5 Results for "

Phe-Asp

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "Phe-Asp" in MCE Product Catalog:

Cat. No.: HY-P4472
CAS No.: 22828-05-3
Synonyms: Phe-Asp
Target:  

Peptides

Research Areas:  

Others

H-Phe-Asp-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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Cat. No.: HY-W009426
CAS No.: 5262-10-2
Target:  

Drug Intermediate

Research Areas:  

Others

Cyclo(Phe-Asp) is an Aspartame (HY-B0361) impurity.
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Cat. No.: HY-P2376
CAS No.: 102567-19-1
Target:  

ADC Linkers

Research Areas:  

Cancer

Arg-Phe-Asp-Ser is a cleavable ADC linker.
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Cat. No.: HY-P11896
CAS No.: 3081054-30-7
Research Areas:  

Neurological Disease

Tyr-c[D-Lys-p-Br-Phe-Phe-Asp]-D-Pro-NH2 is a MOR-selective antagonist with a pA2 value of 9.9. Tyr-c[D-Lys-p-Br-Phe-Phe-Asp]-D-Pro-NH2 blocks G protein- and β-arrestin2-mediated downstream signaling pathways of MOR. Tyr-c[D-Lys-p-Br-Phe-Phe-Asp]-D-Pro-NH2 significantly delays the development of μ-opioid agonist-induced analgesic tolerance by blocking peripheral MOR. Tyr-c[D-Lys-p-Br-Phe-Phe-Asp]-D-Pro-NH2 is applicable to studies related to opioid receptor function and analgesic tolerance .
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Cat. No.: HY-P11895
CAS No.: 3081054-21-6
Research Areas:  

Neurological Disease

Tyr-c [D-Lys-p-F-Phe-Phe-Asp]-D-Pro-NH2 is a multi-opioid receptor (Opioid Receptor) modulator, acting as a MOR/KOR agonist and a DOR antagonist. Tyr-c [D-Lys-p-F-Phe-Phe-Asp]-D-Pro-NH2 activates the G protein-mediated cAMP inhibitory pathway and β-arrestin2 recruitment pathway downstream of MOR, with an EC50 of 159 nM for β-arrestin2 recruitment, an EC50 of 1.1 nM for MOR-mediated calcium mobilization, and an EC50 of 397 nM for KOR. Tyr-c [D-Lys-p-F-Phe-Phe-Asp]-D-Pro-NH2 exhibits potent analgesic activity in vivo. It can be used in studies related to opioid receptor function and analgesia .
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