Kendomycin(Synonyms: (-)-TAN2162)

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Kendomycin (Synonyms: (-)-TAN2162)

Kendomycin ((−)-TAN 2162) 是一种聚酮类的抗生素 (antibiotic)，具有显著的抗菌和肿瘤细胞毒性活性。在低浓度下 (MIC: 5 μg/mL)，Kendomycin 能抑制耐甲氧西林金黄色葡萄球菌 (MRSA) 菌株 COL 的生长。Kendomycin 是内皮素受体 (endothelin receptor) 的拮抗剂和降钙素受体 (calcitonin receptor) 激动剂，具有抗骨质疏松作用。

Kendomycin(Synonyms: (-)-TAN2162)

Kendomycin Chemical Structure

CAS No. : 183202-73-5

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生物活性

Kendomycin ((−)-TAN 2162) is a polyketide antibiotic with remarkable antibacterial and cancer cells cytotoxic activities. Kendomycin tends to be bacteriostatic rather than bactericidal and inhibits the growth of the methicillin-resistant Staphylococcus aureus (MRSA) strain COL at a low concentration (MIC of 5 μg/mL). Kendomycin is a potent antagonist of the endothelin receptor and a calcitonin receptor agonist which plays its role as an anti-osteoporotic agent[1][2].

分子量

486.64

Formula

C29H42O6
CAS 号

183202-73-5
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献

  • [1]. Yasser A Elnakady, et al. Investigations to the Antibacterial Mechanism of Action of Kendomycin. PLoS One. 2016 Jan 21;11(1):e0146165.

    [2]. Yu Yuan, et al. Total synthesis of kendomycin: a macro-C-glycosidation approach. J Am Chem Soc. 2004 Nov 17;126(45):14720-1.

    [3]. Tetsuya Sengoku, et al. Total synthesis of the antibiotic kendomycin: a macrocyclization using the Tsuji-Trost etherification. Angew Chem Int Ed Engl. 2014 Apr 14;53(16):4213-6.

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