poa

Pyrazinamide (Pyrazinecarboxamide), an antimycobacterial, is utilized therapeutically as an antitubercular agent, which is a synthetic pyrazinoic acid amide derivative.

Lipoamide-PEG3-Mal is a PEG-based linker for PROTACs that joins two essential ligands, which are crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Lipoamido-PEG2-OH is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Lipoamido-PEG3-OH, also known as compound TA-TEG-G2CN, is a PEG-based PROTAC linker utilized in PROTAC synthesis. It is instrumental in the creation of a robust, dendronized gold nanoparticle (AuNP)-based drug delivery platform[1].

Lipoamido-PEG4-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Lipoamido-PEG4-azide is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Lipoamide-PEG11-Mal is a PEG-based linker used in PROTACs, joining two essential ligands crucial for the formation of PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system [within cells].

Lipoamido-PEG12-acid is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Lipoamido-PEG24-acid is a PEG-based linker for PROTACs that connects two essential ligands, facilitating selective protein degradation through the ubiquitin-proteasome system within cells.

Lipoamido-PEG8-acid is a PEG-based linker for PROTACs, joining two essential ligands to facilitate PROTAC molecule formation and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Capoamycin is an insotatracine antibiotic investigated for anti tumor properties.

Apoarantoin is a biochemical.

Tempoacmcta is a peptide.

The ApoA-I mimetic peptide (PVLDLFRELLNELLEALKQKLK) exhibits potent activation of lecithin:cholesterol acyl transferase (LCAT). It is also utilized in the synthesis of peptide lipid complexes [1] [2].

Poacic Acid is a plant-derived stilbenoid exhibiting antifungal activity by localizing to the yeast cell wall and disrupting the production and assembly of β-1,3-glucan in fungal cell walls. It shows fungicidal activity against Saccharomyces cerevisiae and plasma membrane-compromised Candida albicans mutants [1].

DAPOA is a click chemistry reagent containing an azido group. It serves as a linker in peptide synthesis and can be further modified on the azido group through Staudinger ligation or click chemistry.

Lipoaconitine is a natural product for research related to life sciences. The catalog number is TN6115 and the CAS number is 81941-14-2.

MDL 72527 (N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride) is a polyamine oxidase (POA) inhibitor

1,1,1,1-Kestohexaose (1,1,1,1-Kestohexose) is a natural product isolated from Poa ampla.

Fructo-oligosaccharide DP7 GF6 (Fructoheptasaccharide) belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=7).