Maduramicin

• 常用名: Maduramicin
• 英文名: Maduramicin
• CAS号: 79356-08-4
• 分子量: 917.13
• 密度: 1.3±0.1 g/cm3
• 沸点: 913.9±65.0 °C at 760 mmHg
• 分子式: C₄₇H₈₀O₁₇
• 熔点: N/A
• 闪点: 255.5±27.8 °C

Maduramicin用途

Maduramicin (Maduramycin) 是从放线菌 Actinomadura rubra 中分离出来的。 Maduramicin 是一种抗球虫药,用于艾美耳球菌,腺苷球菌,鸡血肠球菌和分散肠球菌感染的相关研究。Maduramicin 通过内在和外在途径诱导鸡心肌细胞凋亡 (apoptosis)。

Maduramicin名称

• 英文名: [(2R,3S,4S,5R,6S)-6-{(1R)-1-[(2S,5R,7S,8R,9S)-2-{(2S,2'R,3'S,5R,5'R)-3'-{[(2R,4S,5S,6S)-4,5-Dimethoxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-5'-[(2S,3S,5R,6S)-6-hydroxy-3,5,6-trimethyltetrahydro-2H-pyran-2-yl]-2-methyloctahydro-2,2'-bifuran-5-yl}-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]ethyl}-2-hydroxy-4,5-dimethoxy-3-methyltetrahydro-2H-pyran-2-yl]acetic acid

Maduramicin生物活性

• 描述: Maduramicin (Maduramycin) 是从放线菌 Actinomadura rubra 中分离出来的。 Maduramicin 是一种抗球虫药,用于艾美耳球菌,腺苷球菌,鸡血肠球菌和分散肠球菌感染的相关研究。Maduramicin 通过内在和外在途径诱导鸡心肌细胞凋亡 (apoptosis)。
• 相关类别:
  信号通路 >> 细胞凋亡 >> 细胞凋亡
  研究领域 >> 感染
• 参考文献:

  [1]. McDougald LR, et al. Efficacy of maduramicin ammonium against coccidiosis in turkeys under laboratory and floor-pen conditions.Avian Dis. 1990 Jul-Sep;34(3):634-8.

  [2]. Gao X, et al.Maduramicin induces apoptosis in chicken myocardial cells via intrinsic and extrinsic pathways.Toxicol In Vitro. 2018 Aug;50:190-200.

Maduramicin物理化学性质

• 密度: 1.3±0.1 g/cm3
• 沸点: 913.9±65.0 °C at 760 mmHg
• 分子式: C₄₇H₈₀O₁₇
• 分子量: 917.13
• 闪点: 255.5±27.8 °C
• 精确质量: 916.539551
• PSA: 208.75000
• LogP: 4.34
• InChIKey: RWVUEZAROXKXRT-VQLSFVLHSA-N
• SMILES: COC1CC(OC2CC(C3OC(C)(O)C(C)CC3C)OC2C2(C)CCC(C3(C)CCC4(CC(O)C(C)C(C(C)C5OC(O)(CC(=O)O)C(C)C(OC)C5OC)O4)O3)O2)OC(C)C1OC
• 蒸汽压: 0.0±0.6 mmHg at 25°C
• 折射率: 1.549

Maduramicin靶点实验

查看更多实验

实验名称：DRUGMATRIX: Opiate delta1 (OP1, DOP) radioligand binding (ligand: [3H] Naltrindole) 来源：ChEMBL 靶标：Delta-type opioid receptor External Id：CHEMBL1909180

实验名称：DRUGMATRIX: Nitric Oxide Synthase, Inducible (iNOS) enzyme inhibition (substrate: L-A... 来源：ChEMBL 靶标：Nitric oxide synthase, inducible External Id：CHEMBL1909179

实验名称：DRUGMATRIX: Opiate mu (OP3, MOP) radioligand binding (ligand: [3H] Diprenorphine) 来源：ChEMBL 靶标：Mu-type opioid receptor External Id：CHEMBL1909182

实验名称：DRUGMATRIX: Opiate kappa (OP2, KOP) radioligand binding (ligand: [3H] Diprenorphine) 来源：ChEMBL 靶标：Kappa-type opioid receptor External Id：CHEMBL1909181

实验名称：DRUGMATRIX: Phosphodiesterase PDE3 enzyme inhibition (substrate: [3H]cAMP + cAMP) 来源：ChEMBL 靶标：N/A External Id：CHEMBL1909184

实验名称：DRUGMATRIX: Phorbol Ester radioligand binding (ligand: [3H] PDBu) 来源：ChEMBL 靶标：N/A External Id：CHEMBL1909183

实验名称：DRUGMATRIX: Phosphodiesterase PDE5 enzyme inhibition (substrate: [3H]cGMP + cGMP) 来源：ChEMBL 靶标：cGMP-specific 3',5'-cyclic phosphodiesterase External Id：CHEMBL1909186

实验名称：DRUGMATRIX: Phosphodiesterase PDE4 enzyme inhibition (substrate: [3H]cAMP + cAMP) 来源：ChEMBL 靶标：N/A External Id：CHEMBL1909185

实验名称：DRUGMATRIX: Muscarinic M3 radioligand binding (ligand: [3H] N-Methylscopolamine) 来源：ChEMBL 靶标：Muscarinic acetylcholine receptor M3 External Id：CHEMBL1909172

实验名称：DRUGMATRIX: Muscarinic M2 radioligand binding (ligand: [3H] N-Methylscopolamine) 来源：ChEMBL 靶标：Muscarinic acetylcholine receptor M2 External Id：CHEMBL1909171

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Maduramicin英文别名

• 2-(6-(1-(2-(3'-((4,5-dimethoxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-5'-(6-hydroxy-3,5,6-trimethyltetrahydro-2H-pyran-2-yl)-2-methyloctahydro-[2,2'-bifuran]-5-yl)-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl)ethyl)-2-hydroxy-4,5-dimethoxy-3-methyltetrahydro-2H-pyran-2-yl)acetic acid
• [(2R,3S,4S,5R,6S)-6-{(1R)-1-[(2S,5R,7S,8R,9S)-2-{(2S,2'R,3'S,5R,5'R)-3'-{[(2R,4S,5S,6S)-4,5-Dimethoxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-5'-[(2S,3S,5R,6S)-6-hydroxy-3,5,6-trimethyltetrahydro-2H-pyran-2-yl]-2-methyloctahydro-2,2'-bifuran-5-yl}-9-hydroxy-2,8-dimethyl-1,6-dioxaspiro[4.5]dec-7-yl]ethyl}-2-hydroxy-4,5-dimethoxy-3-methyltetrahydro-2H-pyran-2-yl]acetic acid