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Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP

" in MedChemExpress (MCE) Product Catalog:

By Targets:	ADC Linker (2) PKA (1)
By Research Areas:	Cancer (4) Cardiovascular Disease (1) Inflammation/Immunology (1)

3

Inhibitors & Agonists

6

Peptides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

Fmoc-Val-Cit-PAB-PNP	ADC Linker	Cancer
Fmoc-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Val-Cit-PAB-PNP has superior plasma stability comparable to that of non-cleavable linkers ^[3].

Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP	ADC Linker	Cancer
Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP is a cleavable linker for synthesis of antibody-drug conjugates (ADCs) .

RI-STAD-2	PKA	Cardiovascular Disease Cancer
RI-STAD-2 is a high-affinity interfering peptide that regulates the subunit RI of protein kinase A (PKA). RI-STAD-2 interferes with the binding of AKAPs and PKA-RI by simulating the interaction between AKAPs' α-helix domain and PKA-RI's dimerization/anchoration (D/D) domain, thereby affecting PKA activity and intracellular localization. RI-STAD-2 can be used to study the role of AKAPs interaction with PKA-RI in pathological processes such as cardiovascular disease and cancer .

Cat. No.	Product Name	Target	Research Area

Fmoc-Gly-Pro-Hyp-OH	Peptides	Others
Fmoc-Gly-Pro-Hyp-OH is a tripeptide that can be used in peptide synthesis .

Fmoc-Gly-Pro-Hyp-OH TFA	Peptides	Others
Fmoc-Gly-Pro-Hyp-OH TFA is a tripeptide that can be used in peptide synthesis .

Azido-PEG3-DYKDDDDK	Peptides	Others
Azido-PEG3-DYKDDDDK is a peptide.

Fmoc-Gly-Pro-Hyp(OtBu)-OH TFA	Peptides	Others
Fmoc-Gly-Pro-Hyp(OtBu)-OH (TFA) is a tripeptide that can be used in peptide synthesis .

Fmoc-Thr(GalNAc(Ac)3-β-D)-OH	Peptides	Inflammation/Immunology Cancer
Fmoc-Thr(GalNAc(Ac)3-β-D)-OH inhibits cancer cell growth, through targeting intricate cancer-specific pathways while simultaneously strengthening immunologic response .

RI-STAD-2	PKA	Cardiovascular Disease Cancer
RI-STAD-2 is a high-affinity interfering peptide that regulates the subunit RI of protein kinase A (PKA). RI-STAD-2 interferes with the binding of AKAPs and PKA-RI by simulating the interaction between AKAPs' α-helix domain and PKA-RI's dimerization/anchoration (D/D) domain, thereby affecting PKA activity and intracellular localization. RI-STAD-2 can be used to study the role of AKAPs interaction with PKA-RI in pathological processes such as cardiovascular disease and cancer .

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