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Mikania cordata

Mikania cordata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd3c683beb805248975
Scientific name Mikania cordata
Authority (Burm.f.) B.L.Rob.
First published in Contr. Gray Herb. 104: 65. 1934

Description Top

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Synonyms Top

Scientific name Authority First published in
Mikania sagittata Blanco 54 1837
Eupatorium volubile Norona Verh. Batav. Genootsch. Kunst. Wet. 5, 4 (1790)
Eupatorium cordatum Burm.f. Fl. Ind. : 176 (1768)
Eupatorium volubile Vahl Symb. Bot. iii. 93 (1794)
Mikania volubilis (Vahl) Willd. Sp. Pl., ed. 4 , 3: 1743 (1803)
Mikania carteri Baker Bull. Misc. Inform. Kew 1895: 106 (1895)

Common names Top

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Language Common/alternative name
English heartleaf hempvine
Indonesian sembung rambat
Malay selaput tunggul
Thai ขี้เหล็กย่าน
Chinese 假泽兰
Chinese 蔓澤蘭
Chinese 米甘草

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000134806
USDA Plants MICO16
Tropicos 2701037
KEW urn:lsid:ipni.org:names:160848-2
The Plant List gcc-95578
Open Tree Of Life 44709
NCBI Taxonomy 207834
IPNI 232825-1
iNaturalist 427203
GBIF 5398634
EPPO MIKCO
EOL 489532
USDA GRIN 316382
Wikipedia Mikania_cordata

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
Accumulate and consolidate the traditional vernacular timber preservation technologies through a field survey Mendis MS, Abeyrathna W, Halwatura RU, Amarasekara HS, Somadewa R, Jayasinghe R Heliyon 20-Dec-2023
PMCID:PMC10787270
doi:10.1016/j.heliyon.2023.e23907
PMID:38223715
Loss of plastid ndh genes in an autotrophic desert plant Kharabian-Masouleh A, Furtado A, Alsubaie B, Al-Dossary O, Wu A, Al-Mssalem I, Henry R Comput Struct Biotechnol J 14-Oct-2023
PMCID:PMC10589726
doi:10.1016/j.csbj.2023.10.023
PMID:37867970
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS Life (Basel) 04-Apr-2023
PMCID:PMC10145550
doi:10.3390/life13040948
PMID:37109477
Silver Nanoparticles Synthesized from Abies alba and Pinus sylvestris Bark Extracts: Characterization, Antioxidant, Cytotoxic, and Antibacterial Effects Macovei I, Luca SV, Skalicka-Woźniak K, Horhogea CE, Rimbu CM, Sacarescu L, Vochita G, Gherghel D, Ivanescu BL, Panainte AD, Nechita C, Corciova A, Miron A Antioxidants (Basel) 24-Mar-2023
PMCID:PMC10135277
doi:10.3390/antiox12040797
PMID:37107172
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Immunomodulatory Potency of Eclipta alba (Bhringaraj) Leaf Extract in Heteropneustes fossilis against Oomycete Pathogen, Aphanomyces invadans Kumar V, Das BK, Swain HS, Chowdhury H, Roy S, Bera AK, Malick RC, Behera BK J Fungi (Basel) 21-Jan-2023
PMCID:PMC9963822
doi:10.3390/jof9020142
PMID:36836257
Methods used for the study of endophytic fungi: a review on methodologies and challenges, and associated tips dos Reis JB, Lorenzi AS, do Vale HM Arch Microbiol 20-Oct-2022
PMCID:PMC9584250
doi:10.1007/s00203-022-03283-0
PMID:36264513
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100
Comparative chloroplast genome analysis of Ficus (Moraceae): Insight into adaptive evolution and mutational hotspot regions Zhang ZR, Yang X, Li WY, Peng YQ, Gao J Front Plant Sci 15-Sep-2022
PMCID:PMC9521400
doi:10.3389/fpls.2022.965335
PMID:36186045
Outbreak of Ichthyophthirius multifiliis associated with Aeromonas hydrophila in Pangasianodon hypophthalmus: The role of turmeric oil in enhancing immunity and inducing resistance against co-infection Kumar V, Das BK, Swain HS, Chowdhury H, Roy S, Bera AK, Das R, Parida SN, Dhar S, Jana AK, Behera BK Front Immunol 02-Sep-2022
PMCID:PMC9478419
doi:10.3389/fimmu.2022.956478
PMID:36119096
Medicinal plant sources and traditional healthcare practices of forest-dependent communities in and around Chunati Wildlife Sanctuary in southeastern Bangladesh Rahman MH, Roy B, Chowdhury GM, Hasan A, Saimun MS 07-Jun-2022
PMCID:PMC9170557
doi:10.1007/s42398-022-00230-z
PMID:37521586
Promising antimicrobials from Phoma spp.: progress and prospects Rai M, Zimowska B, Gade A, Ingle P AMB Express 23-May-2022
PMCID:PMC9125353
doi:10.1186/s13568-022-01404-y
PMID:35604500
Pest categorisation of Maconellicoccus hirsutus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Sven Magnusson C, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Antonatos S, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 11-Jan-2022
PMCID:PMC8749475
doi:10.2903/j.efsa.2022.7024
PMID:35035580
On the Edge of Dispensability, the Chloroplast ndh Genes Sabater B Int J Mol Sci 19-Nov-2021
PMCID:PMC8621559
doi:10.3390/ijms222212505
PMID:34830386

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
methyl (1R,4S,5R,9S,10S,13R,15S)-15-benzoyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162995813 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4OC(=O)C5=CC=CC=C5)(C)C(=O)OC 436.60 unknown https://doi.org/10.1016/S0031-9422(00)89343-7
methyl (1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-14-methylidene-15-(2-methylpropanoyloxy)tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162966742 Click to see CC(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)OC)C 402.60 unknown https://doi.org/10.1016/S0031-9422(00)89343-7
Methyl 15-benzoyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162995812 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4OC(=O)C5=CC=CC=C5)(C)C(=O)OC 436.60 unknown https://doi.org/10.1016/S0031-9422(00)89343-7
Methyl 5,9-dimethyl-14-methylidene-15-(2-methylpropanoyloxy)tetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate 162966741 Click to see CC(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)OC)C 402.60 unknown https://doi.org/10.1016/S0031-9422(00)89343-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,8R,9S,10R,13S,14S,17R)-17-[(Z,5R)-5-ethyl-6-methylhept-2-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163186622 Click to see CCC(CC=C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)82193-7
17-(5-ethyl-6-methylhept-2-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 85767808 Click to see CCC(CC=C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)82193-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(3,8-Dimethyl-4,14-dioxo-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-en-12-yl) acetate 14081915 Click to see CC1C2C(CC3(C(O3)CC(C4=CC2OC4=O)OC(=O)C)C)OC1=O 336.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
[(1R,2R,3S,6S,8S,10S,12S)-3,8-dimethyl-4,14-dioxo-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-en-12-yl] acetate 162951801 Click to see CC1C2C(CC3(C(O3)CC(C4=CC2OC4=O)OC(=O)C)C)OC1=O 336.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
[(1R,2R,6S,8S,10S,12S)-8-methyl-3-methylidene-4,14-dioxo-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-en-12-yl] acetate 101324872 Click to see CC(=O)OC1CC2C(O2)(CC3C(C4C=C1C(=O)O4)C(=C)C(=O)O3)C 334.30 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
https://doi.org/10.1016/S0367-326X(01)00318-5
https://doi.org/10.1016/0031-9422(94)00864-P
https://doi.org/10.1055/S-2006-960953
Scandenolide 98927 Click to see CC(=O)OC1CC2C(O2)(CC3C(C4C=C1C(=O)O4)C(=C)C(=O)O3)C 334.30 unknown https://doi.org/10.1016/S0367-326X(01)00318-5
https://doi.org/10.1055/S-2006-960953
https://doi.org/10.1016/0031-9422(94)00864-P
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(10-Hydroxy-3-methyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-8-yl)methyl acetate 162973348 Click to see CC(=O)OCC1=CC(C2C(CC3(C(O3)CC1)C)OC(=O)C2=C)O 322.40 unknown https://doi.org/10.1016/0031-9422(94)00864-P
(1R,2R,3R,6S,8S,10S,12S)-12-hydroxy-3,8-dimethyl-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-ene-4,14-dione 162994780 Click to see CC1C2C(CC3(C(O3)CC(C4=CC2OC4=O)O)C)OC1=O 294.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
(1R,2R,3R,6S,8S,10S)-3,8-dimethyl-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-ene-4,14-dione 45267918 Click to see CC1C2C(CC3(C(O3)CCC4=CC2OC4=O)C)OC1=O 278.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
(3-Methyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-8-yl)methyl acetate 162928149 Click to see CC(=O)OCC1=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C 306.40 unknown https://doi.org/10.1016/0031-9422(94)00864-P
[(1S,3S,5S,8E,11R)-3-methyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-8-yl]methyl acetate 101920249 Click to see CC(=O)OCC1=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C 306.40 unknown https://doi.org/10.1016/0031-9422(94)00864-P
[(1S,3S,5S,8Z,10R,11S)-10-hydroxy-3-methyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-8-yl]methyl acetate 162973349 Click to see CC(=O)OCC1=CC(C2C(CC3(C(O3)CC1)C)OC(=O)C2=C)O 322.40 unknown https://doi.org/10.1016/0031-9422(94)00864-P
[(1S,3S,5S,8Z,11R)-3-methyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradec-8-en-8-yl]methyl acetate 162928150 Click to see CC(=O)OCC1=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C 306.40 unknown https://doi.org/10.1016/0031-9422(94)00864-P
12-Hydroxy-3,8-dimethyl-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-ene-4,14-dione 72508255 Click to see CC1C2C(CC3(C(O3)CC(C4=CC2OC4=O)O)C)OC1=O 294.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
3,8-Dimethyl-5,9,15-trioxatetracyclo[11.2.1.02,6.08,10]hexadec-13(16)-ene-4,14-dione 56671203 Click to see CC1C2C(CC3(C(O3)CCC4=CC2OC4=O)C)OC1=O 278.30 unknown https://doi.org/10.1016/0031-9422(94)00864-P
7-Methyl-12-methylidene-3,6,10,15-tetraoxapentacyclo[12.2.1.02,4.05,7.09,13]heptadec-1(17)-ene-11,16-dione 5140086 Click to see CC12CC3C(C4C=C(C5C(C1O2)O5)C(=O)O4)C(=C)C(=O)O3 290.27 unknown https://doi.org/10.1016/0031-9422(94)00864-P
Deoxymikanolide 14081913 Click to see CC12CC3C(C4C=C(CCC1O2)C(=O)O4)C(=C)C(=O)O3 276.28 unknown https://doi.org/10.1016/0031-9422(94)00864-P
https://doi.org/10.1016/S0305-1978(02)00250-8
https://doi.org/10.1016/S0367-326X(01)00318-5
Dihydromikanolide 442200 Click to see CC1C2C(CC3(C(O3)C4C(O4)C5=CC2OC5=O)C)OC1=O 292.28 unknown https://doi.org/10.1016/S0367-326X(01)00318-5
https://doi.org/10.1016/0031-9422(94)00864-P
https://doi.org/10.1016/S0305-1978(02)00250-8
Mikanolide 442282 Click to see CC12CC3C(C4C=C(C5C(C1O2)O5)C(=O)O4)C(=C)C(=O)O3 290.27 unknown https://doi.org/10.1016/S0367-326X(01)00318-5
https://doi.org/10.1016/S0305-1978(02)00250-8
https://doi.org/10.1016/0031-9422(94)00864-P
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupalitin 3-O-sulfate 44259774 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OS(=O)(=O)O)C3=CC=C(C=C3)O)O)OC 410.40 unknown https://doi.org/10.1016/S0305-1978(02)00250-8
Mikanin 3-O-sulfate 14630674 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OS(=O)(=O)O 424.40 unknown https://doi.org/10.1016/S0305-1978(02)00250-8

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