T1598

Rimantadine hydrochloride (Meradane) is an RNA synthesis inhibitor that is used as an antiviral agent in the prophylaxis and treatment of influenza.

Mal-PEG2-NH-Boc is a PEG-based linker for PROTACs, joining two essential ligands fundamental for forming PROTAC molecules and facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Mal-PEG2-NH2 is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Mal-PEG2-NHS ester is an indestructible ADC linker used for synthesizing ADC compounds.

Mal-PEG2-PFP ester, an alkyl/ether-based PROTAC linker, facilitates the synthesis of PROTACs.

Mal-PEG2-Val-Cit-amido-PAB-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Mal-PEG3-alcohol is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Mal-PEG3-Boc 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.

Mal-PEG3-NHS ester, a noncleavable ADC linker, possesses a Maleimide group. It serves as a crucial component in the synthesis of antibody-drug conjugates[1].

Mal-PEG3-PFP ester is a PEG-based linker for PROTACs, facilitating the combination of two essential ligands, thereby crucial in the formation of PROTAC molecules. This linker promotes selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

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

VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.

VT-1598 tosylate is a selective, orally active antifungal compound that targets CYP51. It demonstrates efficacy against C. auris.