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Veratrum formosanum

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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 UUID6440241c0b515419002582
Scientific name Veratrum formosanum
Authority O.Loes.
First published in Verh. Bot. Vereins Prov. Brandenburg 68: 142 (1926)

Description Top

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Synonyms Top

Scientific name Authority First published in
Veratrum shuehshanarum S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 28(2): 48 (1988)
Veratrum kudoi Masam. J. Soc. Trop. Agric. 4: 193 (1932)
Veratrum formosanum f. albiflorum (Masam.) Masam.
Veratrum formosanum var. albiflorum Masam.

Common names Top

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Language Common/alternative name
Chinese 臺灣藜蘆
Chinese 台湾藜芦

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000751789
Tropicos 18406393
KEW urn:lsid:ipni.org:names:543493-1
The Plant List kew-291315
Missouri Botanical Garden 361133
Open Tree Of Life 1088331
NCBI Taxonomy 203091
IPNI 543493-1
iNaturalist 735123
GBIF 2742159
EOL 1083459

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
Biosynthesis of anticancer phytochemical compounds and their chemistry Dogra A, Kumar J Front Pharmacol 09-Mar-2023
PMCID:PMC10034375
doi:10.3389/fphar.2023.1136779
PMID:36969868
Graphene-Based Sensors for the Detection of Bioactive Compounds: A Review Sainz-Urruela C, Vera-López S, San Andrés MP, Díez-Pascual AM Int J Mol Sci 24-Mar-2021
PMCID:PMC8037795
doi:10.3390/ijms22073316
PMID:33804997
New Highlights of Resveratrol: A Review of Properties against Ocular Diseases Delmas D, Cornebise C, Courtaut F, Xiao J, Aires V Int J Mol Sci 28-Jan-2021
PMCID:PMC7865717
doi:10.3390/ijms22031295
PMID:33525499
Biotechnological Advances in Resveratrol Production and its Chemical Diversity Thapa SB, Pandey RP, Park YI, Sohng JK Molecules 15-Jul-2019
PMCID:PMC6680439
doi:10.3390/molecules24142571
PMID:31311182
Properties of Resveratrol: In Vitro and In Vivo Studies about Metabolism, Bioavailability, and Biological Effects in Animal Models and Humans Gambini J, Inglés M, Olaso G, Lopez-Grueso R, Bonet-Costa V, Gimeno-Mallench L, Mas-Bargues C, Abdelaziz KM, Gomez-Cabrera MC, Vina J, Borras C Oxid Med Cell Longev 28-Jun-2015
PMCID:PMC4499410
doi:10.1155/2015/837042
PMID:26221416
The Sirtuin System: The Holy Grail of Resveratrol? Mohar DS, Malik S J Clin Exp Cardiolog 01-Nov-2012
PMCID:PMC3613783
doi:10.4172/2155-9880.1000216
PMID:23560248
Potential of herbs in skin protection from ultraviolet radiation Korać RR, Khambholja KM Pharmacogn Rev 01-Jul-2011
PMCID:PMC3263051
doi:10.4103/0973-7847.91114
PMID:22279374
Botanical phenolics and brain health Sun AY, Wang Q, Simonyi A, Sun GY Neuromolecular Med 01-Nov-2008
PMCID:PMC2682367
doi:10.1007/s12017-008-8052-z
PMID:19191039
An antiplatelet principle of Veratrum formosanum. Chung MI, Teng CM, Cheng KL, Ko FN, Lin CN Planta Med 01-Jun-1992
doi:10.1055/S-2006-961453
PMID:1409983

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 / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
Angeloylzygadenin 102093836 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1055/S-2006-961453
Angeloylzygadenine 6441115 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1055/S-2006-961453
> 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-2006-961453
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-2006-961453

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Contributors Top

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Collections Top

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