Aloe arborescens

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Collections

Details Top

Internal ID	UUID644024dd32bcb799106001
Scientific name	Aloe arborescens
Authority	Mill.
First published in	Gard. Dict. ed. 8 : n.º 3 (1768)

Description Top

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Aloe arborescens, also known as krantz aloe or candelabra aloe, is a flowering succulent plant that belongs to the same genus as Aloe vera. It is valued by gardeners for its large, green leaves, vibrant flowers, and ability to attract birds, bees, and butterflies. This plant can reach up to 3 meters in height and is native to South Africa, Malawi, Mozambique, and Zimbabwe. It is also found in other parts of the world, including the western Mediterranean, Australia, and California, where it is considered an invasive species. Aloe arborescens is commonly grown in gardens and can tolerate a minimum temperature of 10°C. It is also traditionally used as a living fence or security hedge in Southern Africa. This plant is easy to propagate through cuttings and a cultivar called 'Variegata' has received the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name	Authority	First published in
Catevala arborescens	(Mill.) Medik.	Theodora : 67 (1786)
Aloe arborescens var. frutescens	(Salm-Dyck) Baker	J. Linn. Soc., Bot. 18(no. 108): 175. 1880 [15 Oct 1880]
Aloe arborescens var. milleri	A.Berger	Pflanzenr. IV, 38: 288. 1908
Aloe arborescens var. natalensis	(J.M.Wood & M.S.Evans) A.Berger	Pflanzenr. IV, 38: 290. 1908
Aloe arborescens var. pachystyrsa	A.Berger	Pflanzenr. IV, 38: 292. 1908
Aloe arborescens var. viridifolia	A.Berger	Pflanzenr. IV, 38: 290. 1908
Aloe perfoliata var. arborescens	(Mill.) Aiton	Hort. Kew. 1: 466 (1789)
Aloe salm-dyckiana	Schult. & Schult.f.	Syst. Veg., ed. 15 bis 7: 710 (1829)
Aloe salm-dyckiana var. fulgens	(Tod.) A.Berger	Pflanzenr. IV, 38: 302. 1908

Common names Top

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Filter by language:

Language	Common/alternative name
English	krans aloe
English	candelabra aloe
Afrikaans	kransaalwyn
Arabic	ألوي اربورسنس
Azerbaijani	ağacşəkilli əzvay
Bulgarian	дървовидно алое
Estonian	puis-aaloe
Persian	شاخ بزی
Finnish	rohtoaaloe
French	aloé arborescente
French	aloé candélabre
French	aloès candélabre
French	corne de bélier
Irish	aló aille
Hebrew	אלווי עצי
Upper Sorbian	wohnjowy alowej
Hungarian	fásodó aloé
Indonesian	lidah buaya lilin
Japanese	キダチアロエ
Japanese	アロエ・アルボレッセンス
Japanese	木立アロエ
Lithuanian	medėjantis alavijas
Latvian	kokveida alveja
myv	Алой
nso	sekgopha
Russian	Алоэ древовидное
Slovenian	drevesasta aloja
Swedish	aloë arborescens
Swedish	trädaloe
Swedish	träd-aloe
Swedish	pachidendron africanum
Turkish	testere bitkisi
Ukrainian	Алое деревоподібне
Ukrainian	Алое деревовидне
Chinese	木立芦荟
Chinese	樹蘆薈
Chinese	木立蘆薈
Chinese	樹叢蘆薈
Chinese	树丛芦荟
Chinese	大芦荟
Zulu	inkalane

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Aloe arborescens subsp. arborescens		Unknown
Aloe arborescens subsp. mzimnyati	van Jaarsv. & A.E.van Wyk	Aloe 42(3): 41 (2005)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- South Tropical Africa
  - Malawi
  - Mozambique
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland

Asia-temperate click to expand
- Eastern Asia
  - Korea

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
- New Zealand
  - New Zealand South

Europe click to expand
- Southwestern Europe
  - Baleares
  - France
  - Portugal
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Southwest

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marshall Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000757866
UNII	0EF00WD7LU
USDA Plants	ALAR8
Tropicos	18400127
INPN	81588
Flora of Italy	8391
KEW	urn:lsid:ipni.org:names:529214-1
The Plant List	kew-297073
Open Tree Of Life	720407
Observations.org	114289
NCBI Taxonomy	45385
IUCN Red List	110688013
IPNI	529214-1
iNaturalist	81518
GBIF	2777537
Freebase	/m/0grqty
EPPO	ALFAR
EOL	1085160
Elurikkus	210011
USDA GRIN	2510
Wikipedia	Aloe_arborescens
PFAF	Aloe arborescens
Plantarium	48117

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 chromosome-level genome reveals genome evolution and molecular basis of anthraquinone biosynthesis in Rheum palmatum

Zhang T, Zhou L, Pu Y, Tang Y, Liu J, Yang L, Zhou T, Feng L, Wang X

BMC Plant Biol

10-Apr-2024

PMCID:	PMC11005207
doi:	10.1186/s12870-024-04972-2
PMID:	38594606

Nano-enabled antimicrobial thin films: design and mechanism of action

Finina BF, Mersha AK

RSC Adv

09-Feb-2024

PMCID:	PMC10866018
doi:	10.1039/d3ra07884a
PMID:	38357038

The Potential Application of Aloe Barbadensis Mill. as Chinese Medicine for Constipation: Mini-Review

Huang WR, Fang QH, Yu XB, Ge WH, Yu Y

Drug Des Devel Ther

03-Feb-2024

PMCID:	PMC10849880
doi:	10.2147/DDDT.S446563
PMID:	38328440

A Review of Ethnomedicinal Plants as Potential Anthelmintic Agents to Alternatively Control Gastrointestinal Nematodes of Ruminants in South Africa

Mhlongo LC, Mseleku C, Tenza T, Fomum SW, McGaw LJ, Hassen A, Nsahlai IV

J Parasitol Res

16-Jan-2024

PMCID:	PMC10805549
doi:	10.1155/2024/7955692
PMID:	38268708

Recent Approaches to the Formulation, Uses, and Impact of Edible Coatings on Fresh Peach Fruit

Aaqil M, Peng C, Kamal A, Nawaz T, Gong J

Foods

15-Jan-2024

PMCID:	PMC10815105
doi:	10.3390/foods13020267
PMID:	38254568

Biological Activity of Fermented Plant Extracts for Potential Dermal Applications

Herman A, Herman AP

Pharmaceutics

14-Dec-2023

PMCID:	PMC10748213
doi:	10.3390/pharmaceutics15122775
PMID:	38140115

The vegetation of Holocene coastal dunes of the Cape south coast, South Africa

Cowling RM, Cawthra H, Privett S, Grobler BA

PeerJ

12-Dec-2023

PMCID:	PMC10722985
doi:	10.7717/peerj.16427
PMID:	38107568

Antitumor and Phytochemical Properties of Ferula assa-foetida L. Oleo-Gum–Resin against HT-29 Colorectal Cancer Cells In Vitro and in a Xenograft Mouse Model

Elarabany N, Hamad A, Alzamel NM

Molecules

08-Dec-2023

PMCID:	PMC10746072
doi:	10.3390/molecules28248012
PMID:	38138502

An In Situ Evaluation of Different CAM Plants as Plant Microbial Fuel Cells for Energy Recovery in the Atacama Desert

Madrid FM, Trigo M, Salazar-Avalos S, Carvajal-Funes S, Olivares D, Portillo C, Fuentealba E, Toro N, Carrasco G, Cáceres L, Jamett I, Soliz A

Plants (Basel)

29-Nov-2023

PMCID:	PMC10707800
doi:	10.3390/plants12234016
PMID:	38068652

How Poor Is Aphyllophoroid Fungi Diversity in the Boreal Urban Greenhouses of Eastern Europe?

Shiryaev AG, Zmitrovich IV, Senator SA, Minogina EN, Tkachenko OB

J Fungi (Basel)

17-Nov-2023

PMCID:	PMC10672352
doi:	10.3390/jof9111116
PMID:	37998921

Novel acaricidal and growth-regulating activity of Aloe vera and Rheum rhabarbarum extracts and their oil/water nanoemulsions against the camel tick, Hyalomma dromedarii

Radwan IT, Eltaly RI, Baz MM, Yousif M, Selim A, Taie HA, Manaa EA, Khater HF

Sci Rep

05-Oct-2023

PMCID:	PMC10556011
doi:	10.1038/s41598-023-43776-6
PMID:	37798348

Antibacterial activity of medicinal plants on the management of mastitis in dairy cows: A systematic review

Kaseke TB, Chikwambi Z, Gomo C, Mashingaidze AB, Murungweni C

Vet Med Sci

19-Sep-2023

PMCID:	PMC10650345
doi:	10.1002/vms3.1268
PMID:	37725398

Meta-Topolin-induced mass shoot multiplication and biosynthesis of valuable secondary metabolites in Stevia rebaudiana Bertoni bioreactor culture

Ptak A, Szewczyk A, Simlat M, Błażejczak A, Warchoł M

Sci Rep

19-Sep-2023

PMCID:	PMC10509197
doi:	10.1038/s41598-023-42619-8
PMID:	37726319

Microbiota-derived short chain fatty acids in fermented Kidachi Aloe promote antimicrobial, anticancer, and immunomodulatory activities

Al-Madboly LA, Yagi A, Kabbash A, El-Aasr MA, El-Morsi RM

BMC Microbiol

29-Aug-2023

PMCID:	PMC10464184
doi:	10.1186/s12866-023-02981-z
PMID:	37644400

Identification of a diarylpentanoid-producing polyketide synthase in the biosynthesis of 2-(2-phenylethyl)chromones in agarwood

Morita H, Lee YE, Shi SP

J Nat Med

19-Aug-2023

PMCID:	PMC10465673
doi:	10.1007/s11418-023-01743-5
PMID:	37597060

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
(10R)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one	129628856	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/10.1016/S0305-1978(00)00018-1
(10S)-1,8-dihydroxy-3-(hydroxymethyl)-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one	5458894	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/10.1016/S0305-1978(00)00018-1
(3R)-3,9-dihydroxy-8-methoxy-3-methyl-2,4-dihydroanthracen-1-one	101712954	Click to see CC1(CC2=C(C(=O)C1)C(=C3C(=C2)C=CC=C3OC)O)O	272.29	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
(4S)-4,8,9-trihydroxy-6-methyl-3,4-dihydro-2H-anthracen-1-one	90474413	Click to see CC1=CC2=CC3=C(C(=O)CCC3O)C(=C2C(=C1)O)O	258.27	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one	129628814	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/10.3109/13880209109082880
3,6,9-trihydroxy-8-methyl-3,4-dihydro-2H-anthracen-1-one	102239772	Click to see CC1=CC(=CC2=CC3=C(C(=O)CC(C3)O)C(=C12)O)O	258.27	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
Aloin A	12305761	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/10.1271/BBB1961.51.1723 https://doi.org/10.1007/S10600-009-9405-Z https://doi.org/10.1016/S0305-1978(99)00129-5 https://doi.org/10.1271/BBB1961.55.1627 https://doi.org/10.1080/07929978.1996.10676652 https://doi.org/10.1055/S-2006-962798
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/10.1007/S10600-009-9405-Z https://doi.org/10.1271/BBB1961.51.1723 https://doi.org/10.1271/BBB1961.55.1627 https://doi.org/10.1016/S0305-1978(00)00018-1 https://doi.org/10.1080/07929978.1996.10676652 https://doi.org/10.1016/S0305-1978(99)00129-5
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/10.1007/S10600-009-9405-Z https://doi.org/10.3109/13880209109082880 https://doi.org/10.1271/BBB1961.51.1723 https://doi.org/10.1016/S0305-1978(00)00018-1 https://doi.org/10.1016/S0176-1617(11)81144-2
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
aloesaponarin I	11098986	Click to see CC1=C2C(=CC(=C1C(=O)OC)O)C(=O)C3=C(C2=O)C(=CC=C3)O	312.27	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
Aloesaponol I	44631015	Click to see CC1=C(C(=CC2=CC3=C(C(=O)CC(C3)O)C(=C12)O)O)C(=O)OC	316.30	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
> Benzenoids / Anthracenes / Anthraquinones
2-[(9R)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-yl]-1,8-dihydroxy-6-(hydroxymethyl)anthracene-9,10-dione	162907998	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)C5=C(C6=C(C=C5)C(=O)C7=C(C6=O)C(=CC(=C7)CO)O)O)C=C(C=C3O)CO	686.60	unknown	https://doi.org/10.1021/NP9703104
2-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-yl]-1,8-dihydroxy-6-(hydroxymethyl)anthracene-9,10-dione	162907995	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)C5=C(C6=C(C=C5)C(=O)C7=C(C6=O)C(=CC(=C7)CO)O)O)C=C(C=C3O)CO	686.60	unknown	https://doi.org/10.1021/NP9703104
2-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-9-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-yl]-1,8-dihydroxy-6-(hydroxymethyl)anthracene-9,10-dione	163105987	Click to see C1=CC2=C(C(=C1)O)OC3=C(C2(C4C(C(C(C(O4)CO)O)O)O)C5=C(C6=C(C=C5)C(=O)C7=C(C6=O)C(=CC(=C7)CO)O)O)C=C(C=C3O)CO	674.60	unknown	https://doi.org/10.1021/NP9703104
2-[4,5-Dihydroxy-2-(hydroxymethyl)-10-oxo-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]anthracen-9-yl]-1,8-dihydroxy-6-(hydroxymethyl)anthracene-9,10-dione	14731339	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)C5=C(C6=C(C=C5)C(=O)C7=C(C6=O)C(=CC(=C7)CO)O)O)C=C(C=C3O)CO	686.60	unknown	https://doi.org/10.1021/NP9703104
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/10.1002/PTR.826 https://doi.org/10.1271/BBB1961.55.1627 https://doi.org/10.1007/S10600-009-9405-Z https://doi.org/10.1080/00021369.1991.10870794 https://doi.org/10.3109/13880209109082880 https://doi.org/10.1055/S-2006-962798
Asphodelin	182665	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)C4=C5C(=C(C=C4C)O)C(=O)C6=C(C5=O)C=CC=C6O	506.50	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
Elgonica dimer A	21582596	Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)C5=C(C6=C(C=C5)C(=O)C7=C(C6=O)C(=CC(=C7)CO)O)O)C=C(C=C3O)CO	686.60	unknown	https://doi.org/10.1021/NP9703104
Helminthosporin	97560	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C=CC(=C3C2=O)O)O	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Aloesaponarin II	3085033	Click to see CC1=CC(=CC2=C1C(=O)C3=C(C2=O)C=CC=C3O)O	254.24	unknown	https://doi.org/10.1016/S0031-9422(00)94771-X
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1021/JF990116I
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (2E,4E,6E,10E,16E,18E,20E,22E,24E,26E,36E,44E,50E)-58-amino-13,15,33,35,39,41,43,47,49,53,55-undecahydroxy-2,12,14,30-tetramethyl-31-oxo-29-sulfooxyoctapentaconta-2,4,6,10,16,18,20,22,24,26,36,44,50-tridecaenoate	16109801	Click to see CC(C=CCCC=CC=CC=C(C)C(=O)OC)C(C(C)C(C=CC=CC=CC=CC=CC=CCC(C(C)C(=O)CC(CC(C=CCC(CC(CC(C=CCC(CC(C=CCC(CC(CCCN)O)O)O)O)O)O)O)O)O)OS(=O)(=O)O)O)O	1190.50	unknown	https://doi.org/10.1007/BF00579168
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1021/JF990116I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF990116I
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene	152743364	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	https://doi.org/10.1007/BF00579168
2-(3,7,12,16,20,24-Hexamethylpentacosa-1,3,5,7,9,11,15,19,21,23-decaenyl)-1,3,3-trimethylcyclohexene	162931205	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)CCC=C(C)CCC=C(C)C=CC=C(C)C)C)C	538.90	unknown	https://doi.org/10.1007/BF00579168
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	https://doi.org/10.1007/BF00579168
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1S)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol	448437	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	https://doi.org/10.1007/BF00579168
Violaxanthin	448438	Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C	600.90	unknown	https://doi.org/10.1007/BF00579168
Zeinoxanthin	5281234	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	552.90	unknown	https://doi.org/10.1007/BF00579168
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1271/BBB1961.55.1627 https://doi.org/10.1080/00021369.1991.10870794
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1271/BBB1961.55.1627
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1080/00021369.1991.10870794
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
3-[[1-(4-Aminobutylamino)-1-oxo-3-phenylpropan-2-yl]carbamoyl]oxirane-2-carboxylic acid	19423296	Click to see C1=CC=C(C=C1)CC(C(=O)NCCCCN)NC(=O)C2C(O2)C(=O)O	349.40	unknown	https://doi.org/10.1007/BF00579168
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid	222656	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/S10600-009-9405-Z
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/S10600-009-9405-Z
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-1-butanol	8723	Click to see CCC(C)CO	88.15	unknown	https://doi.org/10.1021/JF990116I
4-Methyl-3-penten-1-ol	136582	Click to see CC(=CCCO)C	100.16	unknown	https://doi.org/10.1021/JF990116I
Isoamyl alcohol	31260	Click to see CC(C)CCO	88.15	unknown	https://doi.org/10.1021/JF990116I
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(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/10.1016/0021-9673(96)00342-1 https://doi.org/10.1007/S10600-009-9405-Z
[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/10.1007/S10600-009-9405-Z
6-[4-hydroxy-2-methyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-methoxypyran-2-one	97290318	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/10.1080/00021369.1991.10870794
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/10.1246/BCSJ.51.842 https://doi.org/10.1016/S0040-4039(00)78048-8 https://doi.org/10.1080/00021369.1991.10870794 https://doi.org/10.1271/BBB1961.51.1723 https://doi.org/10.1007/S10600-009-9192-6 https://doi.org/10.1007/S10600-009-9405-Z
Aloenin	162305	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/10.1007/S10600-009-9405-Z https://doi.org/10.1055/S-2006-962798 https://doi.org/10.1271/BBB1961.51.1723 https://doi.org/10.1016/S0305-1978(99)00129-5 https://doi.org/10.1271/BBB1961.55.1627 https://doi.org/10.1016/0021-9673(96)00342-1 https://doi.org/10.1007/S10600-009-9192-6 https://doi.org/10.1016/S0040-4039(00)78048-8 https://doi.org/10.1016/S0378-4347(00)00524-7 https://doi.org/10.1248/JHS1956.39.5_409 https://doi.org/10.1002/(SICI)1099-1573(199908/09)13:5<401::AID-PTR515>3.0.CO;2-K https://doi.org/10.1016/S0305-1978(00)00018-1 https://doi.org/10.1246/BCSJ.51.842
Aloeresin D	14211225	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)OC	556.60	unknown	https://doi.org/10.1016/S0305-1978(00)00018-1
Aloesin	160190	Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)C3C(C(C(C(O3)CO)O)O)O)O	394.40	unknown	https://doi.org/10.1055/S-2006-962798 https://doi.org/10.1016/S0305-1978(00)00018-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Acetoin	179	Click to see CC(C(=O)C)O	88.11	unknown	https://doi.org/10.1021/JF990116I
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
Csypyrone B2	71519960	Click to see CC(=O)C1=C(C=C(OC1=O)CCCC(=O)O)O	240.21	unknown	https://doi.org/10.1007/BF00579168
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
7-Hydroxy-2,5-dimethyl-4H-1-benzopyran-4-one	5316891	Click to see CC1=CC(=CC2=C1C(=O)C=C(O2)C)O	190.19	unknown	https://doi.org/10.1007/S10600-009-9405-Z
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	https://doi.org/10.1007/S10600-009-9405-Z
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1007/S10600-009-9405-Z
> 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/10.1016/S0031-9422(00)94771-X https://doi.org/10.1055/S-2006-962798 https://doi.org/10.1016/S0176-1617(11)81144-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one	25231268	Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C4C=CC(OC4=C(C(=C3C2=O)O)CC=C(C)C)(C)C)O)C	472.60	unknown	https://doi.org/10.1007/BF00579168

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Aloe arborescens

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