Z-Glu-Tyr-OH

Name: Z-Glu-Tyr-OH
Brand: Creative Peptides
SKU: CP27732
Availability: MadeToOrder

Z-Glu-Tyr-OH can be used for synthesis of peptides on a solid support.

Please kindly note that our products and services can only be used to support research purposes (Not for clinical use).

CAT No: CP27732

CAS No: 988-75-0

Synonyms/Alias: Z-GLU-TYR-OH;988-75-0;Benzyloxycarbonylglutamyltyrosine;Benzyloxycarbonyl-Glu-Tyr;EINECS 213-582-8;NSC 89651;Z-Glu-Tyr;Benzyloxycarbonyl-glutamyl-L-tyrosine;(4S)-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxo-4-(phenylmethoxycarbonylamino)pentanoic acid;MFCD00037189;Z-L-Glu-L-Tyr;SCHEMBL6552944;BDBM36122;AKOS024375447;DA-59274;FG110840;MS-28005;HY-131095;CS-0128297;NS00042566;L-Tyrosine,N-[(phenylmethoxy)carbonyl]-L-a-glutamyl-;N-(N-((Benzyloxy)carbonyl)-L-alpha-glutamyl)-L-tyrosine;(4S)-4-{[(BENZYLOXY)CARBONYL]AMINO}-4-{[(1S)-1-CARBOXY-2-(4-HYDROXYPHENYL)ETHYL]CARBAMOYL}BUTANOIC ACID;

Chemical Name: (4S)-5-[[(1S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]amino]-5-oxo-4-(phenylmethoxycarbonylamino)pentanoic acid

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Specification Technical Data Publications Customer reviews and Q&A

M.F/Formula	C22H24N2O8
M.W/Mr.	444.4
Sequence	One Letter Code:EY Three Letter Code:Cbz-Glu-Tyr-OH
Application	Building Blocks

Long-term Storage Conditions	Soluble in DMSO
Shipping Condition	Room temperature in continental US; may vary elsewhere.
InChI	InChI=1S/C22H24N2O8/c25-16-8-6-14(7-9-16)12-18(21(29)30)23-20(28)17(10-11-19(26)27)24-22(31)32-13-15-4-2-1-3-5-15/h1-9,17-18,25H,10-13H2,(H,23,28)(H,24,31)(H,26,27)(H,29,30)/t17-,18-/m0/s1
InChI Key	XLUMOZQZGPJGTL-ROUUACIJSA-N
Canonical SMILES	C1=CC=C(C=C1)COC(=O)NC(CCC(=O)O)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)O
Isomeric SMILES	C1=CC=C(C=C1)COC(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)O
References	1. Rose Haddoub, et al. Enzymatic Synthesis of Peptides on a Solid Support. Org Biomol Chem

1. Peptides as Active Ingredients: A Challenge for Cosmeceutical Industry

2. An interdomain binding site on HIV-1 Nef interacts with PACS-1 and PACS-2 on endosomes to down-regulate MHC-I

3. Genetic, cellular, and structural characterization of the membrane potential-dependent cell-penetrating peptide translocation pore

4. Uncarboxylated osteocalcin decreases insulin-stimulated glucose uptake without affecting insulin signaling and regulators of mitochondrial biogenesis in myotubes

5. Myotropic activity and immunolocalization of selected neuropeptides of the burying beetle Nicrophorus vespilloides (Coleoptera: Silphidae)

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