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Cyanthillium cinereum

Cyanthillium cinereum - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fcbb964f93186997700
Scientific name Cyanthillium cinereum
Authority (L.) H.Rob.
First published in Proc. Biol. Soc. Washington 103: 252 (1990)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vernonia leptophylla DC. Contr. Bot. India : 6 (1834)
Conyza incana B.Heyne ex DC. Prodr. 5: 24 (1836)
Conyza abbreviata Wall. Numer. List : n.° 3048 (1831)
Isomeria chinensis Wight ex DC. Prodr. 5: 24 (1836)
Monosis elaeagnoides Kunth Index Seminum (B, Berolinensis) : 14 (1848)
Leveillea chinensis Vaniot Bull. Acad. Int. Géogr. Bot. , sér. 3, 13(170-171): 16 (1904)
Vernonia parviflora Reinw. 893 1826
Conyza ivifolia Burm.f. Fl. Indica : 180 (1768)
Conyza chinensis L. Sp. Pl. : 862 (1753)
Chrysocoma violacea Schumach. & Thonn. Beskr. Guin. Pl. : 384 (1827)
Conyza elegantula Wall. Numer. List : n.° 3049 (1831)
Vernonia betonicifolia Baker J. Linn. Soc., Bot. 22: 487 (1887)
Vernonia parviflora Reinw. ex Blume Bijdr. Fl. Ned. Ind. : 893 (1826)
Conyza bellidifolia Wall. Numer. List : n.° 3048 (1831)
Conyza cinerea L. Sp. Pl. : 862 (1753)
Vernonia exilis Miq. J. Bot. Néerl. 1: 98 (1861)
Cacalia kroneana Kuntze Revis. Gen. Pl. 2: 970 (1891)
Eupatorium arboreum Reinw. ex de Vriese Pl. Ind. Bat. Reinw. 129.
Conyza mollis Willd. Sp. Pl., ed. 4 , 3: 1924 (1803)
Erigeron pisonis Burm.f. Fl. Ind. : 180 (1768)
Serratula cinerea Roxb. Hort. Bengal. : 60 (1814)
Vernonia cinerea (L.) Less. Linnaea 4: 291 (1829)
Vernonia villosa W.Wight Contr. U.S. Natl. Herb. 9: 396 (1905)
Vernonia laxiflora Less. Linnaea 6: 646 (1831)
Vernonia villosa W.F.Wright U.S. Dept. Agric. Contrib. Nat. Herb. 9: 396. 190-.
Vernonia kroneana Miq. J. Bot. Néerl. 1: 98 (1861)
Vernonia montana Hook.f. Fl. Brit. India [J. D. Hooker] 3(8): 234, sphalm. 1881 [Mar 1881]
Conyza prolifera Lam. Encycl. 2: 84 (1786)
Claotrachelus rupestris var. glabra Zoll. & Mor. Zoll., Natuur-Geneesk. Arch. Ned.-Indie 2 (1845) 272 1845
Cyanopis erigeroides DC. Contr. Bot. India : 7 (1834)
Cacalia cinerea Kuntze Revis. Gen. Pl. 1: 323 (1891)
Vernonia physalifolia DC. Contr. Bot. India : 6 (1834)
Blumea chinensis DC. Prodr. 5: 444 (1836)
Vernonia cinerea subsp. vialis (DC.) Humbert Fl. Madagasc. 189: 20 (1960)
Eupatorium myosotifolium Jacq. Icon. Pl. Rar. 3: 15 (1793)
Vernonia zollingeriana Sch.Bip. Syst. Verz. : 119 (1855)
Conyza cinerascens Wall. Numer. List : n.° 3062 (1831)
Placus chinensis Baill. Hist. Pl. 8: 303 (1882)
Seneciodes cinereum (L.) Kuntze Lex. Gen. Phan. : 515 (1903)
Blumea esquirolii H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 7: 22 (1909)
Vernonia dendigulensis DC. Prodr. 7: 263 (1838)
Vernonia cyanonioides Walp. Linnaea 14 1840
Vernonia rupestris (Zoll.) Hook.f. ex B.D.Jacks. Index Kew. 1 (1893) 522 1893
Cineraria glaberrima Spreng. ex DC. Prodr. 5: 25 (1836)
Vernonia apocynifolia Baker J. Linn. Soc., Bot. 20: 175 (1883)
Vernonia erigeroides DC. Prodr. 5: 25 (1836)
Cyanthillium cinereum var. cinereum (L.) H.Rob.
Crassocephalum flatmense Hochst. & Steud. ex DC. Prodr. 7(1): 263 (1838)
Vernonia vialis DC. ex Sch.Bip. Zoll. Syst. Verz. (1854) 119 1854
Cacalia rotundifolia Willd. Phytographia 1: 11 (1794)
Vernonia cinerea var. erigeroides (DC.) Domin Biblioth. Bot. 22(89): 651 (1930)
Cyanthillium cinereum var. ovatum Isawumi Compositae Newslett. 26: 16 (1995)
Vernonia cinerea var. parviflora (Reinw. ex Blume) DC. Prodr. 5: 24 (1836)
Cacalia erigerodes Kuntze Revis. Gen. Pl. 2: 970 (1891)
Vernonia abbreviata DC. Prodr. 5: 25 (1836)
Vernonia lentii Volkens & O.Hoffm. Pflanzenw. Ost-Afrikas C: 404 (1895)
Isomeria cinerea Wight ex DC. Prodr. 5: 24 (1836)
Vernonia vialis DC. Prodr. 5: 25 (1836)
Cyanthillium chinense Gleason Bull. Torrey Bot. Club 40: 306 (1913)
Vernonia cinerea var. antoniensis (L.) Bolle 130 1860
Vernonia rhomboidea Edgew. Trans. Linn. Soc. London 20: 62 (1846)
Cacalia exilis Kuntze Revis. Gen. Pl. 2: 970 (1891)
Cacalia chinensis (L.) Kuntze 324 1891
Placus chinensis Kuntze Revis. Gen. Pl. 1: 356 (1891)
Conyza heterophylla Lam. Encycl. 2: 84 (1786)
Centratherum chinense Less. Linnaea 6: 105 (1829)
Cyanopsis decurrens Zoll. & Moritzi Natuur- Geneesk. Arch. Ned.-Indië ii. (1845) 563
Vernonia cinerea var. montana C.B.Clarke Compos. Ind. : 21 (1876)
Vernonia cinerea var. lentii (O.Hoffm.) C.Jeffrey Kew Bull. 43: 224 (1988)

Common names Top

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Language Common/alternative name
English little ironweed
English poovamkurunnila
English an herbal herb.
ace seuriba
Bengali একটি ভেষজ বিরুৎ।
Bengali কুকসিমা
dag nagiyem
Japanese ムラサキムカシヨモギ
Malayalam പൂവാംകുരുന്നില
Malayalam പൂവാംകുറുന്തൽ
Malay pokok tambak bukit
Burmese ကဒူးပြန်
Dutch dạ hương ngưu
Sinhala මොණර කුඩුම්බිය
Thai หญ้าละออง
Tonga fisipuna
Vietnamese dạ hương ngưu
Chinese 夜香牛

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Cyanthillium cinereum var. glabriusculum (DC.) Karthik. & Moorthy Fl. Pl. India : 223 (2009)
Cyanthillium cinereum var. lanatum (J.Kost.) Ghafoor Fl. Australia 37(1): 607 (2015)
Cyanthillium cinereum var. linifolium (Blume) Karthik. & Moorthy Fl. Pl. India : 223 (2009)
Cyanthillium cinereum var. ludens (C.B.Clarke) Karthik. & Moorthy Fl. Pl. India : 223 (2009)
Cyanthillium cinereum var. parviflorum (Reinw. ex Blume) Karthik. & Moorthy Fl. Pl. India : 223 (2009)
Cyanthillium cinereum var. pinnatifidum Ghafoor Fl. Australia 37(1): 607 (2015)
Cyanthillium cinereum var. ugandense (C.Jeffrey) Isawumi Compositae Newslett. 26: 15 (1995)
Cyanthillium cinereum var. viale (DC.) Isawumi Compositae Newslett. 26: 16 (1995)

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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre
    • Western Indian Ocean
      • Chagos Archipelago
      • Comoros
      • Madagascar
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Kazan-retto
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Malaya
      • Maluku
      • Philippines
    • Papuasia
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Southeast
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
    • South-central Pacific
      • Cook Islands
      • Line Islands
      • Marquesas
      • Pitcairn Islands
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Nauru
      • New Caledonia
      • Niue
      • Phoenix Islands
      • Samoa
      • Tokelau-manihiki
      • Tonga
      • Tuvalu
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
    • Caribbean
      • Aruba
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000051035
UNII 1IJV2249O2
Florida Plant Atlas 405
USDA Plants CYCI4
Tropicos 2743180
INPN 448442
KEW urn:lsid:ipni.org:names:962413-1
The Plant List gcc-149577
Open Tree Of Life 1033710
Observations.org 198647
NCBI Taxonomy 211151
IPNI 962413-1
iNaturalist 130374
iNaturalist 448526
GBIF 6445734
Freebase /m/0wzwm7p
Elurikkus 578405
USDA GRIN 406954
Wikipedia Cyanthillium_cinereum
CMAUP NPO33276

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
Traditional Uses, Phytochemistry, and Pharmacological Activities of Vernonia cinerea (L.) Less.: An Updated Review Trang NM, Vinh LB, Phong NV, Yang SY Nutrients 06-May-2024
PMCID:PMC11085347
doi:10.3390/nu16091396
PMID:38732642
Nano-enabled agrochemicals: mitigating heavy metal toxicity and enhancing crop adaptability for sustainable crop production Ghorbani A, Emamverdian A, Pehlivan N, Zargar M, Razavi SM, Chen M J Nanobiotechnology 05-Mar-2024
PMCID:PMC10913482
doi:10.1186/s12951-024-02371-1
PMID:38443975
Little Ironweed and Java Tea in Herbal Toothpaste Reduced Dentine Permeability: An In Vitro Study Vajrabhaya LO, Korsuwannawong S, Harnirattisai C, Teanchai C, Salee W J Int Soc Prev Community Dent 27-Feb-2024
PMCID:PMC10980310
doi:10.4103/jispcd.jispcd_67_23
PMID:38559639
Approaches, Strategies and Procedures for Identifying Anti-Inflammatory Drug Lead Molecules from Natural Products Jamtsho T, Yeshi K, Perry MJ, Loukas A, Wangchuk P Pharmaceuticals (Basel) 22-Feb-2024
PMCID:PMC10974486
doi:10.3390/ph17030283
PMID:38543070
Exploring the potential of Crotalaria juncea flower extracts as a source of antioxidants, antimicrobials, and cytoprotective agents for biomedical applications Mahasawat P, Boukaew S, Prasertsan P BioTechnologia (Pozn) 21-Dec-2023
PMCID:PMC10777724
doi:10.5114/bta.2023.132772
PMID:38213478
Apoptosis-inducing anti-proliferative and quantitative phytochemical profiling with in silico study of antioxidant-rich Leea aequata L. leaves Mostofa MG, Reza AS, Khan Z, Munira MS, Khatoon MM, Kabir SR, Sadik MG, Ağagündüz D, Capasso R, Kazi M, Alam AK Heliyon 10-Dec-2023
PMCID:PMC10759211
doi:10.1016/j.heliyon.2023.e23400
PMID:38170014
The Potentials of Ageratum conyzoides and Other Plants from Asteraceae as an Antiplasmodial and Insecticidal for Malaria Vector: An Article Review Kusman IT, Pradini GW, Ma’ruf IF, Fauziah N, Berbudi A, Achadiyani A, Wiraswati HL Infect Drug Resist 07-Nov-2023
PMCID:PMC10638911
doi:10.2147/IDR.S433328
PMID:37954507
Evaluation of Neutralization Potential of Naja naja and Daboia russelii Snake Venom by Root Extract of Cyanthillium cinereum Suji S, Dinesh M, Keerthi K, Anagha K, Arya J, Anju K Indian J Crit Care Med 01-Nov-2023
PMCID:PMC10626242
doi:10.5005/jp-journals-10071-24567
PMID:37936805
Moringa oleifera Use in Maintaining Oral Health and Its Potential Use in Regenerative Dentistry Shafiq NE, Mahdee AF ScientificWorldJournal 17-Oct-2023
PMCID:PMC10597730
doi:10.1155/2023/8876189
PMID:37881795
The complete chloroplast genome of Elephantopus scaber L. (Vernonioideae, Asteraceae), a useful ethnomedicinal plant in asia Nguyen PA, Khang DT, Nguyen PT, Do HD Mitochondrial DNA B Resour 04-Sep-2023
PMCID:PMC10478624
doi:10.1080/23802359.2023.2252944
PMID:37674912
Medicinal Plants Used in the Management of Sexual Dysfunction, Infertility and Improving Virility in the East African Community: A Systematic Review Kyarimpa C, Nagawa CB, Omara T, Odongo S, Ssebugere P, Lugasi SO, Gumula I Evid Based Complement Alternat Med 12-Aug-2023
PMCID:PMC10439835
doi:10.1155/2023/6878852
PMID:37600549
Pyroptosis Modulators: New Insights of Gasdermins in Health and Disease Allali-Boumara I, Marrero AD, Quesada AR, Martínez-Poveda B, Medina MÁ Antioxidants (Basel) 03-Aug-2023
PMCID:PMC10451529
doi:10.3390/antiox12081551
PMID:37627547
Green Biosynthesis of Zinc Oxide Nanoparticles Using Pluchea indica Leaf Extract: Antimicrobial and Photocatalytic Activities Al-Askar AA, Hashem AH, Elhussieny NI, Saied E Molecules 09-Jun-2023
PMCID:PMC10304739
doi:10.3390/molecules28124679
PMID:37375234
Natural products targeting inflammation-related metabolic disorders: A comprehensive review Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J Heliyon 02-Jun-2023
PMCID:PMC10279840
doi:10.1016/j.heliyon.2023.e16919
PMID:37346355
Economically viable flower drying techniques to sustain flower industry amid COVID-19 pandemic Kumar M, Chaudhary V, Sirohi U, Srivastav AL Environ Dev Sustain 29-May-2023
PMCID:PMC10225293
doi:10.1007/s10668-023-03376-w
PMID:37363010

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 / Toluenes / Tosyl compounds / P-toluenesulfonamides
Tosylphenylalanyl chloromethyl ketone 439647 Click to see CC1=CC=C(C=C1)S(=O)(=O)NC(CC2=CC=CC=C2)C(=O)CCl 351.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Rel-8Alpha-Tigloyloxyhirsutinolide 10384983 Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)CO)C)O)C 378.40 unknown via CMAUP database
Vernolide A 70690655 Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)CO)C)OC)C 392.40 unknown https://doi.org/10.1248/CPB.51.425
https://doi.org/10.1002/CHIN.200337149
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Isomontanic acid 5282610 Click to see CC(C)CCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown https://doi.org/10.1016/S0031-9422(00)80343-X
Octacosanoic acid 10470 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown https://doi.org/10.1016/S1875-5364(19)30114-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4-Acetyloxy-3,6-dimethylidene-2,7-dioxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl)methyl acetate 162925860 Click to see CC(=O)OCC1=CC2C(C(CC(=C)C(=O)CC1)OC(=O)C)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
(4-acetyloxy-7-hydroxy-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-10-yl)methyl acetate 163041127 Click to see CC(=O)OCC1=CC2C(C(CC(=C)C(CC1)O)OC(=O)C)C(=C)C(=O)O2 364.40 unknown https://doi.org/10.1002/JLAC.198719870204
[(3aR,4S,10Z,11aR)-4-acetyloxy-3,6-dimethylidene-2,7-dioxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate 163187577 Click to see CC(=O)OCC1=CC2C(C(CC(=C)C(=O)CC1)OC(=O)C)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
[(3aR,4S,7R,10Z,11aR)-4-acetyloxy-7-hydroxy-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-10-yl]methyl acetate 163185629 Click to see CC(=O)OCC1=CC2C(C(CC(=C)C(CC1)O)OC(=O)C)C(=C)C(=O)O2 364.40 unknown https://doi.org/10.1002/JLAC.198719870204
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
2-(4-acetyloxy-6-ethenyl-6-methyl-3-methylidene-2-oxo-4,5,7,7a-tetrahydro-3aH-1-benzofuran-7-yl)prop-2-enyl acetate 162998829 Click to see CC(=O)OCC(=C)C1C2C(C(CC1(C)C=C)OC(=O)C)C(=C)C(=O)O2 348.40 unknown https://doi.org/10.1002/JLAC.198719870204
2-[(3aR,4S,6S,7R,7aR)-4-acetyloxy-6-ethenyl-6-methyl-3-methylidene-2-oxo-4,5,7,7a-tetrahydro-3aH-1-benzofuran-7-yl]prop-2-enyl acetate 162998830 Click to see CC(=O)OCC(=C)C1C2C(C(CC1(C)C=C)OC(=O)C)C(=C)C(=O)O2 348.40 unknown https://doi.org/10.1002/JLAC.198719870204
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,4aS,8aR,9aR)-3a-hydroxy-8a-methyl-3,5-dimethylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 14707093 Click to see CC12CCCC(=C)C1CC3(C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(90)80185-J
(4-acetyloxy-5a-methyl-3-methylidene-2,6-dioxo-4,5,7,8,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-9-ylidene)methyl acetate 162953165 Click to see CC(=O)OC=C1CCC(=O)C2(C1C3C(C(C2)OC(=O)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
(4-Acetyloxy-6-hydroxy-5a-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-9-ylidene)methyl acetate 162876559 Click to see CC(=O)OC=C1CCC(C2(C1C3C(C(C2)OC(=O)C)C(=C)C(=O)O3)C)O 364.40 unknown https://doi.org/10.1002/JLAC.198719870204
[(E)-[(3aR,4S,5aR,6R,9aS,9bR)-4-acetyloxy-6-hydroxy-5a-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-9-ylidene]methyl] acetate 162876560 Click to see CC(=O)OC=C1CCC(C2(C1C3C(C(C2)OC(=O)C)C(=C)C(=O)O3)C)O 364.40 unknown https://doi.org/10.1002/JLAC.198719870204
[(E)-[(3aR,4S,5aR,9aS,9bR)-4-acetyloxy-5a-methyl-3-methylidene-2,6-dioxo-4,5,7,8,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-9-ylidene]methyl] acetate 162953166 Click to see CC(=O)OC=C1CCC(=O)C2(C1C3C(C(C2)OC(=O)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
3a-hydroxy-8a-methyl-3,5-dimethylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 14707092 Click to see CC12CCCC(=C)C1CC3(C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(4-Acetyloxy-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl)methyl acetate 85140515 Click to see CC(=O)OCC1=CC2C(C(CC(=CCC1)C=O)OC(=O)C)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
[(1S,2R,4R,6S,7Z,10R)-6-acetyloxy-12-(acetyloxymethyl)-4,8-dimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradeca-7,11-dien-10-yl] 2-methylprop-2-enoate 101218858 Click to see CC1=CC(CC2(C(O2)C3C(=C(C(=O)O3)COC(=O)C)C(C1)OC(=O)C(=C)C)C)OC(=O)C 448.50 unknown https://doi.org/10.1016/S0031-9422(00)81290-X
[(3aR,4S,6E,10Z,11aR)-4-acetyloxy-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate 10428712 Click to see CC(=O)OCC1=CC2C(C(CC(=CCC1)C=O)OC(=O)C)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1002/JLAC.198719870204
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) acetate 162983260 Click to see CC(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 304.34 unknown https://doi.org/10.1002/JLAC.198719870204
[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] acetate 101596790 Click to see CC(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 304.34 unknown https://doi.org/10.1002/JLAC.198719870204
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] hexadecanoate 137705088 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1016/S1875-5364(19)30114-1
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP50032A023
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1021/NP50032A023
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1080/14786410500045598
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-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 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1021/NP50035A020
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/10.1021/NP50035A020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-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 137706369 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP50035A020
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/S0031-9422(00)80343-X
https://doi.org/10.1590/S0103-50531999000200015
24-Ethylcholest-5-en-3beta-ol 22012 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/S0031-9422(00)80343-X
https://doi.org/10.1590/S0103-50531999000200015
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP50035A020
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80343-X
https://doi.org/10.1590/S0103-50531999000200015
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1016/S1875-5364(19)30114-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,11S)-6-(acetyloxymethyl)-11-methoxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-methylbut-2-enoate 138114059 Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)COC(=O)C)C)OC)C 434.50 unknown https://doi.org/10.1002/CHIN.200337149
[(1R,2E,8S,10R,11S)-6-(acetyloxymethyl)-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] (2S)-3-chloro-2-hydroxy-2-methylpropanoate 163191043 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)O)C)COC(=O)C)OC(=O)C(C)(CCl)O 458.90 unknown https://doi.org/10.1248/CPB.54.1437
[(1R,2E,8S,10R,11S)-6-(acetyloxymethyl)-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] (E)-4-hydroxy-2-methylbut-2-enoate 101412352 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)O)C)COC(=O)C)OC(=O)C(=CCO)C 436.50 unknown https://doi.org/10.1248/CPB.54.1437
8alpha-(2-Methylacryloyloxy)-1-O-methylhirsutinolide 13-O-acetate 70688595 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)OC)C)COC(=O)C)OC(=O)C(=C)C 420.50 unknown via CMAUP database
8alpha-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate 70686496 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)O)C)COC(=O)C)OC(=O)C(=C)C 406.40 unknown via CMAUP database
8alpha-Tigloyloxyhirsutinolide 13-O-acetate 10002209 Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)COC(=O)C)C)O)C 420.50 unknown via CMAUP database
Vernolide B 70692803 Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)COC(=O)C)C)OC)C 434.50 unknown https://doi.org/10.1248/CPB.51.425
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 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 https://doi.org/10.1016/S0367-326X(99)00052-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1590/S0103-50531999000200015
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(1R,2E,8S,10R,11S)-8-hydroxy-6-(hydroxymethyl)-11-methoxy-1,10-dimethyl-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-5-one 70696889 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)OC)C)CO)O 310.34 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
[(1R,2E,8R,10R,11S)-8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-6-yl]methyl acetate 101995833 Click to see CC(=O)OCC1=C2C(CC(C3(CCC(O3)(C=C2OC1=O)C)O)(C)O)O 354.40 unknown https://doi.org/10.1248/CPB.54.1437
[(2E)-8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-6-yl]methyl acetate 6511409 Click to see CC(=O)OCC1=C2C(CC(C3(CCC(O3)(C=C2OC1=O)C)O)(C)O)O 354.40 unknown https://doi.org/10.1248/CPB.54.1437
8Alpha-Hydroxyhirsutinolide 70690654 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)O)C)CO)O 296.31 unknown via CMAUP database
Hirsutinolide-13-Oacetate 70696890 Click to see CC1CC(C2=C(C(=O)OC2=CC3(CCC1(O3)O)C)COC(=O)C)O 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown https://doi.org/10.1016/S0367-326X(99)00052-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0367-326X(99)00052-0
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Mikanin 15560536 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)81508-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-2-(3,4-dimethoxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-chromen-7-yl 6-O-(6-deoxy-alpha-L-glucopyranosyl)-beta-D-glucopyranoside 16394721 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)OC)O)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1590/S0103-50531999000200015
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1590/S0103-50531999000200015
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1590/S0103-50531999000200015
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/S0367-326X(99)00052-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin 3'-methyl ether 14466294 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC 316.30 unknown https://doi.org/10.1590/S0103-50531999000200015

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