Rutaceae) with Simple Or Unifoliolate Leaves, Including Two New Combinations
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Sistema De Clasificación Artificial De Las Magnoliatas Sinántropas De Cuba
Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA Pedro- Pabfc He.r retira Qltver CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA Y UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA ASPIRANTE: Lie. Pedro Pablo Herrera Oliver Investigador Auxiliar Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente DIRECTORES: CUBA Dra. Nancy Esther Ricardo Ñapóles Investigador Titular Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente ESPAÑA Dr. Andreu Bonet Jornet Piiofesjar Titular Departamento de EGdfegfe Universidad! dte Mearte CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver I. INTRODUCCIÓN 1 II. ANTECEDENTES 6 2.1 Historia de los esquemas de clasificación de las especies sinántropas (1903-2005) 6 2.2 Historia del conocimiento de las plantas sinantrópicas en Cuba 14 III. -
Maculine: a Furoquinoline Alkaloid from the Family Rutaceae: Sources, Syntheses and Biological Activities
The Free Internet Journal Review for Organic Chemistry Archive for Arkivoc 2020, part __, 0-0 Organic Chemistry to be inserted by editorial office Maculine: a furoquinoline alkaloid from the family Rutaceae: sources, syntheses and biological activities Eslam R. El-Sawy,a,b Ahmed B. Abdelwahab,c and Gilbert Kirsch*a a Laboratoire Lorrain de Chimie Moleculaire (L.2.C.M.), Universite de Lorraine, Metz, France b Chemistry of Natural Compounds Department, National Research Centre, Dokki, Cairo, Egypt c Plant Advanced Technologies (PAT), Vandoeuvre-les-Nancy, France Email: [email protected] This paper is dedicated to Prof Jan Bergman for his 80th birthday and his involvement in organic chemistry, and with deep appreciation for over 40 years of friendship Received mm-dd-yyyy Accepted mm-dd-yyyy Published on line mm-dd-yyyy Dates to be inserted by editorial office Abstract Maculine is one of the furoquinolines which are characteristic of the family Rutaceae. Its chemical name is 9-methoxy[1,3]dioxolo[4,5-g]furo[2,3-b]quinoline and it was isolated from several genera of Rutaceae. The present mini- review covers the different sources of maculine, its methods of separation, synthetic pathways and biological activities. Keywords: Maculine, furoquinoline, Rutaceae, alkaloids DOI: https://doi.org/10.24820/ark.5550190.p011.200 Page 1 ©AUTHOR(S) Arkivoc 2020, part _, 0-0 El-Sawy, E. R. et al. Table of Contents 1. Introduction 2. Botanical Sources 3. Organic Synthesis 4. Biological Activity 5. Conclusions References 1. Introduction The Rutaceae family has about 140 genera,1–4 consisting of herbs, shrubs and small trees which grow in all parts of the world, Moluccas, New Guinea, Australia, New Caledonia, Brazil, Cameroon. -
Rutaceae) of Coastal Thicket in the Congo Republic
bioRxiv preprint doi: https://doi.org/10.1101/2021.08.22.457282; this version posted August 22, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Chemistry, Taxonomy and Ecology of the potentially chimpanzee-dispersed Vepris teva sp.nov. (Rutaceae) of coastal thicket in the Congo Republic Moses Langat1, Teva Kami2 & Martin Cheek1 1Science Dept., Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, United Kingdom 2 Herbier National, Institut de Recherche National en Sciences Exactes et Naturelles (IRSEN), Cité Scientifique de Brazzaville, République du Congo ABSTRACT. Continuing a survey of the chemistry of species of the largely continental African genus Vepris, we investigate a species previously referred to as Vepris sp. 1 of Congo. From the leaves of Vepris sp. 1 we report six compounds. The compounds were three furoquinoline alkaloids, kokusaginine (1), maculine (2), and flindersiamine (3), two acridone alkaloids, arborinine (4) and 1-hydroxy-3-methoxy-10-methylacridone (5), and the triterpenoid, ß-amyrin (6). Compounds 1-4 are commonly isolated from other Vepris species, compound 5 has been reported before once, from Malagasy Vepris pilosa, while this is the first report of ß-amyrin from Vepris. This combination of compounds has never before been reported from any species of Vepris. We test the hypothesis that Vepris sp.1 is new to science and formally describe it as Vepris teva, unique in the genus in that the trifoliolate leaves are subsessile, with the median petiolule far exceeding the petiole in length. -
Final Report
Darwin Initiative – Final Report (To be completed with reference to the Reporting Guidance Notes for Project Leaders (http://darwin.defra.gov.uk/resources/reporting/) - it is expected that this report will be a maximum of 20 pages in length, excluding annexes) Darwin project information Project Reference 15034 Project Title Red List Plants of Cameroon Host country(ies) Cameroon UK Contract Holder Royal Botanic Gardens, Kew Institution UK Partner Institution(s) n/a Host Country Partner Herbier National Camerounais, Yaoundé, Cameroon; ERUDEF, Institution(s) ANCO, CWAF, MINEF-MINEP Darwin Grant Value £142,225 Start/End dates of Project July 2006- 4 April 2011 Project Leader Name Martin Cheek Project Website Under development Report Author(s) and date Martin Cheek 5 May 2011 1 Project Background Cameroon forest contains the highest plant species diversity per degree square in Tropical Africa. Many such species are threatened. The project purpose was to provide a sound basis for conserving threatened species throughout Cameroon by assessing the status of every species of plant and making the information available in a variety of formats for different user groups. 2 Project support to the Convention on Biological Diversity (CBD) Since this is a plant project, the GSPC (Global Strategy for Plant Conservation) is the most relevant part of the CBD. GSPC Targets 1 (a working list of all known plant species) and 2 (a preliminary assessment of the conservation status of all known plant species…) were met at national level by the publication of a book with the first taxonomic checklist with IUCN assessments (The Vascular Plants of Cameroon, Onana 2011). -
Chemistry, Taxonomy and Ecology of the Potentially Chimpanzee-Dispersed Vepris Teva Sp.Nov
bioRxiv preprint doi: https://doi.org/10.1101/2021.08.22.457282; this version posted August 22, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Chemistry, Taxonomy and Ecology of the potentially chimpanzee-dispersed Vepris teva sp.nov. (Rutaceae) of coastal thicket in the Congo Republic Moses Langat1, Teva Kami2 & Martin Cheek1 1Science Dept., Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AE, United Kingdom 2 Herbier National, Institut de Recherche National en Sciences Exactes et Naturelles (IRSEN), Cité Scientifique de Brazzaville, République du Congo ABSTRACT. Continuing a survey of the chemistry of species of the largely continental African genus Vepris, we investigate a species previously referred to as Vepris sp. 1 of Congo. From the leaves of Vepris sp. 1 we report six compounds. The compounds were three furoquinoline alkaloids, kokusaginine (1), maculine (2), and flindersiamine (3), two acridone alkaloids, arborinine (4) and 1-hydroxy-3-methoxy-10-methylacridone (5), and the triterpenoid, ß-amyrin (6). Compounds 1-4 are commonly isolated from other Vepris species, compound 5 has been reported before once, from Malagasy Vepris pilosa, while this is the first report of ß-amyrin from Vepris. This combination of compounds has never before been reported from any species of Vepris. We test the hypothesis that Vepris sp.1 is new to science and formally describe it as Vepris teva, unique in the genus in that the trifoliolate leaves are subsessile, with the median petiolule far exceeding the petiole in length. -
Antimicrobial Furoquinoline Alkaloids from Vepris Lecomteana (Pierre) Cheek & T. Heller (Rutaceae)
molecules Article Antimicrobial Furoquinoline Alkaloids from Vepris lecomteana (Pierre) Cheek & T. Heller (Rutaceae) Ariane Dolly Kenmogne Kouam 1,2, Achille Nouga Bissoue 1, Alain Tadjong Tcho 3, Emmanuel Ngeufa Happi 1, Alain François Kamdem Waffo 1, Norbert Sewald 2,* ID and Jean Duplex Wansi 1,* ID 1 Department of Chemistry, University of Douala, Faculty of Sciences, 24157 Douala, Cameroon; [email protected] (A.D.K.K.); [email protected] (A.N.B.); [email protected] (E.N.H.); [email protected] (A.F.K.W.) 2 Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany 3 Department of Chemistry, University of Buea, Faculty of Sciences, 63 Buea, Cameroon; [email protected] * Correspondences:[email protected] (N.S.); [email protected] (J.D.W.); Tel.: +49-521-106-2051 (N.S.); +237-674-725-425 (J.D.W.) Received: 25 November 2017; Accepted: 21 December 2017; Published: 21 December 2017 Abstract: Three new prenylated furoquinoline alkaloids named lecomtequinoline A (1), B (2), and C (3), together with the known compounds anhydroevoxine (4), evoxine (5), dictamnine (6), N-methylflindersine (7), evoxanthine (8), hesperidin, lupeol, b-sitosterol, stigmasterol, b-sitosterol-3-O-b-D-glucopyranoside, stearic acid, and myristyl alcohol, were isolated by bioassay-guided fractionation of the methanolic extracts of leaves and stem of Vepris lecomteana. The structures of compounds were determined by spectroscopic methods (NMR, MS, UV,and IR) and by comparison with previously reported data. Crude extracts of leaves and stem displayed high antimicrobial activity,with Minimum Inhibitory Concentration (MIC) (values of 10.1–16.5 and 10.2–20.5 µg/mL, respectively), against Escherichia coli, Bacillus subtilis, Pseudomonas agarici, Micrococcus luteus, and Staphylococcus warneri, while compounds 1–6 showed values ranging from 11.1 to 18.7 µg/mL or were inactive, suggesting synergistic effect. -
The Hemiptera-Sternorrhyncha (Insecta) of Hong Kong, China—An Annotated Inventory Citing Voucher Specimens and Published Records
Zootaxa 2847: 1–122 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) ZOOTAXA 2847 The Hemiptera-Sternorrhyncha (Insecta) of Hong Kong, China—an annotated inventory citing voucher specimens and published records JON H. MARTIN1 & CLIVE S.K. LAU2 1Corresponding author, Department of Entomology, Natural History Museum, Cromwell Road, London SW7 5BD, U.K., e-mail [email protected] 2 Agriculture, Fisheries and Conservation Department, Cheung Sha Wan Road Government Offices, 303 Cheung Sha Wan Road, Kowloon, Hong Kong, e-mail [email protected] Magnolia Press Auckland, New Zealand Accepted by C. Hodgson: 17 Jan 2011; published: 29 Apr. 2011 JON H. MARTIN & CLIVE S.K. LAU The Hemiptera-Sternorrhyncha (Insecta) of Hong Kong, China—an annotated inventory citing voucher specimens and published records (Zootaxa 2847) 122 pp.; 30 cm. 29 Apr. 2011 ISBN 978-1-86977-705-0 (paperback) ISBN 978-1-86977-706-7 (Online edition) FIRST PUBLISHED IN 2011 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2011 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. This authorization does not extend to any other kind of copying, by any means, in any form, and for any purpose other than private research use. -
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery ¶ ¶ ¶ Gina Porras, Francoiş Chassagne, James T
pubs.acs.org/CR Review Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery ¶ ¶ ¶ Gina Porras, Francoiş Chassagne, James T. Lyles, Lewis Marquez, Micah Dettweiler, Akram M. Salam, Tharanga Samarakoon, Sarah Shabih, Darya Raschid Farrokhi, and Cassandra L. Quave* Cite This: https://dx.doi.org/10.1021/acs.chemrev.0c00922 Read Online ACCESS Metrics & More Article Recommendations *sı Supporting Information ABSTRACT: The crisis of antibiotic resistance necessitates creative and innovative approaches, from chemical identification and analysis to the assessment of bioactivity. Plant natural products (NPs) represent a promising source of antibacterial lead compounds that could help fill the drug discovery pipeline in response to the growing antibiotic resistance crisis. The major strength of plant NPs lies in their rich and unique chemodiversity, their worldwide distribution and ease of access, their various antibacterial modes of action, and the proven clinical effectiveness of plant extracts from which they are isolated. While many studies have tried to summarize NPs with antibacterial activities, a comprehensive review with rigorous selection criteria has never been performed. In this work, the literature from 2012 to 2019 was systematically reviewed to highlight plant-derived compounds with antibacterial activity by focusing on their growth inhibitory activity. A total of 459 compounds are included in this Review, of which 50.8% are phenolic derivatives, 26.6% are terpenoids, 5.7% are alkaloids, and 17% are classified as other metabolites. A selection of 183 compounds is further discussed regarding their antibacterial activity, biosynthesis, structure−activity relationship, mechanism of action, and potential as antibiotics. Emerging trends in the field of antibacterial drug discovery from plants are also discussed. -
Anti-MRSA Constituents from Ruta Chalepensis (Rutaceae)
molecules Article Anti-MRSA Constituents from Ruta chalepensis (Rutaceae) Grown in Iraq, and In Silico Studies on Two of Most Active Compounds, Chalepensin and 6-Hydroxy-rutin 30,7-Dimethyl ether Shaymaa Al-Majmaie 1, Lutfun Nahar 2,* , M. Mukhlesur Rahman 3 , Sushmita Nath 1, Priyanka Saha 4, Anupam Das Talukdar 5, George P. Sharples 1 and Satyajit D. Sarker 1,* 1 Centre for Natural Products Discovery, School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK; [email protected] (S.A.-M.); [email protected] (S.N.); [email protected] (G.P.S.) 2 Laboratory of Growth Regulators, Institute of Experimental Botany ASCR & Palacký University, Šlechtitel ˚u27, 78371 Olomouc, Czech Republic 3 Medicines Research Group, School of Health, Sport and Bioscience, University of East London, Water Lane, London E15 4LZ, UK; [email protected] 4 Cancer Biology and Inflammatory Disease Division, CSIR-Indian Institute of Chemical Biology, Kolkata, West Bengal 700032, India; [email protected] 5 Department of Life Science and Bioinformatics, Assam University, Silchar, Assam 788011, India; Citation: Al-Majmaie, S.; Nahar, L.; [email protected] or [email protected] Rahman, M.M.; Nath, S.; Saha, P.; * Correspondence: [email protected] (L.N.); [email protected] (S.D.S.); Tel.: +44-(0)-15-1231-2096 (S.D.S.) Talukdar, A.D.; Sharples, G.P.; Sarker, S.D. Anti-MRSA Constituents from Abstract: Ruta chalepensis L. (Rutaceae), a perennial herb with wild and cultivated habitats, is well Ruta chalepensis (Rutaceae) Grown in known for its traditional uses as an anti-inflammatory, analgesic, antipyretic agent, and in the Iraq, and In Silico Studies on Two of treatment of rheumatism, nerve diseases, neuralgia, dropsy, convulsions and mental disorders. -
D Án K T H P B O T N Và Phát Tri N Trong Khu D Tr Sinh Quy N
DỰ ÁN K ẾT H ỢP B ẢO T ỒN VÀ PHÁT TRI ỂN TRONG KHU D Ự TR Ữ SINH QUY ỂN KIÊN GIANG KẾT QU Ả KH ẢO SÁT ĐÁNH GIÁ NHANH TH ỰC V ẬT VÀ ĐỘNG V ẬT CÓ X ƯƠ NG S ỐNG Ở CẠN C ỦA KHU D Ự TR Ữ SINH QUY ỂN KIÊN GIANG Cổ r ắn – Anhinga melanogaster Photo: Ngô Xuân T ường Tổng h ợp và hi ệu đính PGS.TS. Nguy ễn Xuân Đặ ng Vi ện Sinh thái và Tài nguyên sinh v ật, Hà N ội 8-2009 MỤC L ỤC DANH M ỤC B ẢNG ................................................................................................................................................. 4 DANH M ỤC HÌNH ................................................................................................................................................... 5 CÁC T Ừ VI ẾT T ẮT................................................................................................................................................. 6 LỜI NÓI ĐẦU ......................................................................................................................................................... 7 TÓM T ẮT BÁO CÁO .............................................................................................................................................. 8 PH ẦN 1. MỤC TIÊU, ĐỊA ĐIỂM, TH ỜI GIAN VÀ PH ƯƠ NG PHÁP NGHIÊN C ỨU ............................................ 14 1.1. M ỤC TIÊU NGHIÊN C ỨU ............................................................................................................................ 14 1.2. TH ỜI GIAN VÀ ĐỊA ĐIẾM KH ẢO SÁT ........................................................................................................ -
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A Pilot Biodiversity Study of the Eastern Frontier Closed Area and North East New Territories, Hong Kong, June-December 2003
A Pilot Biodiversity Study of the eastern Frontier Closed Area and North East New Territories, Hong Kong, June-December 2003 A waterfall at Ng To, Kuk Po April 2004 Kadoorie Farm and Botanic Garden Publication Series: No 1 A Pilot Biodiversity Study of the eastern Frontier Closed Area and North East New Territories, June-December 2003 Editors Captain WONG, Michael LAU, Gary ADES, Bosco CHAN and NG Sai Chit Contributors (in alphabetic order) Gary ADES, Bosco CHAN, Paul CROW, Roger KENDRICK, KWOK Hon Kai, Michael LAU, LEE Kwok Shing, Wicky LEE, NG Sai Chit, Gloria SIU, Ken SO, Captain WONG Citation Kadoorie Farm and Botanic Garden. 2004. A Pilot Biodiversity Study of the eastern Frontier Closed Area and North East New Territories, Hong Kong, June-December 2003. Kadoorie Farm and Botanic Garden Publication Series No.1. Kadoorie Farm and Botanic Garden, Hong Kong Special Adminstrative Region. Copyright © Kadoorie Farm and Botanic Garden Corporation Lam Kam Road, Tai Po, N.T. Hong Kong Special Adminstrative Region April 2004 CONTENTS Page Execuitve Summary 1 Introduction 2 Methodology 5 Results and Discussion 7 Lin Ma Hang 7 San Kwai Tin 14 Kuk Po 16 So Lo Pun 20 Yung Shue Au 24 Mammal occurrence within the study areas: a comparison with 27 existing records for protected areas Summary of Findings 29 Threats 30 Opportunities and Recommendations 32 Acknowledgments 34 References 35 Figures 38 Appendices 40 Plates 67 Executive Summary A 7-day preliminary biodiversity survey was conducted between June and December 2003 at Lin Ma Hang and San Kwai Tin in the Frontier Closed Area (FCA), and Kuk Po, So Lo Pun and Yung Shue Au in North East New Territories (NENT).