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Aloe perfoliata

Aloe perfoliata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Aloe perfoliata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440250239a26338182411
Scientific name Aloe perfoliata
Authority L.
First published in Sp. Pl. : 319 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aloe albispina Haw. Trans. Linn. Soc. London 7: 22 (1804)
Aloe commelyni Willd. Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 5: 282 (1811)
Aloe depressa Salm-Dyck ex Steud. Nomencl. Bot. , ed. 2, 1: 57 (1840)
Aloe flavispina Haw. Trans. Linn. Soc. London 7: 22 (1804)
Aloe mitriformis Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Aloe mitriformis var. albispina (Haw.) A.Berger Pflanzenr. IV, 38: 278. 1908
Aloe mitriformis var. angustior Lam. Encycl. 1: 87. 1784
Aloe mitriformis var. commelyni (Willd.) Baker J. Linn. Soc., Bot. 18: 171. 1880
Aloe mitriformis var. elatior Haw. Trans. Linn. Soc. London 7: 27 (1804)
Aloe mitriformis var. flavispina (Haw.) Baker J. Linn. Soc., Bot. 17: 181. 1878
Aloe mitriformis var. humilior Haw. Trans. Linn. Soc. London 7: 23. 1804
Aloe mitriformis var. humilior Willd. Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 5: 282 1811
Aloe mitriformis var. pachyphylla Baker J. Linn. Soc., Bot. 18: 172. 1880
Aloe mitriformis var. spinosior Haw. Trans. Linn. Soc. London 7: 23 (1804)
Aloe mitriformis var. spinulosa (Salm-Dyck) Baker J. Linn. Soc., Bot. 18: 171. 1880
Aloe mitriformis var. xanthacantha (Willd.) Baker J. Linn. Soc., Bot. 18: 172. 1880
Aloe parvispina Schönland Rec. Albany Mus. 1: 283 (1905)
Aloe perfoliata var. brevifolia Aiton Hort. Kew. 1: 467 (1789)
Aloe perfoliata var. mitriformis (Mill.) Aiton Hort. Kew. 1: 467 (1789)
Aloe reflexa Marum ex Steud. Nomencl. Bot. , ed. 2, 1: 59 (1840)
Aloe spinulosa Salm-Dyck Observ. Bot. Horto Dyck. 3: 4 (1822)
Aloe xanthacantha Willd. Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 5: 282 (1811)
Aloe commelyni var. spinulosa (Salm-Dyck) Baker J. Linn. Soc., Bot. 18(no. 108): 171. 1880 [15 Oct 1880]
Aloe commelyni var. flavispina (Haw.) Baker J. Linn. Soc., Bot. 18(no. 108): 171. 1880 [15 Oct 1880]
Aloe commelyni var. xanthacantha (Willd.) Baker J. Linn. Soc., Bot. 18(no. 108): 172. 1880 [15 Oct 1880]
Aloe commelyni var. pachyphylla Baker J. Linn. Soc., Bot. 18(no. 108): 172. 1880 [15 Oct 1880]

Common names Top

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Language Common/alternative name
Spanish aloe nobilis
Spanish aloe xanthacantha
Spanish aloe spinulosa
Spanish aloe reflexa
Spanish aloe perfoliata var. mitriformis
Spanish aloe perfoliata var. brevifolia
Spanish aloe parvispina
Spanish aloe mitriformis
Spanish aloe flavispina
Spanish aloe distans
Spanish aloe depressa
Spanish aloe commelyni
Spanish aloe albispina
Spanish aloe comptonii
Arabic ألوي متريفورمس
Czech aloe mitriformis
Swedish guldtandsaloe
Ukrainian aloe distans
Ukrainian aloe mitriformis
Vietnamese lô hội lá ngắn
Chinese 不夜城蘆薈
Chinese 不夜城芦荟
Chinese 抱茎芦荟

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000758637
Tropicos 18402404
INPN 81597
Flora of Italy 9858
KEW urn:lsid:ipni.org:names:529765-1
The Plant List kew-297802
Open Tree Of Life 598198
Observations.org 138247
NCBI Taxonomy 1128803
IPNI 529765-1
iNaturalist 84993
GBIF 2777626
Freebase /m/0dlk6g9
EOL 1085477
USDA GRIN 454040
Wikipedia Aloe_perfoliata

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
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
Prevalence, motivation, and associated factors of medicinal herbs consumption in pregnant women from Eastern Mediterranean Regional Office: a systematic review Bouqoufi A, Lahlou L, Ait El Hadj F, Abdessadek M, Obtel M, Khabbal Y Pharm Biol 14-Jul-2023
PMCID:PMC10351469
doi:10.1080/13880209.2023.2229388
PMID:37452524
The use of complementary and alternative medicine during pregnancy: a cross-sectional study from Palestine Quzmar Y, Istiatieh Z, Nabulsi H, Zyoud SH, Al-Jabi SW BMC Complement Med Ther 01-Apr-2021
PMCID:PMC8017862
doi:10.1186/s12906-021-03280-8
PMID:33794888
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430
Complementary and Alternative Medicine-related Drug-induced Liver Injury in Asia Philips CA, Augustine P, Rajesh S, Y PK, Madhu D J Clin Transl Hepatol 02-Sep-2019
PMCID:PMC6783675
doi:10.14218/JCTH.2019.00024
PMID:31608219
Literature Review of Traditional Chinese Medicine Herbs–Induced Liver Injury From an Oncological Perspective With RUCAM Chow HC, So TH, Choi HC, Lam KO Integr Cancer Ther 13-Aug-2019
PMCID:PMC6693029
doi:10.1177/1534735419869479
PMID:31405304
Aloe vera (L.) Webb.: Natural Sources of Antioxidants – A Review Hęś M, Dziedzic K, Górecka D, Jędrusek-Golińska A, Gujska E Plant Foods Hum Nutr 18-Jun-2019
PMCID:PMC6684795
doi:10.1007/s11130-019-00747-5
PMID:31209704
Phyto-assisted synthesis, characterization and applications of gold nanoparticles – A review Santhoshkumar J, Rajeshkumar S, Venkat Kumar S Biochem Biophys Rep 21-Jun-2017
PMCID:PMC5614687
doi:10.1016/j.bbrep.2017.06.004
PMID:28955767
The Mouthwash War - Chlorhexidine vs. Herbal Mouth Rinses: A Meta-Analysis Manipal S, Hussain S, Wadgave U, Duraiswamy P, Ravi K J Clin Diagn Res 01-May-2016
PMCID:PMC4948542
doi:10.7860/JCDR/2016/16578.7815
PMID:27437366
Herbal Hepatotoxicity: Clinical Characteristics and Listing Compilation Frenzel C, Teschke R Int J Mol Sci 27-Apr-2016
PMCID:PMC4881436
doi:10.3390/ijms17050588
PMID:27128912
Herbal hepatotoxicity in traditional and modern medicine: actual key issues and new encouraging steps Teschke R, Eickhoff A Front Pharmacol 23-Apr-2015
PMCID:PMC4407580
doi:10.3389/fphar.2015.00072
PMID:25954198
Aloe vera for treating acute and chronic wounds Dat AD, Poon F, Pham KB, Doust J Cochrane Database Syst Rev 15-Feb-2012
PMCID:PMC9943919
doi:10.1002/14651858.CD008762.pub2
PMID:22336851
Processing, food applications and safety of aloe vera products: a review Ahlawat KS, Khatkar BS J Food Sci Technol 18-Jan-2011
PMCID:PMC3551117
doi:10.1007/s13197-011-0229-z
PMID:23572784
Three new antioxidant C-glucosylanthrones from Aloe nobilis. Lv L, Tian XY, Fang WS J Asian Nat Prod Res 01-Jun-2010
doi:10.1080/10286020.2010.490211
PMID:20552481
BACE1 (beta-secretase) inhibitory chromone glycosides from Aloe vera and Aloe nobilis. Lv L, Yang QY, Zhao Y, Yao CS, Sun Y, Yang EJ, Song KS, Mook-Jung I, Fang WS Planta Med 01-Apr-2008
doi:10.1055/S-2008-1074496
PMID:18543151

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
[(2R,3R,4R,5S,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(9R)-1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-4-yl] acetate 46844573 Click to see CC(=O)OC1C(C(OC(C1O)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)CO)O 476.40 unknown https://doi.org/10.1080/10286020.2010.490211
[(2R,3S,4R,5R,6S)-3-acetyloxy-4,5-dihydroxy-6-[(9R)-1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl]methyl acetate 46844575 Click to see CC(=O)OCC1C(C(C(C(O1)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)O)O)OC(=O)C 518.50 unknown https://doi.org/10.1080/10286020.2010.490211
[(2R,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-[(9R)-1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl]methyl acetate 46844574 Click to see CC(=O)OCC1C(C(C(C(O1)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)OC(=O)C)O)O 518.50 unknown https://doi.org/10.1080/10286020.2010.490211
[3-acetyloxy-4,5-dihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl]methyl acetate 75219052 Click to see CC(=O)OCC1C(C(C(C(O1)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)O)O)OC(=O)C 518.50 unknown https://doi.org/10.1080/10286020.2010.490211
[3,5-dihydroxy-2-(hydroxymethyl)-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-4-yl] acetate 75219050 Click to see CC(=O)OC1C(C(OC(C1O)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)CO)O 476.40 unknown https://doi.org/10.1080/10286020.2010.490211
[5-acetyloxy-3,4-dihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl]methyl acetate 75219051 Click to see CC(=O)OCC1C(C(C(C(O1)C2C3=C(C(=CC(=C3)CO)O)C(=O)C4=C(C=CC(=C24)O)O)OC(=O)C)O)O 518.50 unknown https://doi.org/10.1080/10286020.2010.490211
1,5,8-trihydroxy-3-(hydroxymethyl)-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one 73157760 Click to see C1=CC(=C2C(=C1O)C(C3=C(C2=O)C(=CC(=C3)CO)O)C4C(C(C(C(O4)CO)O)O)O)O 434.40 unknown https://doi.org/10.1080/10286020.2010.490211
5-Hydroxyaloin A 11972367 Click to see C1=CC(=C2C(=C1O)C(C3=C(C2=O)C(=CC(=C3)CO)O)C4C(C(C(C(O4)CO)O)O)O)O 434.40 unknown https://doi.org/10.1080/10286020.2010.490211
> Benzenoids / Phenols / Benzenediols / Resorcinols
2H-Pyran-2-one, 6-(2,4-dihydroxy-6-methylphenyl)-4-methoxy- 5242842 Click to see CC1=CC(=CC(=C1C2=CC(=CC(=O)O2)OC)O)O 248.23 unknown https://doi.org/10.1080/10286020.2010.490211
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[7-hydroxy-2-[(2S)-2-hydroxypropyl]-5-methyl-4-oxochromen-8-yl]-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163191351 Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(C)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 542.50 unknown https://doi.org/10.1055/S-2008-1074496
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[7-hydroxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 5316115 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)O 570.50 unknown https://doi.org/10.1055/S-2008-1074496
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[7-methoxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101701617 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)OC 584.60 unknown https://doi.org/10.1055/S-2008-1074496
[4,5-Dihydroxy-2-[7-hydroxy-2-(2-hydroxypropyl)-5-methyl-4-oxochromen-8-yl]-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 75581317 Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(C)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)O 542.50 unknown https://doi.org/10.1055/S-2008-1074496
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[7-hydroxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73981552 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)O 570.50 unknown https://doi.org/10.1055/S-2008-1074496
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[7-methoxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163002297 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)OC 584.60 unknown https://doi.org/10.1055/S-2008-1074496
1,5-Anhydro-1-[7-hydroxy-5-methyl-4-oxo-2-(2-oxopropyl)-4H-1-benzopyran-8-yl]-2-O-[3-(4-hydroxyphenyl)acryloyl]hexitol 57370126 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)O 540.50 unknown https://doi.org/10.1055/S-2008-1074496
Aloeresin A 5317657 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)O 540.50 unknown https://doi.org/10.1055/S-2008-1074496

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