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Ancistrocladus heyneanus

Ancistrocladus heyneanus - 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 UUID64403c980e552675843328
Scientific name Ancistrocladus heyneanus
Authority Wall. ex J.Graham
First published in Cat. Pl. Bombay : 28 (1839)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Malayalam മോതിരവള്ളി
Marathi करदळ
Chinese 印度钩枝藤
Chinese 海尼钩枝藤

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

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-0000970363
Tropicos 50042014
KEW urn:lsid:ipni.org:names:71944-1
The Plant List kew-8767
Open Tree Of Life 992169
NCBI Taxonomy 122297
IPNI 320533-1
iNaturalist 880761
GBIF 3658991
Freebase /m/0rytm73
EOL 6874709
Wikipedia Ancistrocladus_heyneanus

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
Treating COVID-19 with Medicinal Plants: Is It Even Conceivable? A Comprehensive Review Al-Jamal H, Idriss S, Roufayel R, Abi Khattar Z, Fajloun Z, Sabatier JM Viruses 20-Feb-2024
PMCID:PMC10974729
doi:10.3390/v16030320
PMID:38543686
Biosynthesis of Copper Nanoparticles with Medicinal Plants Extracts: From Extraction Methods to Applications Antonio-Pérez A, Durán-Armenta LF, Pérez-Loredo MG, Torres-Huerta AL Micromachines (Basel) 30-Sep-2023
PMCID:PMC10609153
doi:10.3390/mi14101882
PMID:37893319
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
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 Antiviral Activity of Potential Medicinal Plant Extracts Against Dengue and Chikungunya Viruses Alagarasu K, Patil P, Kaushik M, Chowdhury D, Joshi RK, Hegde HV, Kakade MB, Hoti SL, Cherian S, Parashar D Front Cell Infect Microbiol 07-Apr-2022
PMCID:PMC9021897
doi:10.3389/fcimb.2022.866452
PMID:35463636
Potential of Triterpenic Natural Compound Betulinic Acid for Neglected Tropical Diseases New Treatments Rocha V, Quadros H, Meira C, Silva L, Carvalho D, Hodel K, Moreira D, Soares M Biomedicines 01-Apr-2022
PMCID:PMC9027248
doi:10.3390/biomedicines10040831
PMID:35453582
Asymmetric Synthesis of Axially Chiral C−N Atropisomers Rodríguez‐Salamanca P, Fernández R, Hornillos V, Lassaletta JM Chemistry 25-Mar-2022
PMCID:PMC9314733
doi:10.1002/chem.202104442
PMID:35191558
Computational study to discover potent phytochemical inhibitors against drug target, squalene synthase from Leishmania donovani Wadanambi PM, Mannapperuma U Heliyon 31-May-2021
PMCID:PMC8188062
doi:10.1016/j.heliyon.2021.e07178
PMID:34141935
Betulinic Acid Protects DOX-Triggered Cardiomyocyte Hypertrophy Response through the GATA-4/Calcineurin/NFAT Pathway Yoon JJ, Son CO, Kim HY, Han BH, Lee YJ, Lee HS, Kang DG Molecules 24-Dec-2020
PMCID:PMC7795060
doi:10.3390/molecules26010053
PMID:33374365
Indirect Regeneration and Assessment of Genetic Fidelity of Acclimated Plantlets by SCoT, ISSR, and RAPD Markers in Rauwolfia tetraphylla L.: An Endangered Medicinal Plant Rohela GK, Jogam P, Bylla P, Reuben C Biomed Res Int 11-Apr-2019
PMCID:PMC6487127
doi:10.1155/2019/3698742
PMID:31111050
The effect of betulinic acid on leptin, adiponectin, hepatic enzyme levels and lipid profiles in streptozotocin–nicotinamide-induced diabetic mice Ahangarpour A, Shabani R, Farbood Y Res Pharm Sci 01-Apr-2018
PMCID:PMC5842485
doi:10.4103/1735-5362.223796
PMID:29606968
Extraction efficiency, phytochemical profiles and antioxidative properties of different parts of Saptarangi (Salacia chinensis L.) – An important underutilized plant Ghadage DM, Kshirsagar PR, Pai SR, Chavan JJ Biochem Biophys Rep 24-Aug-2017
PMCID:PMC5613233
doi:10.1016/j.bbrep.2017.08.012
PMID:28955795
Effects of Betulinic Acid on the Male Reproductive System of a Streptozotocin-Nicotinamide-Induced Diabetic Mouse Model Ahangarpour A, Oroojan AA, Khorsandi L, Arzani G, Afshari G World J Mens Health 22-Dec-2016
PMCID:PMC5209562
doi:10.5534/wjmh.2016.34.3.209
PMID:28053951
Studies on the Anti-Inflammatory, Analgesic and Antipyrexic Activities of Betulinic Acid Derived from Tetracera Potatoria Oyebanji BO, Saba AB, Oridupa OA Afr J Tradit Complement Altern Med 02-Nov-2013
PMCID:PMC3957239
PMID:24653551
New Betulinic Acid Derivatives as Potent Proteasome Inhibitors Qian K, Kim SY, Hung HY, Huang L, Chen CH, Lee KH Bioorg Med Chem Lett 26-Jul-2011
PMCID:PMC3171619
doi:10.1016/j.bmcl.2011.07.072
PMID:21856154

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/S0040-4039(98)01935-2
> Benzenoids / Tetralins
Isoshinanolone 443777 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0040-4039(98)01935-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aS,6bS,8aR,12aS,14aR,14bS)-4,4,6b,8a,11,11,12a,14b-octamethyl-1,2,3,4a,5,6a,7,8,9,10,12,13,14,14a-tetradecahydropicen-3-ol 162940792 Click to see CC1(CCC2(CCC3(C(C2(C1)C)CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0040-4020(01)92503-7
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol 12306781 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1016/S0031-9422(00)90546-6
(3R)-7-(1-hydroxy-8-methoxy-3-methylnaphthalen-2-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol 162874829 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 391.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026
(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/S0040-4020(01)92503-7
(3S)-7-(5-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-3,4-dihydroisoquinolin-6-ol 135419358 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)O)C)O 391.50 unknown https://doi.org/10.1016/S0031-9422(96)00358-5
https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026
Ancisheynine 21580079 Click to see CC1=CC2=C(C=CC(=C2C(=C1)OC)OC)[N+]3=C(C4=C(C=C(C=C4C=C3C)OC)OC)C 418.50 unknown https://doi.org/10.1002/CHIN.200346199
https://doi.org/10.1016/S0040-4039(03)01397-2
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/J.PHYTOCHEM.2004.05.026
Ancistrocladine 161741 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026
https://doi.org/10.1016/S0031-9422(00)90546-6
Ancistrocladisine 375958 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)OC 419.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026
Ancistroheynine B 135508453 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 391.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026
Ancistrotanzanine C 11350305 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 407.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.026

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