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Natural Product Research
Formerly Natural Product Letters
Volume 33, 2019 - Issue 5
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Research Articles

5′-Epi-SPA-6952A, a new insecticidal 24-membered macrolide produced by Streptomyces diastatochromogenes SSPRC-11339

Haijing CaoShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
,
Wenjing LiuShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
,
Yuansen ChangShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
,
Hui ChenShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
,
Yang ZhangShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
,
Wenping XuShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, China
&
Liming TaoShanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, ChinaCorrespondence[email protected]
 show all
Pages 659-664 | Received 18 Jul 2017, Accepted 03 Nov 2017, Published online: 20 Nov 2017

References

  • Breckenridge CB. 2001. Chapter 56 – the avermectins: insecticidal and antiparasitic agents. Elsevier Inc; p. 1157–1167.
  • Che W, Shi T, Wu Y, Yang Y. 2013. Insecticide resistance status of field populations of Spodoptera exigua (Lepidoptera: Noctuidae) from China. J Econ Entomol. 106:1855–1862.10.1603/EC13128
  • Chitgupekar SS, Goud KB, Patil RR, Vastrad AS, Nargund VB, Halikatti SI. 2013. Toxicity of newer insecticidal molecules against Spodoptera litura (Fabricius). J Exp Zool India. 16:495–497.
  • Dame ZT, Ruanpanun P. 2017. Production of macrolide antibiotics from a cytotoxic soil Streptomyces sp. strain ZDB. World J Microbiol Biotechnol. 33:9.10.1007/s11274-017-2306-6
  • Fan L, Guo Y, Zhi X, Yu X, Xu H. 2014. Stereoselective synthesis of 2α-chloropicropodophyllotoxins and insecticidal activity of their esters against oriental armyworm, Mythimna separata walker. J Agric Food Chem. 62:3726–3733.10.1021/jf405316w
  • Gao P, Yu C, Li Q. 2012. Study on insecticidal toxicity preparation of monosultap and emamectin benzoate to rice stem borer (Chilo suppressalis walker). Pesticide Sci. Adm. 33:45–47.
  • Guo SS, Zhang WJ, Yang K, Liang JY, You CX, Wang CF, Li YP, Geng ZF, Deng ZW, Du SS. 2016. Repellence of the main components from the essential oil of Glycosmis lucida Wall. ex Huang against two stored product insects. Nat Prod Res. 31:1–4.
  • Hosotani N, Kumagai K, Nakagawa H, Shimatani T, Saji I. 2005. New 24-membered macrolides SPA-6952A and B produced by Streptomyces sp. J Antibio. 58:409–411.10.1038/ja.2005.52
  • James PS, Picton J, Riek RF. 1980. Insecticidal activity of the avermectins. Vet Rec. 106:59.10.1136/vr.106.3.59-a
  • Kim DG, Moon K, Kim SH, Park SH, Park S, Sang KL, Oh KB, Shin J, Oh DC. 2012. Bahamaolides A and B, antifungal polyene polyol macrolides from the marine actinomycete streptomyces sp. J Nat Prod. 75:959–967.10.1021/np3001915
  • Liang F, Subramanyam B, Arthur FH. 2015. Effectiveness of spinosad on four classes of wheat against five stored-product insects. J Econ Entomol. 95:640–650.
  • Qu H, Lv M, Yu X, Lian X, Xu H. 2015. Discovery of some piperine-based phenylsulfonylhydrazone derivatives as potent botanically narcotic agents. Sci Rep. 5:1698.10.1038/srep13077
  • Ranjbari S, Safaralizadeh MH, Aramideh S. 2012. Insecticidal effect of spinosad on larvae of Plutella xylostella L. (Lepidoptera: Plutellidae) under laboratory conditions. Afr J Microbiol Res. 6:552–555.
  • Shishlyannikova TA, Kuzmin AV, Fedorova GA, Shishlyannikov SM, Lipko IA, Sukhanova EV, Belkova NL. 2017. Ionofore antibiotic polynactin produced by Streptomyces sp. 156A isolated from Lake Baikal. Nat Prod Res. 31:639–644.10.1080/14786419.2016.1217203
  • Wang R, Zhi X, Li J, Xu H. 2015. Synthesis of novel oxime sulfonate derivatives of 2′(2′,6′)-(Di)chloropicropodophyllotoxins as insecticidal agents. J Agric Food Chem. 63:6668–6674.10.1021/acs.jafc.5b02036
  • Wang W, Song T, Chai W, Chen L, Chen L, Lian XY, Zhang Z. 2017. Rare polyene-polyol macrolides from mangrove-derived Streptomyces sp. ZQ4BG. Sci Rep. 7:1135.10.1038/s41598-017-01912-z
  • Wongkamhaeng W, Wirawut T. 1978. The armyworm, Mythimna separata (Walker) [a study on its life history and chemical control on corn and sorghum in Thailand]. Rec Nat Prod. 5:108–116.
  • Yang I, Yoon J, Kim D, Hahn D, Nam SJ, Fenical W. 2017. 4 Z - and 4 E -12-deoxydihydrokromycins, two naturally occurring kromycin aglycons of pikromycin from Streptomyces sp. Tetrahedron Lett. 58:2322–2324.10.1016/j.tetlet.2017.03.088
  • Yu X, Che Z, Xu H. 2017. Recent advances in the chemistry and biology of podophyllotoxins. Chem A Eur J. 23:4467–4526.10.1002/chem.201602472
  • Zhang XY, Shen J, Zhou Y, Wei ZP, Gao JM. 2017. Insecticidal constituents from Buddlej aalbiflora Hemsl. Nat Prod Res. 31:1446–1449.10.1080/14786419.2016.1247080
  • Zhang Y, Liu S, Yang X, Yang M, Xu W, Li Y, Tao L. 2016. Staurosporine shows insecticidal activity against Mythimna separata Walker (Lepidoptera: Noctuidae) potentially via induction of apoptosis. Pestic Biochem Physiol. 128:37–44.10.1016/j.pestbp.2015.10.007
  • Zhao PJ, Fan LM, Li GH, Zhu N, Shen YM. 2005. Antibacterial and antitumor macrolides from streptomyces sp. Is9131. Arch Pharm Res. 28:1228–1232.10.1007/BF02978203
  • Zhi-Qin JI, Zhang JW, Wei SP, Wen-Jun WU. 2007. Isolation and identification of the insecticidal ingredients from the Fermentation broth of streptomyces qinlingnensis. Chin J Pest Sci. 1:25–28.

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