (lit.)
storage temp.
−20°C
SMILES string
NCCc1c[nH]c2ccccc12
InChI
1S/C10H12N2/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6,11H2
InChI key
APJYDQYYACXCRM-UHFFFAOYSA-N
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Biochem/physiol Actions
具有血管活性；可能具有神经调质功能。
具有血管活性；可能具有神经调质功能；由色氨酸经 L-芳香氨基酸脱羧酶作用进行脱羧而形成的生物胺。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1A
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
365.0 °F - closed cup
flash_point_c
185 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
A J Greenshaw
Progress in neuro-psychopharmacology & biological psychiatry, 13(3-4), 431-443 (1989-01-01)
1. The relevance of trace amine research is outlined for PEA and T in the context of psychotherapeutic drug action, particularly in relation to the actions of MAO-inhibitor antidepressant drugs. 2. Evidence for the neuronal localization of these amines and
Tryptamine may couple dopaminergic and serotonergic transmission in the brain.
A V Juorio et al.
General pharmacology, 21(5), 613-616 (1990-01-01)
D D Mousseau
Metabolic brain disease, 8(1), 1-44 (1993-03-01)
Although early interest in the biomedical relevance of tryptamine has waned in recent years, it is clear from the above discussion that the study of tryptamine is worthy of serious consideration as a factor in neuropsychiatric disorders. The study of
Kenji Sakota et al.
The Journal of chemical physics, 137(22), 224311-224311 (2012-12-20)
Rearrangement of intermolecular hydrogen bond in a monohydrated tryptamine cation, [TRA(H(2)O)(1)](+), has been investigated in the gas phase by IR spectroscopy and quantum chemical calculations. In the S(0) state of TRA(H(2)O)(1), a water molecule is hydrogen-bonded to the N atom
Weslee S Glenn et al.
Journal of the American Chemical Society, 133(48), 19346-19349 (2011-11-05)
Installing halogens onto natural products can generate compounds with novel or improved properties. Notably, enzymatic halogenation is now possible as a result of the discovery of several classes of halogenases; however, applications are limited because of the narrow substrate specificity
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