Imperata cylindrica - Unknown
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Internal ID UUID644030ed6988f922238002
Scientific name Imperata cylindrica
Authority (L.) P.Beauv.
First published in Ess. Agrostogr. : 165 (1812)

Description Top

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Imperata cylindrica, also known as cogongrass or kunai grass, is a perennial rhizomatous grass native to tropical and subtropical regions of Asia, Micronesia, Melanesia, Australia, Africa, and Southern Europe. It has also been introduced to Latin America, the Caribbean, and the Southeastern United States. This highly flammable grass can spread rapidly by colonizing disturbed areas and encouraging frequent wildfires. It is known by various names in different languages and is used for thatching, soil stabilization, and traditional medicine. However, it is also considered an invasive weed in many areas and is difficult to control due to its adaptability and allelopathic tendencies. Efforts are being made to eradicate it through the use of herbicides and biological control methods. Imperata cylindrica has a long history of taxonomic confusion and has been described under various names, including Lagurus cylindricus by Linnaeus in 1759.

Synonyms Top

Scientific name Authority First published in
Arundo epigeios Forssk. ex Steud. Nomencl. Bot. , ed. 2, 1: 144 (1840)
Calamagrostis lagurus Koeler Descr. Gramin. : 112 (1802)
Imperata allang Jungh. Tijdschr. Natuurl. Gesch. Physiol. 7: 295 (1840)
Imperata angolensis Fritsch Bull. Herb. Boissier , sér. 2, 1: 1096 (1901)
Imperata arundinacea Cirillo Pl. Rar. Neapol. 2: XXVI (1792)
Imperata arundinacea var. africana Andersson Öfvers. Kongl. Vetensk.-Akad. Förh. 12: 159 1855
Imperata arundinacea var. europaea Andersson Öfvers. Kongl. Vetensk.-Akad. Förh. 12: 159. 1855
Imperata arundinacea var. indica Andersson Öfvers. Kongl. Vetensk.-Akad. Förh. 12: 159. 1855
Imperata arundinacea var. koenigii Benth. Fl. Hongk. : 419 (1861)
Imperata arundinacea var. latifolia Hook.f. Fl. Brit. India 7: 106 1896
Imperata arundinacea var. pedicellata (Steud.) Debeaux Rech. Fl. Pyr. Or. 1: ?. 1878
Imperata cylindrica f. pallida Honda J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 3: 374 1930
Imperata cylindrica subsp. koenigii (Retz.) Tzvelev Zlaki SSSR 691. 1976
Imperata cylindrica var. africana (Andersson) C.E.Hubb. Joint Publ. Imp. Agric. Bur. 7: 10 1944
Imperata cylindrica var. europaea (Andersson) Asch. & Graebn. Syn. Mitteleur. Fl. 2(1): 37 1898
Imperata cylindrica var. koenigii (Retz.) Perkins Fragm. Fl. Philipp. 137. 1904 [30 Jun 1904]
Imperata cylindrica var. latifolia (Hook.f.) C.E.Hubb. Joint Publ. Imp. Agric. Bur. 7: 14 1944
Imperata cylindrica var. major (Nees) C.E.Hubb. Grasses of Mauritius & Rodriguez 1940
Imperata cylindrica var. parviflora Batt. & Trab. Bull. Soc. Bot. France 53: 32. 1906
Imperata cylindrica var. pedicellata (Steud.) Debeaux Actes Soc. Linn. Bordeaux 32: 52. 1878
Imperata cylindrica var. thunbergii (Retz.) T.Durand & Schinz Consp. Fl. Afric. 5: 693. 1894
Imperata dinteri Pilg. Bot. Jahrb. Syst. 48: 342 (1912)
Imperata filifolia Nees ex Steud. Syn. Pl. Glumac. 1: 405 (1854)
Imperata koenigii P.Beauv. Ess. Agrostogr. : 165 (1812)
Imperata koenigii var. major Nees Fl. Afr. Austral. Ill. : 90 (1841)
Imperata laguroides (Pourr.) Roux Nat. Monspel., Sér. Bot. 9: 177 (1958)
Imperata latifolia (Hook.f.) L.Liu Vasc. Pl. Hengduan Mount. 2: 2299 (1994)
Imperata pedicellata Steud. Flora 29: 22 (1846)
Imperata praecoquis Honda Bot. Mag. (Tokyo) 53: 385 (1939)
Imperata robustior A.Chev. Rev. Int. Bot. Appl. Agric. Trop. 29: 114 (1949)
Imperata sieberi Opiz Naturalientausch 10: 190 (1825)
Imperata sisca Beauv. ex Steud. Nomencl. Bot. , ed. 2, 1: 805 (1841)
Imperata thunbergii (Retz.) Nees Fl. Afr. Austral. Ill. 89. 1841 (1841)
Lagurus cylindricus L. Syst. Nat. ed. 10 , 2: 878 (1759)
Saccharum cylindricum Lam. Encycl. 1: 594 (1785)
Saccharum diandrum J.Koenig ex Retz. Observ. Bot. 5: 16 (1789)
Saccharum europaeum Pers. Syn. Pl. 1: 103 (1805)
Saccharum indum Pers. Syn. Pl. 1: 103 (1805)
Saccharum koenigii Retz. Observ. Bot. 5: 16 (1789)
Saccharum laguroides Pourr. Mém. Acad. Sci. Toulouse 3: 326 (1788)
Saccharum sisca Cav. Icon. 3: 47 (1794)
Saccharum spicatum Thunb. Fl. Jap. (Thunberg) 42 (1784); J. & C. Presl, Rel. Haenk. i. 346.
Saccharum spicatum Burm. ex Kunth Enum. Pl. 1: 477 (1833)
Saccharum thunbergii Retz. Observ. Bot. 5: 17 (1789)
Imperata arundinacea var. glabrescens Büse Pl. Jungh. 366. 1854
Imperata thunbergii Beauv Ess. Agrostogr. 165. 1812
Saccharum cylindricum var. europaeum Pers. Syn. Pl. 1: 103 1805

Common names Top

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Language Common/alternative name
English satin tail
English kura-kura
English kunai grass
English japanese bloodgrass
English cotton wool grass
English cogon grass, cotton grass, thatch grass
English cogon grass
English blady grass
English alang-alang
English cogongrass
Spanish marciega
Spanish marciega menor
Spanish cogon
Spanish cogón
Spanish cogon de filipinas
Spanish cogón de filipinas
Arabic حلف
Azerbaijani silindrik hülpə
azb سیلیندریک هولپه
ban ambengan
Bulgarian цилиндрична императа
bjn halalang
Bambara jɔlen
Bengali উলুঘাস
Catalan xisca
Czech imperáta válcovitá
Czech kunai
dag piriŋkpaŋ
German japanisches blutgras
German blutgras
Estonian alang-alang
Estonian jaapani mererohi
Estonian harilik alang
Persian زلف شیطان
Finnish silkkiheinä
French paillote
French paillotte
gor padengo
Hausa tofa (shuka)
Hebrew משיין גליליני
Indonesian alang-alang
Indonesian ilalang
Japanese チガヤ
Japanese 白茅
Japanese ボウコン
Japanese ツバナ
jv alang-alang
jv wit alang-alang
Korean
mad lang-alang
min alang-alang
Malayalam കോഗൺ ഗ്രാസ്സ്
Malay lalang
Burmese သက်ကယ်
Burmese သက်ငယ်
Nepali सिरु
nia o'o
Dutch japans bloedgras
Dutch alang alang
Dutch alang-alang
pam ilib
pwn ravuc
Russian Аланг-аланг
Russian Императа цилиндрическая
Sango pêrë
su eurih
Swahili mtimbi
tay lupitux mangurusngurus
Telugu దర్భ గడ్డి
Thai หญ้าคา
Vietnamese cỏ tranh
war kogon
Chinese 黄茅根
Chinese 大白茅(丝茅)
Chinese 白茅根
Chinese 白茅

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

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-0000875631
UNII V13X168O65
Florida Plant Atlas 1407
Flora of Alabama 4847
USDA Plants IMCY
Tropicos 25509715
Flora of Italy 7815
KEW urn:lsid:ipni.org:names:30138371-2
The Plant List kew-420125
Missouri Botanical Garden 285406
PFAF Imperata cylindrica
Open Tree Of Life 740074
Observations.org 118924
NCBI Taxonomy 80369
Nature Serve 2.133529
IPNI 60462577-2
iNaturalist 164056
GBIF 5289712
Freebase /m/06378z
EPPO IMPCY
EOL 1114980
Elurikkus 210200
US Library of Congress sh89003901
USDA GRIN 19864
Wikipedia Imperata_cylindrica
CMAUP NPO23628

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
Unveiling allelopathic dynamics and impacts of invasive Erigeron bonariensis and Bidens pilosa on plant communities and soil parameters Balah MA, Al-Andal A, Radwan AM, Donia AE Sci Rep 03-May-2024
PMCID:PMC11065986
doi:10.1038/s41598-024-57552-7
PMID:38698043
Impacts of Soil Properties on Species Diversity and Structure in Alternanthera philoxeroides-Invaded and Native Plant Communities Wu H, Liu Y, Zhang T, Xu M, Rao B Plants (Basel) 25-Apr-2024
PMCID:PMC11085794
doi:10.3390/plants13091196
PMID:38732411
Qingfei mixture modulates the immune responses in lung cancer through modulating mTOR signaling and gut microbiota-derived short-chain fatty acids Qian X, Chen Z, Ji XM, Ji YL, Wang J, Liu YC, Zhou XC, Li QL, Li CY, Zhang AQ Heliyon 16-Apr-2024
PMCID:PMC11041045
doi:10.1016/j.heliyon.2024.e29404
PMID:38660245
Liangxue-Qushi-Zhiyang Decoction Ameliorates DNCB-Induced Atopic Dermatitis in Mice through the MAPK Signaling Pathway Based on Network Pharmacology Zhang L, Zhang H, Niu X, Zhang X, Chen X, Lei S, Ma S, Sun Z ACS Omega 10-Apr-2024
PMCID:PMC11044150
doi:10.1021/acsomega.3c09218
PMID:38680355
Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
Leveraging the sugarcane CRISPR/Cas9 technique for genetic improvement of non-cultivated grasses Li C, Iqbal MA Front Plant Sci 27-Mar-2024
PMCID:PMC11004347
doi:10.3389/fpls.2024.1369416
PMID:38601306
Rice false smut pathogen: implications for mycotoxin contamination, current status, and future perspectives Zhou L, Mubeen M, Iftikhar Y, Zheng H, Zhang Z, Wen J, Khan RA, Sajid A, Solanki MK, Sohail MA, Kumar A, Massoud EE, Chen L Front Microbiol 20-Mar-2024
PMCID:PMC10996400
doi:10.3389/fmicb.2024.1344831
PMID:38585697
Optimization of ultrasound-assisted extraction of Imperata cylindrica polysaccharides and evaluation of its anti-oxidant and amelioration of uric acid stimulated cell apoptosis Yu W, Li J, Xiong Y, Wang J, Liu J, Baranenko D, Zhang Y, Lu W Ultrason Sonochem 06-Mar-2024
PMCID:PMC10951092
doi:10.1016/j.ultsonch.2024.106844
PMID:38479187
Definitive Review of Nanobiochar Chaubey AK, Pratap T, Preetiva B, Patel M, Singsit JS, Pittman CU Jr, Mohan D ACS Omega 04-Mar-2024
PMCID:PMC10955718
doi:10.1021/acsomega.3c07804
PMID:38524436
Phyto-pharmacological evaluation and characterization of the methanolic extract of the Baccaurea motleyana Müll. Arg. seed: promising insights into its therapeutic uses Shompa SA, Hasnat H, Riti SJ, Islam MM, Nur F, Alam S, Shao C, Wang S, Geng P, Mamun AA Front Pharmacol 29-Feb-2024
PMCID:PMC10937468
doi:10.3389/fphar.2024.1359815
PMID:38487168
Transcriptomics, proteomics, and metabolomics interventions prompt crop improvement against metal(loid) toxicity Raza A, Salehi H, Bashir S, Tabassum J, Jamla M, Charagh S, Barmukh R, Mir RA, Bhat BA, Javed MA, Guan DX, Mir RR, Siddique KH, Varshney RK Plant Cell Rep 27-Feb-2024
PMCID:PMC10899315
doi:10.1007/s00299-024-03153-7
PMID:38411713
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Isolation and Identification of Allelopathic Substances from Forsythia suspensa Leaves, and Their Metabolism and Activity Kato-Noguchi H, Takahashi Y, Tojo S, Teruya T Plants (Basel) 20-Feb-2024
PMCID:PMC10935053
doi:10.3390/plants13050575
PMID:38475422
Isolation and identification of allelochemicals and their activities and functions Kato-Noguchi H J Pestic Sci 20-Feb-2024
PMCID:PMC10912975
doi:10.1584/jpestics.D23-052
PMID:38450087
Ethnobotanical study on ritual plants used by Hani people in Yunnan, China Ma X, Luo D, Xiong Y, Huang C, Li G J Ethnobiol Ethnomed 13-Feb-2024
PMCID:PMC10865556
doi:10.1186/s13002-024-00659-y
PMID:38350958

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 / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
3,3a-Didehydrolycoran-1alpha,2beta-diol 3978 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-alpha-Hydrastine 442247 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OCO3 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+/-)-Isocorypalmine 10220 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Benzylacetone 17355 Click to see CC(=O)CCC1=CC=CC=C1 148.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate 54675866 Click to see C1=CC(=C(C=C1C(=O)O)O)[O-] 153.11 unknown via CMAUP database
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3-Hydroxy-4,5-dimethoxybenzoic acid 74709 Click to see COC1=CC(=CC(=C1OC)O)C(=O)O 198.17 unknown via CMAUP database
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/JF902310J
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
cylindol A 10425993 Click to see COC(=O)C1=CC(=C(C=C1)O)OC2=C(C=CC(=C2)C(=O)OC)O 318.28 unknown https://doi.org/10.1021/NP50111A019
Cylindol B 157798 Click to see COC(=O)C1=C(C=CC(=C1)OC2=CC(=C(C=C2)O)C(=O)OC)O 318.28 unknown https://doi.org/10.1021/NP50111A019
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2,4-Di-tert-butylphenol 7311 Click to see CC(C)(C)C1=CC(=C(C=C1)O)C(C)(C)C 206.32 unknown via CMAUP database
2,6-Di-t-butyl-4-hydroxytoluene 10220096 Click to see CC1=C(C=C(C=C1C(C)(C)C)O)C(C)(C)C 220.35 unknown via CMAUP database
Butylated Hydroxytoluene 31404 Click to see CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C 220.35 unknown via CMAUP database
> Benzenoids / Indanes
Cylindrene 190914 Click to see CC(C)C1=C2CCC(C2=CC(=C1)C(=O)C)(C)O 232.32 unknown https://doi.org/10.1021/NP50110A010
> Benzenoids / Phenol ethers / Anisoles
1-(3,4,5-Trimethoxyphenyl)propane-1,2,3-triol 74033649 Click to see COC1=CC(=CC(=C1OC)OC)C(C(CO)O)O 258.27 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
N-[2-(4-Hydroxyphenyl)ethyl]benzamide 577614 Click to see C1=CC=C(C=C1)C(=O)NCCC2=CC=C(C=C2)O 241.28 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-4-vinylphenol 332 Click to see COC1=C(C=CC(=C1)C=C)O 150.17 unknown via CMAUP database
4-Hydroxy-2-methoxybenzaldehyde 519541 Click to see COC1=C(C=CC(=C1)O)C=O 152.15 unknown via CMAUP database
5-Ethenyl-2-methoxyphenol 10441857 Click to see COC1=C(C=C(C=C1)C=C)O 150.17 unknown https://doi.org/10.1021/JF902310J
cis-Isoeugenol 1549041 Click to see CC=CC1=CC(=C(C=C1)O)OC 164.20 unknown via CMAUP database
Isoeugenol 853433 Click to see CC=CC1=CC(=C(C=C1)O)OC 164.20 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1021/JF902310J
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
Imperanene 10903632 Click to see COC1=C(C=CC(=C1)CC(CO)C=CC2=CC(=C(C=C2)O)OC)O 330.40 unknown https://doi.org/10.1021/NP50115A022
> Lignans, neolignans and related compounds / Lignan lactones
Graminone B 10001150 Click to see COC1=CC(=CC(=C1)O)C2C3C(CO2)C(OC3=O)C4=CC(=C(C(=C4)OC)OC)O 402.40 unknown https://doi.org/10.1021/NP50114A020
Graminonea 101915994 Click to see COC1=CC(=CC(=C1)O)C2C3COC(C3C(=O)O2)C4=CC(=CC(=C4)OC)O 372.40 unknown https://doi.org/10.1021/NP50114A020
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic acid 10465 Click to see CCCCCCCCCCCCCCCCC(=O)O 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Pentadecanoic Acid 13849 Click to see CCCCCCCCCCCCCCC(=O)O 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown via CMAUP database
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown via CMAUP database
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown via CMAUP database
Undecanoic Acid 8180 Click to see CCCCCCCCCCC(=O)O 186.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Hexadecanamide 69421 Click to see CCCCCCCCCCCCCCCC(=O)N 255.44 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,7R)-1-methoxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 100930976 Click to see CC1CCC2C1C(OC=C2C=O)OC 196.24 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Arundoin 12308619 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C 440.70 unknown via CMAUP database
Cylindrin 189045 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C 440.70 unknown via CMAUP database
Fernenol 12305178 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
Isoarborinol 12305182 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 38349717 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Obacunone 119041 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown via CMAUP database
Zapoterin 441812 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)C(CC4(C35C(O5)C(=O)OC4C6=COC=C6)C)O)C)C 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(-)-Simiarenol 42608302 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown via CMAUP database
Simiarenol 12442794 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCC(C5(C)C)O)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Monomethyl proline 6951137 Click to see C[NH+]1CCCC1C(=O)[O-] 129.16 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Methyltartronic acid 136386 Click to see CC(C(=O)O)(C(=O)O)O 134.09 unknown https://doi.org/10.1021/JF902310J
Oxalic Acid 971 Click to see C(=O)(C(=O)O)O 90.03 unknown https://doi.org/10.1080/00128325.1974.11662643
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(S)-3,4-Dihydroxybutyric acid 10920498 Click to see C(C(CO)O)C(=O)O 120.10 unknown via CMAUP database
3,4-Dihydroxybutanoic acid 150929 Click to see C(C(CO)O)C(=O)O 120.10 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
N,N-Dimethylhistamine 12656 Click to see CN(C)CCC1=CN=CN1 139.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
Casimiroedine 5281818 Click to see CN(CCC1=CN(C=N1)C2C(C(C(C(O2)CO)O)O)O)C(=O)C=CC3=CC=CC=C3 417.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3',4'-Dimethoxyacetophenone 14328 Click to see CC(=O)C1=CC(=C(C=C1)OC)OC 180.20 unknown via CMAUP database
3',5'-Dimethoxyacetophenone 95997 Click to see CC(=O)C1=CC(=CC(=C1)OC)OC 180.20 unknown via CMAUP database
Acetosyringone 17198 Click to see CC(=O)C1=CC(=C(C(=C1)OC)O)OC 196.20 unknown via CMAUP database
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1021/JF902310J
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-(2-Phenylethyl)chromone 441964 Click to see C1=CC=C(C=C1)CCC2=CC(=O)C3=CC=CC=C3O2 250.29 unknown https://doi.org/10.1021/NP0503808
5-Hydroxy-2-(2-Phenylethyl)Chromen-4-One 11536299 Click to see C1=CC=C(C=C1)CCC2=CC(=O)C3=C(C=CC=C3O2)O 266.29 unknown https://doi.org/10.1021/NP0503808
5-Hydroxy-2-[2-(2-Hydroxyphenyl)Ethyl]Chromone 11822089 Click to see C1=CC=C(C(=C1)CCC2=CC(=O)C3=C(C=CC=C3O2)O)O 282.29 unknown https://doi.org/10.1021/NP0503808
5-Hydroxy-2-styryl-chromen-4-one 6477677 Click to see C1=CC=C(C=C1)C=CC2=CC(=O)C3=C(C=CC=C3O2)O 264.27 unknown https://doi.org/10.1021/NP0503808
5-Hydroxy-2-styrylchromone 497595 Click to see C1=CC=C(C=C1)C=CC2=CC(=O)C3=C(C=CC=C3O2)O 264.27 unknown https://doi.org/10.1021/NP0503808
> Organoheterocyclic compounds / Benzoxazoles / Benzoxazolones
Coixol 10772 Click to see COC1=CC2=C(C=C1)NC(=O)O2 165.15 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
2,3-Dihydrobenzofuran 10329 Click to see C1COC2=CC=CC=C21 120.15 unknown https://doi.org/10.1021/JF902310J
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidinethiones
Zapotidine 12445018 Click to see CN1CCC2=CN=CN2C1=S 167.23 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
1,7-Dioxadispiro[4.0.4.2]dodeca-3,9-diene-2,8-dione 10496 Click to see C1CC2(C13C=CC(=O)O3)C=CC(=O)O2 192.17 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(S)-3-Hydroxy-4,4-dimethyldihydrofuran-2(3H)-one 736053 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
DL-Pantolactone 989 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
Pantolactone 439368 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(16beta)-4,12-Didehydro-9,10-(methylenedioxy)galanthan-1alpha,2beta,3alpha-triol 101649371 Click to see C1C=C2C3N1CC4=CC5=C(C=C4C3C(C(C2O)O)O)OCO5 303.31 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
5,7-Dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,17,18-triol 14413773 Click to see C1C=C2C3N1CC4=CC5=C(C=C4C3C(C(C2O)O)O)OCO5 303.31 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
Dehydroanhydrolycorine 10999422 Click to see C1C2=CC3=C(C=C2C4=CC=CC5=C4N1C=C5)OCO3 249.26 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown via CMAUP database
2-(2'-Hydroxy-4'-methoxyphenyl)-5,8-dimethoxy-3-propyl-1h-quinolin-4-one 24766568 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=C(C=C(C=C3)OC)O 369.40 unknown via CMAUP database
5-Hydroxy-1-methyl-2-phenylquinolin-4(1H)-one 71307707 Click to see CN1C2=C(C(=CC=C2)O)C(=O)C=C1C3=CC=CC=C3 251.28 unknown via CMAUP database
5,6-Dimethoxy-2-(2',5',6'-trimethoxyphenyl)-1h-quinolin-4-one 11132423 Click to see COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC 371.40 unknown via CMAUP database
5,6-dimethoxy-2-(3-methoxyphenyl)-1H-quinolin-4-one 11109704 Click to see COC1=C(C2=C(C=C1)NC(=CC2=O)C3=CC(=CC=C3)OC)OC 311.30 unknown via CMAUP database
5,6-Dimethoxy-2-(3,4-dimethoxyphenyl)-1h-quinolin-4-one 11131642 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(N2)C=CC(=C3OC)OC)OC 341.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3'-methoxyphenyl)-3-propyl-1h-quinolin-4-one 24766570 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=CC=C3)OC 353.40 unknown via CMAUP database
5,8-Dimethoxy-2-(3',4'-dimethoxyphenyl)-3-propyl-1h-quinolin-4-one 24766569 Click to see CCCC1=C(NC2=C(C=CC(=C2C1=O)OC)OC)C3=CC(=C(C=C3)OC)OC 383.40 unknown via CMAUP database
Eduleine 253834 Click to see CN1C(=CC(=O)C2=C1C=C(C=C2)OC)C3=CC=CC=C3 265.31 unknown via CMAUP database
Eduline 622180 Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3 265.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
Casimiroin 124075 Click to see CN1C(=O)C=C(C2=C1C3=C(C=C2)OCO3)OC 233.22 unknown via CMAUP database
Edulitine 826073 Click to see COC1=CC=CC2=C1NC(=O)C=C2OC 205.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
Isoferulic acid 736186 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/JF902310J
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Siderin 185740 Click to see CC1=CC(=CC2=C1C(=CC(=O)O2)OC)OC 220.22 unknown https://doi.org/10.4268/CJCMM20121523
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-[(E,6S)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-one 92475864 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)CCC(C(C)(C)O)O 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
8-Hydroxybergapten 3083726 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)O 232.19 unknown via CMAUP database
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Luteolinidin 441701 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2)O)O)O)O 271.24 unknown https://doi.org/10.1038/2131033A0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
7-Hydroxy-4'-methoxyflavane 3483299 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O 256.30 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
Broussin 442277 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O 256.30 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
5-methoxy-2-(4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 74977228 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3OC)O 286.32 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
5-Methoxy-2-(4-methoxyphenyl)chromen-7-one 162910514 Click to see COC1=CC=C(C=C1)C2=CC=C3C(=CC(=O)C=C3OC)O2 282.29 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
5-Methoxyflavone 94525 Click to see COC1=CC=CC2=C1C(=O)C=C(O2)C3=CC=CC=C3 252.26 unknown via CMAUP database
7-Hydroxy-5,4'-dimethoxyflavan 44257196 Click to see COC1=CC=C(C=C1)C2CCC3=C(O2)C=C(C=C3OC)O 286.32 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
3',5,6-Trimethoxyflavone 44257599 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=CC=C3)OC)OC 312.30 unknown via CMAUP database
5,6-Dimethoxyflavone 14349486 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3)OC 282.29 unknown via CMAUP database
5,6,2'-Trimethoxyflavone 14484690 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC=CC=C3OC)OC 312.30 unknown via CMAUP database
Zapotin 629965 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC 342.30 unknown via CMAUP database
Zapotinin 44257595 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C=CC(=C3O)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
2,4-Dihydroxy-4',6-dimethoxychalcone 74819284 Click to see COC1=CC=C(C=C1)C(=O)C=CC2=C(C=C(C=C2OC)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)81561-7
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database

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