抗螺旋體鏈絲菌素结构式
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常用名 | 抗螺旋體鏈絲菌素 | 英文名 | (-)-borrelidin |
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CAS号 | 7184-60-3 | 分子量 | 489.644 | |
密度 | 1.1±0.1 g/cm3 | 沸点 | 710.3±60.0 °C at 760 mmHg | |
分子式 | C28H43NO6 | 熔点 | 143-145℃ | |
MSDS | 中文版 美版 | 闪点 | 383.4±32.9 °C |
抗螺旋體鏈絲菌素用途Borrelidin (Treponemycin) 是从 Streptomyces rochei 中分离的一种含氮大环内酯类抗生素,能作为抑制细菌和真核 threonyl-tRNA 合成酶的抑制剂,通过诱导细胞凋亡和介导 G1 期阻滞作用来靶向 ALL 细胞。Borrelidin (Treponemycin) 是一种出芽酵母细胞周期蛋白依赖性激酶 (CDK) Cdc28/Cln2 的抑制剂,其 IC50 值为 24 μM。Borrelidin (Treponemycin) 是一种强效的血管生成抑制剂,其 IC50 值为 0.8 nM,可诱导血管形成细胞凋亡。Borrelidin (Treponemycin) 具有较强的抗疟活性,对恶性疟原虫 K1 株和 FCR3 株作用的 IC50 值分别为 1.9 nM 和 1.8 nM。 |
中文名 | 抗螺旋体链丝菌素 |
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英文名 | borrelidin |
中文别名 | 疏螺体素 | 疏螺旋体素 | 抗螺旋體鏈絲菌素 |
英文别名 | 更多 |
描述 | Borrelidin (Treponemycin) 是从 Streptomyces rochei 中分离的一种含氮大环内酯类抗生素,能作为抑制细菌和真核 threonyl-tRNA 合成酶的抑制剂,通过诱导细胞凋亡和介导 G1 期阻滞作用来靶向 ALL 细胞。Borrelidin (Treponemycin) 是一种出芽酵母细胞周期蛋白依赖性激酶 (CDK) Cdc28/Cln2 的抑制剂,其 IC50 值为 24 μM。Borrelidin (Treponemycin) 是一种强效的血管生成抑制剂,其 IC50 值为 0.8 nM,可诱导血管形成细胞凋亡。Borrelidin (Treponemycin) 具有较强的抗疟活性,对恶性疟原虫 K1 株和 FCR3 株作用的 IC50 值分别为 1.9 nM 和 1.8 nM。 |
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相关类别 | |
靶点 |
IC50:24μM (Cdc28/Cln2)[2] |
参考文献 |
密度 | 1.1±0.1 g/cm3 |
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沸点 | 710.3±60.0 °C at 760 mmHg |
熔点 | 143-145℃ |
分子式 | C28H43NO6 |
分子量 | 489.644 |
闪点 | 383.4±32.9 °C |
精确质量 | 489.309052 |
PSA | 127.85000 |
LogP | 4.31 |
外观性状 | 白色至灰白色粉末 |
蒸汽压 | 0.0±5.1 mmHg at 25°C |
折射率 | 1.539 |
储存条件 | 库房通风低温干燥,与食品原料分开存放 |
水溶解性 | DMSO: 1 mg/mL |
Further characterization of Bacillus subtilis antibiotic biosensors and their use for antibacterial mode-of-action studies.
Antimicrob. Agents Chemother. 55(4) , 1784-6, (2011) We further examined the usefulness of previously reported Bacillus subtilis biosensors for antibacterial mode-of-action studies. The biosensors could not detect the tRNA synthetase inhibitors mupiroci... |
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Total synthesis of borrelidin.
J. Org. Chem. 72 , 2744, (2007) The total synthesis of borrelidin has been achieved. The best feature of our synthetic route is macrocyclization at C11-C12 for the construction of an 18-membered ring after esterification between two... |
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Iterative deoxypropionate synthesis based on a copper-mediated directed allylic substitution: formal total synthesis of borrelidin (C3-C11 fragment).
Chemistry 12(25) , 6684-91, (2006) A new iterative strategy for the flexible preparation of any oligodeoxypropionate stereoisomer is presented which relies on an o-DPPB-directed copper mediated allylic substitution employing enantiomer... |
Borrelidin |
Cyclopentanecarboxylic acid, 2-[(2S,4Z,6Z,8R,9S,11R,13S,15S,16S)-7-cyano-8,16-dihydroxy-9,11,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6-dien-2-yl]-, (1R,2R)- |
Borrelidine |
Quinquangulin K 031 |
2-(7-CYANO-8,16-DIHYDROXY-9,11,13,15-TETRAMETHYL-18-OXOOXACYCLOOCTADECA-4,6-DIEN-2-YL)-CYCLOPENTANECARBOXYLIC ACID |
Quinquangulin K 182 |
Cyclopentanecarboxylic acid, 2-[(2S,4E,6Z,8R,9S,11R,13S,15S,16S)-7-cyano-8,16-dihydroxy-9,11,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6-dien-2-yl]-, (1R,2R)- |
(1R,2R)-2-[(2S,4Z,6Z,8R,9S,11R,13S,15S,16S)-7-Cyano-8,16-dihydroxy-9,11,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6-dien-2-yl]cyclopentanecarboxylic acid |
(1R,2R)-2-[(2S,4E,6Z,8R,9S,11R,13S,15S,16S)-7-Cyano-8,16-dihydroxy-9,11,13,15-tetramethyl-18-oxooxacyclooctadeca-4,6-dien-2-yl]cyclopentanecarboxylic acid |
(-)-borrelidine |
TREPONEMYCIN |