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Aloe castellorum

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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 UUID644024e3ce001592438410
Scientific name Aloe castellorum
Authority J.R.I.Wood
First published in Kew Bull. 38: 25 (1983)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aloe hijazensis Lavranos & Collen. Cact. Succ. J. (Los Angeles) 72: 23 (2000)

Common names Top

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Language Common/alternative name
Afrikaans aloe hijazensis
German aloe hijazensis

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-0000758007
Tropicos 100145317
KEW urn:lsid:ipni.org:names:901422-1
The Plant List kew-297211
Open Tree Of Life 3997075
NCBI Taxonomy 1389495
IPNI 901422-1
GBIF 2777509
EOL 1085221

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
Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA Saudi J Biol Sci 04-Mar-2021
PMCID:PMC8176062
doi:10.1016/j.sjbs.2021.02.076
PMID:34121869
Molecular perspective and anticancer activity of medicinal plants Ahamed A, Panneerselvam A, Alaklabi A, Arif IA, Ambikapathy V, Thajuddin N Saudi J Biol Sci 17-Dec-2019
PMCID:PMC6997859
doi:10.1016/j.sjbs.2019.11.043
PMID:32210686
Museomics Clarifies the Classification of Aloidendron (Asphodelaceae), the Iconic African Tree Aloes Malakasi P, Bellot S, Dee R, Grace OM Front Plant Sci 15-Oct-2019
PMCID:PMC6803536
doi:10.3389/fpls.2019.01227
PMID:31681358
New bioactive compounds from Aloe hijazensis. Abd-Alla HI, Shaaban M, Shaaban KA, Abu-Gabal NS, Shalaby NM, Laatsch H Nat Prod Res 01-Jan-2009
doi:10.1080/14786410802242851
PMID:19521919

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes
Aloin B 14989 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)CO)O)O)O)C=C(C=C3O)CO 418.40 unknown https://doi.org/10.1080/14786410802242851
Barbaloin 313325 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)CO)O)O)O)C=C(C=C3O)CO 418.40 unknown https://doi.org/10.1080/14786410802242851
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Methyl 8-hydroxy-1,3-dimethyl-9,10-dioxoanthracene-2-carboxylate 163013386 Click to see CC1=CC2=C(C(=C1C(=O)OC)C)C(=O)C3=C(C2=O)C=CC=C3O 310.30 unknown https://doi.org/10.1080/14786410802242851
> Benzenoids / Anthracenes / Anthraquinones
1-Hydroxy-5-methoxy-3-methylanthracene-9,10-dione 92446318 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)OC 268.26 unknown https://doi.org/10.1080/14786410802242851
1-Hydroxy-6-methoxy-8-methyl-anthraquinone 129830911 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C2=O)C=CC=C3O)OC 268.26 unknown https://doi.org/10.1080/14786410802242851
1,5-Dihydroxy-3-methylanthraquinone 5316800 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O 254.24 unknown https://doi.org/10.1080/14786410802242851
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/10.1080/14786410802242851
CID 4483734 4483734 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1080/14786410802242851
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1080/14786410802242851
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1080/14786410802242851
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1080/14786410802242851
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/10.1080/14786410802242851
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-methoxy-6-oxopyran-2-yl)-3-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163195165 Click to see CC1=CC(=CC(=C1C2=CC(=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 718.70 unknown https://doi.org/10.1080/14786410802242851
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[2-(4-methoxy-6-oxopyran-2-yl)-3-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 78410330 Click to see CC1=CC(=CC(=C1C2=CC(=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 718.70 unknown https://doi.org/10.1080/14786410802242851
6-[2-[(7,8-Dihydroxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy]-4-hydroxy-6-methylphenyl]-4-methoxypyran-2-one 162890995 Click to see CC1OCC2C(O1)C(C(C(O2)OC3=C(C(=CC(=C3)O)C)C4=CC(=CC(=O)O4)OC)O)O 436.40 unknown https://doi.org/10.1080/14786410802242851
6-[2-[[(2R,4aR,6S,7R,8R,8aS)-7,8-dihydroxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-4-hydroxy-6-methylphenyl]-4-methoxypyran-2-one 162890996 Click to see CC1OCC2C(O1)C(C(C(O2)OC3=C(C(=CC(=C3)O)C)C4=CC(=CC(=O)O4)OC)O)O 436.40 unknown https://doi.org/10.1080/14786410802242851
6-[4-hydroxy-2-methyl-6-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-methoxypyran-2-one 124578088 Click to see CC1=CC(=CC(=C1C2=CC(=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O)O 410.40 unknown https://doi.org/10.1080/14786410802242851
6-[4-Hydroxy-2-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-methoxypyran-2-one 13984205 Click to see CC1=CC(=CC(=C1C2=CC(=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O)O 410.40 unknown https://doi.org/10.1080/14786410802242851
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3,4-Dihydro-6,8-dihydroxy-3-(2'acetyl-3,5-dihydroxyphenyl)methyl isocoumarin 78384911 Click to see CC(=O)C1=C(C=C(C=C1O)O)CC2CC3=C(C(=CC(=C3)O)O)C(=O)O2 344.30 unknown https://doi.org/10.1080/14786410802242851
Feralolide 5317333 Click to see CC(=O)C1=C(C=C(C=C1O)O)CC2CC3=C(C(=CC(=C3)O)O)C(=O)O2 344.30 unknown https://doi.org/10.1080/14786410802242851
> Organoheterocyclic compounds / Quinolines and derivatives / Haloquinolines / Chloroquinolines
4,7-Dichloroquinoline 6866 Click to see C1=CC2=C(C=CN=C2C=C1Cl)Cl 198.05 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1080/14786410802242851
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1080/14786410802242851
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1080/14786410802242851
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1080/14786410802242851
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/14786410802242851
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786410802242851
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1080/14786410802242851
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 6426859 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786410802242851
5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5885565 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/14786410802242851

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