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Cat. No.	Product Name	Target	Signaling Pathways
T9111	8-Azaadenosine	Adenosine deaminase	Metabolism
	8-Azaadenosine 是 ADAR1抑制剂和是 A-to-I 编辑抑制剂。它可阻断 RNA 编辑并抑制甲状腺癌细胞的增殖、3D 生长、侵袭和迁移。
T40153	BAMEA-O16B BAMEA-O16B
	BAMEAO16B is a lipid nanoparticle that incorporates disulfide bonds for efficient delivery of Cas9 mRNA and sgRNA into cells. In the intracellular environment, BAMEAO16B responds to reduction by releasing RNA, facilitating genome editing. This compound is valuable for gene editing research purposes.
T79763	UNC9512	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	UNC9512是一种针对甲基赖氨酸读取器p53结合蛋白1 (53BP1) 的有效拮抗剂, 适用于探究53BP1在DNA修复、基因编辑及肿瘤发生等生物学过程的功能。
T74879	306-N16B
	306-N16B 是一种脂质纳米颗粒，可实现 Cas9 mRNA 和 sgRNA 的系统性协同递送。306-N16B 可将 mRNA 转运至肺内皮细胞。306-N16B 可用于基因组编辑疗法的研究。
T60520	Cas9-IN-3
	Cas9-IN-3 是一种有效的Cas9抑制剂，IC50值为28 μM。CRISPR/Cas 系统彻底改变了多个物种的基因编辑。
T38320	93-O17S 93-O17S
	93-O17S is a chalcogen-containing cationic lipidoid.1It has been used in the synthesis of lipid nanoparticles (LPNs) for the delivery of Cre recombinase and ribonucleoproteins for genome editing in mice. LPNs containing 93-O17S have been used for the intratumoral delivery of cGAMP to enhance cross-presentation of tumor antigens and stimulation of interferon genes (STING) activation in a B16/F10 murine melanoma model.2 1.Li, Y., Yang, T., Yu, Y., et al.Combinatorial library of chalcogen-containin...
T74445	ZA3-Ep10
	ZA3-Ep10是一种两性离子的脂质，用于合成脂质纳米颗粒，用于体内 RNA 传递和非病毒 CRISPR/Cas 基因编辑。
T38319	93-O17O 93-O17O
	93-O17O is a chalcogen-containing cationic lipidoid.1,2It has been used in the generation of lipid nanoparticles (LPNs). LPNs containing 93-O17O localize to the spleen after intravenous injection into mice.1LPNs containing 93-O17O have been used for the delivery of Cre recombinase and ribonucleoproteins for genome editing in mice and for the intratumoral delivery of cGAMP to enhance cross-presentation of tumor antigens.3,2 1.Zhao, X., Chen, J., Qiu, M., et al.Imidazole-based synthetic lipidoids ...
T72764	8-Azanebularine
	8-Azanebularine是通过将C6位的氨基替换为氢的化合物，能在高浓度(IC50=15 mM)下抑制ADAR2活性。该化合物在人类ADAR2识别的RNA结构中插入，展示出高亲和力(KD=2 nM)。因此，8-Azanebularine可应用于研究ADAR催化的RNA编辑过程。