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Cyclea barbata

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644014ccc9c0f806346292
Scientific name Cyclea barbata
Authority Miers
First published in Contr. Bot. 3: 237 (1871)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyclea ciliata Craib Bull. Misc. Inform. Kew 1922: 230 (1922)

Common names Top

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Language Common/alternative name
Indonesian cincau (tumbuhan)
Malayalam സൈക്ളിയ ബാർബേറ്റ
su cingcau
Chinese 银不换
Chinese 毛叶轮环藤
Chinese 毛葉輪環藤

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000632046
Tropicos 50098970
KEW urn:lsid:ipni.org:names:580678-1
The Plant List kew-2750007
Open Tree Of Life 867903
NCBI Taxonomy 152373
IPNI 580678-1
iNaturalist 347715
GBIF 3830078
EOL 5517385
Wikipedia Cyclea_barbata
CMAUP NPO3849

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
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
Dietary Fiber from Soybean (Glycine max) Husk as Fat and Phosphate Replacer in Frankfurter Sausage: Effect on the Nutritional, Physicochemical and Nutraceutical Quality Araujo-Chapa AP, Urías-Orona V, Niño-Medina G, Muy-Rangel D, de la Garza AL, Castro H Molecules 26-Jun-2023
PMCID:PMC10343251
doi:10.3390/molecules28134997
PMID:37446659
Babesiosis: Current status and future perspectives in Pakistan and chemotherapy used in livestock and pet animals Azhar M, Gadahi JA, Bhutto B, Tunio S, Vistro WA, Tunio H, Bhutto S, Ram T Heliyon 18-Jun-2023
PMCID:PMC10333442
doi:10.1016/j.heliyon.2023.e17172
PMID:37441378
Comparative Investigation of Chemical Constituents of Kernels, Leaves, Husk, and Bark of Juglans regia L., Using HPLC-DAD-ESI-MS/MS Analysis and Evaluation of Their Antioxidant, Antidiabetic, and Anti-Inflammatory Activities Bourais I, Elmarrkechy S, Taha D, Badaoui B, Mourabit Y, Salhi N, Alshahrani MM, Al Awadh AA, Bouyahya A, Goh KW, Tan CS, El Hajjaji S, Dakka N, Iba N Molecules 16-Dec-2022
PMCID:PMC9788639
doi:10.3390/molecules27248989
PMID:36558122
Antibacterial and Antifungal Alkaloids from Asian Angiosperms: Distribution, Mechanisms of Action, Structure-Activity, and Clinical Potentials Sulaiman M, Jannat K, Nissapatorn V, Rahmatullah M, Paul AK, de Lourdes Pereira M, Rajagopal M, Suleiman M, Butler MS, Break MK, Weber JF, Wilairatana P, Wiart C Antibiotics (Basel) 24-Aug-2022
PMCID:PMC9495154
doi:10.3390/antibiotics11091146
PMID:36139926
Role of ethno-phytomedicine knowledge in healthcare of COVID-19: advances in traditional phytomedicine perspective Nasir Ahmed M, Hughes K Beni Suef Univ J Basic Appl Sci 04-Aug-2022
PMCID:PMC9362587
doi:10.1186/s43088-022-00277-1
PMID:35966214
Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones Arif Y, Singh P, Bajguz A, Hayat S Int J Mol Sci 04-Aug-2022
PMCID:PMC9369314
doi:10.3390/ijms23158664
PMID:35955797
Synthesis, Computational Pharmacokinetics Report, Conceptual DFT-Based Calculations and Anti-Acetylcholinesterase Activity of Hydroxyapatite Nanoparticles Derived From Acorus Calamus Plant Extract Pradeep S, Jain AS, Dharmashekara C, Prasad SK, Akshatha N, Pruthvish R, Amachawadi RG, Srinivasa C, Syed A, Elgorban AM, Al Kheraif AA, Ortega-Castro J, Frau J, Flores-Holguín N, Shivamallu C, Kollur SP, Glossman-Mitnik D Front Chem 07-Oct-2021
PMCID:PMC8529163
doi:10.3389/fchem.2021.741037
PMID:34692640
Tetrandrine suppresses the growth of human osteosarcoma cells by regulating multiple signaling pathways Wang N, Yang S, Tan T, Huang Y, Chen Y, Dong C, Chen J, Luo X Bioengineered 03-Sep-2021
PMCID:PMC8806773
doi:10.1080/21655979.2021.1967034
PMID:34477474
Medicinal Plants Used for Treating Mild Covid-19 Symptoms Among Thai Karen and Hmong Phumthum M, Nguanchoo V, Balslev H Front Pharmacol 20-Jul-2021
PMCID:PMC8329454
doi:10.3389/fphar.2021.699897
PMID:34354592
Anticholinesterase Activity of Eight Medicinal Plant Species: In Vitro and In Silico Studies in the Search for Therapeutic Agents against Alzheimer's Disease Uddin MJ, Russo D, Rahman MM, Uddin SB, Halim MA, Zidorn C, Milella L Evid Based Complement Alternat Med 25-Jun-2021
PMCID:PMC8260289
doi:10.1155/2021/9995614
PMID:34257698
Immunomodulatory and Antioxidant Activities of Select Indonesian Vegetables, Herbs, and Spices on Human Lymphocytes Safriani N, Rungkat FZ, Yuliana ND, Prangdimurti E Int J Food Sci 06-Mar-2021
PMCID:PMC7960050
doi:10.1155/2021/6340476
PMID:33748265
Findings of Research Misconduct N/A Fed Regist 04-Feb-2021
PMCID:PMC7862038
PMID:33568876
Wild food plants and fungi sold in the markets of Luang Prabang, Lao PDR Łuczaj Ł, Lamxay V, Tongchan K, Xayphakatsa K, Phimmakong K, Radavanh S, Kanyasone V, Pietras M, Karbarz M J Ethnobiol Ethnomed 26-Jan-2021
PMCID:PMC7835671
doi:10.1186/s13002-020-00423-y
PMID:33499871
The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A Acta Pharm Sin B 16-Oct-2020
PMCID:PMC8343124
doi:10.1016/j.apsb.2020.10.012
PMID:34386319

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(6aR)-2,11-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 739273 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=CC=C4)OC)O)OC 311.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
1,2-dimethoxy-12-methyl-5,6,11b,13-tetrahydro-4bH-[1,3]benzodioxolo[5,6-c]phenanthridin-5-ol 3446460 Click to see CN1CC2=C(C=CC(=C2OC)OC)C3C1C4=CC5=C(C=C4CC3O)OCO5 369.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(-)-Cycleapeltine 3084718 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50091A004
https://doi.org/10.1021/NP50101A020
(-)-Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50101A020
(14S)-6,20,21,25-tetramethoxy-15-methyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-1(30),3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-tridecaene 5315989 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6=NCCC7=CC(=C(O3)C=C76)OC)OC)OC)OC 606.70 unknown via CMAUP database
(14S)-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 10054445 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC 608.70 unknown via CMAUP database
(1R,14R)-9,20,25-trimethoxy-30-methyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 23259240 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6)OC)O)OC)OC 594.70 unknown https://doi.org/10.1021/NP50101A020
(1R,14S)-9,20,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 5458555 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
(1S,14R)-10,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9,11,18,20,22(33),24,26,31,34-dodecaen-21-ol 161315820 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=C(CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)C=C5)OC)OC 608.70 unknown https://doi.org/10.1021/NP50101A020
(1S,14S,30R)-9,20,21,25-tetramethoxy-15,30-dimethyl-30-oxido-7,23-dioxa-15-aza-30-azoniaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene 102121490 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C=C7CC[N+]6(C)[O-])OC)O3)C=C5)OC)OC 638.70 unknown https://doi.org/10.1002/ARDP.19773100204
1-Isotetrandrine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Cycleabarbatine 192607 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)O)OC)OC)OC 608.70 unknown https://doi.org/10.1021/NP50101A020
Fangchinoline 73481 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1055/S-0028-1097974
Homoaromoline 99620 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP50091A004
Isofangchinoline 321937 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1055/S-0028-1097974
Limacine 7656034 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50101A020
Tetrandrine 73078 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50101A020
Tetrandrine N2'-oxide 44559015 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C=C7CC[N+]6(C)[O-])OC)O3)C=C5)OC)OC 638.70 unknown https://doi.org/10.1021/NP50101A020
https://doi.org/10.1002/ARDP.19773100204
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50091A004
https://doi.org/10.1055/S-0028-1097974
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
Tetraneurin A 174868 Click to see CC(=O)OCC1CCC2C(C3(C1(CCC3=O)O)C)OC(=O)C2=C 322.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
1,2,3,4,5-Cyclohexanepentol 101715 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown https://doi.org/10.1002/ARDP.19823150104
Cyclohexane-1,2,3,4,5-pentol 12309654 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown https://doi.org/10.1002/ARDP.19823150104
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide 5318530 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O 505.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(1R,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.218,21.18,12.027,31.016,35]heptatriaconta-3(37),4,6(36),8(35),9,11,18,20,24,26,31,33-dodecaen-32-ol 154495894 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(CO3)C=C7)N(CCC6=CC(=C5OC)OC)C)O)OC 622.70 unknown https://doi.org/10.1021/NP50101A020
12-O-Methylcurine 16637550 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)OC)O3)N(CCC6=CC(=C5O)OC)C)OC 608.70 unknown https://doi.org/10.1021/NP50101A020
Curine 253793 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)N(CCC6=CC(=C5O)OC)C)OC 594.70 unknown https://doi.org/10.1021/NP50101A020
Isochondrodendrine 197726 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5O)OC)C)O)OC 594.70 unknown https://doi.org/10.1021/NP50101A020
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Coclaurine 440989 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1021/NP50101A020
(R)-N-Methylcoclaurine 440595 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1021/NP50101A020
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1021/NP50101A020
Csh 068 259676 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Thamnolic acid 4316933 Click to see CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2C)C(=O)O)O)C=O)O)O)C(=O)O)OC 420.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database

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