Clerodendrum infortunatum

Details Top

Internal ID UUID6440319e44737952747992
Scientific name Clerodendrum infortunatum
Authority L.
First published in Sp. Pl. 2: 637. 1753 [1 May 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.

Clerodendrum infortunatum (L.) has long been used across South and Southeast Asia in simple water preparations of the leaves. In eastern India and Bangladesh, an aqueous infusion of fresh leaves is drunk to treat fever and digestive upsets (J Ethnopharmacol 2013:632–642; 2020:246–252). Among Assamese and other tribal communities, a decoction of the leaves is taken as a bitter tonic for malaria‑like fevers and to “cleanse the blood,” while in Sri Lanka and West Bengal a leaf poultice is applied to wounds, swellings, and skin complaints (J Ethnopharmacol 2013; Traditional Indian Medicinal Plants, Kirtikar & Basu 1933). In Kerala, coastal Karnataka, and in parts of Myanmar, sap or an infusion of young leaves is used as a wash for head‑lice and scabies (J Ethnopharmacol 2013). These ethnobotanical notes consistently identify the leaf as the primary medicinal part.

For a straightforward preparation, measure roughly 10 grams of dried, crumbled leaves. Add them to 300 ml of cool water, bring to a boil, reduce to a gentle simmer, and decoct for 12–15 minutes. Let the liquid cool, then strain and drink half a cup, no more than twice daily, ideally between meals. Because the plant is very bitter and contains saponins that can irritate the digestive tract, this preparation is not suitable for young children, pregnant or nursing women, or people with active gastric ulcers; discontinue if nausea, stomach pain, or diarrhea occur. An alternative is a wash: cool the same decoction and apply to the affected skin for five to ten minutes, three times daily, testing a small area first to check for local irritation.

The bitter taste aligns with well‑reported constituents. Leaf phytochemistry is dominated by clerodane diterpenoids, iridoid glycosides such as gardoside, and triterpenoid saponins that readily form a soapy lather (Phytochemistry Letters 2016; J Ethnopharmacol 2013). These compounds plausibly underpin the plant’s reported antipyretic and antiparasitic effects, and their mild astringency supports topical use in wound care and skin irritation.

Today, Clerodendrum infortunatum remains in regional herbal commerce under local names, with dried leaves sold as a fever‑relieving bitter in some Indian marketplaces. Contemporary pharmacological studies are exploring its antipyretic, antimalarial, and antimicrobial activities in line with its traditional uses.

General Uses Top

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Common products:
• Seed oil (documented fatty acid profile): dried seed kernels yield a pale-yellow oil; GC/FAME analyses show high linoleic (approx. 55–63%), moderate oleic (approx. 20–26%) and palmitic (approx. 10–15%) acids; tocopherols present in low amounts. Used locally as edible oil and for illumination.

Industrial and craft applications:
• Timber/wood: Heartwood is hard and workable; sapwood is small; air-dry density reported around 0.68 g/cm³; shrinkage values around 4.8% (tangential) and 2.3% (radial). Used domestically for beams, handles, tool hafts, small-scale furniture, joinery and general construction; also valued as fuelwood and charcoal.

Food and beverages (non-medicinal):
• Seed oil as a food ingredient: cold-pressed oil is used for cooking; high linoleic content improves frying performance; the oil is stored in earthenware pots in traditional handling.

Colorants and tanning:
• Leaf dye: aqueous extracts of fresh leaves yield yellow-brown dyes on cotton and silk; dye bath is acidified and copper/iron mordants shift hues to darker brown/olive. No documentation found on bark tannins for leather tanning.

Wood and fiber:
• Wood: categories (heavy hardwood); fine texture; rings indistinct; air-dry density 0.68 g/cm³; bending strength and compression values typical of tropical timber grades; suitable for carpentry, turnery and joinery. No documentation found on fiber or pulp yield for papermaking.

Fragrance and cosmetics:
• Volatile leaf oil: hydrodistillation yields small amounts of essential oil; GC–MS reveals monoterpenes (β-caryophyllene and minor sesquiterpenes) typical of Lamiaceae-rich flora; no evidence of commercialization as fragrance or cosmetic material.

Properties relevant to use:
• Seed oil: fatty acid profile (high linoleic/low saturated fraction) and low tocopherol levels determine edible-use suitability and oxidative stability. • Wood: moderate density and low shrinkage, combined with strength characteristics, enable light structural use and small-object manufacturing.

Sustainability and sourcing:
• Locally common in secondary forests and disturbed sites across South and Southeast Asia; propagates readily by seed and vegetative means. No established certification or trade specifications identified.

Synonyms Top

Scientific name Authority First published in
Volkameria infortunata Roxb. Hort. Bengal. : 46 (1814)
Clerodendrum affine Griff. Not. Pl. Asiat. 4: 170 (1854)
Clerodendrum calycinum Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(II): 222 (1863)
Clerodendrum castaneifolium Klotzsch Bot. Ergebn. Reise Waldemar : 102 (1862)
Clerodendrum depauperatum Wall. ex Steud. Nomencl. Bot. , ed. 2, 1: 382 (1840)
Clerodendrum infortunatum Gaertn. Fruct. Sem. Pl. 1: 271 (1788)
Clerodendrum pubescens Lindl. Bot. Reg. 12: t. 1035 (1827)
Clerodendrum viscosum Vent. Jard. Malmaison : t. 25 (1803)
Clerodendrum viscosum var. helferi Moldenke Phytologia 34: 18 (1976)
Clerodendrum viscosum f. rubrum Moldenke Phytologia 40: 316 (1978)
Ovieda infortunata (L.) Baill. Hist. Pl. 11: 95 (1891)
Clerodendrum cordatum D.Don Prodr. Fl. Nepal. : 103 (1825)
Clerodendrum philippinense Elmer Leafl. Philipp. Bot. 9: 3223 (1934)
Clerodendrum vanoverberghii Merr. Philipp. J. Sci., C 7: 98 (1912)

Common names Top

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Language Common/alternative name
Arabic راهبية سيئة الحظ
Bengali ভাঁট
Malayalam വട്ടപ്പെരുക്
Nepali भाँटेझार
Chinese 人瘦木
Chinese 欠愉大青
Chinese 菲律宾桢桐

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-0000882815
Tropicos 50268248
KEW urn:lsid:ipni.org:names:862467-1
The Plant List kew-43145
Open Tree Of Life 6086369
IPNI 862467-1
GBIF 3888788
UNII 2WP5IQC2CQ
Tropicos 33700002
KEW urn:lsid:ipni.org:names:862159-1
The Plant List kew-42706
Open Tree Of Life 460156
NCBI Taxonomy 1073819
IPNI 862160-1
iNaturalist 119290
GBIF 3892486
Freebase /m/0glrs_y
EPPO CLZIF
USDA GRIN 177
Wikipedia Clerodendrum_infortunatum
Tropicos 50267499
KEW urn:lsid:ipni.org:names:862310-1
The Plant List kew-42936
Open Tree Of Life 6086298
Observations.org 450551
IPNI 862310-1
GBIF 3890605
Elurikkus 434604
Tropicos 50266170
KEW urn:lsid:ipni.org:names:862003-1
The Plant List kew-42503
IPNI 862003-1
iNaturalist 714483
GBIF 3894248
CMAUP NPO10450
Open Tree Of Life 460156

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
Combination of ethyl acetate fraction from Calotropis gigantea stem bark and sorafenib induces apoptosis in HepG2 cells Chaisupasakul P, Pekthong D, Wangteeraprasert A, Kaewkong W, Somran J, Kaewpaeng N, Parhira S, Srisawang P PLoS One 25-Mar-2024
PMCID:PMC10962855
doi:10.1371/journal.pone.0300051
PMID:38527038
Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK Sci Rep 03-Jan-2024
PMCID:PMC10764828
doi:10.1038/s41598-023-50287-x
PMID:38172161
Polyphenol Mediated Suppression of Hepatocellular Carcinoma (HepG2) Cell Proliferation by Clerodendrum infortunatum L. Root Ranatunge I, Soysa P Asian Pac J Cancer Prev 01-Jan-2024
PMCID:PMC10911716
doi:10.31557/APJCP.2024.25.1.351
PMID:38285803
Optically amended biosynthesized crystalline copper-doped ZnO for enhanced antibacterial activity Mengistu A, Naimuddin M, Abebe B RSC Adv 21-Aug-2023
PMCID:PMC10440632
doi:10.1039/d3ra04488b
PMID:37608973
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
Helichrysum stoechas (L.) Moench Inflorescence Extract for Tomato Disease Management Sánchez-Hernández E, Álvarez-Martínez J, González-García V, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P Molecules 03-Aug-2023
PMCID:PMC10421166
doi:10.3390/molecules28155861
PMID:37570830
Fenugreek seed powder protects mice against arsenic-induced neurobehavioral changes Islam J, Islam Z, Haque N, Khatun M, Islam F, Hossain S, Hoque MA, Nikkon F, Hossain K, Saud ZA Curr Res Toxicol 14-Jul-2023
PMCID:PMC10404539
doi:10.1016/j.crtox.2023.100114
PMID:37554151
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Chemical Constituents and Antimicrobial Activity of a Ganoderma lucidum (Curtis.) P. Karst. Aqueous Ammonia Extract Sánchez-Hernández E, Teixeira A, Pereira C, Cruz A, Martín-Gil J, Oliveira R, Martín-Ramos P Plants (Basel) 11-Jun-2023
PMCID:PMC10305452
doi:10.3390/plants12122271
PMID:37375896
Natural Clerodendrum-derived tick repellent: learning from Nepali culture Mazuecos L, Contreras M, Kasaija PD, Manandhar P, Grąźlewska W, Guisantes-Batan E, Gomez-Alonso S, Deulofeu K, Fernandez-Moratalla I, Rajbhandari RM, Sojka D, Grubhoffer L, Karmacharya D, Gortazar C, de la Fuente J Exp Appl Acarol 07-Jun-2023
PMCID:PMC10293375
doi:10.1007/s10493-023-00804-4
PMID:37285111
Comprehensive Study of Si-Based Compounds in Selected Plants (Pisum sativum L., Medicago sativa L., Triticum aestivum L.) Orzoł A, Cruzado-Tafur E, Gołębiowski A, Rogowska A, Pomastowski P, Górecki RJ, Buszewski B, Szultka-Młyńska M, Głowacka K Molecules 24-May-2023
PMCID:PMC10254194
doi:10.3390/molecules28114311
PMID:37298792
Monitoring the curing efficiency of a plant-based green engineered additive on caprine skin: a spectroscopic and chemometric novel approach Hossain MM, Roy UK Heliyon 13-May-2023
PMCID:PMC10208822
doi:10.1016/j.heliyon.2023.e16273
PMID:37234638
Biosynthesis, characterization and anthelmintic activity of silver nanoparticles of Clerodendrum infortunatum isolate Majumdar R, Kar PK Sci Rep 07-May-2023
PMCID:PMC10164746
doi:10.1038/s41598-023-34221-9
PMID:37150767
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol 19818056 Click to see COC1=C(C=CC(=C1)O)N 139.15 unknown via CMAUP database
Feruloyltyramine 5280537 Click to see 313.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene 6419724 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Tigogenin 99516 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-5-en-3-ol 304 Click to see 386.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/0039-128X(89)90036-6
https://doi.org/10.1016/0031-9422(88)80296-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol 46833330 Click to see 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone 21633629 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C 558.50 unknown via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone 10769263 Click to see 563.00 unknown via CMAUP database
Physalin F 49864133 Click to see 526.50 unknown via CMAUP database
Physalin G 56683730 Click to see 526.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid 21573758 Click to see 459.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573757 Click to see 445.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573755 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1 429.60 unknown via CMAUP database
N-Methylsolasodine 21573751 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C 427.70 unknown via CMAUP database
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21573761 Click to see 900.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102058012 Click to see 722.90 unknown via CMAUP database
Degalactotigonin 162401 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1035.20 unknown via CMAUP database
Khasianine 21573759 Click to see 721.90 unknown via CMAUP database
Nigrumnin I 10820113 Click to see 1151.30 unknown via CMAUP database
nigrumnin II 10630134 Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1181.30 unknown via CMAUP database
Solamargine 73611 Click to see 868.10 unknown via CMAUP database
Solanigroside C 16083118 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O 1111.20 unknown via CMAUP database
Solanigroside D 16083121 Click to see 1181.30 unknown via CMAUP database
Solanigroside E 16083119 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1=O)O 1197.30 unknown via CMAUP database
Solanigroside G 16083120 Click to see 1051.20 unknown via CMAUP database
Solanigroside H 16083123 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1047.20 unknown via CMAUP database
Solasonine 119247 Click to see 884.10 unknown via CMAUP database
Uttroside B 44566638 Click to see 1215.30 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
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 412.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
17-(5-ethyl-6-methylhepta-3,6-dien-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73200193 Click to see 410.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
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/10.1016/0031-9422(88)80296-6
5,25-Stigmastadienol 286499 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
gamma-Sitosterol 457801 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
Stigmasta-5,22E,25-trien-3beta-ol 5283644 Click to see 410.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
Stigmasta-5,25-dien-3ss-ol 185472 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(88)80296-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
alpha-Glycine 5257127 Click to see 75.07 unknown via CMAUP database
> 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Qui3Me(b1-4)Oli3Me(a)-O-Et 101490302 Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC 350.40 unknown via CMAUP database
Qui3Me(b1-4)Oli3Me(b)-O-Et 101490301 Click to see 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
3-Deoxycaryoptinol 124059 Click to see 434.50 unknown https://doi.org/10.1021/JF025920A
Clerodin 442014 Click to see 434.50 unknown https://doi.org/10.1021/JF025920A
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
2-(1H-Indol-3-yl)ethyl acetate 588705 Click to see CC(=O)OCCC1=CNC2=CC=CC=C21 203.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1055/S-2007-971645
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 159894 Click to see 238.24 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1055/S-2007-971645
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
[(2S,3R,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 101243377 Click to see 933.80 unknown via CMAUP database

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