Commiphora socotrana
Table of Contents
Details Top
Internal ID | UUID644013081a288461537817 |
Scientific name | Commiphora socotrana |
Authority | Engl. |
First published in | Monogr. Phan. 4: 536 (1883) |
Description Top
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Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Balsamodendrum socotranum | Balf.f. | Proc. Roy. Soc. Edinburgh 11: 505 (1882) |
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
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Africa click to expand
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Northeast Tropical Africa
- Socotra
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Northeast Tropical Africa
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000617476 |
Tropicos | 100314948 |
KEW | urn:lsid:ipni.org:names:127817-1 |
The Plant List | kew-2733684 |
Open Tree Of Life | 6124539 |
IUCN Red List | 30418 |
IPNI | 127817-1 |
iNaturalist | 190824 |
GBIF | 3993248 |
Wikipedia | Commiphora_socotrana |
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 | ||||
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7-O-methylaloeresin A--a new chromone glycoside from Commiphora socotrana. | Blitzke T, Schmidt J, Masaoud M | Nat Prod Lett | 01-Jan-2001 |
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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 / Anthracenes / Anthraquinones | |||||
Aloe emodin | 10207 | Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO | 270.24 | unknown | https://doi.org/10.1080/10575630108041254 |
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives | |||||
3,4,5-Trimethoxybenzoic Acid | 8357 | Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O | 212.20 | unknown | https://doi.org/10.1080/10575630108041254 |
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides | |||||
7-O-Methylaloeresin A | 637110 | Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)C3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)OC | 554.50 | unknown | https://doi.org/10.1080/10575630108041254 |
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins | |||||
Cianidanol | 9064 | Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O | 290.27 | unknown | https://doi.org/10.1080/10575630108041254 |
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones | |||||
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one | 667495 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O | 272.25 | unknown | https://doi.org/10.1080/10575630108041254 |
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one | 932 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O | 272.25 | unknown | https://doi.org/10.1080/10575630108041254 |
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols | |||||
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one | 662 | Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O | 288.25 | unknown | https://doi.org/10.1080/10575630108041254 |
Aromadendrin | 122850 | Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O | 288.25 | unknown | https://doi.org/10.1080/10575630108041254 |
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids | |||||
Flavanone, 3,5,7-trihydroxy-4'-methoxy- | 586387 | Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O | 302.28 | unknown | https://doi.org/10.1080/10575630108041254 |
Isosakuranetin | 160481 | Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O | 286.28 | unknown | https://doi.org/10.1080/10575630108041254 |
Collections Top
In private collections | 0 |
In public collections | 0 |