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3-Carboxypropyl-CoA (3-Carboxypropyl coenzyme A) 属于辅酶 A 的衍生物。

3-Hydroxy-5-methylhex-4-enoyl-CoA (3-Hydroxy-5-methylhex-4-enoyl-coenzyme A) 是辅酶 A 的一种衍生物。

2-(2-Naphthylmethyl)succinyl-CoA (Naphthyl-2-methyl-succinyl-CoA) 是辅酶 A 的一种衍生物。

(R)-3-Hydroxydecanoyl-CoA ((R)-3-Hydroxydecanoyl-coenzyme A) 是一种 3-羟基脂肪酰辅酶 A。

(Z)-2,3-Dehydroadipoyl-CoA ((Z)-2,3-Dehydroadipoyl-coenzyme A) 是一种具有顺式结构的2-烯酰辅酶 A。

(R)-3-Hydroxytetradecanoyl-CoA ((R)-3-Hydroxytetradecanoyl-coenzyme A) 是一种化合物，属于3-羟基脂肪酰辅酶 A，由辅酶 A 的巯基和 (R)-3-羟基十四烷酸的羧基缩合形成。

(Methylenecyclopropyl)acetyl-CoA (S-(2-Methylenecyclopropyl)acetyl-CoA) 是辅酶A的一个衍生物。

2,6-Dihydroxycyclohexane-1-carbonyl-CoA (2,6-Dihydroxycyclohexane-1-carbonyl-coenzyme A) 是一种酰基辅酶 A。

(R)-2-Hydroxybutanoyl-CoA ((R)-2-Hydroxybutanoyl-coenzyme A) 是羟基脂肪酰辅酶 A 的一种形式。

(R)-3-Hydroxypimelyl-CoA ((R)-3-Hydroxypimelyl coenzyme A) 是辅酶 A 的一种衍生物。

3,5,7-Trioxododecanoyl-CoA (3,5,7-Trioxododecanoyl-coenzyme A) 是一种氧化的脂肪酰辅酶 A。

12-Hydroxyoctadecanoyl-CoA (12-Hydroxyoctadecanoyl-coenzyme A) 是一种羟基脂肪酰辅酶 A。

12-Methyltridecanoyl-CoA (12-Methyltridecanoyl-coenzyme A) 是一种由辅酶 A 衍生而成的化合物。

11Z-Tetradecenoyl-CoA 是辅酶 A 的一种衍生物。

N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide 是化合物TT3 的类似物。TT3 是一种可电离的类脂材料，专门用于传递mRNA。

NH2-PEG8-COOMe 是一种用于药物递送研究的生化试剂。

TCL065是一种可离子化阳离子脂质（pKa = 6.3），用于在体内和体外生成脂质纳米颗粒（LNPs）以递送mRNA和单向导RNA（sgRNA）。含有TCL065的LNPs，可封装靶向dystrophin外显子45供体位点的sgRNA，与含有TCL065的LNPs封装靶向dystrophin外显子45剪接受体位点的sgRNA一起使用，能够恢复从杜氏肌营养不良症（DMD）患者分离的诱导多能干细胞（iPS）分化的成肌细胞中的dystrophin表达。含有TCL065的LNPs，封装编码Cas9核酸酶的mRNA，与含有TCL065并封装靶向Rosa26位点的单向导RNA的LNPs联合使用，已用于在小鼠腓肠肌中诱导CRISPR介导的基因编辑。

S-[2-[[2-(1H-Indol-3-yl)ethyl]amino]-2-oxoethyl]-COA (S-[2-[[2-(1H-Indol-3-yl)ethyl]amino]-2-oxoethyl]-coenzyme A) 是辅酶 A 的一种衍生形式。

Thiol-PEG4-NH2 (SH-PEG4-NH2) 是一种 PEG 衍生物，由巯基 (-SH) 和 NH2 基团通过1 个 PEG 单元连接而成。巯基具有高度活性，能够与多种分子进行特异性反应，形成稳定的共价键。

Fumarprotocetraric acid是一种可用于生命科学研究的天然产物。

Sabinyl Acetate是一种可用于生命科学研究的天然产物。

Resmethrin, a synthetic pyrethroid insecticide, is used against a variety of insects.

CCW 28-3 is a novel potent covalent BRD4 degrader, degrading BRD4 in a proteasome- and RNF4-dependent manner without inhibiting RNF4 autoubiquitination activity.

cis-VZ 185 is a negative control for VZ 185.

Quizartinib, also know as AC220 and AC010220, is an orally available FLT3 / STK1 inhibitor with potential antineoplastic activity. Class III receptor tyrosine kinase inhibitor AC220 selectively inhibits class III receptor tyrosine kinases, including FMS-related tyrosine kinase 3 (FLT3/STK1), colony-stimulating factor 1 receptor (CSF1R/FMS), stem cell factor receptor (SCFR/KIT), and platelet derived growth factor receptors (PDGFRs), resulting in inhibition of ligand-independent leukemic cell proliferation and apoptosis. Mutations in FLT3, resulting in constitutive activation, are the most frequent genetic alterations in acute myeloid leukemia (AML) and occur in approximately one-third of AML cases.

2-(2,6-Dioxopiperidin-3-yl)-5-ethynylisoindoline-1,3-dione 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 T64589，CAS号为 2154356-63-3。

Methanesulfonato(diadamantyl-n-butylphosphino)-2'-amino-1,1'-biphenyl-2-yl)palladium(II) 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 T64620。

Amyloid precursor c-terminal peptide has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. APP is best known as the precursor molecule whose proteolysis generates beta-amyloid (Aβ), a 37 to 49 amino acid peptide whose am

Dap-NE hydrochloride为一种二肽盐酸盐，功能作为可降解（cleavable）的ADC Linker。该化合物适用于抗体（Antibody）与毒素分子（Cytotoxin）的连接，用以合成抗体偶联活性分子（ADC）。

N-Carbobenzoxy-L-homoserine (N-(Benzyloxycarbonyl)-L-homoserine) 作为一种带有 N-Carbobenzoxy保护基团的L-homoserine，常用作连接子 (ADC Linker) 以用于抗体药物偶联物 (Antibody-Drug Conjugates (ADCs)) 的合成。

Propargyl-PEG4-CH2CO2-NHS is a PEG derivative containing a propargyl group and an NHS group. The hydrophilic PEG spacer increases solubility in aqueous media.

TAT-PDHPS1是一种针对Yes-associated protein (YAP) 信号的肽抑制剂。它由内源性肽PDHPS1和能穿透细胞的肽序列TAT组成。PDHPS1与蛋白磷酸酶2磷酸酶激活因子(PTPA)结合, 激活蛋白磷酸酶2A (PP2A)。该激活促进YAP的磷酸化和抑制YAP靶向基因的表达。TAT-PDHPS1能够抑制体外卵巢癌细胞的增殖和小鼠皮下异种移植肿瘤模型中的卵巢肿瘤生长。

Pyraziflumid is a fungicide. Pyraziflumid is a novel member of succinate dehydrogenase inhibitor fungicides (SDHI). The average EC50 value was 0.0561 (±0.0263)μg/ml for mycelial growth. There was no cross-resistance between pyraziflumid and the widely used fungicides carbendazim, dimethachlon and the phenylpyrrole fungicide fludioxonil.

Cilazapril, also known as Ro 31 2848, is a potent ACE inhibitor used for hypertension. Cilazapril is a prodrug that is hydrolyzed after absorption to its main metabolite cilazaprilat. Cilazapril is a monoethyl ester, which acts as an angiotensin-converting enzyme (ACE) inhibitor. The inhibitor functions by inhibiting the ability of ACE to cleave bonds of angiotensin I and Hip-His-Leu. It is known that the diacid form of Cilazapril is more potent that enalapril at inhibiting ACE.

Avorelin acetate is a luteinizing hormone releasing hormone (LH-RH) agonist.

Vernolepin is a natural reversible plant growth inhibitor.