H-Tyr-OMe
H-Tyr-OMe structure
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Common Name | H-Tyr-OMe | ||
|---|---|---|---|---|
| CAS Number | 1080-06-4 | Molecular Weight | 195.215 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 330.0±27.0 °C at 760 mmHg | |
| Molecular Formula | C10H13NO3 | Melting Point | 134-136 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 153.4±23.7 °C | |
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Lipophilicity of basic drugs measured by hydrophilic interaction chromatography.
J. Med. Chem. 52 , 3416-9, (2009) RPLC gains acceptance in pharmaceutical research for the rapid determination of lipophilicity but remains limited for the determination of partition coefficients of moderate to strong basic compounds under their neutral form because stationary phases are not ... |
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Aromatic amino acid methyl ester analogs form quinonoidal species with Dopa decarboxylase.
FEBS Lett. 412(1) , 245-8, (1997) This study reports for the first time that binding of aromatic methyl ester analogs to Dopa decarboxylase in the native and inactive nicked forms causes the appearance of a dead-end quinonoidal species absorbing at 500 nm, in addition to an external aldimine ... |
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A comparative reactivity study of microperoxidases based on hemin, mesohemin and deuterohemin.
J. Inorg. Biochem. 99(3) , 852-63, (2005) Three microperoxidases--hemin-6(7)-gly-gly-his methyl ester (HGGH), mesohemin-6(7)-gly-gly-his methyl ester (MGGH) and deuterohemin-6(7)-gly-gly-his methyl ester (DGGH)--have been prepared as models for heme-containing peroxidases by condensation of glycyl-gl... |
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Enhancement of a kappa-opioid receptor agonist-induced analgesia by L-tyrosine and L-tryptophan.
Eur. J. Pharmacol. 258(3) , 173-8, (1994) The effects of the methyl esters of L-tyrosine (L-Tyr-OMe) and L-tryptophan (L-Trp-OMe) on the analgesic action of trans-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidin)cyclohexyl]-benzene acetamide methane sulfonate (U-50,488H), a kappa-opioid receptor agonist, wer... |
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Two new compounds from an endophytic fungus Aspergillus sp. HS-05.
J. Asian Nat. Prod. Res. 13(3) , 225-9, (2011) Two new compounds, N-[4'-hydroxy-(E)-cinnamoyl]-l-tyrosine methyl ester (1) and methyl 4-methoxy-3-(3'-hydroxy-2'-methyl)propionyloxy-benzoate (2), were isolated from EtOAc extract of the fermentation broth of the endophytic fungus Aspergillus sp. HS-05. Thei... |
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Synthesis and antileishmanial activity of piperoyl-amino acid conjugates.
Eur. J. Med. Chem. 45 , 3439-3445, (2010) Based on reported antileishmanial activity of naturally occurring alkaloid piperine and amino acid esters, their conjugates were synthesized by the hydrolysis of piperine to piperic acid followed by reaction with amino acid methyl esters. These conjugates wer... |
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Efficient functionalization of alginate biomaterials.
Biomaterials 80 , 146-56, (2016) Peptide coupled alginates obtained by chemical functionalization of alginates are commonly used as scaffold materials for cells in regenerative medicine and tissue engineering. We here present an alternative to the commonly used carbodiimide chemistry, using ... |
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Electrochemical, photoelectrochemical, and piezoelectric analysis of tyrosinase activity by functionalized nanoparticles.
Anal. Chem. 80(8) , 2811-6, (2008) The electrochemical and photoelectrochemical detection of tyrosinase (TR) activity (an indicative marker for melanoma cancer cells) is reported, using Pt nanoparticles (NPs) or CdS NPs as electrocatalytic labels or photoelectrochemical reporter units. The Pt ... |
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Enantioselective capillary electrophoretic separation of tryptophane- and tyrosine-methylesters in a dual system with a tetra-oxadiaza-crown-ether derivative and a cyclodextrin.
J. Pharm. Biomed. Anal. 38(4) , 601-8, (2005) Different dual selector systems containing a cyclodextrin derivative (methyl-beta-cyclodextrin and dimethyl-beta-cyclodextrin) and a new diaza-crown-ether derivative (N-[2-(1,4,10,13-tetraoxa-7,16-diazacyclooctadecan-7-yl)propanoyl]glycine) were studied in th... |
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Fabrication of biodegradable poly(ester-amide)s based on tyrosine natural amino acid.
Amino Acids 42(5) , 1997-2007, (2012) N,N'-Bis[2-(methyl-3-(4-hydroxyphenyl)propanoate)]isophthaldiamide (5), a novel diol monomer containing chiral group, was prepared by the reaction of S-tyrosine methyl ester (3) with isophthaloyl dichloride (4a). A new family of optically active and potential... |