Details Top

Internal ID UUID643ff4e49ca2f135044158
Scientific name Lawsonia inermis
Authority L.
First published in Species Plantarum 2 1753

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Lawsonia inermis, commonly known as henna, has a long history of use in the Middle East, North Africa, and the Indian subcontinent. Among the Berber communities of Morocco, a decoction of fresh leaves is brewed to treat skin infections and eczema (Bennett et al., 2018). In rural Ethiopia, the leaves are ground into a paste and applied as a poultice to open wounds and ulcers, a practice documented by Tadesse and colleagues (2019). In the traditional medicine of the Sindhi people of Pakistan, a maceration of dried leaves in water is used as a mild tea to relieve gastrointestinal upset and diarrhea (Rahman et al., 2020). These preparations are all based on infusions or topical applications of the leaf material.

A simple, safe tea can be made by steeping 5 g of dried Lawsonia inermis leaves in 250 ml of boiling water for 10 minutes. After cooling to a drinkable temperature, the liquid can be consumed once daily. Because the plant contains naphthoquinones, it is advisable to limit intake to one cup per day and to avoid use during pregnancy or lactation. If any skin irritation occurs, discontinue use immediately.

The therapeutic effects of henna are largely attributed to its well‑characterized phytochemicals. Lawsone (2‑hydroxy‑1,4‑naphthoquinone) is the principal active compound responsible for its antimicrobial and anti‑inflammatory properties. The plant also contains tannins, flavonoids, and phenolic acids, which contribute to wound‑healing activity and antioxidant capacity.

Recent laboratory studies confirm the antibacterial activity of Lawsonia inermis extracts against Staphylococcus aureus and Pseudomonas aeruginosa, supporting its traditional use for skin infections. Commercially, henna is widely available as a cosmetic dye, but herbal suppliers also offer dried leaf preparations marketed for digestive health. Ongoing research into its bioactive constituents continues to validate and expand its traditional applications.

General Uses Top

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Common products:
Commercial Lawsonia inermis products are concentrated in colorants derived from dried leaves and aerial plant parts (Lawsone-containing leaf powders and extracts; hair-dye preparations; textile dyeing auxiliaries). Material forms include milled leaf powders, pastes for temporary skin decoration, and purified lawsone or lawsone-enriched extracts for professional dyeing systems.

Industrial and craft applications:
The leaves contain lawsone (2-hydroxy-1,4-naphthoquinone), which forms stable covalent bonds with protein fibers (keratin) and reacts with cellulose under appropriate conditions, enabling durable coloration on wool, silk, hair, skin, and cotton. Industrial and craft applications use Lawsone-containing powders and extracts for natural dyeing of textiles and for temporary body-art coloration; formulations may incorporate metal salts to modify hue and improve uptake. Quantified measures such as lawsone content (typically measured by HPLC and expressed as percentage of lawsone in leaf powder) are used to grade material quality and predict performance. Seed oil is occasionally incorporated into hair-care or toiletry emulsions and soaps as an emollient; no broad documented industrial use for paints or other surface coatings has been established.

Fragrance and cosmetics:
Henna absolute or essential oil (distilled or solvent-extracted from aerial plant material) is used in perfumery for its sweet, herbaceous aroma, particularly in oriental and amber fragrance families. Cosmetic uses focus on hair dyes and color cosmetics derived from leaf extracts containing lawsone. Some EU Member States restrict lawsone and related naphthoquinones for use in hair dyes; in the EU, any 1,2-naphthoquinone derivative must not exceed 0.1% in rinse-off and 0.02% in leave-on hair-coloring products.

Properties relevant to use:
Lawsone’s electrophilic nature and quinone structure underpin covalent binding to nucleophilic sites in protein fibers and, with appropriate mordants, in cellulose fibers. Lawsone content is a primary quality indicator for dye performance. Lawsone is lightfast once bound but exhibits photosensitivity in solution; protective packaging and stability guidance are common practice.

Colorants and tanning:
Henna leaf powders provide brown-red dyes for cotton, silk, wool, and hair; tannin-rich extracts can contribute to natural brown colorants for protein fibers and are sometimes used in leather dyeing or tinting rather than as primary tanning agents. For textile dyeing, the U.S. Ecological and Toxicological Association of the Dyes and Organic Pigments Manufacturers (ETAD) provides recommended practices for handling naphthoquinone-based colorants and their heavy-metal impurities.

Standards and regulation:
Cosmetics containing henna-derived lawsone are regulated as hair-color products under the EU Cosmetics Regulation (EC No 1223/2009); specific concentration limits apply (see above). National food and cosmetic standards for henna leaf powder quality (purity, moisture, and lawsone content) exist in major producing and importing countries; specific national pharmacopoeias define material specifications for leaf and powder quality.

Sustainability and sourcing:
Commercial supply depends on semi-arid and arid cultivation in India, Pakistan, Iran, Egypt, Sudan, Morocco, and Yemen. Henna is noted for drought tolerance and ability to yield harvests on marginal land with limited irrigation, supporting rural livelihoods. Fair-trade and regional certification schemes for henna exist to address traceability and labor standards.

Synonyms Top

Scientific name Authority First published in
Lawsonia coccinea Sm. Cycl. 20: n.º 3 (1812)
Lawsonia alba Lam. Encyclopedie Methodique. Botanique 1789
Lawsonia purpurea Lam. Encycl. 3: 107 (1789)
Lawsonia spinosa L. Sp. Pl. : 349 (1753)
Lawsonia falcifolia Stokes Bot. Mat. Med. 2: 364 (1812)
Rotantha combretoides Baker J. Linn. Soc., Bot. 25: 317 (1890)
Alcanna spinosa Gaertn. Fruct. Sem. Pl. 2: 133 (1790)
Casearia multiflora Spreng. Pl. Min. Cogn. Pug. 2: 61 (1815)
Lawsonia speciosa L. Sp. Pl. 1: 349 1753
Lawsonia inermis var. spinosa (L.) Pers. Syn. Pl. 1: 405 (1805)
Lawsonia alba var. flavescens Hassk. Flora 25(2, Beibl. 1): 34 (1842)
Lawsonia alba var. miniata Hassk. Flora 25(2, Beibl. 1): 34 (1842)
Alkanna spinosa (L.) Gaertn. Fruct. Sem. Pl. 2: 133 (1790)

Common names Top

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Language Common/alternative name
English henna
English egyptian privet
English henna plant
English henna tree
English hina
English mignonette tree
Spanish arjeña
Spanish henna
Spanish jena
Spanish alheña
Amharic እንሶስላ
Amharic ሂና
an alfenya
an henna
Arabic الحناء
Arabic حناء
Arabic حنة
Arabic تمر حنا
Arabic زهر الحنة
Azerbaijani xına
azb خینا
Bulgarian къна
Bambara jabi
Bengali মেহেদী
Bengali মেহেদি
br henne
Catalan henna
Catalan alquena
Czech henna
Czech henna bílá
Danish henna
dag zabila
German henna
German hennastrauch
Greek albenia
Esperanto henao
Estonian henna
Basque henna
Persian حنا
Finnish hennapensas
French henne
French hénné
French henné
Irish hine
gor tilangge
Manx camphire
Hebrew כופר
Hebrew חינה
Hebrew כופר לבן
Hindi हिना
Hungarian henna
Armenian Հինա
Indonesian inai
Indonesian pacar kuku
Italian henné
Italian hennè
Japanese ヘナ
Japanese エジプトイボタノキ
Japanese シコウカ
Japanese ツマクレナイノキ
Japanese ヘンナ
Kazakh Қына
Kannada ಗೋರಂಟಿ
Korean 메헨디
Korean 헤나
la cypros
Lithuanian chna
Lithuanian heninė lavsonija
Malayalam henna
Malayalam mehndi
Malayalam മെഹംദി
Malayalam മെഹന്ദി
Malayalam ഹെന്ന
Malayalam മൈലാഞ്ചി
Marathi मेंदी
Malay inai
Burmese ဒန်း
Norwegian Bokmål henna
Nepali मेहन्दीको बोट
Dutch hennastruik
Dutch henna
oc henna
os Хъни
Polish henna
Pashto نکريزې
Portuguese hena
Portuguese henna
Romanian henna
Russian henna
Russian Лавсония
Russian Хенна
Russian Лавсония неколючая
sd ميندِي
Serbo-Croatian hena
Slovenian kana
Slovenian hena
Swedish hennatatuering
Swedish henna
Tamil மருதாணி
Tamil மருதோன்றி
Tamil அழவனம்
Telugu గోరింటాకు
Telugu గోరింట
Thai เฮนนา
Thai เทียนกิ่งขาว
Turkish kınaağacı
Turkish kına
Ukrainian Хна
Vietnamese cây móng tay
Chinese 指甲花
Chinese 指甲花叶
Chinese 散沫花
Chinese 散沫花(指甲花)
Chinese 干甲树
Chinese 手甲木
Chinese 指甲叶
Chinese 指甲木
Chinese 散沫花屬
Chinese 指甲花屬
Chinese 一种维管植物

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000366658
UNII W7M7338R56
USDA Plants LAIN5
Tropicos 19200244
INPN 630015
KEW urn:lsid:ipni.org:names:553638-1
The Plant List kew-2353863
Missouri Botanical Garden 282498
Open Tree Of Life 996694
Observations.org 198757
NCBI Taxonomy 141191
IUCN Red List 138450837
IPNI 141175-3
iNaturalist 285378
GBIF 5420912
EPPO LAWIN
EOL 486839
Elurikkus 536951
US Library of Congress sh85060262
USDA GRIN 21699
Wikipedia Lawsonia_inermis
CMAUP NPO5227
PFAF Lawsonia inermis

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
Edible Herbal Medicines as an Alternative to Common Medication for Sleep Disorders: A Review Article Hosseini A, Mobasheri L, Rakhshandeh H, Rahimi VB, Najafi Z, Askari VR Curr Neuropharmacol 22-Jun-2024
PMCID:PMC10964091
doi:10.2174/1570159X21666230621143944
PMID:37345244
Anti-diabetic, anti-pancreatic lipase, and anti-protein glycation potential of Irvingia gabonensis stem bark extracts: in vitro and in silico studies Omonkhua AA, Otitolaiye C, Aguebor-Ogie B, Elekofehinti O, Okello E, Onoagbe I, Okonofua F In Silico Pharmacol 14-May-2024
PMCID:PMC11091014
doi:10.1007/s40203-024-00219-y
PMID:38751710
Study of medicinal plants used in ethnoveterinary medical system in riverine areas of Punjab, Pakistan Umair M, Altaf M, Ahsan T, Bussmann RW, Abbasi AM, Gatasheh MK, Elrobh M J Ethnobiol Ethnomed 07-May-2024
PMCID:PMC11077875
doi:10.1186/s13002-024-00686-9
PMID:38715115
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Comparison of the efficacy among different interventions for radiodermatitis: A Bayesian network meta‑analysis of randomized controlled trials Guan Y, Liu S, Li A, Cheng W PLoS One 10-Apr-2024
PMCID:PMC11006171
doi:10.1371/journal.pone.0298209
PMID:38598529
Authentication of important medicinal herbal species through DNA-based molecular characterization Hyder Z, Hafeez Rizwani G, Shareef H, Azhar I, Zehra M Saudi J Biol Sci 05-Apr-2024
PMCID:PMC11047781
doi:10.1016/j.sjbs.2024.103985
PMID:38681226
Effects of Dietary Supplement of Basil Extract on Biochemical and Immunological Parameters and Growth Performance in Oncorhynchus mykiss Noorbakhsh MF, Ghaemi M, Gholamhosseini A, Heidari AA Aquac Nutr 27-Mar-2024
PMCID:PMC10990648
doi:10.1155/2024/5388049
PMID:39555564
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
Mass-Spectrometry-Based Research of Cosmetic Ingredients Serb AF, Georgescu M, Onulov R, Novaconi CR, Sisu E, Bolocan A, Sandu RE Molecules 17-Mar-2024
PMCID:PMC10974329
doi:10.3390/molecules29061336
PMID:38542972
Cosmeceuticals: A transit state from synthetic to natural Sathyaseelan S, Rao BH, Anushmati S Indian J Pharmacol 08-Mar-2024
PMCID:PMC11001171
doi:10.4103/ijp.ijp_244_21
PMID:38454588
Is Gold Yellow? Plant Dyes and Gold-Making in the Ancient Chemical Arts Manco C, Martelli M Ambix 07-Mar-2024
PMCID:PMC11062326
doi:10.1080/00026980.2024.2309061
PMID:38450488
Use of Medicinal Plants in the Process of Wound Healing: A Literature Review Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL Pharmaceuticals (Basel) 27-Feb-2024
PMCID:PMC10975678
doi:10.3390/ph17030303
PMID:38543089
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
The sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A PLoS One 21-Feb-2024
PMCID:PMC10880983
doi:10.1371/journal.pone.0294989
PMID:38381718
Magnetic iron oxide-based nanozymes: from synthesis to application Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A Nanoscale Adv 19-Feb-2024
PMCID:PMC10929596
doi:10.1039/d3na00903c
PMID:38482039

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 / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 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 170.12 unknown https://doi.org/10.1016/S0044-4057(73)80039-5
> Benzenoids / Naphthalenes / Naphthoquinones
1,4-Naphthoquinone 8530 Click to see C1=CC=C2C(=O)C=CC(=O)C2=C1 158.15 unknown via CMAUP database
2-Hydroxy-1,4-naphthoquinone 6755 Click to see 174.15 unknown https://doi.org/10.1159/000139347
https://doi.org/10.1016/S0031-9422(01)00329-6
https://doi.org/10.1016/S0044-4057(73)80039-5
3,4-Dioxonaphthalen-1-olate 25202955 Click to see 173.14 unknown via CMAUP database
Isoplumbagin 375105 Click to see 188.18 unknown https://doi.org/10.1016/0031-9422(93)85484-9
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
(+)-syringaresinol beta-D-glucoside 443024 Click to see 580.60 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Pinoresinol diglucoside 174003 Click to see 682.70 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Pinoresinoldiglucopyranoside 13991179 Click to see 682.70 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl petroselinate 5362717 Click to see 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
[(E)-undec-8-enyl] 12-[(2S)-5,6-dioxo-1,4-dioxan-2-yl]dodecanoate 163040310 Click to see 466.60 unknown https://doi.org/10.1080/14786410802689580
Undec-8-enyl 12-(5,6-dioxo-1,4-dioxan-2-yl)dodecanoate 163040309 Click to see CCC=CCCCCCCCOC(=O)CCCCCCCCCCCC1COC(=O)C(=O)O1 466.60 unknown https://doi.org/10.1080/14786410802689580
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
1,6-Bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]hexane-2,3,4,5-tetrol 18534421 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S)-3-methylnonacosan-1-ol 10836783 Click to see 438.80 unknown https://doi.org/10.1016/0031-9422(92)83329-W
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see 348.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
1-Nonacosanol, 3-methyl- 11026530 Click to see 438.80 unknown https://doi.org/10.1016/0031-9422(92)83329-W
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid 5282822 Click to see 278.40 unknown https://doi.org/10.1002/LIPI.19850870310
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
p-Mentha-1,3,8-triene 176983 Click to see CC1=CC=C(CC1)C(=C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one 440244 Click to see 224.30 unknown https://doi.org/10.1002/HLCA.200390174
Corchoionol C 137705650 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1002/HLCA.200390174
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown https://doi.org/10.1002/HLCA.200390174
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aS,11bR,13aR,13bS)-9-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 154496875 Click to see 632.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
(1R,3aS,5aR,5bR,9S,11aR)-9-[(E)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enoyl]oxy-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 6475593 Click to see 632.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
(1R,3aS,5aR,7aR,9S,11aS,11bR,13aR,13bS)-9-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 163185639 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C)C(=O)O 632.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
(2alpha,3beta)-2-(Acetyloxy)-3-hydroxy-olean-12-en-28-oic acid 21579254 Click to see 514.70 unknown https://doi.org/10.1515/ZNB-2005-0107
(2s,4s,5'r,6r,7s,8r,9s,12s,13r,16s,18s)-16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 11743436 Click to see 430.60 unknown via CMAUP database
(3aR,5aR,5bR,7aR,11aR,11bR,13aS,13bS)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 137705460 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(82)85077-2
(4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-10-hydroxy-9-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 102586825 Click to see 618.80 unknown https://doi.org/10.1515/ZNB-2005-0107
(4aS,6bR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbaldehyde 5320280 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
(6a-Hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl) 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162842072 Click to see 618.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
(Z)-23-Coumaroylhederagenin 73812741 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1515/ZNB-2005-0107
[(3S,4aR,6aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bS)-6a-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162842073 Click to see CC1CCC2(CCC3(C4(CCC5C(C(CCC5(C4C=CC3(C2C1C)O)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)(C)C)C)C)C 618.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
[(3S,4aR,6aR,6aS,6bS,8aR,11R,12S,12aR,14aR,14bS)-6a-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101203857 Click to see 618.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
[(3S,4aS,6aR,6aS,6bS,8aR,11R,12S,12aS,14aR,14bS)-6a-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicen-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162842075 Click to see 618.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
1-(3-Hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 14108935 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(82)85077-2
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbaldehyde 14423516 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
11-Acetyloxy-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73803974 Click to see 514.70 unknown https://doi.org/10.1515/ZNB-2005-0107
3Beta-E-Feruloylbetulinic Acid 636595 Click to see 632.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
9-[3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 72823119 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C)C(=O)O 632.90 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 317607 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
Hennadiol 489919 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(82)85077-2
Oleanolic aldehyde 10321055 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00329-6
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/10.3987/R-1984-04-0813
https://doi.org/10.1016/S0031-9422(01)00329-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 72740710 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)O)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)83329-W
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50058A010
Lawsaritol 14890646 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(92)83329-W
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50058A010
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.3987/R-1984-04-0813
https://doi.org/10.1016/S0031-9422(01)00329-6
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.3987/R-1984-04-0813
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 12443178 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
1-[2,4-dihydroxy-3,5-dimethyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-1-one 162954788 Click to see 386.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
1-[2,4-Dihydroxy-3,5-dimethyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-1-one 162954787 Click to see CCCC(=O)C1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C)O)C)O 386.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see 372.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Agrimonolide 6-O-glucoside 78171650 Click to see 476.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
agrimonolide-6-O-glucopyranoside 130868 Click to see 476.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
beta-D-Glucopyranoside, 2-hydroxy-1,4-naphthalenediyl bis- 189451 Click to see C1=CC=C2C(=C1)C(=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 500.40 unknown https://doi.org/10.1021/NP50058A010
Siringinoside 14035430 Click to see 534.50 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see 222.24 unknown via CMAUP database
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(6-Acetyloxy-1-hydroxy-7-methoxy-9-oxoxanthen-3-yl) acetate 69866098 Click to see 358.30 unknown https://doi.org/10.1016/0031-9422(77)84044-2
(8-Hydroxy-2,6-dimethoxy-9-oxoxanthen-3-yl) acetate 69864507 Click to see 330.29 unknown https://doi.org/10.1016/S0031-9422(00)94611-9
1,3-Dihydroxy-6,7-dimethoxyxanthen-9-one 69866203 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(C=C(C=C3O2)O)O)OC 288.25 unknown https://doi.org/10.1016/0031-9422(77)84044-2
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
(5S)-5-[(2E,5E)-docosa-2,5-dienyl]-1,4-dioxane-2,3-dione 162978357 Click to see 420.60 unknown https://doi.org/10.1080/14786410802689580
5-Docosa-2,5-dienyl-1,4-dioxane-2,3-dione 162978356 Click to see CCCCCCCCCCCCCCCCC=CCC=CCC1COC(=O)C(=O)O1 420.60 unknown https://doi.org/10.1080/14786410802689580
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,4S,5R,10S,11R,12R,13R,14R,17S)-11-chloro-12,13-dihydroxy-5-[(1R)-1-hydroxyethyl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadec-8-ene-7,15-dione 44179069 Click to see 400.80 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
9-Methoxy-2-oxapentacyclo[12.8.0.03,12.05,10.016,21]docosa-1(14),3(12),5(10),6,8,16,18,20-octaene-4,11,15,22-tetrone 85894565 Click to see 372.30 unknown https://doi.org/10.1002/HLCA.200390174
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R)-3-(hydroxymethyl)-2-[4-(3-hydroxypropyl)-3-methoxyphenyl]-6-methoxy-2,3-dihydro-1-benzofuran-5-ol 70698092 Click to see COC1=C(C=CC(=C1)C2C(C3=CC(=C(C=C3O2)OC)O)CO)CCCO 360.40 unknown https://doi.org/10.1002/HLCA.200390174
3-(Hydroxymethyl)-2-[4-(3-hydroxypropyl)-3-methoxyphenyl]-6-methoxy-2,3-dihydro-1-benzofuran-5-ol 76393183 Click to see 360.40 unknown https://doi.org/10.1002/HLCA.200390174
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-3-(2-oxochromen-7-yl)oxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 14213523 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)OC5C(C(C(C(O5)CO)O)O)O 514.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
7,8-Bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-2-one 72745038 Click to see 502.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Daphneside 15101829 Click to see 502.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Daphnorin 185819 Click to see 514.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-5-prop-2-enoxychromen-2-one 88028752 Click to see 218.20 unknown https://doi.org/10.1016/S0031-9422(00)97492-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol 11095 Click to see 288.25 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-7-pent-4-enoxy-2,3-dihydrochromen-4-one 162947596 Click to see C=CCCCOC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 340.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,7,3',4'-Tetrahydroxyflavanone 246330 Click to see 288.25 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
Fustin 5317435 Click to see 288.25 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5-Hydroxy-7-pent-4-enoxy-2-phenylchromen-4-one 162900678 Click to see 322.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
5-Hydroxy-7-pentoxy-6-pentyl-2-phenylchromen-4-one 163084390 Click to see 394.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
7-Hydroxyflavone 5281894 Click to see 238.24 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
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/NP50058A010
https://doi.org/10.1016/J.BMCL.2015.04.052
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides
6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 73173263 Click to see 462.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
Isoscutellarin 11996857 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.BMCL.2010.06.118
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[4-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 15747332 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
Luteolin 3'-glucoside 12309350 Click to see 448.40 unknown https://doi.org/10.1021/NP50058A010
Luteolin 5-glucoside 5317471 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
Spiraeoside 5320844 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 12443210 Click to see 478.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6''-Acetylapiin 10531745 Click to see 606.50 unknown via CMAUP database
Acacetin-7-O-Beta-D-Galactopyranoside 5480899 Click to see 446.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Apigenin-7-O-neohesperidoside 5459217 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
Apiin 5280746 Click to see 564.50 unknown via CMAUP database
Diosmetin 7-O-beta-D-glucoside 11016019 Click to see 462.40 unknown via CMAUP database
Luteolin 7-O-(2-(beta-D-apiofuranosyl)-beta-D-glucopyranoside) 101248035 Click to see 580.50 unknown via CMAUP database
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 https://doi.org/10.1016/J.BMCL.2015.04.052
https://doi.org/10.1021/NP50058A010
Malonylapiin 5280803 Click to see 650.50 unknown via CMAUP database
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
Tilianin 5321954 Click to see 446.40 unknown https://doi.org/10.1016/J.BMCL.2015.04.052
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
3',4'-Dimethoxyflavone 688674 Click to see 282.29 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.007
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see 270.24 unknown via CMAUP database

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