modified mmaf-c-5-cooh

5-ETHYL-4,5,6,7-TETRAHYDRO-THIAZOLO[5,4-C]PYRIDIN-2-YLAMINE 靶向 PLK1。

3-(9-Chloro-3-methyl-4-oxoisoxazolo[4,3-c]quinolin-5(4H)-yl)-N-(3,4,5-trimethoxyphenyl)benzeneacetamide抑制多药耐药蛋白（MRP1）。

Pomalidomide-PEG4-C-COOH (E3 Ligase Ligand-Linker Conjugates 1) 包含基于 Pomalidomide 的 cereblon 配体和 4 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。

Thalidomide-5-NH2-CH2-COOH (compound 114) 是原肌球蛋白受体激酶的选择性抑制剂。它是 E3 连接酶的配体，具有研究一种或多种疾病的潜力。

2-Bromo-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine 是一种片段分子，在生命科学相关研究中具有广泛的应用。

Modified MMAF-C5-COOH is a drug-linker conjugate for ADC.

5'-O-Benzoyl-2'-O,4'-C-methyleneuridine is a Nucleoside Derivative - LNA related nucleoside; Protected nucleoside with NH2/OH open.

5'-O-Benzoyl-3'-O-(4-methoxybenzoyl)-2'-O,4'-C-methyleneuridine is a Nucleoside Derivative - LNA-related nucleoside.

Nucleoside Derivatives - 5’-Modified nucleosides; 6-Modified purine nucleosides; N-Methylated nucleosides

5-Methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid hydrochloride 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 T66095，CAS号为 720720-96-7。

5’(R)-C-Methyl-5-fluorouridine 是尿嘧啶核苷类似物，具有潜在抗癫痫能力。该类似物用于研究抗惊厥和抗焦虑活性，进而开发新型降压药物。

Nucleoside Derivatives - 2’-Modified nucleosides, 5-Modified pyrimidine nucleosides

Nucleosides and Reagents - Fluoro-modified nucleoside; 2’-C-methyl nucleoside; ; 5-Modified pyrimidine nucleoside

1-(2-C-b-Methyl-b-D-ribofuranosyl)-5-nitropyridine-2(1H)-one is a Pyridine nucleoside; 2'-C-Methyl nucleoside.

5'(R)-C-Methylguanosine is a Nucleoside Derivative - 5'-Modified nucleoside.

2'-C-Methyl-5-methyluridine is a 2'-C-Methyl nucleoside; 5-Modified pyrimidine nucleoside.

Rev 2’-O-MOE-C(Bz)-5’-amidite; N4-Benzoyl-3'-O-(4,4’-dimethoxy trityl)-2'-O-(2-methoxyethyl)cytidine-5’-CED phosphoramidite 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 TNU1531。

Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene][[5-[(dimethylamino)sulfonyl]-2-(1-methylethoxy-O)phenyl]methylene-C]ruthenium(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 T66135。

MC-Alkyl-Hydrazine Modified MMAF is a potent antitumor drug-linker conjugate for ADC, incorporating Modified MMAF, a tubulin inhibitor, through a noncleavable MC-Alkyl-Hydrazine linkage[1].

5'(R)-C-Methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside.

2',3',5'-Tri-O-benzoyl-2'-C-methyl-5-methyluridine is a 2'-C-Methyl nucleoside; 5-Modified pyrimidine nucleoside.

N-Trityl-N4-benzoyl-morpholino-C-5'-O-phosphoramidite is a Nucleoside Derivative - Morpholino nucleoside; Phosphoramidite.

5-O-Benzoyl-1,2,3-tri-O-acetyl-4-C-fluoromethyl-D-ribofuranose is a Carbohydrate Derivative.

Nucleoside Derivatives - 5’-Modified nucleosides, 5-Modified pyrimidine nucleosides

5-O-Benzoyl-1,2,3-tri-O-acetyl-4-C-methyl-D-ribofuranose is a Carbohydrate Derivative.

tert-Butyl 4,6-dihydropyrrolo[3,4-c]pyrazole-5(2H)-carboxylate 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 T66374，CAS号为 1280210-79-8。

2'-C-Methyl-5-methoxyuridine is a 2'-C-Methyl nucleoside; 5-Modified pyrimidine nucleoside.

Rev 2’-O-MOE-C(Bz)-5’-amidite 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物，主要针对惰性淋巴系统恶性肿瘤。其抗癌机制包括抑制 DNA 合成和诱导细胞凋亡 (apoptosis)。

5’-O-Benzoyl-3’-O-(4-methoxybenzyl)-2’-O,4’-C-methyleneuridine 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物，主要针对惰性淋巴系统的恶性肿瘤。其作用机制主要通过抑制 DNA 合成和诱导细胞凋亡 (apoptosis) 实现。

5-Chloro-3-phenylbenzo[c]isoxazole 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 T66589，CAS号为 719-64-2。

5-Iodo-2'-C-methyl uridine is a 2'-C-Methyl nucleoside; Halo-nucleoside.

5-O-Benzoyl-4-C-hydroxymethyl-2,3-O-isopropylidene-1-O-methyl-beta-D-ribofuranose is a Carbohydrate Derivative.

Nucleoside Derivatives - 5’-Modified nucleosides; 3-Deazauridines

2',3',5'-Tri-O-benzoyl-2'-C-methyl-5-methoxyuridine is a 2'-C-Methyl nucleoside; 5-Modified pyrimidine nucleoside.

5-Methyl-2'-O,4'-C-methylenecytidine is a Nucleoside Derivative - LNA-related nucleoside.

Nucleoside Derivative –4’-Modified nucleosides; Protected nucleosides with NH2 OH group

3'-beta-C-Methyl-5-methyluridine is a Nucleoside Derivative - 3'-Modified nucleoside.

7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine is a building block.1It has been used in the synthesis of PI3K inhibitors. 1.Scott, W.J., Hentemann, M.F., Rowley, R.B., et al.Discovery and SAR of novel 2,3-dihydroimidazo[1,2-c]quinazoline PI3K inhibitors: Identification of copanlisib (BAY 80-6946)ChemMedChem.11(14)1517-1530(2016)

4'-C-Methyl-5-methylcytidine is a Nucleoside Derivative - 4'-Modified nucleoside.

5-Fluoro-4'-C-methyluridine is a Nucleoside Derivative - 4'-Modified nucleoside; Fluoro-modified nucleoside; 5-Modified pyrimidine nucleoside.

2'-beta-C-Ethynyl-5-methyluridine is a Nucleoside Derivative - 2'-Modified nucleoside.

Ald-Ph-amido-PEG3-C-COOH is a noncleavable linker utilized in the formation of antibody-drug conjugates (ADCs).

Scaffolds and Templates; Heterocyclic Compounds - Fused polyheterocycles

5-Fluoro-3'-beta-C-methyluridine is a Nucleoside Derivative - 3'-Modified nucleoside, 5-Modified pyrimidine nucleoside, Fluoro-modified nucleoside.

1-(2,3,5-Tribenzoyl-2-C-b-methyl-b-D-ribofuranosyl)-5-nitropyridine-2(1H)-one is a Pyridine nucleoside; 2'-C-Methyl nucleoside.

3'-Deoxy-3'-a-C-methyl-5-fluorouridine is a Nucleoside Derivative - 3'-Modified nucleoside, 5-Modified pyrimidine nucleoside, Fluoro-modified nucleoside.

CathepsinC-IN-5 (compound SF38) 为一高效、选择性、口服活性的组织蛋白酶 C (Cat C) 抑制剂，其针对Cat C、Cat L、Cat S、Cat B、Cat K 的IC50s 分别为 59.9 nM、4.26 µM、>5 µM、>5 µM、>5 µM。该化合物能够抑制骨髓和血液中的Cat C活性，降低中性粒细胞丝氨酸蛋白酶（NSP）的激活，并展现抗炎活性。

Nucleoside Derivatives - 2’-Modified nucleosides; Scaffolds and Templates;Bi-Tricyclic nucleosides