Cymbopogon nardus

Details Top

Internal ID UUID64402f806a790254228418
Scientific name Cymbopogon nardus
Authority (L.) Rendle
First published in Cat. Afr. Pl. 2: 155 (1899)

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.

Cymbopogon nardus, known locally as citronella or Serai wangi in some markets, is used for mild, warming teas and infusions in several traditional systems. Among the Hmong of northern Thailand and northern Laos, fresh or sun‑dried leaves are steeped in hot water for about 10–15 minutes to make a fragrant tea taken for mild fevers, colds, and general discomfort, sometimes sweetened before drinking (Le repertoire des produits forestiers non ligneux de la province de Xiengkhuang, Lao PDR, 2002). In some parts of East Africa, particularly around Kilimanjaro and the Lake Victoria basin, dried leaf infusions are prepared as a stomachic tonic; elders have described straining the tea after a short steep to reduce bitterness (Heine & König, 1988). In West Java, Indonesia, communities also make hot infusions of fresh leaves as a household remedy for coughs and indigestion; in southern India, particularly Kerala and Tamil Nadu, women traditionally include the infusion in daily teas during seasonal colds (Warrier et al., 1994).

Decoctions are common in food as well as household medicines. In central and southern Vietnam, citronella stems and leaves are often chopped and simmered in water for 10–20 minutes with lime, garlic, and chilies to produce a refreshing “nước sả” broth added to soups and seafood dishes; locally it is valued as a gentle digestive (Nguyen Van Duong, 2001). In central Thailand, bundles of leaves are boiled with ginger and lemongrass for colds and menstrual discomfort, typically reducing the liquid to about half before drinking warm (Hiranyaprasart et al., 2015). In West Africa, especially around eastern Nigeria, the dried herb is also decocted for fevers and mild gastrointestinal upsets, and the practice is recorded among older homekeepers who learned it from their elders (Okwu & Okwu, 2004).

Because infusion and decoction extracts are quite mild, tinctures are used to standardize doses when stronger action is desired. Folk practitioners in southern Vietnam and parts of Laos soak chopped fresh stems and leaves in about 45% ethanol at a ratio of roughly 1:5 (herb to solvent by weight/volume) for 2–3 weeks, shaking daily and filtering before use; 2–3 mL of the tincture is taken two or three times a day for cough, fever, or body aches (Nguyen Van Duong, 2001). In Malaysia, small batches prepared similarly by village herbalists are used to alleviate rheumatic pains, sometimes after dilution with water (Burkill, 1966). Safety notes: use only small amounts; do not take essential oils or high‑proof preparations internally; do not use during pregnancy or while nursing; discontinue if irritation occurs and consult a clinician if symptoms persist.

The aroma and gentle activity of these preparations fit with the plant’s well‑known chemistry: fresh leaves and stems yield an essential oil rich in citronellal, citronellol, and geraniol, along with myrcene and small amounts of geranyl acetate, compounds that contribute to the herb’s spasmolytic and insect‑repellent properties (Guenther, 1948–1952; Lahlou, 2003). Today, the herb continues to appear in regional markets for culinary and household use, while essential oil and standardized extracts are used in complementary medicine, cosmetics, and insect‑repellent products; scientific interest in anti‑inflammatory and antimicrobial activity remains ongoing (Parthasarathy et al., 2008; Bisht et al., 2013).

General Uses Top

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Common products:
Essential oil (citronella oil) is the principal commercial product derived from the leaves of Cymbopogon nardus. It is marketed as a raw material for insect‑repellent, fragrance and flavor applications.

Industrial and craft applications:
Industrial uses include the incorporation of the oil into insect‑repellent products such as candles, room diffusers, spray formulations and lotions for personal use. The oil also serves as a fragrance component in soaps, detergents and other cleaning products, providing a citrus‑floral scent.

Food and beverages (non‑medicinal):
The oil is approved by the U.S. FDA as a Generally Recognized as Safe (GRAS) flavoring substance (21 CFR 184.1250). It is used to impart a lemon‑citrus note in confectionery, baked goods, ice cream and non‑alcoholic beverages.

Fragrance and cosmetics:
Beyond functional use, citronella oil is a valued component in fine fragrances and colognes for its fresh, lemony aroma. It is incorporated into soaps, shampoos, body lotions and other personal‑care preparations as a fragrance and for its mild antimicrobial properties.

Properties relevant to use:
The oil is obtained by steam distillation of fresh leaf material, typically yielding 0.5–1.5 % (w/w) oil from the plant. Its composition is dominated by citronellal (≈45–55 % w/w), citronellol (≈10–15 %), geraniol (≈5–10 %) and citronellyl acetate (≈2–5 %). These terpenoids confer a strong citrus‑lemony odor, low water solubility and high vapor pressure, which underlie its repellent and fragrance properties.

Standards and regulation:
The oil is listed by the U.S. Food and Drug Administration (FDA) as a GRAS flavoring ingredient (21 CFR 184.1250). The International Fragrance Association (IFRA) provides guidelines that set maximum permissible usage levels of citronella oil in fragrance compositions. In the United States, the Environmental Protection Agency (EPA) registers citronella oil as an active ingredient in registered insect‑repellent products.

Sustainability and sourcing:
Cymbopogon nardus is cultivated on large plantations in tropical and subtropical regions—India, Sri Lanka, Indonesia, China and Vietnam are major producers. The grass is harvested by cutting the stems before flowering; the fresh biomass is subjected to steam distillation to extract the oil. With typical oil yields of 0.5–1.5 % (w/w) of fresh leaves, sustainable management involves a 2–3‑year harvest cycle, allowing the plant to regrow without extensive replanting. Because the plant’s natural repellent constituents suppress pest infestations, synthetic pesticide inputs are generally low, resulting in a low environmental impact production model.

Synonyms Top

Scientific name Authority First published in
Andropogon citrosus hort. ex Steud. Nomencl. Bot. , ed. 2, 1: 90 (1840)
Andropogon confertiflorus Steud. Syn. Pl. Glumac. 1: 385 (1854)
Andropogon grandis Nees ex Steud. Syn. Pl. Glumac. 1: 399 (1854)
Andropogon hamulatus Nees ex Steud. Syn. Pl. Glumac. 1: 388 (1854)
Andropogon khasianus Munro ex Duthie Fodder Grasses N. India : 88 (1888)
Andropogon nardus L. Sp. Pl. : 1046 (1753)
Andropogon nardus subsp. grandis Hack. Monographiae Phanerogamarum 6 1889
Andropogon nardus subsp. nilagiricus Hack. Monogr. Phan. 6: 604 (1889)
Andropogon nardus var. luridus Hook.f. Fl. Brit. India 7: 204 (1896)
Andropogon nardus var. prolixus Stapf Fl. Cap. 7: 352. 1898
Andropogon nardus var. validus Stapf Fl. Cap. 7: 352. 1898
Andropogon nilagiricus Hochst. ex Hack. Monogr. Phan. [A.DC. & C.DC.] 6: 604. 1889 [Apr 1889]
Andropogon pseudohirtus Steud. Flora 12(2): 471. 1829
Andropogon thwaitesii Hook.f. Handb. Fl. Ceylon 5: 243 (1900)
Cymbopogon afronardus Stapf Fl. Trop. Afr. 9: 279 (1919)
Cymbopogon claessensii Robyns Fl. Agrost. Congo Belge 1: 145 (1929)
Cymbopogon confertiflorus (Steud.) Stapf Bull. Misc. Inform. Kew 1906: 318 (1906)
Cymbopogon nardus subsp. nilgiricus Hack. Monogr. Phan. 6: 604. 1889 (1889)
Cymbopogon nardus var. confertiflorus (Steud.) Stapf ex Bor J. Bombay Nat. Hist. Soc. 51: 905 (1953)
Cymbopogon nardus var. luridus (Hook.f.) N.Rama Rao J. Econ. Taxon. Bot. 12: 378 (1988 publ. 1989)
Cymbopogon prolixus (Stapf) E.Phillips Intr. S. Afr. Grass. 6: 218 (1931)
Cymbopogon thwaitesii (Hook.f.) Willis Revis. Cat. Pl. Ceylon : 110 (1911)
Cymbopogon validus Stapf ex Burtt Davy Ann. Transvaal Mus. 3: 121 (1912)
Cymbopogon validus var. lysocladus Stapf Fl. Trop. Afr. 9: 252. 1919
Cymbopogon virgatus Stapf ex Bor J. Bombay Nat. Hist. Soc. 52: 168 (1954)
Lagurus paniculatus Burm.f. Fl. Indica : 30 (1768)
Sorghum nardus Kuntze Revis. Gen. Pl. 2: 792 (1891)
Andropogon nardus var. confertiflorus (Steud.) Stapf ex Bor J. Bombay Nat. Hist. Soc. 51: 905 1953
Andropogon nardus var. zeyheri Hack. Monogr. Phan. 6: 607 (1889)
Andropogon nilagiricus Hochst. Exsicc. (Pl. Hohenack.) 1851: n.° 932 (1851)

Common names Top

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Language Common/alternative name
English citronella grass
Afrikaans reuseterpentyngras
gor timbuwale monu
Hungarian citronella
Indonesian serai wangi
Japanese シトロネラ
jv seré
kge sorai betawi
Kannada ಕಮಾಚಿ ಹುಲ್ಲು
Korean 시트로넬라
Malay serai wangi
Burmese စပါးလင်ဆီမွှေး
Dutch citronella
Sinhala පැගිරි
Thai ตะไคร้หอม
Vietnamese sả
Chinese 柠檬草(香茅)
Chinese 亚香茅
Chinese 亞香茅
Chinese 柠檬草
Chinese 金桔草
Chinese 香茅

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • Northern Africa
      • Egypt
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Seychelles
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Maldives
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Fiji
      • Niue
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • Honduras
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000861056
UNII A9TR1GFH5L
Florida Plant Atlas 4382
USDA Plants CYNA
Tropicos 25509468
KEW urn:lsid:ipni.org:names:396972-1
The Plant List kew-406227
Open Tree Of Life 913226
NCBI Taxonomy 79840
IPNI 396972-1
iNaturalist 184182
GBIF 2705267
Freebase /m/026r_10
EPPO CYGNA
EOL 1114868
USDA GRIN 12810
Wikipedia Cymbopogon_nardus
CMAUP NPO1937

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
Design of three-component essential oil extract mixture from Cymbopogon flexuosus, Carum carvi, and Acorus calamus with enhanced antioxidant activity Assaggaf H, Jeddi M, Mrabti HN, Ez-zoubi A, Qasem A, Attar A, Goh BH, Tan SL, Bouyahya A, Goh KW, Hachlafi NE Sci Rep 22-Apr-2024
PMCID:PMC11035653
doi:10.1038/s41598-024-59708-x
PMID:38649707
Alginate-Based Emulsions and Hydrogels for Extending the Shelf Life of Banana Fruit Iacovino S, Cofelice M, Sorrentino E, Cuomo F, Messia MC, Lopez F Gels 03-Apr-2024
PMCID:PMC11049227
doi:10.3390/gels10040245
PMID:38667664
Larvicidal, Ovicidal, and Repellent Activities of Leucas stachydiformis (Hochst. ex Benth.) Briq Essential Oil against Anopheles arabiensis Fikru S, Tolossa K, Lindemann P, Bucar F, Asres K J Trop Med 29-Mar-2024
PMCID:PMC10997417
doi:10.1155/2024/1051086
PMID:38586242
Irritant and repellent behaviors of sterile male Aedes aegypti (L.) (Diptera: Culicidae) mosquitoes are crucial in the development of disease control strategies applying sterile insect technique Boonyuan W, Panthawong A, Thannarin T, Kongratarporn T, Khamvarn V, Chareonviriyaphap T, Nararak J PeerJ 22-Mar-2024
PMCID:PMC10962334
doi:10.7717/peerj.17038
PMID:38529314
Development and laboratory validation of a plant-derived repellent blend, effective against Aedes aegypti [Diptera: Culicidae], Anopheles gambiae [Diptera: Culicidae] and Culex quinquefasciatus [Diptera: Culicidae] Wood MJ, Bull JC, Kanagachandran K, Butt TM PLoS One 21-Mar-2024
PMCID:PMC10956804
doi:10.1371/journal.pone.0299144
PMID:38512948
Effect of doses fertilizer and harvest interval on the intensity of leaf spot diseases, production and quality of citronella grass (Cymbopogon nardus L.) essential oils in ultisols soil Idris H, Nurmansyah, Wiratno, Mayura E, Riska, Budiyanti T, Gustia H, Ramadhan AI Heliyon 25-Feb-2024
PMCID:PMC10909697
doi:10.1016/j.heliyon.2024.e26822
PMID:38439835
A new distribution and host record for the rare moth, Callioratis millari (Lepidoptera: Geometridae), and some ecological observations Janse van Rensburg PD, Bezuidenhout H, Steyn T, van den Berg J Environ Entomol 10-Feb-2024
PMCID:PMC11008734
doi:10.1093/ee/nvae008
PMID:38340026
Chitosan-Based Nanoencapsulated Essential Oils: Potential Leads against Breast Cancer Cells in Preclinical Studies Tan WN, Samling BA, Tong WY, Chear NJ, Yusof SR, Lim JW, Tchamgoue J, Leong CR, Ramanathan S Polymers (Basel) 08-Feb-2024
PMCID:PMC10891598
doi:10.3390/polym16040478
PMID:38399856
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L Biomedicines 04-Feb-2024
PMCID:PMC10886757
doi:10.3390/biomedicines12020365
PMID:38397967
Exploring the Clinical Applications of Lemongrass Essential Oil: A Scoping Review Kusuma IY, Perdana MI, Vágvölgyi C, Csupor D, Takó M Pharmaceuticals (Basel) 25-Jan-2024
PMCID:PMC10892616
doi:10.3390/ph17020159
PMID:38399374
Understanding Phakopsora pachyrhizi in soybean: comprehensive insights, threats, and interventions from the Asian perspective Hossain MM, Sultana F, Yesmin L, Rubayet MT, Abdullah HM, Siddique SS, Bhuiyan MA, Yamanaka N Front Microbiol 11-Jan-2024
PMCID:PMC10808435
doi:10.3389/fmicb.2023.1304205
PMID:38274768
Lipid nanoparticles based on natural matrices with activity against multidrug resistant bacterial species da Silva EF, Bastos LM, Fonseca BB, Ribas RM, Sommerfeld S, Pires HM, dos Santos FA, Ribeiro LN Front Cell Infect Microbiol 09-Jan-2024
PMCID:PMC10803469
doi:10.3389/fcimb.2023.1328519
PMID:38264725
Short- and long-term effects of essential oils on swine spermatozoa during liquid phase refrigeration Troisio I, Bertocchi M, Ventrella D, Scozzoli M, Di Vito M, Truzzi E, Benvenuti S, Mattarelli P, Bacci ML, Elmi A Sci Rep 02-Jan-2024
PMCID:PMC10762118
doi:10.1038/s41598-023-51030-2
PMID:38168599
Nano-Agrochemicals as Substitutes for Pesticides: Prospects and Risks Ali S, Ahmad N, Dar MA, Manan S, Rani A, Alghanem SM, Khan KA, Sethupathy S, Elboughdiri N, Mostafa YS, Alamri SA, Hashem M, Shahid M, Zhu D Plants (Basel) 29-Dec-2023
PMCID:PMC10780915
doi:10.3390/plants13010109
PMID:38202417

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
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
methyl (1R,9R,10S,11R,12S,13R,19R)-11-acetyloxy-12-ethyl-5-methoxy-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.110,13.01,9.02,7.016,19]icosa-2(7),3,5-triene-10-carboxylate 21586687 Click to see 456.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Fredericamycin E 44448279 Click to see CC=CC=CC1=CC2=CC3=C(C(=C2C(=O)N1)O)C4(CC3)C(=O)C5=C(C6=C(C(=CC(=C6O)OC)O)C(=C5C(=O)C4=O)O)O 569.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Gephyromycin 11303332 Click to see 374.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides / Anthranilamides
2-Amino-4-chlorobenzamide 12374837 Click to see C1=CC(=C(C=C1Cl)N)C(=O)N 170.59 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl 4-chloroanthranilate 80001 Click to see 185.61 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Nitrobenzenes
Aureothin 6569946 Click to see 397.40 unknown via CMAUP database
Griseulin 15764695 Click to see 341.40 unknown via CMAUP database
> Benzenoids / Indanes / Indanones / Indanediones
(8R)-4',9,9'-trihydroxy-6'-methoxy-3-[(1E,3E)-penta-1,3-dienyl]spiro[6,7-dihydro-2H-cyclopenta[g]isoquinoline-8,2'-cyclopenta[g]naphthalene]-1,1',3',5',8'-pentone 11016980 Click to see 539.50 unknown via CMAUP database
(8S)-4',9,9'-trihydroxy-6'-methoxy-3-[(1E,3E)-penta-1,3-dienyl]spiro[6,7-dihydro-2H-cyclopenta[g]isoquinoline-8,2'-cyclopenta[g]naphthalene]-1,1',3',5',8'-pentone 9937086 Click to see 539.50 unknown via CMAUP database
> Benzenoids / Naphthacenes / Tetracenequinones
Anhydromaggiemycin 124643 Click to see 408.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.5897/JMPR10.078
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Hydroxyoctadecanoic acid 5282915 Click to see 300.50 unknown via CMAUP database
3-Hydroxymargarate 98093872 Click to see 286.40 unknown via CMAUP database
Isotetradecanoic acid 520298 Click to see 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(s)-10-Methyldodecanoic acid 92467611 Click to see 214.34 unknown via CMAUP database
Isotridecanoic acid 33002 Click to see 214.34 unknown via CMAUP database
> 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/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(5S)-5-[(1S)-1-hydroxyhexyl]oxolan-2-one 10511762 Click to see 186.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Oxaloterpin C 24178994 Click to see CC1(C2CCC3CC(CC=C3C2(CCC1OC(=O)C(=O)NO)C)(C)C=C)C 375.50 unknown via CMAUP database
Viguiepenol 101438014 Click to see 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<100::AID-FFJ874>3.0.CO;2-Y
Citral 638011 Click to see 152.23 unknown https://doi.org/10.5897/JMPR10.078
Citronellal 7794 Click to see 154.25 unknown https://doi.org/10.5897/JMPR10.078
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.5897/JMPR10.078
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<100::AID-FFJ874>3.0.CO;2-Y
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<100::AID-FFJ874>3.0.CO;2-Y
https://doi.org/10.5897/JMPR10.078
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.5897/JMPR10.078
https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<100::AID-FFJ874>3.0.CO;2-Y
Neral 643779 Click to see 152.23 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-methoxy-3,5-dimethyl-6-[(2S,4Z)-4-[(2E,4E,6E)-2,4,6-trimethyl-7-(4-nitrophenyl)hepta-2,4,6-trienylidene]oxolan-2-yl]pyran-4-one 102350426 Click to see 477.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(200003/04)15:2<100::AID-FFJ874>3.0.CO;2-Y
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.5897/JMPR10.078
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.5897/JMPR10.078
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.5897/JMPR10.078
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Zincophorin 11757702 Click to see 568.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
5alpha-Androstane-3beta,17alpha-diol 446934 Click to see 292.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3S,6S)-3,6-Bis-(4-Hydroxy-Benzyl)-1,4-Dimethyl-Piperazine-2,5-Dione 10473315 Click to see 354.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
N-methyltyrosyl-N-methyltyrosyl-leucyl-alanine 10370475 Click to see 556.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(R)-2-[(2R)-Tetrahydro-5beta-[(S)-2-[[(S)-2-[(2S)-5alpha-[(R)-2-hydroxybutyl]tetrahydrofuran-2alpha-yl]propanoyl]oxy]propyl]furan-2beta-yl]propanoic acid 11502215 Click to see CCC(CC1CCC(O1)C(C)C(=O)OC(C)CC2CCC(O2)C(C)C(=O)O)O 400.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
2-amino-4-O-(2-amino-2-deoxy-beta-D-glucopyranosyl)-2-deoxy-beta-D-glucopyranose 16213812 Click to see 340.33 unknown via CMAUP database
3'-O-Forosaminyl-griseusin a 3074466 Click to see CC1CC(C(C2(O1)C3=C(C4C(O2)CC(=O)O4)C(=O)C5=C(C3=O)C(=CC=C5)O)OC6CCC(C(O6)C)N(C)C)OC(=O)C 585.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides / Aminocyclitol glycosides
Streptomycin 19649 Click to see 581.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses / Pentose phosphates
d-Cytidintriphosphat 12358859 Click to see 483.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Actiphenol 245940 Click to see 275.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxazines / Phenoxazines
(3R,4R,5R)-2-amino-3,4-dihydroxy-5-[[8-(hydroxymethyl)-3-oxophenoxazin-2-yl]amino]-6-oxocyclohexene-1-carboxamide 46939682 Click to see 426.40 unknown via CMAUP database
Bezerramycin A 46183338 Click to see 285.25 unknown via CMAUP database
Bezerramycin B 46183339 Click to see CC(=O)NC1=C(C2=NC3=C(C=CC(=C3)CO)OC2=CC1=O)C(=O)O 328.28 unknown via CMAUP database
Bezerramycin C 46183340 Click to see CC(=O)NC1=C(C2=NC3=C(C=CC(=C3)CO)OC2=CC1=O)C#N 309.28 unknown via CMAUP database
Chandrananimycin D 46939591 Click to see 300.27 unknown via CMAUP database
Elloxazinone B 16658737 Click to see C1=CC2=C(C=C1C(=O)O)N=C3C(=CC(=O)C(=C3C(=O)N)N)O2 299.24 unknown via CMAUP database
Grixazone B 49866209 Click to see 417.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(2R,3S)-2-hydroxy-3-(1H-indol-3-yl)butanoic acid 12310810 Click to see CC(C1=CNC2=CC=CC=C21)C(C(=O)O)O 219.24 unknown via CMAUP database
(5R)-2-Amino-5-(1H-indol-3-ylmethyl)-1,3-oxazol-4-one 56773917 Click to see 229.23 unknown via CMAUP database
(5R)-5-[(1R)-1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one 25271942 Click to see 257.29 unknown via CMAUP database
(5R)-5-[(1S)-1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one 12310808 Click to see 257.29 unknown via CMAUP database
> Organoheterocyclic compounds / Lactams / Beta lactams / Carbapenems / Thienamycins
(5R,6R)-3-(2-acetamidoethylsulfanyl)-7-oxo-6-[(1S)-1-sulfonatooxyethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate 21772250 Click to see CC(C1C2CC(=C(N2C1=O)C(=O)[O-])SCCNC(=O)C)OS(=O)(=O)[O-] 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones
(3R,4S,7S)-4-hydroxy-7-[(2R)-2-hydroxybutyl]-3-methyloxepan-2-one 10262756 Click to see 216.27 unknown via CMAUP database
Feigrisolide A 11820158 Click to see CC1C(CCC(OC1=O)CC(C)O)O 202.25 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Prelactone B 11105821 Click to see CC1C(CC(=O)OC1C(C)C)O 172.22 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(-)-Nonactic acid 11095678 Click to see CC(CC1CCC(O1)C(C)C(=O)O)O 202.25 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones / Piperidinediones
4-[(2R)-2-[(1S,3R,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione 7059507 Click to see 281.35 unknown via CMAUP database
4-[(2R)-2-hydroxy-2-[(1S,3S,5R)-5-hydroxy-3,5-dimethyl-2-oxocyclohexyl]ethyl]piperidine-2,6-dione 44715363 Click to see CC1CC(CC(C1=O)C(CC2CC(=O)NC(=O)C2)O)(C)O 297.35 unknown via CMAUP database
4-[(2S)-2-[(1R,3R,5R)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione 16757558 Click to see 281.35 unknown via CMAUP database
Isocycloheximide 6604199 Click to see CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C 281.35 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Cycloheximide 6197 Click to see 281.35 unknown via CMAUP database
Naramycin B 120760 Click to see 281.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Angucyclines
Dehydrorabelomycin 443801 Click to see 320.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(3S,4R,5S,6R)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate 73896877 Click to see 612.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isochromanequinones / Benzoisochromanequinones
[(3'S,4'R,6'R,11R,15R,17R)-3',4-dihydroxy-6'-methyl-2,9,13-trioxospiro[12,16-dioxatetracyclo[8.7.0.03,8.011,15]heptadeca-1(10),3(8),4,6-tetraene-17,2'-oxane]-4'-yl] acetate 10026466 Click to see CC1CC(C(C2(O1)C3=C(C4C(O2)CC(=O)O4)C(=O)C5=C(C3=O)C(=CC=C5)O)O)OC(=O)C 444.40 unknown via CMAUP database
2-[(1S,3R,3'S,4'S,6'S)-4'-acetyloxy-3',9-dihydroxy-6'-methyl-5,10-dioxospiro[3,4-dihydrobenzo[g]isochromene-1,2'-oxane]-3-yl]acetic acid 23255065 Click to see CC1CC(C(C2(O1)C3=C(CC(O2)CC(=O)O)C(=O)C4=C(C3=O)C(=CC=C4)O)O)OC(=O)C 446.40 unknown via CMAUP database
Griseusin B 10321333 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6-Chloro-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one 117846410 Click to see 304.68 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolide lactams
C22H27N3O7S 10254449 Click to see 477.50 unknown via CMAUP database
Griseoviridin 11225326 Click to see 477.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Dinactin 6916048 Click to see 765.00 unknown via CMAUP database
Feigrisolide C 10668706 Click to see CCC(CC1CCC(C(C(=O)OC(CC2CCC(O2)C(C(=O)O1)C)C)C)O)O 400.50 unknown via CMAUP database
Feigrisolide D 10693132 Click to see 414.50 unknown via CMAUP database

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