Lipids

BP Lipid 424 is a symmetric polar lipid featuring a two unsaturated oleic acid tails and a DBCO group for click chemistry. This compound may be used for bioconjugation and surface modification applications, or as a useful synthetic scaffold for novel lipids. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

Val-Cit-PAB-MMAE is a derivatized linker-payload that can be used in the creation of antibody-drug conjugates (ADCs). It contains a cathepsin-cleavable Val-Ala dipeptide and an MMAE payload, which is a synthetic antineoplastic agent that can be attached to a monoclonal antibody (MAB) which directs it toward cancer cells. The azide moiety can react with alkyne, BCN, and DBCO via Click Chemistry to yield a stable triazole linkage. The PEG spacer enhances the water-solubility of the compound and may aid in optimizing DMPK properties. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

An ionizable lipid featuring a two biodegredable ester linkages to unsaturated oleic acid tails. Additional features include a core hydroxyl group to promote hydrogen-bonding with neighboring lipids. This compound may be used in the formulation of lipid nanoparticles (LNP's) for delivery applications. Reagent grade, for research purpose.

Phthalimidooxy-PEG4-NHS ester is a protected aminooxy compound with an NHS ester-linked to a Phthalimide moiety via four discrete PEG units. It enables the installation of a hydrophilic, protected aminooxy group on peptides, proteins, small molecules, and amine-functionalized surfaces. Upon deprotection, the aminooxy group forms stable oxime bonds with aldehydes and ketones. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

Tetra(-amido-PEG11-DBCO)pentaerythritol constitutes a branched PEG linker with terminal DBCO groups that react azides via copper-free catalyzed click chemistry. The PEG arms elevate hydrophilicity and help fine-tune DMPK properties.

m-PEG12-amido-PEG24-DSPE serves as a polyPEG compound conjugated with DSPE. The DSPE-PEGs have been FDA approved for medical applications. The hydrophobic properties of the DSPE allow for the encapsulation and congregation of other hydrophobic drugs. The hydrophilic PEG linkers improve the water solubility of the overall compound allowing for the delivery of the drug.

MAL-PEG24-amido-PEG24-TFP ester functions as a long heterobifunctional PEG linker featuring a terminal thiol-reactive maleimide group and TFP ester, which can react with primary amine groups and is less susceptible to undergo hydrolysis compared to NHS ester. The PEG chain elevates the hydrophilicity of the compound and helps fine-tune DMPK properties.

m-PEG25-DSPE represents a polyPEG reagent conjugated with DSPE, approved by the FDA for medical applications. The hydrophobic DSPE encapsulates hydrophobic drugs, while the hydrophilic PEG linkers enhance water solubility for effective drug delivery.

DBCO-PEG24-amido-PEG24-DSPE represents a polyPEG lipid with a terminal DBCO group that reacts azides via copper-free catalyzed click chemistry and DSPE, which is approved by the FDA for medical applications. The hydrophobic DSPE encapsulates hydrophobic drugs, while the hydrophilic PEG linkers increase water solubility for effective drug delivery.