Scientific name	Authority	First published in
Sabdariffa rubra	Kostel.	Allg. Med.-Pharm. Fl. 5: 1857 (1836)
Sabdariffa digitata	Kostel.	Allg. Med.-Pharm. Fl. 5: 1857 (1836)
Abelmoschus cruentus	Walp.	Repert. Bot. Syst. 1: 310 (1842)
Furcaria sabdariffa	Ulbr.	Veg. Erde 9(III 2): 402 (1921)
Hibiscus cruentus	Bertol.	Fl. Guatimal. : 28 (1840)
Hibiscus digitatus	Cav.	Diss. 3: 151 (1787)
Hibiscus fraternus	L.	Pl. Surin. : 90 (1775)
Hibiscus gossypiifolius	Mill.	Gard. Dict. ed. 8 : n.º 10 (1768)
Hibiscus masuianus	De Wild. & T.Durand	Bull. Soc. Roy. Bot. Belgique , Compt. Rend. 38: 20 (1899)
Hibiscus sanguineus	Griff.	Not. Pl. Asiat. 4: 520 (1854)
Hibiscus palmatilobus	Baill.	Bull. Mens. Soc. Linn. Paris 1: 509 (1885)
Hibiscus digitatus var. kerrianus	DC.	Prodr. 1: 453 (1824)

Common names Top

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Filter by language:

Language	Common/alternative name
English	roselle
Spanish	rosa de jamaica
Spanish	rosa de abisinia
Spanish	flor de jamaica
Spanish	jamaica
anp	roselle (plant)
Arabic	كركديه
Arabic	الكركديه
Assamese	টেঙামৰা
Azerbaijani	məkkə çayı
Azerbaijani	rozella
Azerbaijani	məkkə teli
azb	مکَه چایی
Bengali	চুকাই
Catalan	rosa de jamaica
Catalan	cànem de guinea
Czech	ibišek súdánský
dag	birili
German	roselle
German	sudan-eibisch
German	sabdariff-eibisch
German	karkade
German	bissap
German	afrikanische malve
Esperanto	sabdarifo
Persian	روزل
Finnish	teehibiskus
French	roselle
French	oseille de guinée
French	ketmie acide
French	karkadé
French	carcadé
French	carcade
French	bissap
Gujarati	અંબાડી
Hausa	zobo
Hebrew	היביסקוס עב-גביע
Hungarian	rozella
Indonesian	rosela
Indonesian	rosella
Italian	carcadè
Italian	karkadè
Japanese	ローゼル
jv	rosela
Korean	로젤
ln	ngai ngai
Lithuanian	jamaikinė kinrožė
Malayalam	പുളിവെണ്ട
Malayalam	roselle
Malayalam	മീൻപുളി
Malayalam	മത്തിപ്പുളി
mnw	လဂဝ်
Marathi	अंबाडी
Malay	asam belanda
Malay	roselle
Malay	asam susur
Burmese	ချဉ်ပေါင်
Nepali	बेलचन्दन
Dutch	roselle
os	Розеллæ (зайæгой)
Polish	ketmia szczawiowa
Portuguese	vinagreira
Portuguese	caruru-azedo
pwn	yuzilu
Russian	Гибискус сабдарифа
Russian	Гибискус сабдариффа
Russian	Красный щавель
Russian	Розелла
Russian	Ямайский щавель
Russian	Суданская роза
sd	کٽنبڙو
Sango	dongö
su	rosella
Swedish	rosellhibiskus
Telugu	గోంగూర
Thai	กระเจี๊ยบแดง
Thai	กระเจี๊ยบเปรี้ยว
Turkish	hibisküs
Turkish	karabamya
Turkish	kerkede
Chinese	扶桑叶
Chinese	洛神花
Chinese	洛神果
Chinese	山茄子
Chinese	玫瑰茄
Chinese	洛神葵

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Tanzania
- Northeast Tropical Africa
  - Chad
  - Somalia
  - Sudan
- Northern Africa
  - Egypt
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Namibia
  - Northern Provinces
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Mali
  - Mauritania
  - Niger
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cameroon
  - Central African Republic
  - Congo
  - Gabon
  - Gulf Of Guinea Islands
  - Zaïre
- Western Indian Ocean
  - Comoros
  - Mauritius
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Taiwan
- Western Asia
  - Iraq

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Thailand
  - Vietnam
- Papuasia
  - Solomon Islands

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- Southwestern Pacific
  - Fiji
  - Vanuatu

Southern America click to expand
- Brazil
  - Brazil Southeast
- Caribbean
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - El Salvador
  - Guatemala
- Northern South America
  - Venezuela
- Western South America
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000723020
UNII	UH3Z91Y49Y
USDA Plants	HISA2
Tropicos	19600047
INPN	629855
KEW	urn:lsid:ipni.org:names:326388-2
The Plant List	kew-2850461
Plantarium	18729
Open Tree Of Life	120930
Observations.org	142124
NCBI Taxonomy	183260
Nature Serve	2.155606
IPNI	326388-2
iNaturalist	163773
GBIF	3152582
Freebase	/m/05pyzn
EPPO	HIBSA
EOL	487306
US Library of Congress	sh85115429
USDA GRIN	19078
Wikipedia	Roselle_(plant)

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_037953265.1	ASM3795326v1	Contig	KAIST	2024-04-03	141.3x	2.20 Gb

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

Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC)

Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO

3 Biotech

05-Apr-2024

PMCID:	PMC10997672
doi:	10.1007/s13205-024-03970-3
PMID:	38585410

Antidiabetic Property Optimization from Green Leafy Vegetables Using Ultrasound-Assisted Extraction to Improve Cracker Production

Maser WH, Maiyah N, Karnjanapratum S, Nukthamna P, Thompson AK, Huda N, Moula Ali AM, Bavisetty SC

Prev Nutr Food Sci

31-Mar-2024

PMCID:	PMC10987381
doi:	10.3746/pnf.2024.29.1.47
PMID:	38576886

Maximizing Curcuminoid Extraction from Curcuma aromatica Salisb. Rhizomes via Environmentally Friendly Microwave-Assisted Extraction Technique Using Full Factorial Design

Suksaeree J, Monton C

Int J Food Sci

25-Mar-2024

PMCID:	PMC10985645
doi:	10.1155/2024/4566123
PMID:	38566754

Anthocyanins from Lycium ruthenicum Murray Mitigate Cadmium-Induced Oxidative Stress and Testicular Toxicity by Activating the Keap1/Nrf2 Signaling Pathway

Dong M, Lu J, Xue H, Lou Y, Li S, Liu T, Ding Z, Chen X

Pharmaceuticals (Basel)

01-Mar-2024

PMCID:	PMC10975946
doi:	10.3390/ph17030322
PMID:	38543108

The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil

da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC

J Ethnobiol Ethnomed

26-Feb-2024

PMCID:	PMC10895823
doi:	10.1186/s13002-024-00667-y
PMID:	38409039

Monitor the freshness of shrimp by smart halochromic films based on gelatin/pectin loaded with pistachio peel anthocyanin nanoemulsion

Taheri-Yeganeh A, Ahari H, Mashak Z, Jafari SM

Food Chem X

20-Feb-2024

PMCID:	PMC10901912
doi:	10.1016/j.fochx.2024.101217
PMID:	38426072

Targets and Effects of Common Biocompounds of Hibiscus sabdariffa (Delphinidin-3-Sambubiosid, Quercetin, and Hibiscus Acid) in Different Pathways of Human Cells According to a Bioinformatic Assay

Zúñiga-Hernández SR, García-Iglesias T, Macías-Carballo M, Pérez-Larios A, Gutiérrez-Mercado YK, Camargo-Hernández G, Rodríguez-Razón CM

Nutrients

19-Feb-2024

PMCID:	PMC10893457
doi:	10.3390/nu16040566
PMID:	38398890

Green Solvents for Extraction of Natural Food Colorants from Plants: Selectivity and Stability Issues

Tzanova MT, Yaneva Z, Ivanova D, Toneva M, Grozeva N, Memdueva N

Foods

16-Feb-2024

PMCID:	PMC10887973
doi:	10.3390/foods13040605
PMID:	38397582

Unique properties of titanium dioxide quantum dots assisted regulation of growth and biochemical parameters of Hibiscus sabdariffa plants

Abdelhameed RE, Abdalla H, Ibrahim MA

BMC Plant Biol

16-Feb-2024

PMCID:	PMC10870679
doi:	10.1186/s12870-024-04794-2
PMID:	38365586

High electrochemical performance of nickel cobaltite@biomass carbon composite (NiCoO@BC) derived from the bark of Anacardium occidentale for supercapacitor application

Diop M, Ndiaye BM, Dieng S, Ngom BD, Chaker M

RSC Adv

14-Feb-2024

PMCID:	PMC10865185
doi:	10.1039/d3ra08138a
PMID:	38362084

In Vivo Diuretic Activity and Anti-Hypertensive Potential of Hibiscus sabdariffa Extract by Inhibition of Angiotensin-Converting Enzyme and Hypertension Precursor Enzymes

Sanou A, Konaté K, Belemnaba L, Sama H, Kaboré K, Dakuyo R, Nitiéma M, Dicko MH

Foods

09-Feb-2024

PMCID:	PMC10888337
doi:	10.3390/foods13040534
PMID:	38397511

Evaluation of Bioactive Effects of Five Plant Extracts with Different Phenolic Compositions against Different Therapeutic Targets

Villegas-Aguilar MD, Sánchez-Marzo N, Fernández-Ochoa Á, Del Río C, Montaner J, Micol V, Herranz-López M, Barrajón-Catalán E, Arráez-Román D, Cádiz-Gurrea MD, Segura-Carretero A

Antioxidants (Basel)

08-Feb-2024

PMCID:	PMC10886104
doi:	10.3390/antiox13020217
PMID:	38397815

The potential effect of natural antioxidants on endothelial dysfunction associated with arterial hypertension

Caminiti R, Carresi C, Mollace R, Macrì R, Scarano F, Oppedisano F, Maiuolo J, Serra M, Ruga S, Nucera S, Tavernese A, Gliozzi M, Musolino V, Palma E, Muscoli C, Rubattu S, Volterrani M, Federici M, Volpe M, Mollace V

Front Cardiovasc Med

02-Feb-2024

PMCID:	PMC10869541
doi:	10.3389/fcvm.2024.1345218
PMID:	38370153

Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review

Islam Shawon S, Nargis Reyda R, Qais N

Heliyon

01-Feb-2024

PMCID:	PMC10864916
doi:	10.1016/j.heliyon.2024.e25340
PMID:	38356556

Analyses of phytochemical compounds in the flowers and leaves of Spiraea japonica var. fortunei using UV-VIS, FTIR, and LC-MS techniques

Yılmazer Keskin S, Avcı A, Fajriana Febda Kurnia H

Heliyon

01-Feb-2024

PMCID:	PMC10848007
doi:	10.1016/j.heliyon.2024.e25496
PMID:	38327478

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
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/S0304-3835(98)00010-X https://doi.org/10.1016/0009-2797(96)03721-0 https://doi.org/10.1016/S0006-2952(00)00322-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	https://doi.org/10.1021/JF00123A022
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1021/JF00123A022
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	https://doi.org/10.1021/JF00123A022
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1021/JF00123A022
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1021/JF00123A022
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	https://doi.org/10.1021/JF00123A022
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1021/JF00123A022
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Gossypol	3503	Click to see CC1=CC2=C(C(=C(C(=C2C(C)C)O)O)C=O)C(=C1C3=C(C4=C(C=C3C)C(=C(C(=C4C=O)O)O)C(C)C)O)O	518.60	unknown	https://doi.org/10.1021/JF00123A022 https://doi.org/10.21608/BFSA.1998.67837
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,8S,9R,10R,13S,14S,17S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162906455	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1055/S-0028-1097275
2,15-Dimethyl-14-(6-methylheptan-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol	304	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1055/S-0028-1097275
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9R,10R,13S,14S,17S)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	163015450	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1055/S-0028-1097275
(3S,9R,10S,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	163000932	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.1055/S-0028-1097275
(3S,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	247705	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	https://doi.org/10.1055/S-0028-1097275
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1055/S-0028-1097275
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,5S,9S,10R,13S,14R,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162958784	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-0028-1097275
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-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	162965363	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1055/S-0028-1097275
(3S,8S,9R,10R,13S,14S,17S)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	163081991	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-0028-1097275
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	521229	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-0028-1097275
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-0028-1097275
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/10.1055/S-0028-1097275
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(2S,3R)-3-hydroxy-3-methoxycarbonyl-5-oxooxolane-2-carboxylic acid	9930500	Click to see COC(=O)C1(CC(=O)OC1C(=O)O)O	204.13	unknown	https://doi.org/10.1271/BBB.64.1041
3-Hydroxy-3-methoxycarbonyl-5-oxooxolane-2-carboxylic acid	85069821	Click to see COC(=O)C1(CC(=O)OC1C(=O)O)O	204.13	unknown	https://doi.org/10.1271/BBB.64.1041
allo-Hydroxycitric acid lactone	6481826	Click to see C1C(=O)OC(C1(C(=O)O)O)C(=O)O	190.11	unknown	https://doi.org/10.1271/BBB.64.1041
Hydroxycitric acid lactone, (-)-(P)	9859390	Click to see C1C(=O)OC(C1(C(=O)O)O)C(=O)O	190.11	unknown	https://doi.org/10.1271/BBB.64.1041
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-Maltose	439341	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1021/JF00123A022
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Gossypetin	5280647	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O	318.23	unknown	https://doi.org/10.1039/CT9099501855
Hibiscetin	15559735	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O	334.23	unknown	https://doi.org/10.1039/CT9099501855 https://doi.org/10.1007/BF03051846
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5,8-trihydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12310325	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	480.40	unknown	https://doi.org/10.1007/BF03170544
Gossypitrin	6452123	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	480.40	unknown	https://doi.org/10.1007/BF03170544

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Hibiscus sabdariffa

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