critical

BAI1 是一种选择性凋亡因子BAX 变构抑制剂。它结合 BAX 并变构抑制其激活，具有潜力研究 BAX 依赖性细胞死亡介导的疾病。

Ritodrine hydrochloride (NSC 291565) 是一种 β-2肾上腺素受体激动剂。

Ethyl oleate 是由油酸和乙醇的缩合形成的脂肪酸酯。它是纳米结构脂质载体 (NLC) 中的液体脂质成分。其中 NLC 是一种口服有活性的反式阿魏酸的给药载体。

L-Glutamic acid monosodium salt monohydrate （MSG monohydrate）是一种重要的食品添加剂，具有胃肠道保护作用，在营养代谢、能量需求、免疫响应、氧化应激、信号通路调节及突触传递中有重要作用。L-Glutamic acid monosodium salt monohydrate 诱导小鼠肝脏和脑组织氧化应激、DNA损伤和细胞凋亡。L-Glutamic acid monosodium salt monohydrate 可通过多种机制保护非甾体抗炎药及幽门螺杆菌引起的胃肠道损伤。

Ampicillin sodium (Domicillin) 是Ampicillin 的钠盐形式，是Ampicillin 的广谱半合成衍生物。它通过与青霉素结合蛋白结合来抑制细菌细胞壁的合成，从而抑制肽聚糖的合成，肽聚糖是细菌细胞壁的关键成分。

Abametapir (BRN 0123183) 是一种金属蛋白酶抑制剂，能够靶向对卵孵化和虱子发育至关重要的金属蛋白酶。

SKF-96365 hydrochloride (SKF96365) 是store-operated Ca2+entry 抑制剂，也是TRP channel 阻滞剂。它显著抑制豚鼠离体心脏 hERG、hKCNQ1 hKCNE1、hKir2.1 和 hKv4.3 电流，延长QTc 间期。它通过诱导结直肠癌细胞的细胞周期阻滞和凋亡起抗肿瘤作用。

1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中，具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。

Pulsatilla saponin D (Hederacolchiside A) 是从朝鲜白头翁根部分离得到的一种天然产物，具有抗癌活性。

NADP，也称为烟酰胺腺嘌呤二核苷酸磷酸，是各种代谢过程中电子转移所必需的重要氧化还原辅因子。 它在促进细胞能量产生和维持细胞内氧化还原平衡方面发挥着关键作用。

Necrosulfonamide ((E)-Necrosulfonamide) 是一种坏死性凋亡抑制剂，通过选择性靶向(MLKL)，可阻止 MLKL-RIP1-RIP3 坏死小体复合体与其下游效应子相互作用。MLKL 是诱导坏死过程中 RIP3 的重要底物。

M2I-1 是Mad2抑制剂，靶向的 Mad2 与 Cdc20 的结合，该结合是纺锤体装配检查点内必不可少的蛋白-蛋白相互作用。

HIV-1 integrase inhibitor 8 是一种 HIV-1 整合酶抑制剂，整合是HIV 复制的必要步骤。

16,16-Dimethyl prostaglandin E2 is an orally active vertebrate Hematopoietic stem cells homeostasis critical regulator. It can act through EP2 EP4 and has an interaction with the Wnt pathway.

Guanosine-5'-triphosphate disodium salt (5'-GTP disodium salt) 是肌原性细胞分化的增强剂，也是翻译和其他重要细胞过程的能量来源。

Afabicin is the prodrug of Debio1452. Debio1452 is an inhibitor FabI, an enzyme critical to fatty acid biosynthesis in staphylococci.

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

Aminooxy-PEG4-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Aminooxy-PEG8-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

APN-C3-PEG4-alkyne is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azide-PEG7-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG1-PFP ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG5-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Bis-PEG4-sulfonic acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.