T3629
DL-间酪氨酸
≥98% (HPLC)
别名:
(±)-2-氨基-3-(3-羟基苯基)丙酸, 3-(3-羟基苯基)-DL-丙氨酸
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关于此项目
线性分子式:
HOC6H4CH2CH(NH2)CO2H
化学文摘社编号:
分子量:
181.19
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
212-270-9
MDL number:
Beilstein/REAXYS Number:
2416853
产品名称
DL-间酪氨酸, crystalline
InChI key
JZKXXXDKRQWDET-UHFFFAOYSA-N
InChI
1S/C9H11NO3/c10-8(9(12)13)5-6-2-1-3-7(11)4-6/h1-4,8,11H,5,10H2,(H,12,13)
SMILES string
NC(Cc1cccc(O)c1)C(O)=O
assay
≥98% (HPLC)
form
crystalline
color
off-white to yellow
mp
280-285 °C (dec.) (lit.)
solubility
1 M HCl: soluble
application(s)
detection
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Catecholamines and dihydroxyphenylalanine in metamorphosing larvae of the nudibranch Phestilla sibogae Bergh (Gastropoda: Opisthobranchia).
Pires A, Coon SL, Hadfield MG.
J. Comp. Physiol., 181, 187-194 (1997)
A Pappa-Louisi et al.
Methods in molecular biology (Clifton, N.J.), 828, 101-114 (2011-11-30)
The combined use of a dual-UV detector as well as a fluorimetric and a multielectrode electrochemical detector (equipped with a dual electrode, consisting of a conventional size 3 mm diameter glassy carbon electrode (GCE) and of a pair of 30
P Manini et al.
The Journal of organic chemistry, 66(15), 5048-5053 (2001-07-21)
In 0.1 M phosphate buffer at pH 7.4 and 37 degrees C, the tyrosine metabolite L-3,4-dihydroxyphenylalanine (L-DOPA) reacts smoothly with D-glucose to afford, besides diastereoisomeric tetrahydroisoquinolines 1 and 2 by Pictet-Spengler condensation, a main product shown to be the unexpected
Tengfang Huang et al.
Phytochemistry, 75, 60-66 (2011-12-24)
m-Tyrosine is a non-protein amino acid that is structurally similar to the common protein amino acids p-tyrosine and phenylalanine. Copious amounts of m-tyrosine can be found in root exudates of the fine fescue cultivar, Festuca rubra L. ssp. commutata (Chewings
Philip H Elsinga et al.
Current medicinal chemistry, 13(18), 2139-2153 (2006-08-22)
The dopaminergic system plays a major role in neurological and psychiatric disorders such as Parkinson's disease, Huntington's disease, tardive dyskinea and schizophrenia. Knowledge on altered dopamine synthesis, receptor densities and status are important for understanding the mechanisms underlying the pathogenesis
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