Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H12N2O2 |
| Molecular Weight | 180.2038 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CC1=CC=C(O)C=C1)C(N)=O
InChI
InChIKey=PQFMNVGMJJMLAE-QMMMGPOBSA-N
InChI=1S/C9H12N2O2/c10-8(9(11)13)5-6-1-3-7(12)4-2-6/h1-4,8,12H,5,10H2,(H2,11,13)/t8-/m0/s1
| Molecular Formula | C9H12N2O2 |
| Molecular Weight | 180.2038 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| In vitro selection of DNA aptamers that bind L-tyrosinamide. | 2001 Oct |
|
| Spectroscopic properties of tyrosyl radicals in dipeptides. | 2002 May 15 |
|
| Probing the binding specificity of C-type lectins in vivo. | 2003 |
|
| Antineoplastic agents. 487. Synthesis and biological evaluation of the antineoplastic agent 3,4-methylenedioxy-5,4'-dimethoxy-3'-amino-Z-stilbene and derived amino acid amides. | 2003 Feb 13 |
|
| Chemolabile cellular microarrays for screening small molecules and peptides. | 2004 |
|
| Immobilized DNA aptamers as target-specific chiral stationary phases for resolution of nucleoside and amino acid derivative enantiomers. | 2004 Feb 15 |
|
| Influence of alkyl group on amide nitrogen atom on fluorescence quenching of tyrosine amide and N-acetyltyrosine amide. | 2004 Oct 1 |
|
| Enzymatic copolymerization alters the structure of unpolymerized mixtures of the biomimetic monomers: the amphiphilic decyl ester of L-tyrosine and L-tyrosineamide--an AFM investigation of nano- to micrometer-scale structure differences. | 2004 Sep-Oct |
|
| NF-kappaB pathway protects cochlear hair cells from aminoglycoside-induced ototoxicity. | 2005 Mar 1 |
|
| Simultaneous delivery of doxorubicin and gemcitabine to tumors in vivo using prototypic polymeric drug carriers. | 2009 Jul |
|
| Glycan labeling strategies and their use in identification and quantification. | 2010 Aug |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 16 21:57:05 UTC 2022
by
admin
on
Fri Dec 16 21:57:05 UTC 2022
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| Record UNII |
05LU01CS4T
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| Record Status |
Validated (UNII)
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| Record Version |
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4985-46-0
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05LU01CS4T
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151243
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21412
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DB03380
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DTXSID70198120
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| Related Record | Type | Details | ||
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ENANTIOMER -> ENANTIOMER |
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