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Pinalia pandurata

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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 UUID64403553ee4c3630043208
Scientific name Pinalia pandurata
Authority (Schltr.) Ormerod
First published in Malesian Orchid J. 7: 85 (2011)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eria pandurata Schltr. Repert. Spec. Nov. Regni Veg. Beih. 1: 659 (1912)

Common names Top

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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-0000922211
KEW urn:lsid:ipni.org:names:77110301-1
The Plant List kew-467776
Open Tree Of Life 3979632
IPNI 77110301-1
GBIF 7601848

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)!
Title Authors Publication Released IDs
A cyanogenic glycoside from Canthium schimperianum. Schwarz B, Wray V, Proksch P Phytochemistry 01-Jun-1996
doi:10.1016/0031-9422(96)00018-0
PMID:8768318

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 / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1016/0031-9422(96)00018-0
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1016/0031-9422(96)00018-0
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1016/0031-9422(96)00018-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(96)00018-0
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(96)00018-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one 4053302 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0
5-Hydroxy-7-methoxyflavanone 4101463 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/0031-9422(96)00018-0

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Collections Top

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