69575
O-Methyl-D-tyrosine
≥99.0% (NT)
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C10H13NO3
Numer CAS:
Masa cząsteczkowa:
195.22
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
3201704
MDL number:
Pomoc techniczna
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Pozwól nam pomócassay
≥99.0% (NT)
optical activity
[α]20/D +7.0±1°, c = 1% in 5 M HCl
SMILES string
COc1ccc(C[C@@H](N)C(O)=O)cc1
InChI
1S/C10H13NO3/c1-14-8-4-2-7(3-5-8)6-9(11)10(12)13/h2-5,9H,6,11H2,1H3,(H,12,13)/t9-/m1/s1
InChI key
GEYBMYRBIABFTA-SECBINFHSA-N
Klasa składowania
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
L Wang et al.
Science (New York, N.Y.), 292(5516), 498-500 (2001-04-21)
A unique transfer RNA (tRNA)/aminoacyl-tRNA synthetase pair has been generated that expands the number of genetically encoded amino acids in Escherichia coli. When introduced into E. coli, this pair leads to the in vivo incorporation of the synthetic amino acid
M Manning et al.
Journal of peptide science : an official publication of the European Peptide Society, 7(9), 449-465 (2001-10-06)
We report the solid phase synthesis of four pairs of L- and D-thienylalanine (Thi/D-Thi) position two modified analogues of the following four oxytocin (OT) antagonists: des-9-glycinamide [1-(beta-mercapto-beta,beta-pentamethylene propionic acid), 2-O-methyltyrosine, 4-threonine]ornithine-vasotocin (desGly(NH2)9,d (CH2)5[Tyr(Me)2,Thr4]OVT) (A); the Tyr-(NH2)9 analogue of (A), d(CH2)5[Tyr(Me)2,Thr4,Tyr-(NH2)9]OVT
S E Shoelson et al.
The Journal of biological chemistry, 264(14), 7831-7836 (1989-05-15)
The receptors for insulin and epidermal growth factor undergo tyrosine autophosphorylation in response to ligand stimulation, while pp60v-src is an unregulated tyrosine kinase. In this report we show that each of the kinases phosphorylates an exogenous peptide that corresponds to
Jeffrey K Takimoto et al.
ACS chemical biology, 6(7), 733-743 (2011-05-07)
Unnatural amino acids (Uaas) can be translationally incorporated into proteins in vivo using evolved tRNA/aminoacyl-tRNA synthetase (RS) pairs, affording chemistries inaccessible when restricted to the 20 natural amino acids. To date, most evolved RSs aminoacylate Uaas chemically similar to the
Deqiang Zhang et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(10), 6579-6584 (2002-05-16)
Although incorporation of amino acid analogs provides a powerful means of producing new protein structures with interesting functions, many amino acid analogs cannot be incorporated easily by using the wild-type aminoacyl-tRNA synthetase (aaRS). To be able to incorporate specific amino
Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.
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