xl-147 derivative 1

L-Threonine derivative-1 是乙酰水杨酸-L-苏氨酸酯，具有潜在的镇痛活性。

Betulinic acid derivative-1 demonstrates potent inhibition of osteoclast (OC) differentiation, achieving an IC50 value of 1.86 μM.

Kobusine derivative-1，一种Kobusine衍生物，展现出了对癌细胞显著的抗增殖活性。

Heterocyclyl carbamate derivative 1, a heterocyclyl carbamate derivative, is used for the research of neurological diseases and inflammatory.

Pyridazinediones-derivative-1 has potential in treating neurodegenerative disorders.

Ebselen derivative 1 (Compound 19) 作为一种口服活性的谷胱甘肽过氧化物酶 (GPx) 模拟物，在体外和体内均显示出对顺铂诱导的毛细胞 (HC) 损伤的显著保护效果。它不仅可有效减轻毛细胞的氧化应激和凋亡 (apoptosis)，还能减轻铁死亡。此化合物被广泛用于研究顺铂诱导的听力损失。

BCL-xL BCL-2 ligand 1 (compound 72-1) 作为BCL-xL和BCL-2蛋白的配体，能够通过连接子与E3连接酶结合，从而形成PROTAC。

Hydrocarbon chain derivative 1 has inhibitory activities against lipid synthesis.

OT antagonist 1 demethyl derivative, a demethyl derivative of OT antagonist 1, is a selective Oxytocin antagonist with a Ki of 50 nM.

Benzylbenzofuran derivative-1 (Compound 8)是从Silene conoidea中分离的一种苯甲酰基苯并呋喃衍生物。

PROTACBcl-xL ligand-1 是Bcl-xL 的配体，可用于PROTAC 的合成。

PROTACBcl-xL degrader-1是一种针对Bcl-xL（Bcl-2家族成员）的PROTAC，具备配体结合基团、linker以及IAPE3连接酶结合基团。这种化合物是一个有效的Bcl-xL降解剂，对人血小板和MyLa 1929细胞显示出明显的毒性，其IC50值分别为62 nM和8.5 μM。

Carbazole derivative 1 is used to reduce androgen or oestrogen levels in mammals.

Diarylalkane derivative 1 is used for the research of pancreatitis.

Cyclosporin A-Derivative 1 (Free base) is a crystalline intermediate derived from the opening of cyclosporin A.

Benzamide Derivative 1 苯甲酰胺衍生物，具有胃动力学活性。Benzamide Derivative 1可用于研究胃肠疾病。

Hemiasterlin Derivative-1, a derivative of hemiasterlin, is utilized in the synthesis of Antibody-Drug Conjugates (ADC).

Oleanolic acid derivative 1 is a modified form of oleanolic acid.

Glycerol derivative 1 is a Glycerol derivative.

Cyclosporin A-Derivative 1 is a crystalline intermediate derived from the opening of cyclosporin A.

Exendin derivative 1, a 39-amino acid peptide, is a chemical compound known for its significant biological activity and therapeutic potential.

PI3K-IN-1 (Voxtalisib Analogue) 是 PI3K 抑制剂，PI3K-IN-1(25 μM) 能够阻断 PI3K Akt 信号通路。