Ancistrocladus tectorius - Unknown
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Internal ID UUID64403c9fa0c29251576031
Scientific name Ancistrocladus tectorius
Authority (Lour.) Merr.
First published in Lingnan Sci. J. 6: 329 (1928 publ. 1930)

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Synonyms Top

Scientific name Authority First published in
Bembix tectoria Lour. Fl. Cochinch. : 346 (1790)
Ancistrocladus extensus var. pinangianus (Wall. ex Planch.) King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42: 137 1893
Ancistrocladus carallioides Craib Bull. Misc. Inform. Kew 1925: 19 (1925)
Ancistrocladus cochinchinensis Gagnep. Notul. Syst. (Paris) 1: 115 (1909)
Ancistrocladus extensus Wall. ex Planch. Ann. Sci. Nat., Bot. , sér. 3, 13: 318 (1849)
Ancistrocladus hainanensis Hayata Icon. Pl. Formosan. 3: 46 (1913)
Ancistrocladus harmandii Gagnep. Notul. Syst. (Paris) 1: 114 (1909)
Ancistrocladus pinangianus Wall. ex Planch. Ann. Sci. Nat., Bot. , sér. 3, 13: 318 (1849)
Ancistrocladus stelligerus Wall. ex A.DC. Prodr. 16(2): 603 (1868)

Common names Top

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Language Common/alternative name
Vietnamese trung quân lợp nhà
Chinese 钩枝藤
Chinese 本叶藤
Chinese 本蓬藤

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000970482
Tropicos 1400016
KEW urn:lsid:ipni.org:names:71950-1
The Plant List kew-8778
Open Tree Of Life 784356
NCBI Taxonomy 714108
IPNI 71950-1
iNaturalist 427903
GBIF 3659000
Freebase /m/0gg523d
EPPO BNSTE
EOL 2889986
USDA GRIN 458420
Wikipedia Ancistrocladus_tectorius

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Ancistrocladus tectorius Extract Inhibits Obesity by Promoting Thermogenesis and Mitochondrial Dynamics in High-Fat Diet-Fed Mice Kim M, Paik JH, Lee H, Kim MJ, Eum SM, Kim SY, Choi S, Park HY, Jeong HG, Jeong TS Int J Mol Sci 27-Mar-2024
PMCID:PMC11011498
doi:10.3390/ijms25073743
PMID:38612554
Naphthylisoquinoline alkaloids, a new structural template inhibitor of Nav1.7 sodium channel Wang QQ, Wang L, Zhang WB, Tang CP, Chen XQ, Zheng YM, Yao S, Gao ZB, Ye Y Acta Pharmacol Sin 04-May-2023
PMCID:PMC10462648
doi:10.1038/s41401-023-01084-9
PMID:37142682
Development of a P450 Fusion Enzyme for Biaryl Coupling in Yeast Zetzsche LE, Chakrabarty S, Narayan AR ACS Chem Biol 31-Oct-2022
PMCID:PMC10082971
doi:10.1021/acschembio.2c00690
PMID:36315613
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
In Vitro Selective Antibacterial and Antiproliferative Effects of Ethanolic Extracts from Cambodian and Philippine Plants Used in Folk Medicine for Diarrhea Treatment Kudera T, Fiserova B, Korytakova M, Doskocil I, Salmonova H, Tulin EE, Nguon S, Bande MM, Kokoska L Front Pharmacol 26-Nov-2021
PMCID:PMC8661004
doi:10.3389/fphar.2021.746808
PMID:34899301
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Revisiting the linkage between ethnomedical use and development of new medicines: A novel plant collection strategy towards the discovery of anticancer agents Henkin JM, Sydara K, Xayvue M, Souliya O, Kinghorn AD, Burdette JE, Chen WL, Elkington BG, Soejarto DD 25-Oct-2017
PMCID:PMC5686776
doi:10.5897/jmpr2017.6485
PMID:29152156
Countercurrent Separation of Natural Products: An Update Friesen JB, McAlpine JB, Chen SN, Pauli GF J Nat Prod 15-Jul-2015
PMCID:PMC4517501
doi:10.1021/np501065h
PMID:26177360
Spasmolytic activity of p-menthane esters Luciana N. Andrade Academic Journals 16-Jan-2012
doi:10.5897/JMPR11.1074
Cytotoxic and antibacterial activities of endophytic fungi isolated from plants at the National Park, Pahang, Malaysia Hazalin NA, Ramasamy K, Lim SM, Wahab IA, Cole AL, Abdul Majeed AB BMC Complement Altern Med 21-Nov-2009
PMCID:PMC2785751
doi:10.1186/1472-6882-9-46
PMID:19930582
Isolation, Structure Elucidation, and Total Synthesis of Ancistrocline, an Alkaloid of<i>Ancistrocladus tectorius</i> G. Bringmann, L. Kinzinger, H. Busse, C. Zhao Georg Thieme Verlag KG 07-Nov-2008
doi:10.1055/S-2006-961729
Traditional Medicinal Plants of Thailand, V. Ancistrotectorine, a New Naphthalene-Isoquinoline Alkaloid from Ancistrocladus tectorius Nijsiri Ruangrungsi, Varima Wongpanich, Payom Tantivatana, Heather J. Cowe, Philip J. Cox, Shinji Funayama, Geoffrey A. Cordell American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A003
Isoquinoline alkaloids from Ancistrocladus tectorius A. Montagnac, A.Hamid A. Hadi, F. Remy, M. Païs Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(94)00936-N

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Naphthalenes / Naphthoquinones
Plumbagin 10205 Click to see CC1=CC(=O)C2=C(C1=O)C=CC=C2O 188.18 unknown https://doi.org/10.1016/S0031-9422(96)00510-9
> Benzenoids / Tetralins
Isoshinanolone 443777 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0031-9422(96)00510-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1R,2S,3S,4S,5S,8R,9S,10R,11R,14R,16S,17R,18R,19R)-2,19-diacetyloxy-3-hydroxy-5-methyl-12-methylidene-4-(2-methylpropanoyloxy)-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-10-yl] benzoate 163104266 Click to see CC(C)C(=O)OC1C(C(C23C4C1(CN5C4CC67C2C(C(C(C6C35)OC(=O)C8=CC=CC=C8)C(=C)C7)OC(=O)C)C)OC(=O)C)O 619.70 unknown https://doi.org/10.1055/S-2006-957970
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(96)00510-9
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00510-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1S,3S)-5-(4-hydroxy-5-methoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 15767943 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)O)OC 393.50 unknown https://doi.org/10.1016/0031-9422(94)00936-N
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375943 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1055/S-2006-957970
(3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol 136676242 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 405.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6
2-[(1R,3R)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-7-yl]-8-methoxy-3-methylnaphthalen-1-ol 162848346 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 421.50 unknown https://doi.org/10.1021/NP50040A003
4-[(1R,3S)-6,8-dimethoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-7-yl]-8-methoxy-3-methylnaphthalen-1-ol 162946598 Click to see CC1CC2=CC(=C(C(=C2C(N1)C)OC)C3=C4C=CC=C(C4=C(C=C3C)O)OC)OC 407.50 unknown https://doi.org/10.1021/NP000091D
5-(4,5-Dimethoxy-2-methylnaphthalen-1-yl)-6,8-dimethoxy-1,3-dimethylisoquinoline 14684438 Click to see CC1=CC(=C2C(=C1C3=C(C=C(C4=C3C=C(N=C4C)C)OC)OC)C=CC=C2OC)OC 417.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6
5-(4,5-Dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,2,3-trimethyl-3,4-dihydroisoquinolin-6-one 163192420 Click to see CC1CC2=C(C(=O)C=C(C2=C(N1C)C)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 419.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6
7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 375952 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)OC 421.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6
7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-6-ol 162963746 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 421.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6
Ancistrocladidine 193880 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 405.50 unknown https://doi.org/10.1016/0031-9422(90)85241-7
Ancistrocline 158203 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 421.50 unknown https://doi.org/10.1055/S-2006-961729
Ancistrotectoriline A 10093654 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 421.50 unknown https://doi.org/10.1021/NP000091D
Ancistrotectorine 179169 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 421.50 unknown https://doi.org/10.5897/JMPR11.1074
https://doi.org/10.1021/NP50040A003
Dioncophylline A 443773 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1055/S-2006-957970
O-Methylancistrocladinine 11212280 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 419.50 unknown https://doi.org/10.1016/S0031-9422(97)00110-6

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