Aspalathus linearis

Upload a new image!

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	UUID643fde9292a1f215066275
Scientific name	Aspalathus linearis
Authority	(Burm.f.) R.Dahlgren
First published in	Opera Bot.9: 283 (1963)

Description Top

Suggest a correction or write a new one!

No description added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Lebeckia candolleana	Walp.	Linnaea13: 477 (1840)
Aspalathus linearis subsp. linearis	(Burm.f.) R.Dahlgren
Aspalathus corymbosa	E.Mey.	Linnaea7: 159 (1832)
Aspalathus linearis subsp. pinifolia	(Marloth) R.Dahlgren	Opera Bot.9: 283 (1963)
Borbonia pinifolia	Marloth	Trans. Roy. Soc. South Africa2: 238 (1912)
Lebeckia linearis	(Burm.f.) DC.	Prodr.2: 137 (1825)
Aspalathus cognata	C.Presl	Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 556 (1845)
Genista contaminata	Poir.	J.B.A.M.de Lamarck, Encycl., Suppl. 2: 721 (1812)
Psoralea linearis	Burm.f.	Fl. Indica, Prodr. Fl. Cap.: 22 (1768)
Aspalathus tenuifolia	DC.	Prodr.2: 143 (1825)
Achyronia tenuifolia	(DC.) Kuntze	Revis. Gen. Pl.1: 157 (1891)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	rooibos
Spanish	aspalathus cognata
Spanish	rooibos
Spanish	psoralea linearis
Spanish	lebeckia linearis
Spanish	borbonia pinifolia
Spanish	aspalathus tenuifolia
Spanish	aspalathus linearis subsp. pinifolia
Spanish	aspalathus corymbosa
Afrikaans	rooibos
Arabic	رويبوس
Bulgarian	ройбос
br	te ruz
Catalan	rooibos
Czech	rooibos
Czech	roibos
Danish	rooibos
German	roibos
German	roibosh
German	rooi
German	rooibosch
German	rooibostee
German	rooibusch
German	rooibush
German	rotbuschtee
German	rooibos
Esperanto	rojbos-arbusto
Estonian	rooibos
Estonian	tee-punapõõsas
Basque	rooibos
Persian	راوند
Finnish	punapensas
Finnish	rooibos
French	rooibos
Galician	rooibos
Hebrew	רויבוש
Hungarian	rooibos
Hungarian	vörös fokföldirekettye
Indonesian	rooibos
Italian	rooibos
Japanese	ルイボスティー
Japanese	ルイボス
Kazakh	Ройбұш
Kazakh	Ройбос
Korean	루이보스
Korean	루이보스 차
lb	rooibos
Lithuanian	rooibos
Latvian	rooibos tēja
Malay	rooibos
Malay	roobois
Norwegian Bokmål	rooibos
Dutch	rooibos
Dutch	rooibosthee
Norwegian Nynorsk	rooibos
Polish	czerwonokrzew
Polish	rooibos
Portuguese	chá de rooibos
Portuguese	arbusto vermelho
Portuguese	chá de arbusto
Portuguese	chá de arbusto vermelho
Portuguese	chá vermelho
Portuguese	chá vermelho da África do sul
Portuguese	roibos
Portuguese	rooibosch
Portuguese	rooibos
Romanian	rooibos
Russian	Ройбос
Russian	Аспалатус линейный
Russian	Ройбош
Russian	Ройбуш
Slovenian	roiboos
Slovenian	rooibos
Serbian	Ројбос
Serbian	Роибос
Serbian	Рооибос
Swedish	rooibos
Swedish	rött te
Swedish	roibus
Swedish	roibos
Thai	โรยบอส
Turkish	rooibos
Ukrainian	Ройбуш
Vietnamese	chè rooibos
Chinese	南非茶
Chinese	博士茶
Chinese	路易波士茶
Chinese	松雀花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
- Southern Africa
  - Cape Provinces

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000211610
UNII	O17JQA1A9Z
USDA Plants	ASLI14
Tropicos	50326573
KEW	urn:lsid:ipni.org:names:475647-1
The Plant List	ild-6704
Open Tree Of Life	406601
NCBI Taxonomy	155124
IPNI	475647-1
iNaturalist	447656
GBIF	5348220
Freebase	/m/013v0m
EPPO	ASQLI
EOL	702617
US Library of Congress	sh85115345
USDA GRIN	310979
Wikipedia	Rooibos
CMAUP	NPO27761

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

Afriplex GRTTM extract attenuates hepatic steatosis in an in vitro model of NAFLD

Gabuza K, Mabuda TI, Patel O, Khuboni N, van Aarde R, Riedel S, Sangweni NF, Windvogel S, Johnson R, Muller CJ

PLoS One

17-Apr-2024

PMCID:	PMC11023570
doi:	10.1371/journal.pone.0297572
PMID:	38630788

Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines

Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW

J Fungi (Basel)

26-Jan-2024

PMCID:	PMC10890244
doi:	10.3390/jof10020105
PMID:	38392777

Pyrrolizidine alkaloid contamination of food in Africa: A review of current trends and implications

Letsyo E, Madilo FK, Effah-Manu L

Heliyon

03-Jan-2024

PMCID:	PMC10789634
doi:	10.1016/j.heliyon.2024.e24055
PMID:	38230234

Stevens’ Cure (Umckaloabo)—the vindication of a patent medicine

Brendler T, Stander MA, van Wyk BE

Front Pharmacol

03-Jan-2024

PMCID:	PMC10791834
doi:	10.3389/fphar.2023.1294997
PMID:	38235116

Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China

Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y

J Ethnobiol Ethnomed

02-Jan-2024

PMCID:	PMC10763305
doi:	10.1186/s13002-023-00645-w
PMID:	38169414

Translation of preclinical ethnomedicine data in LMICs: the example of rooibos

Pretorius L, Smith C

Front Pharmacol

19-Dec-2023

PMCID:	PMC10763253
doi:	10.3389/fphar.2023.1328828
PMID:	38174224

The health benefits of rooibos tea in humans (aspalathus linearis)-a scoping review

AFRIFA D, ENGELBRECHT L, EIJNDE BO, TERBLANCHE E

J Public Health Afr

01-Dec-2023

PMCID:	PMC10774856
doi:	10.4081/jphia.2023.2784
PMID:	38204815

JON 62nd Meeting 2023 Anchorage ABSTRACTS

N/A

J Nematol

16-Oct-2023

PMCID:	PMC10578804
doi:	10.2478/jofnem-2023-0047
PMID:	37849470

Cancer stem cells of head and neck squamous cell carcinoma; distance towards clinical application; a systematic review of literature

Sun Q, Chen X, Luo H, Meng C, Zhu D

Am J Cancer Res

15-Sep-2023

PMCID:	PMC10560931
PMID:	37818051

Soil water dynamics and biomass production of young rooibos (Aspalathus linearis) plants

van Schalkwyk R, Hoffman JE, Hardie AG, van Zyl JL

Sci Rep

13-Sep-2023

PMCID:	PMC10499911
doi:	10.1038/s41598-023-41666-5
PMID:	37704653

Kombucha: Challenges for Health and Mental Health

Batista P, Rodrigues Penas M, Vila-Real C, Pintado M, Oliveira-Silva P

Foods

08-Sep-2023

PMCID:	PMC10530084
doi:	10.3390/foods12183378
PMID:	37761087

Investigating the efficacy of topical application of Ipomoea carnea herbal cream in preventing skin damage induced by UVB radiation in a rat model

Sundar M, Lingakumar K

Heliyon

23-Aug-2023

PMCID:	PMC10472012
doi:	10.1016/j.heliyon.2023.e19161
PMID:	37662739

A Review on the Impact of Oxidative Stress and Medicinal Plants on Leydig Cells

Monageng E, Offor U, Takalani NB, Mohlala K, Opuwari CS

Antioxidants (Basel)

04-Aug-2023

PMCID:	PMC10451682
doi:	10.3390/antiox12081559
PMID:	37627554

Biomedical Applications of Biosynthesized Nickel Oxide Nanoparticles

Berhe MG, Gebreslassie YT

Int J Nanomedicine

27-Jul-2023

PMCID:	PMC10390717
doi:	10.2147/IJN.S410668
PMID:	37534055

Tea film formation in artificial tap water

Giacomin CE, Chen RY, Hack E, Fischer P

Soft Matter

19-Jul-2023

PMCID:	PMC10411494
doi:	10.1039/d3sm00169e
PMID:	37491884

Phytochemical Profile Top

Add a new one!

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 / Benzene and substituted derivatives
Methyl phenylacetate	7559	Click to see COC(=O)CC1=CC=CC=C1	150.17	unknown	https://doi.org/10.1021/JF00062A024
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl benzoate	7150	Click to see COC(=O)C1=CC=CC=C1	136.15	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate	4133	Click to see COC(=O)C1=CC=CC=C1O	152.15	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	via CMAUP database
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
3,5-Dihydroxybenzoic acid	7424	Click to see C1=C(C=C(C=C1O)O)C(=O)O	154.12	unknown	via CMAUP database
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1007/BF02858780
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid	338	Click to see C1=CC=C(C(=C1)C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methylbenzaldehyde	7725	Click to see CC1=CC=C(C=C1)C=O	120.15	unknown	https://doi.org/10.1021/JF00062A024
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1021/JF00062A024
> 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/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Naphthalenes
1-Methylnaphthalene	7002	Click to see CC1=CC=CC2=CC=CC=C12	142.20	unknown	https://doi.org/10.1021/JF00062A024
2-Methylnaphthalene	7055	Click to see CC1=CC2=CC=CC=C2C=C1	142.20	unknown	https://doi.org/10.1021/JF00062A024
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Ethylphenol	31242	Click to see CCC1=CC=C(C=C1)O	122.16	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol	996	Click to see C1=CC=C(C=C1)O	94.11	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see CC1=CC=C(C=C1)O	108.14	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)-	688030	Click to see COC1=C(C=CC(=C1)C(CO)O)O	184.19	unknown	via CMAUP database
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1021/JF00062A024
Guaiacol	460	Click to see COC1=CC=CC=C1O	124.14	unknown	https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00062A024
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(+)-Secoisolariciresinol	6336781	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl hexanoate	7824	Click to see CCCCCC(=O)OC	130.18	unknown	https://doi.org/10.1021/JF00062A024
Methyl octanoate	8091	Click to see CCCCCCCC(=O)OC	158.24	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
alpha-(beta-D-Glucopyranosyloxy)-trans-cinnamic acid	53385591	Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O	326.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl acetate	1549025	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptanol	8129	Click to see CCCCCCCO	116.20	unknown	https://doi.org/10.1021/JF00062A024
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1021/JF00062A024
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1021/JF00062A024
1-Octen-3-OL	18827	Click to see CCCCCC(C=C)O	128.21	unknown	https://doi.org/10.1021/JF00062A024
2-Heptanol	10976	Click to see CCCCCC(C)O	116.20	unknown	https://doi.org/10.1021/JF00062A024
2-Octanol	20083	Click to see CCCCCCC(C)O	130.23	unknown	https://doi.org/10.1021/JF00062A024
Hept-2-en-1-ol	36504	Click to see CCCCC=CCO	114.19	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF00062A024
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF00062A024
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00062A024
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00062A024
beta-Terpineol	8748	Click to see CC(=C)C1CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1021/JF00062A024
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Emericolin A	6480207	Click to see CC1CC(C2C1CC3(CCC4(CCC(C4C3CC=C2C=O)C(=C)C)C)C)O	370.60	unknown	https://doi.org/10.1016/J.MRGENTOX.2007.03.009
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hexyl acetate	8908	Click to see CCCCCCOC(=O)C	144.21	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organic oxides
beta-Cyclocitral	9895	Click to see CC1=C(C(CCC1)(C)C)C=O	152.23	unknown	https://doi.org/10.1021/JF00062A024
Safranal	61041	Click to see CC1=C(C(CC=C1)(C)C)C=O	150.22	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Hepten-3-OL	21057	Click to see CCCCC(C=C)O	114.19	unknown	https://doi.org/10.1021/JF00062A024
3-Heptanol	11520	Click to see CCCCC(CC)O	116.20	unknown	https://doi.org/10.1021/JF00062A024
4-Heptanol	11513	Click to see CCCC(CCC)O	116.20	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool, oxide	102611	Click to see CC(=CCCC(C)(C1CO1)O)C	170.25	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hepten-1-al	17167	Click to see CCCCC=CC=O	112.17	unknown	https://doi.org/10.1021/JF00062A024
2-Octenal	5283324	Click to see CCCCCC=CC=O	126.20	unknown	https://doi.org/10.1021/JF00062A024
4-Heptenal, (4Z)-	71590	Click to see CCC=CCCC=O	112.17	unknown	https://doi.org/10.1021/JF00062A024
Dodecanal	8194	Click to see CCCCCCCCCCCC=O	184.32	unknown	https://doi.org/10.1021/JF00062A024
Heptanal	8130	Click to see CCCCCCC=O	114.19	unknown	https://doi.org/10.1021/JF00062A024
Non-2-enal	17166	Click to see CCCCCCC=CC=O	140.22	unknown	https://doi.org/10.1021/JF00062A024
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1021/JF00062A024
Oct-2-enal	16900	Click to see CCCCCC=CC=O	126.20	unknown	https://doi.org/10.1021/JF00062A024
Undecanal	8186	Click to see CCCCCCCCCCC=O	170.29	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
2-Methyl-2-hepten-4-one	31138	Click to see CCCC(=O)C=C(C)C	126.20	unknown	https://doi.org/10.1021/JF00062A024
Damascenone	5366074	Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C	190.28	unknown	https://doi.org/10.1021/JF00062A024
Oct-3-en-2-one	15475	Click to see CCCCC=CC(=O)C	126.20	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Salicylaldehyde	6998	Click to see C1=CC=C(C(=C1)C=O)O	122.12	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Heptanone	8051	Click to see CCCCCC(=O)C	114.19	unknown	https://doi.org/10.1021/JF00062A024
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	https://doi.org/10.1021/JF00062A024
2-Octanone	8093	Click to see CCCCCCC(=O)C	128.21	unknown	https://doi.org/10.1021/JF00062A024
3-Heptanone	7802	Click to see CCCCC(=O)CC	114.19	unknown	https://doi.org/10.1021/JF00062A024
4-Heptanone	31246	Click to see CCCC(=O)CCC	114.19	unknown	https://doi.org/10.1021/JF00062A024
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Methylacetophenone	8500	Click to see CC1=CC=C(C=C1)C(=O)C	134.17	unknown	https://doi.org/10.1021/JF00062A024
Acetophenone	7410	Click to see CC(=O)C1=CC=CC=C1	120.15	unknown	https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole	7222	Click to see C1=CC=C2C(=C1)N=CS2	135.19	unknown	https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid	54670067	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	https://doi.org/10.1007/BF02858780
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran	19602	Click to see CCCCCC1=CC=CO1	138.21	unknown	https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine	2519	Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C	194.19	unknown	https://doi.org/10.1007/BF02858780
> Organoheterocyclic compounds / Lactones / Delta valerolactones
delta-Valerolactone	10953	Click to see C1CCOC(=O)C1	100.12	unknown	https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(S)-4-Nonanolide	441574	Click to see CCCCCC1CCC(=O)O1	156.22	unknown	https://doi.org/10.1021/JF00062A024
Gamma-nonalactone	7710	Click to see CCCCCC1CCC(=O)O1	156.22	unknown	https://doi.org/10.1021/JF00062A024
gamma-Octalactone	7704	Click to see CCCCC1CCC(=O)O1	142.20	unknown	https://doi.org/10.1021/JF00062A024
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)-	5274623	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO	360.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)86894-6
Sinapinic acid	637775	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O	224.21	unknown	via CMAUP database
> 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	via CMAUP database
> 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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/JF0347721 https://doi.org/10.1016/0027-5107(95)00116-6 https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1016/S0031-9422(00)86894-6 https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one	162904319	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(00)00182-5
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one	162904320	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(00)00182-5
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one	44715644	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(00)00182-5
2,3-Dihydro-5,7-dihydroxy-6-(beta-D-glucopyranosyl)-2beta-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one	45271033	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	via CMAUP database
Eriodictyol-6-glucoside	102370911	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	https://doi.org/10.1016/S0031-9422(00)00182-5
Hemiphloin	160711	Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	via CMAUP database
Isoorientin	114776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF0347721
Isovitexin	162350	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF0347721 https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside	122221847	Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O	450.40	unknown	via CMAUP database
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JF0347721
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-[2,4,6-Trihydroxy-3-(beta-D-glucopyranosyloxy)phenyl]-3-(4-hydroxyphenyl)-1-propanone	102467789	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	452.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF0347721 https://doi.org/10.1016/S0031-9422(00)86894-6
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JF0347721
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Quercetin 3-O-robinobioside	10371536	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1021/JF0347721 https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-(3,4-Dihydroxyphenyl)-1-(3-beta-D-glucopyranosyl-2,4,6-trihydroxyphenyl)-1-propanone	16752601	Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.PHYMED.2008.11.009 https://doi.org/10.1016/S0031-9422(00)86894-6 https://doi.org/10.1021/JF0347721 https://doi.org/10.1016/J.MRGENTOX.2007.03.009 https://doi.org/10.1016/0308-8146(95)00166-2
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one	133562015	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	https://doi.org/10.1016/0308-8146(95)00166-2
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one	154497759	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(00)00182-5
3'-C-glucosylphloretin	73830082	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	https://doi.org/10.1016/J.MRGENTOX.2007.03.009
Aspalathin	11282394	Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.MRGENTOX.2007.03.009
Nothofagin	21722188	Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O	436.40	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Aspalathus linearis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top