Planta Med 2017; 83(09): 805-811
DOI: 10.1055/s-0043-100382
Natural Product Chemistry and Analytical Studies
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Antichlamydial Dimeric Indole Derivatives from Marine Actinomycete Rubrobacter radiotolerans

Jian Lin Li*
1   School of Pharmacy, Nantong University, Nantong, China
,
Dandan Chen*
1   School of Pharmacy, Nantong University, Nantong, China
2   Department of Pharmacy, The Second Peopleʼs Hospital of Nantong, Nantong, China
,
Lei Huang
1   School of Pharmacy, Nantong University, Nantong, China
,
Min Ni
1   School of Pharmacy, Nantong University, Nantong, China
,
Yu Zhao
1   School of Pharmacy, Nantong University, Nantong, China
,
Huizhou Fan
3   Robert Wood Johnson Medical School, Rutgers University, Piscataway, New Jersey, USA
,
Xiaofeng Bao
1   School of Pharmacy, Nantong University, Nantong, China
› Author Affiliations
Further Information

Publication History

received 26 September 2016
revised 19 December 2016

accepted 29 December 2016

Publication Date:
17 January 2017 (online)

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Abstract

Chlamydiae are widely distributed pathogens of human populations, which can lead to serious reproductive and other health problems. In our search for novel antichlamydial metabolites from marine derived-microorganisms, one new (1) and two known (2, 3) dimeric indole derivatives were isolated from the sponge-derived actinomycete Rubrobacter radiotolerans. The chemical structures of these metabolites were elucidated by NMR spectroscopic data as well as CD calculations. All three metabolites suppressed chlamydial growth in a concentration-dependent manner. Among them, compound 1 exhibited the most effective antichlamydial activity with IC50 values of 46.6 ~ 96.4 µM in the production of infectious progeny. Compounds appeared to target the mid-stage of the chlamydial developmental cycle by interfering with reticular body replication, but not directly inactivating the infectious elementary body.

* These two authors contributed equally to this work.


Supporting Information

1H, 13C, and 2D NMR data of compound 1 and concentration-response curves for generating IC50 values of the three compounds on each Chlamydia are available as Supporting Information.