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。

Lipoamide dehydrogenase, porcine 是一种关键的生物催化剂，用于新生物催化技术。酶工程专注于提高酶反应动力学、底物选择性以及在恶劣条件下（例如低或高 pH）的活性。通过对这些酶进行修饰，加入刺激响应性，可以实现对活性的动态控制。

DAPOA DCHA 是一种叠氮化物的点化学试剂，用于多肽合成，作为连接剂。通过 Staudinger 连接法或点击化学可以对其叠氮基团进行进一步修饰。这种材料可作为树状结构的构建砌块，含有 Azide 基团，能够与含有 Alkyne 基团的分子进行铜催化的叠氮-炔环加成反应（CuAAc）。此外，它也能与含有 DBCO 或 BCN 基团的分子发生环张力促进的炔-叠氮环加成反应（SPAAC）。

Thioctamide (Thioctic acid amide) 是 6, 8-dithiooctanoic amide 的俗称。它是 6, 8-dithiooctanoic amide 的功能形式，其中羧基通过酰胺键（包含 -NH2）与蛋白质（或任何其他胺）连接。

Flibanserin (Girosa) 一种具有口服活性的 5-HT1A 受体激动剂和 5-HT2A 受体拮抗剂，Ki 值分别为 1 和 49 nM。它与多巴胺 D4 受体结合，Ki 值在 4 到 24 nM 之间。它是一种血清素能抗抑郁药，用于治疗性欲减退症。

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。