Boc-Tyr-Otbu

Name: Boc-Tyr-Otbu | 18938-60-8
Brand: US-CATO
SKU: S57CPTD788141_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD788141_10_MG

Vendor: US-CATO

Product Information

Product Name

Boc-Tyr-Otbu

Brand Name

US-CATO

Product Number

CPTD788141

CAS

18938-60-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

15512828

IUPAC Name

tert-butyl (2S)-3-(4-hydroxyphenyl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoate

InChI Key

WGJGINMQCMATNP-AWEZNQCLSA-N

SMILES

CC(C)(C)OC(=O)C@H(CC1=CC=C(C=C1)O)NC(=O)OC(C)(C)C

References Data Source From Pubchem

Tranilast-tyrosine hybrid molecule exhibits dual activity: suppression of epithelial-mesenchymal transition and induction of cytotoxicity in cancer cells

Publication Name: Medicinal Chemistry Research

Publication Date: 2022-07-29

DOI: 10.1007/s00044-022-02939-2

Photorelease of tyrosine from a-carboxy-6-nitroveratryl (aCNV) derivatives

Publication Name: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Publication Date: 2012-03-01

DOI: 10.1039/c2pp05320a

Lipid Peroxyl Radicals Mediate Tyrosine Dimerization and Nitration in Membranes

Publication Name: Chemical Research in Toxicology

Publication Date: 2010-02-19

DOI: 10.1021/tx900446r

Preparation of two triflate precursors for O-(2-[18F] fluoroethyl)-L-tyrosine used in positron emission tomography (PET)

Publication Name: Science in China Series B: Chemistry

Publication Date: 2009-12-20

DOI: 10.1007/s11426-009-0195-8

Tyrosine nitration, dimerization, and hydroxylation by peroxynitrite in membranes as studied by the hydrophobic probe N-t-BOC-l-tyrosine tert-butyl ester

Publication Name: Methods in enzymology

Publication Date: 2008

DOI: 10.1016/s0076-6879(08)01212-3

Boc-Tyr-Otbu

Product Information

General Information

References Data Source From Pubchem

Tranilast-tyrosine hybrid molecule exhibits dual activity: suppression of epithelial-mesenchymal transition and induction of cytotoxicity in cancer cells

Photorelease of tyrosine from a-carboxy-6-nitroveratryl (aCNV) derivatives

Lipid Peroxyl Radicals Mediate Tyrosine Dimerization and Nitration in Membranes

Preparation of two triflate precursors for O-(2-[18F] fluoroethyl)-L-tyrosine used in positron emission tomography (PET)

Tyrosine nitration, dimerization, and hydroxylation by peroxynitrite in membranes as studied by the hydrophobic probe N-t-BOC-l-tyrosine tert-butyl ester

Boc-Tyr-Otbu

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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Boc-Tyr-Otbu

Product Information

General Information

References Data Source From Pubchem

Tranilast-tyrosine hybrid molecule exhibits dual activity: suppression of epithelial-mesenchymal transition and induction of cytotoxicity in cancer cells

Photorelease of tyrosine from a-carboxy-6-nitroveratryl (aCNV) derivatives

Lipid Peroxyl Radicals Mediate Tyrosine Dimerization and Nitration in Membranes

Preparation of two triflate precursors for O-(2-[18F] fluoroethyl)-L-tyrosine used in positron emission tomography (PET)

Tyrosine nitration, dimerization, and hydroxylation by peroxynitrite in membranes as studied by the hydrophobic probe N-t-BOC-l-tyrosine tert-butyl ester

Boc-Tyr-Otbu

Related Product

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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