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Helietta apiculata

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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 UUID64401ffa144d9127163834
Scientific name Helietta apiculata
Authority Benth.
First published in Hooker's Icon. Pl. 14: 67. 1882

Description Top

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Synonyms Top

Scientific name Authority First published in
Esenbeckia cuspidata Engl. Beibl. Bot. Jahrb. Syst. 54: 28 (1896)
Helietta cuspidata Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 4: 1285 (1904)
Helietta cuspidata f. gracilis Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 4: 1285 (1904)
Helietta cuspidata f. latifolia Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 4: 1285 (1904)
Helietta cuspidata f. subobtusa Chodat & Hassl. Bull. Herb. Boissier ser. 2, 4: 1285. 1904
Helietta longifoliata Britton Ann. New York Acad. Sci. 7: 69 (1892)
Esenbeckia cuspidata Mitt. Hooker's J. Bot. Kew Gard. Misc. 8: 263 1856

Common names Top

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Language Common/alternative name
gn yvyra ovi

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-0000718163
Tropicos 28101320
KEW urn:lsid:ipni.org:names:77221758-1
The Plant List kew-2843303
Open Tree Of Life 5747575
NCBI Taxonomy 2364054
IUCN Red List 211565585
iNaturalist 969070
GBIF 7802673
CMAUP NPO20865

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
Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties Szewczyk A, Pęczek F Int J Mol Sci 15-Aug-2023
PMCID:PMC10454094
doi:10.3390/ijms241612811
PMID:37628986
Phenolic Compounds in Bacterial Inactivation: A Perspective from Brazil Kauffmann AC, Castro VS Antibiotics (Basel) 24-Mar-2023
PMCID:PMC10135396
doi:10.3390/antibiotics12040645
PMID:37107007
Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV Int J Mol Sci 02-Feb-2023
PMCID:PMC9917851
doi:10.3390/ijms24032839
PMID:36769163
Essential Oils of Aromatic Plant Species from the Atlantic Rainforest Exhibit Extensive Chemical Diversity and Antimicrobial Activity Perigo CV, Haber LL, Facanali R, Vieira MA, Torres RB, Bernacci LC, Guimarães EF, Baitello JB, Sobral ME, Quecini V, Marques MO Antibiotics (Basel) 19-Dec-2022
PMCID:PMC9774909
doi:10.3390/antibiotics11121844
PMID:36551501
Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH Life (Basel) 11-Nov-2022
PMCID:PMC9696702
doi:10.3390/life12111852
PMID:36430987
Can floral nectars reduce transmission of Leishmania? Palmer-Young EC, Schwarz RS, Chen Y, Evans JD PLoS Negl Trop Dis 12-May-2022
PMCID:PMC9098005
doi:10.1371/journal.pntd.0010373
PMID:35551517
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
A hidden deadly venomous insect: First eco-epidemiological assessment and risk mapping of lonomism in Argentina Casafús MG, Favalesso MM, Gritti MA, Coronel JM, Guimarães AT, Elisa Peichoto M PLoS Negl Trop Dis 01-Jul-2021
PMCID:PMC8279340
doi:10.1371/journal.pntd.0009542
PMID:34197465
Pest categorisation of Diaphorina citri Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Kertesz V, Streissl F, MacLeod A EFSA J 06-Jan-2021
PMCID:PMC7786542
doi:10.2903/j.efsa.2021.6357
PMID:33437319
Use of Natural Products in Leishmaniasis Chemotherapy: An Overview Gervazoni LF, Barcellos GB, Ferreira-Paes T, Almeida-Amaral EE Front Chem 23-Nov-2020
PMCID:PMC7732490
doi:10.3389/fchem.2020.579891
PMID:33330368
Biodiversity and threats in non-protected areas: A multidisciplinary and multi-taxa approach focused on the Atlantic Forest Avigliano E, Rosso JJ, Lijtmaer D, Ondarza P, Piacentini L, Izquierdo M, Cirigliano A, Romano G, Nuñez Bustos E, Porta A, Mabragaña E, Grassi E, Palermo J, Bukowski B, Tubaro P, Schenone N Heliyon 27-Aug-2019
PMCID:PMC6722266
doi:10.1016/j.heliyon.2019.e02292
PMID:31497670
Protective Effect of Pitao (Pitavia punctata (R. & P.) Molina) Polyphenols against the Red Blood Cells Lipoperoxidation and the In Vitro LDL Oxidation Castro RI, Forero-Doria O, Soto-Cerda L, Peña-Neira A, Guzmán L Evid Based Complement Alternat Med 30-Jul-2018
PMCID:PMC6091293
doi:10.1155/2018/1049234
PMID:30151018
Emerging therapeutic targets for treatment of leishmaniasis Sundar S, Singh B Expert Opin Ther Targets 09-May-2018
PMCID:PMC6047532
doi:10.1080/14728222.2018.1472241
PMID:29718739
Anti-Leishmania Activity of Osthole Kermani EK, Sajjadi SE, Hejazi SH, Arjmand R, Saberi S, Eskandarian AA Pharmacognosy Res 01-Mar-2016
PMCID:PMC4821100
doi:10.4103/0974-8490.178650
PMID:27114685
Recent Developments in Drug Discovery for Leishmaniasis and Human African Trypanosomiasis Nagle AS, Khare S, Kumar AB, Supek F, Buchynskyy A, Mathison CJ, Chennamaneni NK, Pendem N, Buckner FS, Gelb MH, Molteni V Chem Rev 03-Nov-2014
PMCID:PMC4633805
doi:10.1021/cr500365f
PMID:25365529

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 / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2002-32898
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epi-alpha-bisabolol 1201551 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2002-32898
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1055/S-2002-32898
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1055/S-2002-32898
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2002-32898
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1055/S-2002-32898
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol 547972 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1055/S-2002-32898
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1055/S-2002-32898
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2002-32898
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2002-32898
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1055/S-2002-32898
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/10.1055/S-2002-32898
> 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/10.1055/S-2002-32898
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2002-32898
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2002-32898
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromenopyridines
2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-9H-pyrano[3,2-g]quinolin-8-one 134830748 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=C(C(=O)N3)C(C)(C)C=C)C 295.40 unknown https://doi.org/10.1055/S-2002-32898
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8,16-Dimethoxy-4,13-dioxa-2-azatetracyclo[7.7.0.03,7.011,15]hexadeca-1(9),2,5,7,10,15-hexaene 162877064 Click to see COC1=C2COCC2=CC3=C1N=C4C(=C3OC)C=CO4 271.27 unknown https://doi.org/10.1055/S-2002-32898
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1055/S-2002-32898
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1055/S-2002-32898
Maculosidine 68222 Click to see COC1=CC2=C(C(=C1)OC)N=C3C(=C2OC)C=CO3 259.26 unknown https://doi.org/10.1055/S-2002-32898
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C 227.26 unknown https://doi.org/10.1055/S-2002-32898
> Phenylpropanoids and polyketides / Coumarins and derivatives
Rutacultin 182049 Click to see CC(C)(C=C)C1=CC2=CC(=C(C=C2OC1=O)OC)OC 274.31 unknown https://doi.org/10.1055/S-2002-32898
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-6-(1,1-Dimethyl-allyl)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one 17753871 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown https://doi.org/10.1055/S-2002-32898
Chalepin 119066 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown https://doi.org/10.1055/S-2002-32898
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(3R)-3-hydroxy-2,2-dimethyl-7-(2-methylbut-3-en-2-yl)-3,4-dihydropyrano[3,2-g]chromen-8-one 92470573 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)O)C 314.40 unknown https://doi.org/10.1055/S-2002-32898
7-Hydroxy-8,8-dimethyl-3-(2-methylbut-3-en-2-yl)-7,8-dihydro-2H,6H-benzo[1,2-b:5,4-b']dipyran-2-one 14133590 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)O)C 314.40 unknown https://doi.org/10.1055/S-2002-32898
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one 15939939 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)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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