Details Top

Internal ID UUID6440065848fb0468632128
Scientific name Abutilon indicum
Authority (L.) Sweet
First published in Hort. Brit. : 54 (1826)

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.

Abutilon indicum is a small shrub widely distributed in South Asia, where its roots and leaves have been used in classical medicinal traditions. In Ayurvedic practice the dried root bark is recorded as a diuretic and for urinary discomfort, prepared as a decoction taken after food, while in Unani medicine the root is used similarly for urinary tract complaints (Pharmacopoeia of India, 1996; Wealth of India, 1985). In central and southern India the leaves are made into a soothing tea for sore throat and cough (Jain and Singh, 2010). In East Africa the leaves are also infused as a tea to ease bronchial irritation (Giday et al., 2003), and in southern China the whole plant is taken as a decoction for similar respiratory relief (Chinese Materia Medica, 1999). On the western coast of India fresh leaves are crushed and applied as a poultice to soothe inflamed wounds or hemorrhoids (Sharma et al., 2012).

A practical preparation frequently cited is a mild infusion for urinary comfort: place 5–8 g of chopped dried root bark in 250 ml near‑boiling water, cover and steep for 10–15 minutes, then strain and drink 1 cup after meals, 1–2 times daily. A diuretic tincture is also common: 1:5 (w/v) root bark in 45% ethanol, macerated for 4 weeks, shaken daily; typical adult dose is 2–4 ml (about 40–80 mg root equivalent) taken with water once or twice daily. For coughs and colds a leaf infusion is used, similar in method to the root‑bark tea but using 4–6 g of fresh or dried leaves per cup. Do not exceed the stated amounts of the 1:5 tincture; the plant is considered mildly diuretic and should be avoided in pregnancy or in renal disease unless advised by a clinician.

The activity aligns with constituents well established for Abutilon indicum, notably soluble mucilages that form demulcent films, flavonoids such as quercetin that confer free‑radical scavenging and anti‑inflammatory actions, and tannins that can reduce irritation and microbial load on mucous membranes (Reddy et al., 2010; Narayanan et al., 2015). These profiles support the documented use as a soothing demulcent for urinary and respiratory mucosa.

Modern interest persists through validation of anti‑inflammatory and antimicrobial effects in the literature, and preparations of A. indicum are still sold or compounded by several Ayurvedic and Unani pharmacies in India, while ethnobotanical surveys continue to record tea and poultice applications in traditional communities (Kumar et al., 2013).

General Uses Top

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Common products:
• Bast fiber from stems for coarse twine and cordage; short fibers for paper pulp and matting; seed oil for technical applications.

Industrial and craft applications:
• Bast fiber used for twine, coarse cordage, and sacking/matting; fiber strength and length suit low-grade rope and coarse textiles.

Colorants and tanning:
• No documented non-medicinal colorants or tanning uses.

Wood and fiber:
• Stem bast fiber (bast fiber) for cordage, rope, and coarse textile applications; fiber dimensions and cellulose content support manual spinning and weaving for rustic textiles and matting.

Fragrance and cosmetics:
• No documented fragrance/cosmetics uses.

Properties relevant to use:
• Fiber: bast fiber with cellulose/lignin composition suitable for coarse cordage and pulp; tenacity and flexibility appropriate for manual twine and rope. Seed oil: primarily linoleic and oleic acids; physicochemical parameters (acid value, iodine value, saponification value) typical of semi-drying oils used in non-edible technical products.

Standards and regulation:
• No plant-specific standards identified.

Sustainability and sourcing:
• Seed oil as a minor, non-food product with low industrial scale; widely available as a weed in South Asia, favoring wild or semi-wild collection.

Synonyms Top

Scientific name Authority First published in
Sida eteromischos Cav. Diss. 2: 55 (1786)
Sida coronata Scop. Delic. Fl. Faun. Insubr. 3: 1 (1788)
Sida meridionalis Salisb. Prodr. Stirp. Chap. Allerton : 382 (1796)
Sida guilleminiana Steud. Nomencl. Bot. , ed. 2, 2: 577 (1841)
Sida pubescens Cav. Diss. 1: 33 (1785)
Abutilon album Hill Brit. Herb. 49 (1756); Druce in Rep. Bot. Exch. Cl. Brit. Isles, 1913, iii. 437.
Abutilon arborescens Medik. Malvenfam. : 29 (1787)
Abutilon asiaticum (L.) Sweet Hort. Brit. : 53 (1826)
Abutilon asiaticum var. subasperum Fosberg Micronesica 2: 149 (1966 publ. 1967)
Abutilon asiaticum var. supraviride Fosberg Micronesica 2: 149 (1966 publ. 1967)
Abutilon cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 12: 185 (1913)
Abutilon croizatianum Moscoso Cat. Fl. Domingensis 1: 356 (1943)
Abutilon cunninghamii Benth. Fl. Austral. 1: 205 (1863)
Abutilon cysticarpum Hance Ann. Bot. Syst. (Walpers) 2(1): 157. 1851 [15-16 Dec 1851]
Abutilon elongatum Moench Suppl. Meth. (Moench) 205. 1802
Abutilon frutescens Medik. Malvenfam. : 29 (1787)
Abutilon hirsutissimum Moench Suppl. Meth. (Moench) 205. 1802 [2 May 1802]
Abutilon indicum var. albidum (Willd.) Baker f. J. Bot. 31: 213 (1893)
Abutilon indicum var. asiaticum (L.) Griseb. Fl. Brit. W. I. : 78 (1859)
Abutilon indicum var. populifolium (Lam.) Wight & Arn. Prodr. Fl. Ind. Orient. 1: 56. 1834 [10 Oct 1834]
Abutilon indicum var. welwitschii Baker f. J. Bot. 31: 213 (1893)
Abutilon leiospermum Griseb. Fl. Brit. W. I. : 79 (1859)
Abutilon populifolium (Lam.) Sweet Hort. Brit. : 53 (1826)
Abutilon pubescens (Cav.) Urb. Repert. Spec. Nov. Regni Veg. 16: 32. 1919
Abutilon subpapyraceum Hochr. Annuaire Conserv. Jard. Bot. Genève 6: 23 (1902)
Abutilon vesicarium (Cav.) Sweet Hort. Brit. : 54 (1826)
Beloere cistiflora Shuttlew. Smithsonian Contr. Knowl. 3(5): 21, footnote. 1852 [Mar 1852] ; in A. Gray, Pl. Wright. 1: 21. Mar 1852.
Sida indica L. Cent. Pl. II. 26. 1756 [2 Jun 1756]
Sida asiatica L. Cent. Pl. II : 26 (1756)
Sida populifolia Lam. Encycl. 1: 7 (1783)
Sida vesicaria Cav. Diss. 2, Secunda Diss. Bot. 55 (t. 14, f. 3). 1786 [Jan-Apr 1786]
Abutilon indicum var. indicum (L.) Sweet Illustrations of the Botany of Captain Cook's Voyage Round the World 1 1900
Sida albida Willd. Enum. Pl. : 722 (1809)

Common names Top

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Language Common/alternative name
English indian mallow/country mallow
English monkeybush
ace jeuleupa
Arabic أبو طيلون هندي
Arabic أبي طيلون هندي
Arabic أبا طيلون هندي
Bengali দেশি পেটারি
Bengali পোটারী
French mauve indienne
Indonesian kembang sore
Japanese タカサゴイチビ
Kannada ಕುರುವೆಗಿಡ
Malayalam ഊർപ്പം
Malayalam ഊരം
Marathi पेटारी
Malay kembang lohor
nan bō-á-tún
Oriya ପେଡିପେଡିକା
Oriya ପେଡ଼ିପେଡ଼ିକା
Oriya ଅତିବଳା
Tamil வட்டத்துத்தி
Tamil துத்திக்கீரை
Telugu దువ్వెన బెండ
Thai ครอบฟันสี
Vietnamese cây cối xay
Vietnamese cối xay
Chinese 冬葵子
Chinese 磨盘根
Chinese 磨盘草子
Chinese 磨子树
Chinese 磨谷子
Chinese 磨龙子
Chinese 磨盘草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Abutilon indicum subsp. albescens (Miq.) Borss.Waalk. Blumea 14: 173 (1966)
Abutilon indicum subsp. indicum

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
    • Macaronesia
      • Madeira
    • West-central Tropical Africa
      • Rwanda
    • Western Indian Ocean
      • Chagos Archipelago
      • Comoros
      • Mauritius
      • Rodrigues
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Kazan-retto
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
    • Western Asia
      • Afghanistan
      • Iraq
      • Palestine
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
  • Australasia
    • Australia
      • Norfolk Island
      • Northern Territory
      • Queensland
      • Western Australia
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Wake Island
    • South-central Pacific
      • Line Islands
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Howland-baker Islands
      • Nauru
      • Niue
      • Tokelau-manihiki
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil North
    • Caribbean
      • Cuba
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Windward Islands
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000511989
UNII 995RVR7OMH
USDA Plants ABIN3
Tropicos 19601227
INPN 445748
KEW urn:lsid:ipni.org:names:1101632-2
The Plant List kew-2610698
Open Tree Of Life 851840
NCBI Taxonomy 318060
Nature Serve 2.153793
IPNI 1101632-2
iNaturalist 157844
GBIF 3152634
Freebase /m/026lrhv
EPPO ABUIN
EOL 592448
USDA GRIN 746
Wikipedia Abutilon_indicum
CMAUP NPO24749

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
Ethnobotanical survey of medicinal plants used by various ethnic tribes of Mizoram, India Ralte L, Singh YT PLoS One 10-May-2024
PMCID:PMC11086894
doi:10.1371/journal.pone.0302792
PMID:38728345
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
CTAB Protocol for Obtaining High-Quality Total RNA from Hibiscus rosa-sinensis and Other Related Plants of the Family Malvaceae Kaushik N, Noorani MS, Shukla K, Mirza MA, Dhir S, Alotaibi AS, Siddiqui ZH ACS Omega 22-Apr-2024
PMCID:PMC11080010
doi:10.1021/acsomega.4c00877
PMID:38737072
Green synthesis, characterization and applications of Phyllanthus emblica fruit extract mediated chromium oxide nanoparticles Fatima E, Arooj I, Javeed M, Yin J Discov Nano 16-Apr-2024
PMCID:PMC11019192
doi:10.1186/s11671-024-04006-8
PMID:38625606
Leaf functional traits and resource use strategies facilitate the spread of invasive plant Parthenium hysterophorus across an elevational gradient in western Himalayas Sharma P, Rathee S, Ahmad M, Siddiqui MH, Alamri S, Kaur S, Kohli RK, Singh HP, Batish DR BMC Plant Biol 02-Apr-2024
PMCID:PMC10985864
doi:10.1186/s12870-024-04904-0
PMID:38561674
Phytol from Scoparia dulcis prevents NF-κB-mediated inflammatory responses during macrophage polarization Duraisamy P, Angusamy A, Ravi S, Krishnan M, Martin LC, Manikandan B, Sundaram J, Ramar M 3 Biotech 17-Feb-2024
PMCID:PMC10874368
doi:10.1007/s13205-024-03924-9
PMID:38375513
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
Surface engineered nanohybrids in plasmonic photothermal therapy for cancer: Regulatory and translational challenges Debnath M, Debnath SK, Talpade MV, Bhatt S, Gupta PP, Srivastava R Nanotheranostics 12-Feb-2024
PMCID:PMC10911973
doi:10.7150/ntno.92639
PMID:38444744
Photocatalytic Degradation of Rhodamine-B and Water Densification via Eco-Friendly Synthesized Cr2O3 and Ag@Cr2O3 Using Garlic Peel Aqueous Extract Alqarni LS, Alghamdi MD, Alshahrani AA, Alotaibi NF, Moustafa SM, Ashammari K, Alruwaili IA, Nassar AM Nanomaterials (Basel) 31-Jan-2024
PMCID:PMC10857512
doi:10.3390/nano14030289
PMID:38334561
Unveiling the cytotoxic and anti-proliferative potential of green-synthesized silver nanoparticles mediated by Colletotrichum gloeosporioides Gupta P, Singh S, Rai N, Verma A, Tiwari H, Kamble SC, Gautam HK, Gautam V RSC Adv 30-Jan-2024
PMCID:PMC10825743
doi:10.1039/d3ra06145k
PMID:38292267
Exploring the excellence of commercial Brahmi products from Thai online markets: Unraveling phytochemical contents, antioxidant properties and DNA damage protection Nopparat J, Sujipuli K, Ratanasut K, Weerawatanakorn M, Prasarnpun S, Thongbai B, Laothaworn W, Inthima P Heliyon 17-Jan-2024
PMCID:PMC10831600
doi:10.1016/j.heliyon.2024.e24509
PMID:38304802
Green and cost-effective biofabrication of copper oxide nanoparticles: Exploring antimicrobial and anticancer applications Gebreslassie YT, Gebremeskel FG Biotechnol Rep (Amst) 12-Jan-2024
PMCID:PMC10835232
doi:10.1016/j.btre.2024.e00828
PMID:38312482
Evaluation of the Ethanolic Leaf Extract of Abutilon indicum on Isonicotinic Acid Hydrazide-Induced Proinflammatory Marker Gene Expression Changes Sunil M, Vedavijaya T, Thakur RS, Sree P K, Ramana Yella V, Babu Sayana S Cureus 07-Dec-2023
PMCID:PMC10771030
doi:10.7759/cureus.50102
PMID:38186405
Characterization of Sesuvium sesuvioides Using High-Performance Liquid Chromatography and Validation of Its In Vivo Anti-hyperthyroidism Effect via Suppressing Oxidative Stress and Inflammatory Markers Sajid-ur-Rehman M, Ishtiaq S, Khan MS, Jabeen Q, Youssef FS, Ahmed SA, Elhady SS, Ashour ML ACS Omega 22-Nov-2023
PMCID:PMC10701866
doi:10.1021/acsomega.3c06630
PMID:38075807
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1055/S-0028-1097714
> 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/10.7897/2230-8407.089160
> 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/10.1055/S-0028-1097714
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1055/S-0028-1097714
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1055/S-0028-1097714
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1055/S-0028-1097714
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1055/S-0028-1097714
Octacosane 12408 Click to see 394.80 unknown https://doi.org/10.1055/S-0028-1097714
Pentacosane 12406 Click to see 352.70 unknown https://doi.org/10.1055/S-0028-1097714
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1055/S-0028-1097714
Triacontane 12535 Click to see 422.80 unknown https://doi.org/10.1055/S-0028-1097714
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1055/S-0028-1097714
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.7897/2230-8407.089160
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.7897/2230-8407.089160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.7897/2230-8407.089160
7-(5-Formyl-3,6,7-trihydroxy-1-methyl-8-propan-2-ylnaphthalen-2-yl)-2,3,8-trihydroxy-6-methyl-4-propan-2-ylnaphthalene-1-carbaldehyde 25201041 Click to see 518.60 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.7897/2230-8407.089160
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.7897/2230-8407.089160
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(+)-Alantolactone 72724 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(89)80379-6
https://doi.org/10.7897/2230-8407.089160
(+)-Isoalantolactone 73285 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(89)80379-6
https://doi.org/10.7897/2230-8407.089160
Bohlmann K2631 327378 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(89)80379-6
Isohelenin 605266 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(89)80379-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Methyl Betulinate 73493 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Guggulsterone 6450278 Click to see 312.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(1S)-1-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3,16-dioxo-2,6,7,8,9,11,12,14,15,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl] acetate 91597955 Click to see 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3R,5S,8R,9S,10S,13S,14S,17R)-17-ethyl-10,13-dimethyl-16-oxo-1,2,3,4,5,6,7,8,9,11,12,14,15,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] acetate 15767893 Click to see 360.50 unknown via CMAUP database
[(8R,9S,10R,13S,14S,16S,17Z)-17-ethylidene-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-16-yl] acetate 101929524 Click to see CC=C1C(CC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)OC(=O)C 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Threonine 205 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Allothreonine 99289 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
(+-)-Aspartic Acid 424 Click to see 133.10 unknown https://doi.org/10.1055/S-0028-1097714
L-Aspartic Acid 5960 Click to see 133.10 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid 611 Click to see 147.13 unknown https://doi.org/10.1055/S-0028-1097714
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
DL-Histidine 773 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1055/S-0028-1097714
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
DL-leucine 857 Click to see 131.17 unknown https://doi.org/10.1055/S-0028-1097714
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1055/S-0028-1097714
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
DL-Serine 617 Click to see 105.09 unknown https://doi.org/10.1055/S-0028-1097714
L-Serine 5951 Click to see 105.09 unknown https://doi.org/10.1055/S-0028-1097714
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
(2R,3S,4R,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoic acid 25021697 Click to see C(=O)C(C(C(C(C(=O)O)O)O)O)O 194.14 unknown https://doi.org/10.1055/S-0028-1097714
Galactopyranuronic acid, D- 152867 Click to see 194.14 unknown https://doi.org/10.1055/S-0028-1097714
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1055/S-0028-1097714
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1055/S-0028-1097714
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1055/S-0028-1097714
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1055/S-0028-1097714
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(1R,2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 5316222 Click to see 755.70 unknown via CMAUP database
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5,8-trihydroxy-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10254562 Click to see 480.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10345073 Click to see 480.40 unknown via CMAUP database

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