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Pholidota yunnanensis

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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 UUID643fe726e0115035867591
Scientific name Pholidota yunnanensis
Authority Rolfe
First published in J. Linn. Soc., Bot. 36: 24 (1903)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pholidota kouytcheensis Gagnep. Bull. Mus. Natl. Hist. Nat. , sér. 2, 3: 145 (1931)

Common names Top

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Language Common/alternative name
Chinese 石枣子
Chinese 云南石仙桃

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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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-0000269944
Tropicos 50026834
KEW urn:lsid:ipni.org:names:650706-1
The Plant List kew-152834
Open Tree Of Life 654352
NCBI Taxonomy 169181
IPNI 650706-1
iNaturalist 1095616
GBIF 5323555
EOL 1135022

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
New stilbenoids from Pholidota yunnanensis and their inhibitory effects on nitric oxide production. Guo XY, Wang J, Wang NL, Kitanaka S, Liu HW, Yao XS Chem Pharm Bull (Tokyo) 01-Jan-2006
doi:10.1248/CPB.54.21
PMID:16394543

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 / Phenanthrenes and derivatives / Hydrophenanthrenes
7-[4-Hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol 11705759 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C(C=C(C=C4OC)O)CCC5=CC(=CC=C5)O)C(=C1)O 484.50 unknown https://doi.org/10.1248/CPB.54.21
7-[4-Hydroxy-2-[2-(4-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol 163105339 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C(C=C(C=C4OC)O)CCC5=CC=C(C=C5)O)C(=C1)O 484.50 unknown https://doi.org/10.1248/CPB.54.21
Phoyunnanin E 11503968 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C(C=C(C5=C4CCC6=C5C=CC(=C6)O)O)OC)C(=C1)O 482.50 unknown https://doi.org/10.1248/CPB.54.21
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(2,3-Dimethoxyphenyl)ethenyl]-5-methoxyphenol 73025850 Click to see COC1=CC=CC(=C1OC)C=CC2=CC(=CC(=C2)OC)O 286.32 unknown https://doi.org/10.1248/CPB.54.21
3-[2-(3-Hydroxy-5-methoxyphenyl)ethenyl]-2-methoxyphenol 72988360 Click to see COC1=CC(=CC(=C1)O)C=CC2=C(C(=CC=C2)O)OC 272.29 unknown https://doi.org/10.1248/CPB.54.21
3-[2-(3-Hydroxy-5-methoxyphenyl)ethenyl]-2,6-dimethoxyphenol 72993730 Click to see COC1=C(C(=C(C=C1)C=CC2=CC(=CC(=C2)OC)O)OC)O 302.32 unknown https://doi.org/10.1248/CPB.54.21
4-[2-(3-Hydroxy-5-methoxyphenyl)ethenyl]-2,3-dimethoxyphenol 73006688 Click to see COC1=CC(=CC(=C1)O)C=CC2=C(C(=C(C=C2)O)OC)OC 302.32 unknown https://doi.org/10.1248/CPB.54.21
Phoyunbene A 11522311 Click to see COC1=C(C(=C(C=C1)C=CC2=CC(=CC(=C2)OC)O)OC)O 302.32 unknown https://doi.org/10.1248/CPB.54.21
Phoyunbene B 11558520 Click to see COC1=CC(=CC(=C1)O)C=CC2=C(C(=C(C=C2)O)OC)OC 302.32 unknown https://doi.org/10.1248/CPB.54.21
Phoyunbene C 11507326 Click to see COC1=CC(=CC(=C1)O)C=CC2=C(C(=CC=C2)O)OC 272.29 unknown https://doi.org/10.1248/CPB.54.21
Phoyunbene D 11601663 Click to see COC1=CC=CC(=C1OC)C=CC2=CC(=CC(=C2)OC)O 286.32 unknown https://doi.org/10.1248/CPB.54.21

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