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
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
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
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)
Paola Manini et al.
Carbohydrate research, 340(18), 2719-2727 (2005-10-19)
The reactions of 5-S-cysteinyldopa, L-alpha-methyldopa and DL-m-tyrosine with D-glucose were investigated at 90 degrees C in phosphate buffer at pH ranging from 5.0 to 9.0. Whereas gave mainly the double Maillard condensation product N,N'-bis(1''-deoxy-D-fructos-1''-yl)-5-S-cysteinyldopa, as an inseparable mixture of beta-D-fructopyranosyl
Jae B Park et al.
Cancer letters, 202(2), 161-171 (2003-12-04)
N-Cinnamoyltyramine, N-caffeoyltyramine, N-feruloyltyramine, and N-sinapoyltyramine were synthesized and investigated to identify the most potent compound with anti-proliferation effect on HL-60, U937 and Jurkat cells. N-Caffeoyltyramine was the most potent with GI(50)=10 microM. The treatment of the cells with N-caffeoyltyramine activated
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