poa

Pyrazinamide (Pyrazinecarboxamide) 是一种口服抗结核类抗生素。它是一种前药，通过结核分枝杆菌pncA 基因编码的 PZase/烟酰胺酶转化为活性吡嗪酸形式。

Lipoamide-PEG3-Mal 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.

Lipoamido-PEG2-OH 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.

Lipoamido-PEG3-OH, also known as compound TA-TEG-G2CN, is a PEG-based PROTAC linker utilized in PROTAC synthesis. It is instrumental in the creation of a robust, dendronized gold nanoparticle (AuNP)-based drug delivery platform[1].

Lipoamido-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.

Lipoamido-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.

Lipoamide-PEG11-Mal 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.

Lipoamido-PEG12-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.

Lipoamido-PEG24-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.

Lipoamido-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.

Capoamycin is an insotatracine antibiotic investigated for anti tumor properties.

Apoarantoin is a biochemical.

Tempoacmcta is a peptide.

ApoA-I mimetic peptide (PVLDLFRELLNELLEALKQKLK) 显示出高效激活卵磷脂：胆固醇酰基转移酶（LCAT）的功能，适用于合成肽 脂质复合物。

Poacic Acid 是一种植物衍生且具有抗真菌活性的二苯乙烯类化合物，定位于酵母细胞壁，破坏真菌细胞壁中 β-1,3-葡聚糖的生产和组装。Poacic Acid 对酿酒酵母具有杀菌活性，对质膜受损的突变体具有杀菌活性白色念珠菌。

DAPOA 是一款含叠氮基的点击化学试剂,广泛应用于多肽合成,作为连接剂使用.该化合物可通过 Staudinger 连接法或点击化学技术在叠氮基团上进行进一步的修饰.

Lipoaconitine 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6115，CAS号为 81941-14-2。

Tocofersolan (TPGS) 是合成的 α-生育酚的聚乙二醇衍生物。

Fmoc-Asp-OAll (Fmoc-L-aspartic acid a-allyl ester) 是一种天冬氨酸衍生物。

DCH36_06 ((5E)-1-(3-chloro-4-methylphenyl)-5-[(2E)-3-(furan-2-yl)prop-2-en-1-ylidene]-2-thioxodihydropyrimidine-4,6(1H,5H)-dione) 是一种选择性p300/CBP 抑制剂，介导 p300/CBP 抑制导致白血病细胞中 H3K18 的低乙酰化，有抗肿瘤活性，对p300和CBP 的IC50分别为 0.6 μM 和 3.2 μM。

TPO agonist 1 is a thrombopoietin agonist. It would be useful as promoters of thrombopoiesis and megakaryocytopoiesis to treat thrombocytopenia.

PPO-allene 是一类共价肉毒杆菌毒素 (BoNT) 轻链抑制剂，IC50值为20.9 μM。PPO-allene 以0.3 mg/kg的剂量静脉注射时，在小鼠体内的半衰期大约为1.5小时。

Epothilone A (Epo A) 是紫杉醇和管蛋白聚合物结合的一种竞争性抑制剂，其Ki 值为 0.6-1.4 μM。

Fmoc-Asp(OAll)-OH 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T65759，CAS号为 146982-24-3。