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Chuquiraga ulicina

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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 UUID643fc729b7b38863295418
Scientific name Chuquiraga ulicina
Authority Hook.
First published in Companion Bot. Mag. 1: 110 (1835)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Chuquiraga ulicina subsp. ulicina Companion Bot. Mag. 1: 110 (1835)

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

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Database ID/link to page
World Flora Online wfo-0000012144
KEW urn:lsid:ipni.org:names:194400-1
Open Tree Of Life 13225
NCBI Taxonomy 171767
iNaturalist 865942
GBIF 4227844
IPNI 194400-1

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)!
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Title Authors Publication Released IDs
A Review on Recent Trends in Green Synthesis of Gold Nanoparticles for Tuberculosis Gupta A, Pandey S, Yadav JS Adv Pharm Bull 07-Nov-2020
PMCID:PMC7961233
doi:10.34172/apb.2021.002
PMID:33747849
CONSTITUENTS OF CHUQUIRAGA ATACAMENSIS AND C. ULICINA M. HOENEISEN, ALEJANDRA ROJAS, M. BITTNER, J. BECERRA, M. SILVA, J. JAKUPOVIC SciELO Agencia Nacional de Investigacion y Desarrollo (ANID) 04-Aug-2009
doi:10.4067/S0366-16442000000100007
Pentacyclic triterpenes from Chuquiraga ulicina. Flagg ML, Valcic S, Montenegro G, Gomez M, Timmermann BN Phytochemistry 01-Dec-1999
doi:10.1016/S0031-9422(99)00362-3
PMID:10647216

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 / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate 162901456 Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC 521.60 unknown https://doi.org/10.4067/S0366-16442000000100007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,5R,6aR,6aR,6bR,8aS,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,5-diol 15484407 Click to see CC1C2C3CCC4C5(CCC(C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)O)C 442.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
(4aR,5R,6aR,6aR,6bR,8aS,12S,12aR,14aR,14bR)-5-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydropicen-3-one 15484405 Click to see CC1C2C3CCC4C5(CCC(=O)C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
(5-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-yl) acetate 85260893 Click to see CC1C2C3CCC4C5(CCC(C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)OC(=O)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
(5-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-yl) hexadecanoate 85211577 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(C(=CCC5(CCC4(C3(CC(C2C1(C)C)O)C)C)C)C)C)C 681.10 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 145706026 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.4067/S0366-16442000000100007
[(1R,7aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 45050622 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
[(3S,4aR,5R,6aR,6aR,6bR,8aS,12S,12aR,14aR,14bR)-5-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-yl] acetate 15484404 Click to see CC1C2C3CCC4C5(CCC(C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)OC(=O)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
[(3S,4aR,5R,6aR,6aR,6bR,8aS,12S,12aR,14aR,14bR)-5-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-yl] hexadecanoate 15484406 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(C(=CCC5(CCC4(C3(CC(C2C1(C)C)O)C)C)C)C)C)C 681.10 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picene-3,5-diol 85260290 Click to see CC1C2C3CCC4C5(CCC(C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)O)C 442.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
5-Hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydropicen-3-one 85162810 Click to see CC1C2C3CCC4C5(CCC(=O)C(C5C(CC4(C3(CCC2(CC=C1C)C)C)C)O)(C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.4067/S0366-16442000000100007
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.4067/S0366-16442000000100007
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(99)00362-3
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/10.4067/S0366-16442000000100007
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.4067/S0366-16442000000100007
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.4067/S0366-16442000000100007

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