DC66528 |
9A1P9 |
9A1P9 is a multi-tail ionizable cationic phospholipid. 9A1P9 induces membrane destabilization. 9A1P9 can be used for CRISPR-Cas9 gene editing in mice. |
|
DC66529 |
ALC-0315 analogue-1 |
ALC-0315 analogue-1 (compound P-10) is a cationic lipid. ALC-0315 analogue-1 is the raw material for synthesis of cationic liposome. |
|
DC60619 |
12T-O14 |
|
|
DC60632 |
Lipid TG6A |
TG6A is a biodegradable and ionizable glycerolipid for cmRNA delivery. TG6A-LNP exhibits above 9-fold and 41-fold higher EGFP protein expression in MSCs than DLin-MC3-DMA-LNP and ALC-0315-LNP, respectively. |
|
DC82210 |
A1-D1-5 |
Lipid A1-D1-5 is an ionizable lipid-like substance used for RNA interference therapy in heat-stable ionizable lipid-like nanoparticles (iLAND) for the treatment of hyperlipidemia. |
|
DC60636 |
Acid-degradable Cationic Lipid (ADC)
Featured
|
Acid-degradable Cationic Lipid (ADC) composed of cationic lipid is synthesized with the azido-acetal linker and used to generate RD-LNPs, which significantly improves the performance of LNP-mRNA complexes in vitro and in vivo. |
|
DC60639 |
Acid-degradable Anionic Lipid (ADA)
Featured
|
ADA (Acid-Degradable Anionic Lipids) is revolutionizing mRNA delivery with its unique azido-acetal linker, enabling rapid hydrolysis in endosomes (pH ~6.0). This breakthrough technology ensures efficient endosomal escape, significantly enhancing mRNA delivery to target cells. ADA-LNPs excel in delivering mRNA to the spleen and liver, making them ideal for immune-related therapies.By degrading into biocompatible byproducts, ADA minimizes long-term tissue persistence and toxicity.ADA-LNPs outperform traditional LNPs, delivering mRNA more effectively to immune cells like macrophages and B cells. |
|
DC66648 |
CP-LC-1143
Featured
|
Lipid CP-LC-1143 is an ionizable cationic amino lipid derived from homocysteine, a naturally occurring amino acid. This lipid has demonstrated an efficient delivery and high protein expression of different kinds of RNA (mRNA, cRNA and saRNA) in vivo, with no signs of toxicity. |
|
DC66649 |
CP-LC-1254 |
|
|
DC66650 |
CP-LC-0729 |
Lipid CP-LC-0729, an ionizable cationic amino lipid synthesized from homocysteine—a naturally occurring amino acid—has been shown to exhibit superior efficacy in the delivery and subsequent protein expression of various RNA modalities, including messenger RNA (mRNA), circular RNA (cRNA), and self-amplifying RNA (saRNA) in vivo. Importantly, CP-LC-0729 demonstrates an exemplary safety profile, with no observable toxicological effects in preclinical studies.
Comparative analyses reveal that CP-LC-0729 significantly surpasses MC3, a widely utilized benchmark lipid nanoparticle formulation, in terms of protein expression efficiency. Specifically, CP-LC-0729 achieves a striking 32-fold enhancement in protein expression within lung tissue relative to MC3, underscoring its pronounced tissue selectivity and targeting efficacy for pulmonary applications. These findings suggest that CP-LC-0729 represents a highly promising candidate for the development of RNA-based therapeutics, particularly in the context of lung-targeted delivery systems, where its combination of high efficiency and low toxicity offers significant translational potential. |
|
DC66651 |
CP-LC-0743 |
Lipid CP-LC-0743 is an ionizable cationic amino lipid derived from homocysteine, a naturally occurring amino acid. This lipid has demonstrated an efficient delivery and high protein expression of different kinds of RNA (mRNA, cRNA and saRNA) in vivo, with no signs of toxicity. |
|
DC66652 |
CP-LC-0867 |
|
|
DC66653 |
C9-200 |
C9-200 is an ionizable cationic lipid that has been used in the formation of lipid nanoparticles (LNPs).1 LNPs containing C9-200 and encapsulating mRNA encoding erythropoietin (EPO) increase serum EPO levels in mice. LNPs containing C9-200 and encapsulating mRNA encoding the Cas9 nuclease and small-guide RNA (sgRNA) targeting transthyretin (TTR) induce 3-fold higher hepatic insertion and deletion (indel) formation than LNPs containing C12-200 (Item No. 36699) and encapsulating mRNA encoding Cas9 in mice. |
|
DC66654 |
Lipid N2-3L |
|
|
DC66655 |
YHS-12 |
YHS-12 is an ionizable cationic lipid (pKa = 6.506) that has been used in the generation of lipid nanoparticles (LNPs) for the delivery of siRNA and mRNA in vitro and in vivo.1 LNPs containing YHS-12 and the macrophage targeting peptide CRVLRSGSC and encapsulating mRNA encoding chimeric antigen receptor targeting methicillin-resistant S. aureus (MRSA) and siRNA targeting caspase-11 increase the phagocytosis rate of MRSA in RAW 264.7 macrophages and primary mouse bone marrow-derived macrophages (BMDMs). Intravenous administration of these LNPs decreases blood bacterial burden and increases survival in a model of sepsis using cyclophosphamide-induced immunosuppressed mice. |
|
DC60662 |
Si6-C14b |
|
|
DC60663 |
Si5-N14
Featured
|
Si5-N14 is a lipid-based molecule engineered with siloxane groups, designed specifically for efficient mRNA delivery to the lungs. The incorporation of siloxane units boosts the cellular uptake of mRNA-loaded lipid nanoparticles (LNPs) and enhances their ability to escape from endosomes. These properties significantly increase the overall effectiveness of mRNA delivery, making Si5-N14 a promising tool for targeted therapeutic applications. |
|
DC60664 |
Si12-C10 |
|
|
DC60670 |
CL4F11-ζ-2 |
|
|
DC60671 |
THP1 |
THP1 is a tetrahydropyrimidine ionizable lipid for mRNA delivery. THP1 demonstrates higher transfection efficiency comparable to DLin-MC3-DMA (MC3). THP1 LNPs also demonstrates the ability to edit genes in specific liver tissues in a tdTomato transgenic mouse model. |
|
DC60673 |
(+)CP-LC-0729 |
|
|
DC60683 |
Lipid-168
Featured
|
Lipid168 is an ionizable lipid nanoparticle (LNP) optimized for in vivo mRNA delivery to human hematopoietic stem cells (HSCs). Designed through systematic structural modifications of head and tail groups in Library A, Lipid-168 demonstrated superior bone marrow (BM) targeting efficiency compared to prior candidates (e.g., LNP-028). When encapsulating ABE8e mRNA and sgRNA targeting the HBG promoter (LNP 168-ABE8e-HBG), it achieved 42.6% base editing efficiency in transfusion-dependent β-thalassemia (TDT) patient-derived HSCs engrafted in NCG-X mice, restoring γ-globin expression and globin chain balance in erythroid cells. To mitigate liver tropism, miR-122T sequences were incorporated into the mRNA 3’UTR, reducing hepatic editing from 71% to 19% while maintaining BM efficacy. In Ai14 mice, LNP-168-Cre-miR-122T mediated efficient tdTomato activation in BM cell subsets, including multipotent progenitors (80% editing). Proteomic analysis revealed a unique protein corona enriched with albumin, fibronectin, and fibrinogen, potentially enhancing BM targeting. Safety assessments showed transient inflammatory cytokine spikes (e.g., TNF-α, IL-6) and liver enzyme elevations post-injection, resolving within 48 hours without cumulative toxicity or anti-Cas9/PEG antibodies. Lipid-168 represents a promising non-viral platform for in vivo HSC editing, enabling one-time treatment of blood disorders without cell mobilization or preconditioning. |
|
DC60684 |
Lipid I97 |
|
|
DC60685 |
313O13 |
|
|
DC60686 |
313oi10 |
|
|
DC99010 |
CAPSTAN Lipid A-11
Featured
|
Compound A-11 (Lipid A11) is a novel ionizable cationic lipid for used for tLNP(targeting antibody LNP) targeting to T cell,with pKa range 6-7, high encapsulation efficiency and high T cell transfection, compared to benchmark ATX-126 and other lipids. |
|
DC67110 |
DOTMA |
DOTMA is a cationic lipid that has been used as a non-viral vector for gene therapy. DOTMA is used as a component of liposomes to encapsulate siRNA, microRNA, and oligonucleotides and for in vitro gene transfection. DOTMA promotes effective interaction between liposomes and cell membranes by inducing positive charge on the liposomes. DOTMA showed good gene transfection effect both in vitro and in vivo. |
|
DC67116 |
80-O14B |
|
|
DC67117 |
113-N16B
Featured
|
113-N16B is an ionizable cationic lipid used for the generation of lipid nanoparticles (LNPs). 113-N16B delivers mRNA preferentially to pulmonary endothelial cells. |
|
DC67118 |
PNI 132 |
|
|