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Cocculus hirsutus

Cocculus hirsutus - 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 UUID644012623c122660795806
Scientific name Cocculus hirsutus
Authority (L.) W.Theob.
First published in Burmah , ed. 3, 2: 657 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Menispermum hastatum Lam. Encycl. 4: 98 (1797)
Menispermum hirsutum L. Sp. Pl. : 341 (1753)
Menispermum myosotoides L. Sp. Pl. : 341 (1753)
Cebatha hirsuta (L.) Kuntze Revis. Gen. Pl. 1: 9 (1891)
Cebatha villosa C.Chr. Dansk Bot. Ark. iv. No. 3, 37 (1922).
Cocculus aristolochiae DC. Syst. Nat. 1: 520 (1817)
Cocculus hastatus DC. Syst. Nat. 1: 522 (1817)
Cocculus holopeira-torridus Broun & R.E.Massey Fl. Sudan : 53 (1929)
Cocculus linnaeanus Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 43: 62 (1874)
Cocculus sepium Colebr. Trans. Linn. Soc. London 13: 58 (1821)
Cocculus villosus DC. Syst. Nat. [Candolle] 1: 525. 1817 [1818 publ. 1-15 Nov 1817]
Holopeira villosa (Lam.) Miers Ann. Mag. Nat. Hist. , ser. 3, 19: 28 (1867)
Cocculus hirsutus (L.) Diels Pflanzenr. (Engler) IV. 94(Heft 46): 236. 1910 [6 Dec 1910]

Common names Top

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Language Common/alternative name
English broom creeper
English bushveld moonseed creeper
English python climber
Afrikaans bosveld-halfmaanranke
Arabic عنيبية وبرية
Malayalam പാതാളഗരുഡക്കൊടി
Marathi वासनवेल
Chinese 多毛木防己

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

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-0000613546
KEW urn:lsid:ipni.org:names:941634-1
The Plant List kew-2729659
Open Tree Of Life 591388
NCBI Taxonomy 421226
IPNI 580559-1
iNaturalist 582499
GBIF 3829491
EPPO COUHI
EOL 2877918
USDA GRIN 423360
Wikipedia Cocculus_hirsutus

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
Green synthesis of Piper nigrum copper-based nanoparticles: in silico study and ADMET analysis to assess their antioxidant, antibacterial, and cytotoxic effects Kiranmayee M, Rajesh N, Vidya Vani M, Khadri H, Mohammed A, Chinni SV, Ramachawolran G, Riazunnisa K, Moussa AY Front Chem 05-Sep-2023
PMCID:PMC10509375
doi:10.3389/fchem.2023.1218588
PMID:37736256
From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds Isopencu GO, Covaliu-Mierlă CI, Deleanu IM Plants (Basel) 16-Jul-2023
PMCID:PMC10386126
doi:10.3390/plants12142661
PMID:37514275
Comment on Villalva et al. Antioxidant, Anti-Inflammatory, and Antibacterial Properties of an Achillea millefolium L. Extract and Its Fractions Obtained by Supercritical Anti-Solvent Fractionation against Helicobacter pylori. Antioxidants 2022, 11, 1849 Frański R, Beszterda-Buszczak M Antioxidants (Basel) 07-Jun-2023
PMCID:PMC10295287
doi:10.3390/antiox12061226
PMID:37371956
A multivariate and quantitative assessment of medicinal plants used by the indigenous Malayali tribes in the Javadhu hills of Tiruvannamalai district, Tamil Nadu, India Silambarasan R, Sasidharan S, Nair J H, Kumar S N, R A, Nair AS, Selavinayagam KT Heliyon 18-Apr-2023
PMCID:PMC10256831
doi:10.1016/j.heliyon.2023.e15607
PMID:37305490
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
The wound healing effect of botanicals and pure natural substances used in in vivo models El-Sherbeni SA, Negm WA Inflammopharmacology 22-Feb-2023
PMCID:PMC10140094
doi:10.1007/s10787-023-01157-5
PMID:36811778
Sinococuline, a bioactive compound of Cocculus hirsutus has potent anti-dengue activity Shukla R, Ahuja R, Beesetti H, Garg A, Aggarwal C, Chaturvedi S, Nayyar K, Arora U, Lal AA, Khanna N Sci Rep 19-Jan-2023
PMCID:PMC9852271
doi:10.1038/s41598-023-27927-3
PMID:36658277
Hemisynthetic alkaloids derived from trilobine are antimalarials with sustained activity in multidrug-resistant Plasmodium falciparum Nardella F, Dobrescu I, Hassan H, Rodrigues F, Thiberge S, Mancio-Silva L, Tafit A, Jallet C, Cadet-Daniel V, Goussin S, Lorthiois A, Menon Y, Molinier N, Pechalrieu D, Long C, Sautel F, Matondo M, Duchateau M, Médard G, Witkowski B, Scherf A, Halby L, Arimondo PB iScience 11-Jan-2023
PMCID:PMC9883252
doi:10.1016/j.isci.2023.105940
PMID:36718363
Phytochemical Profiling of Sambucus nigra L. Flower and Leaf Extracts and Their Antimicrobial Potential against Almond Tree Pathogens Sánchez-Hernández E, Balduque-Gil J, González-García V, Barriuso-Vargas JJ, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P Int J Mol Sci 06-Jan-2023
PMCID:PMC9866908
doi:10.3390/ijms24021154
PMID:36674670
Management of Dengue: An Updated Review Tayal A, Kabra SK, Lodha R Indian J Pediatr 27-Dec-2022
PMCID:PMC9793358
doi:10.1007/s12098-022-04394-8
PMID:36574088
Ayurvedic Management of Prurigo nodularis at scalp: A case report Javed D J Ayurveda Integr Med 28-Nov-2022
PMCID:PMC9707002
doi:10.1016/j.jaim.2022.100668
PMID:36455368
Cardio-protective effect of Cocculus hirsutus in experimental hypertension in rats Gunjegaonkar SM, Khakal VR, Joshi AA, Nargund SL, Shinde SD, Khan NS J Ayurveda Integr Med 17-Nov-2022
PMCID:PMC9678779
doi:10.1016/j.jaim.2022.100652
PMID:36403501
Chickpea (Cicer arietinum L.) Biology and Biotechnology: From Domestication to Biofortification and Biopharming Koul B, Sharma K, Sehgal V, Yadav D, Mishra M, Bharadwaj C Plants (Basel) 30-Oct-2022
PMCID:PMC9654780
doi:10.3390/plants11212926
PMID:36365379
Phytochemicals as potential inhibitors for COVID-19 revealed by molecular docking, molecular dynamic simulation and DFT studies Puthanveedu V, Muraleedharan K Struct Chem 13-Jun-2022
PMCID:PMC9189813
doi:10.1007/s11224-022-01982-4
PMID:35729939
Clinical safety and pharmacokinetic evaluation of aqueous extract of Cocculus hirsutus, an anti-viral phytopharmacetical drug as a potential for the treatment of dengue and COVID-19 Dar SK, Kumar S, Maiti S, Dhawan S, Joglekar S, Arora U, Kalra R, Madan S, Lal AA, Singamaneni V, Gupta P, Nandi U, Singh D, Khuroo AH Heliyon 13-May-2022
PMCID:PMC9098428
doi:10.1016/j.heliyon.2022.e09416
PMID:35582330

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
> Alkaloids and derivatives / Aporphines
Magnoflorine 73337 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1080/10575639308043793
> Alkaloids and derivatives / Corynanthean-type alkaloids
Hirsutine 3037884 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown https://doi.org/10.1021/NP50074A037
> Lignans, neolignans and related compounds
Isotrilobine 12310578 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)OC)OC 576.70 unknown https://doi.org/10.1080/10575639308043793
Trilobine 169007 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O4)C(=C(C=C8CCN7)OC)O3)C=C6 562.70 unknown https://doi.org/10.1080/10575639308043793
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown https://doi.org/10.1016/S0031-9422(00)84788-3
Ginnol 16057860 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown https://doi.org/10.1016/S0031-9422(00)84788-3
Nonacosan-10-ol 25240035 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown https://doi.org/10.1016/S0031-9422(00)84788-3
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1080/10575639308043793
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1080/10575639308043793
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
(1R,17S)-5,6-dihydroxy-17-methoxy-10-azatetracyclo[8.8.0.01,14.03,8]octadeca-3,5,7,14-tetraen-9-one 163106500 Click to see COC1CC=C2CCCN3C2(C1)CC4=CC(=C(C=C4C3=O)O)O 315.40 unknown https://doi.org/10.1021/NP50074A037
(1R,17S)-5,6,17-trimethoxy-10-azatetracyclo[8.8.0.01,14.03,8]octadeca-3,5,7,14-tetraen-9-one 13946037 Click to see COC1CC=C2CCCN3C2(C1)CC4=CC(=C(C=C4C3=O)OC)OC 343.40 unknown https://doi.org/10.1016/S0040-4020(01)87792-9
5,6-Dihydroxy-17-methoxy-10-azatetracyclo[8.8.0.01,14.03,8]octadeca-3,5,7,14-tetraen-9-one 163106499 Click to see COC1CC=C2CCCN3C2(C1)CC4=CC(=C(C=C4C3=O)O)O 315.40 unknown https://doi.org/10.1021/NP50074A037
https://doi.org/10.1080/10575639308043793
5,6,17-Trimethoxy-10-azatetracyclo[8.8.0.01,14.03,8]octadeca-3,5,7,14-tetraen-9-one 13946036 Click to see COC1CC=C2CCCN3C2(C1)CC4=CC(=C(C=C4C3=O)OC)OC 343.40 unknown https://doi.org/10.1080/10575639308043793
https://doi.org/10.1016/S0040-4020(01)87792-9
6-Hydroxy-5,17-dimethoxy-10-azatetracyclo[8.8.0.01,14.03,8]octadeca-3,5,7,14-tetraen-9-one 163106840 Click to see COC1CC=C2CCCN3C2(C1)CC4=CC(=C(C=C4C3=O)O)OC 329.40 unknown https://doi.org/10.1080/10575639308043793
https://doi.org/10.1016/S0031-9422(00)95239-7
methyl (12aR,12bR)-2,3-dimethoxy-6-oxo-5,8,10,11,12,12b-hexahydroisoindolo[1,2-a]isoquinoline-12a-carboxylate 162977514 Click to see COC1=C(C=C2C3C4(CCCC=C4CN3C(=O)CC2=C1)C(=O)OC)OC 357.40 unknown https://doi.org/10.1016/0031-9422(93)85490-I
Methyl 2,3-dimethoxy-6-oxo-5,8,10,11,12,12b-hexahydroisoindolo[1,2-a]isoquinoline-12a-carboxylate 162977513 Click to see COC1=C(C=C2C3C4(CCCC=C4CN3C(=O)CC2=C1)C(=O)OC)OC 357.40 unknown https://doi.org/10.1016/0031-9422(93)85490-I
https://doi.org/10.1080/10575639308043793
methyl 3'-ethyl-1-hydroxy-6',7'-dimethoxy-2'-methyl-3,4'-dioxospiro[1,4,5,6-tetrahydroindene-2,1'-3H-isoquinoline]-3a-carboxylate 162873283 Click to see CCC1C(=O)C2=CC(=C(C=C2C3(N1C)C(C4=CCCCC4(C3=O)C(=O)OC)O)OC)OC 443.50 unknown https://doi.org/10.1080/10575639308043793
> Organoheterocyclic compounds / Tetrahydroisoquinolines
5,16-Dimethoxy-10-azatetracyclo[8.7.0.01,13.03,8]heptadeca-3,5,7,13-tetraen-6-ol 163105271 Click to see COC1CC=C2CCN3C2(C1)CC4=CC(=C(C=C4C3)O)OC 301.40 unknown https://doi.org/10.1021/NP50080A016
https://doi.org/10.1080/10575639308043793
Jamtine 11739413 Click to see COC1=C(C=C2C3C4(CCCC=C4CN3CCC2=C1)C(=O)OC)OC 343.40 unknown https://doi.org/10.3987/R-1987-05-1251
Jamtine-N-oxide 12114535 Click to see COC1=C(C=C2C3C4(CCCC=C4C[N+]3(CCC2=C1)[O-])C(=O)OC)OC 359.40 unknown https://doi.org/10.3987/R-1987-05-1251
https://doi.org/10.1080/10575639308043793
> Phenylpropanoids and polyketides / Depsides and depsidones
10-Chloro-3,9-dihydroxy-1-(2-hydroxybutan-2-yl)-4,7-dimethylbenzo[b][1,4]benzodioxepin-6-one 71437138 Click to see CCC(C)(C1=CC(=C(C2=C1OC3=C(C(=CC(=C3Cl)O)C)C(=O)O2)C)O)O 378.80 unknown https://doi.org/10.1080/10575639308043793

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