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Narcissus tazetta

Narcissus tazetta - Unknown
Part: Unknown
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 UUID64401ddbd92b4694375135
Scientific name Narcissus tazetta
Authority L.
First published in Sp. Pl. : 290 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hermione ambigena Salisb. Trans. Hort. Soc. London 1: 361 (1812)
Hermione biancae Tod. Index Seminum Panorm. 1857: 43. 1858 [10 Jan 1858] ; cf. Linnaea, 29: 746 (-747) 1858.
Hermione brevistyla Herb. Amaryllidaceae : 324 (1837)
Hermione cerina Haw. Syn. Pl. Succ. 329. 1812
Hermione crenularis Salisb. Trans. Hort. Soc. London 1: 363 (1812)
Hermione discolor Jurd. & Fourr. Brev. Pl. Nov. ii. 111. 1868
Hermione fistulosa Haw. Syn. Pl. Succ. 330. 1812
Hermione floribunda Salisb. Trans. Hort. Soc. London 1: 362. 1812
Hermione grandiflora Haw. Syn. Pl. Succ. 330. 1812
Hermione italica Herb. Amaryllidaceae 325.
Hermione leucojifolia Salisb. Trans. Hort. Soc. London 1: 359 (1812)
Hermione polyantha Haw. Monogr. Narciss. 11. 1831 (1831)
Hermione stylosa Salisb. Trans. Hort. Soc. London 1: 360 (1812)
Hermione taxetta (L.) Haw. Suppl. Pl. Succ. : 142 (1819)
Hermione tereticaulis (Haw.) Haw. Suppl. Pl. Succ. : 140 (1819)
Hermione trewiana Sweet Brit. Fl. Gard. [Sweet] Ser. II. t. 118.
Jonquilla tasetta Raf. Fl. Tellur. 4: 21 (1838)
Narcissus tazettus St.-Lag. Ann. Soc. Bot. Lyon 7: 130 (1880)
Narcissus timbali Gaut. Herb. Comm. Agr. Narb. 18; ex Timb. in Bull. Soc. Sc. Phys. & Nat. Toul. iii.(1875-76) 143.
Narcissus flos-lactis Steud. Nomencl. Bot. [Steudel], ed. 2. 2: 181. 1841
Patrocles orientalis Salisb. Gen. Pl. : 100 (1866)
Pancratium tazetta Sessé & Moc. Fl. Mexic. , ed. 2: 85 (1894)
Tityrus primulaceus Salisb. Gen. Pl. 101. 1866 (1866)
Narcissus tazetta var. cypri (Haw.) Boiss. Fl. Orient. 5: 151. 1882
Narcissus tazetta subsp. cypri (Haw.) Holmboe Stud. Veg. Cyprus 53. 1914 (1914)
Narcissus tazetta var. syriacus (Boiss. & Gaill.) Boiss. Fl. Orient. 5: 150. 1882
Narcissus tazetta subsp. canaliculatus (Guss.) Nyman Consp. Fl. Eur. 711. 1882 (1882)
Narcissus patulus subsp. etruscus (Parl.) Nyman Consp. Fl. Eur. 711. 1882 (1882)
Narcissus patulus subsp. ricasolianus (Parl.) Nyman Consp. Fl. Eur. 711. 1882 (1882)
Narcissus patulus subsp. vergellensis (Parl.) Nyman Consp. Fl. Eur. 711. 1882 (1882)
Narcissus patulus subsp. siculus (Parl.) Nyman Consp. Fl. Eur. 711. 1882 (1882)
Narcissus tazetta subsp. eutazetta Briq. Prodr. Fl. Corse 326. 1910 (1910)
Narcissus tazetta subsp. patulus (Loisel.) Baker Handb. Amaryll. 7. 1888 (1888)
Narcissus linnaeanus subsp. ganymedoides (Jord. & Fourr.) Rouy Fl. France 13: 45. 1912 (1912)
Narcissus linnaeanus var. antipolensis (Jord. & Fourr.) Rouy Fl. France 13: 49. 1912
Hermione multiflora var. aurantia Haw. Suppl. Pl. Succ. 146. 1819
Narcissus papyraceus var. sequentis (Tod.) Nyman Consp. Fl. Eur. 711. 1882
Narcissus tazetta var. varians (Guss. ex Parl.) Nyman Consp. Fl. Eur. 711. 1882
Narcissus neglectus var. commutatus (Parl.) Nyman Consp. Fl. Eur. 711. 1882
Narcissus patulus var. timbalii (Gaut. ex Timb.-Lagr.) Nyman Consp. Fl. Eur. Suppl. 2: 298. 1890
Narcissus tazetta var. mediterraneus (Jord. & Fourr.) Baker Gard. Chron. 1869: 1015.
Narcissus citrinus (Haw.) Schult.f. Syst. Veg., ed. 15 bis [Roemer & Schultes] 7(2): 968. 1830 [late 1830]
Narcissus tazetta var. orientalis (L.) hort.

Common names Top

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Language Common/alternative name
English cream narcissus
Spanish narciso de ramillete
Spanish narciso coronado
Spanish inclintinas
Spanish juncos blancos hediondos
Spanish meado de burro
Spanish narciso amarillo
Spanish narciso de alger
Spanish narciso hediondo
Spanish narciso de manojo
Spanish narciso del campo amarillo
Spanish varica de san josé
Spanish varica de san jose
Spanish narciso temprano
Spanish narciso sobredorado
Arabic رنجس
Arabic نرجس
Arabic نرجس شائع
Azerbaijani tazet nərgizgülü
cdo cūi-siĕng
Czech taceta
Czech narcis taceta
Welsh cenhinen-bedr glystyrog
German strauß-narzisse
German tazette
German strauss-narzisse
German mehrblütige narzisse
German bukett-narzisse
Persian نرگس
Finnish tasetti
French narcisse à bouquet
Hebrew נרקיס מצוי
Croatian višecvjetni sunovrat
Japanese スイセン
Kabyle tixlulin
Malayalam നാർസിസസ് ടസെറ്റ
Polish narcyz wielokwiatowy
Russian Нарцисс букетный
Russian Тацет
Turkish Çin nergisi
Vietnamese thủy tiên
Chinese 欧洲水仙
Chinese 多花水仙

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Narcissus tazetta subsp. aureus (Jord. & Fourr.) Baker Handb. Amaryll. : 9 (1888)
Narcissus tazetta subsp. canariensis (Burb.) Baker Handb. Amaryll. : 8 (1888)
Narcissus tazetta subsp. chinensis (M.Roem.) Masamura & Yanagih. Trans. Nat. Hist. Soc. Formosa 31: 329 (1941)
Narcissus tazetta subsp. corcyrensis (Herb.) Baker Handb. Amaryll. 7. 1888 (1888)
Narcissus tazetta subsp. italicus (Ker Gawl.) Baker Handb. Amaryll. : 8 (1888)
Narcissus tazetta subsp. tazetta Unknown

Varieties (abbr. var.) Top

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No variety added yet.

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
    • Macaronesia
      • Azores
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Australasia
    • Australia
      • Norfolk Island
      • South Australia
      • Tasmania
      • Western Australia
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
    • Northwestern U.S.A.
      • Oregon
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Louisiana
      • Mississippi
      • North Carolina
      • South Carolina
      • Virginia
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000700066
UNII S2T09UI8K0
Florida Plant Atlas 1941
Flora of Alabama 4432
USDA Plants NATA2
Tropicos 1200058
INPN 109309
Flora of Italy 6997
KEW urn:lsid:ipni.org:names:66240-1
The Plant List kew-282289
PFAF Narcissus tazetta
Open Tree Of Life 103379
Observations.org 147234
NCBI Taxonomy 54860
NBN Atlas NBNSYS0000014810
Nature Serve 2.143249
IPNI 66240-1
iNaturalist 56027
GBIF 2858963
Freebase /m/0fm2ph
EPPO NARTA
EOL 1010901
Elurikkus 318922
Calflora (Californian flora) 8638
USDA GRIN 25053
Wikipedia Narcissus_tazetta
CMAUP NPO17954

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
Physiological, Biochemical, and Molecular Analyses Reveal Dark Heartwood Formation Mechanism in Acacia melanoxylon Zhang R, Bai X, Chen Z, Chen M, Li X, Zeng B, Hu B Int J Mol Sci 02-May-2024
PMCID:PMC11084464
doi:10.3390/ijms25094974
PMID:38732191
Integrative analysis of the metabolome and transcriptome provides insights into the mechanisms of lignan biosynthesis in Herpetospermum pedunculosum (Cucurbitaceae) Zhu Z, Chen D, Sun M, Xiao M, Huang P, Ren D, Yang Y, Zhang Z, Zhao Q, Li R BMC Genomics 29-Apr-2024
PMCID:PMC11059704
doi:10.1186/s12864-024-10306-1
PMID:38684979
Functional Characterization of PmDXR, a Critical Rate-Limiting Enzyme, for Turpentine Biosynthesis in Masson Pine (Pinus massoniana Lamb.) Li R, Zhu L, Chen P, Chen Y, Hao Q, Zhu P, Ji K Int J Mol Sci 17-Apr-2024
PMCID:PMC11050515
doi:10.3390/ijms25084415
PMID:38673998
Integration of Wnt-inhibitory activity and structural novelty scoring results to uncover novel bioactive natural products: new Bicyclo[3.3.1]non-3-ene-2,9-diones from the leaves of Hymenocardia punctata Quiros-Guerrero LM, Marcourt L, Chaiwangrach N, Koval A, Ferreira Queiroz E, David B, Grondin A, Katanaev VL, Wolfender JL Front Chem 04-Apr-2024
PMCID:PMC11024435
doi:10.3389/fchem.2024.1371982
Identification and Expression Analysis of R2R3-MYB Transcription Factors Associated with Flavonoid Biosynthesis in Panax quinquefolius Song G, Yan Y, Guo C, Chen J, Wang Y, Wang Y, Zhang J, Gao C, Lian J, Piao X, Di P Int J Mol Sci 26-Mar-2024
PMCID:PMC11011825
doi:10.3390/ijms25073709
PMID:38612520
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Identification of Viruses Infecting Phalaenopsis Orchids Using Nanopore Sequencing and Development of an RT-RPA-CRISPR/Cas12a for Rapid Visual Detection of Nerine Latent Virus Lee HJ, Kim HJ, Cho IS, Jeong RD Int J Mol Sci 25-Feb-2024
PMCID:PMC10931582
doi:10.3390/ijms25052666
PMID:38473916
Volatile Organic Compounds Emitted by Flowers: Ecological Roles, Production by Plants, Extraction, and Identification Lo MM, Benfodda Z, Molinié R, Meffre P Plants (Basel) 31-Jan-2024
PMCID:PMC10857460
doi:10.3390/plants13030417
PMID:38337950
Characterization of the Heat Shock Transcription Factor Family in Lycoris radiata and Its Potential Roles in Response to Abiotic Stresses Wang N, Shu X, Zhang F, Song G, Wang Z Plants (Basel) 17-Jan-2024
PMCID:PMC10819275
doi:10.3390/plants13020271
PMID:38256823
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
The R2R3-MYB Transcriptional Repressor TgMYB4 Negatively Regulates Anthocyanin Biosynthesis in Tulips (Tulipa gesneriana L.) Hu X, Liang Z, Sun T, Huang L, Wang Y, Chan Z, Xiang L Int J Mol Sci 01-Jan-2024
PMCID:PMC10779166
doi:10.3390/ijms25010563
PMID:38203734
Understanding the Lost: Reconstruction of the Garden Design of Villa Peretti Montalto (Rome, Italy) for Urban Valorization Bartoli F, D’Amato L, Nucera A, Albani Rocchetti G, Caneva G Plants (Basel) 26-Dec-2023
PMCID:PMC10780482
doi:10.3390/plants13010077
PMID:38202385
Which Plant Species for Green Roofs in the Mediterranean Environment? Leotta L, Toscano S, Romano D Plants (Basel) 27-Nov-2023
PMCID:PMC10708222
doi:10.3390/plants12233985
PMID:38068621
Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics Paudel S, Mishra N, Agarwal R Pharmaceuticals (Basel) 26-Nov-2023
PMCID:PMC10746110
doi:10.3390/ph16121652
PMID:38139779
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11S,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 154496716 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1248/CPB.29.3381
Haemanthamine 441593 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/0031-9422(91)80051-2
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
1-(14-Hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-4-yl)ethanone 72477006 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 315.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
1-[(14S)-14-hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-4-yl]ethanone 163093250 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 315.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
1-[(1R,12R,14S)-14-hydroxy-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-4-yl]ethanone 163093251 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 315.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
Epigalantamine 676392 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.3987/R-1986-08-2089
Epigalanthamin 3449 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.3987/R-1986-08-2089
https://doi.org/10.1016/0031-9422(91)80051-2
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1055/S-2006-957740
https://doi.org/10.1016/0031-9422(91)80051-2
Lycoramine 443723 Click to see CN1CCC23CCC(CC2OC4=C(C=CC(=C34)C1)OC)O 289.40 unknown https://doi.org/10.3987/R-1986-08-2089
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthindole-type amaryllidaceae alkaloids
[6-(1-Methyl-1H-indol-7-yl)-2H-1,3-benzodioxol-5-yl]methanol 71369229 Click to see CN1C=CC2=C1C(=CC=C2)C3=CC4=C(C=C3CO)OCO4 281.30 unknown https://doi.org/10.1002/CBDV.201400309
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
9-Hydroxy-10-methoxy-1-methyl-2,3,5,5a,11b,11c-hexahydroisochromeno[3,4-g]indol-7-one 3844472 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC 301.34 unknown https://doi.org/10.1002/ARDP.19943270908
9-O-Demethylhomolycorine 388787 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)O)OC 301.34 unknown https://doi.org/10.1248/CPB.29.3381
https://doi.org/10.1002/ARDP.19943270908
Homolycorine 160473 Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)OC)OC 315.40 unknown https://doi.org/10.1248/CPB.29.3381
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
[(1S,15R,17S,18S,19R)-18-acetyloxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9-trien-17-yl] acetate 45483145 Click to see CC(=O)OC1CC2CCN3C2C(C1OC(=O)C)C4=CC5=C(C=C4C3)OCO5 373.40 unknown https://doi.org/10.1002/CBER.19560891042
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1248/CPB.29.3381
https://doi.org/10.1016/0031-9422(91)80051-2
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1R,11R,13S,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-ol 95907135 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
(1R,13S,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 92246662 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
(1S,11R,13R,16S,18S)-11,18-dimethoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 10926024 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)OC)OCO5 345.40 unknown https://doi.org/10.1002/CBDV.201400309
(1S,11S,13R,16S,18S)-18-methoxy-11,15-dimethyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 162817593 Click to see CC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 329.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-ol 10314625 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown via CMAUP database
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 23259454 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5 315.40 unknown https://doi.org/10.1002/CBDV.201400309
3-Epimacronine 375117 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(=O)O2)OCO5 329.30 unknown https://doi.org/10.1002/CBDV.201400309
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol 419046 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
Pretazettine 73360 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(O2)O)OCO5 331.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
https://doi.org/10.1159/000226558
https://doi.org/10.1016/B978-0-12-013320-8.50007-1
Sekisanin 443682 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/0031-9422(91)80051-2
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1248/CPB.29.3381
https://doi.org/10.1002/CBER.19560891042
Tazettine 271607 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1002/CBER.19560891042
https://doi.org/10.1016/0031-9422(91)80051-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.3109/13880209409083015
Methyl Anthranilate 8635 Click to see COC(=O)C1=CC=CC=C1N 151.16 unknown https://doi.org/10.3109/13880209409083015
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.3109/13880209409083015
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown https://doi.org/10.3109/13880209409083015
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.3109/13880209409083015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.3109/13880209409083015
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.3109/13880209409083015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.3109/13880209409083015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.3109/13880209409083015
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.3109/13880209409083015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.3109/13880209409083015
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.3109/13880209409083015
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101675599 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O 1427.50 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101675600 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1427.50 unknown via CMAUP database
(3R,4S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carboxylic acid 101618891 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 957.10 unknown via CMAUP database
(3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101675598 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)(C)C)O)O)O)CO)O)O)O 957.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 101606373 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)O)C)C(=C)C)O)O)O)CO)O)O)O 927.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675597 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1C)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)O 1075.20 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675278 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21630094 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1075.20 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101675601 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)O)O)C)C)(C)C)O)O)O)CO)O)O)O 959.10 unknown via CMAUP database
3alpha,11alpha-Dihydroxylup-20(29)-ene-23,28-dioic acid 28-[6-O-[4-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl]-beta-D-glucopyranosyl] ester 101606374 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CC(C7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)O)C(=C)C)O)O)O)CO)O)O)O 973.10 unknown via CMAUP database
Acankoreoside A 10795959 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)C(=C)C)O)O)O)CO)O)O)O 957.10 unknown via CMAUP database
Asiaticoside 11954171 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
Scheffoleoside A 101675595 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)O)O)C)C)(C)C)O)O)O)CO)O)O)O 959.10 unknown via CMAUP database
Scheffursoside B 101675277 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 957.10 unknown via CMAUP database
Schoffoleoside B 101675596 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)C=O)O)O)C)C)(C)C)O)O)O)CO)O)O)O 957.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
1'-OH-4-Keto-gamma-carotene/(Carotenoid K) 14730338 Click to see CC1=C(C(CCC1=O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCCC(C)(C)O)C)C 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-sulfooxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21582889 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OS(=O)(=O)O)C)C(=O)O 536.80 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
(5R,9R,10R,13R,14R,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methyl-5-oxoheptan-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162843958 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1002/CBER.19560891042
3Alpha-Hydroxylup-20(29)-Ene-23,28-Dioic Acid 14466871 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)C(=O)O 486.70 unknown via CMAUP database
3alpha,11alpha-Dihydroxylup-20(29)-ene-23,28-dioic acid 14866192 Click to see CC(=C)C1CCC2(C1C3CC(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)O)C(=O)O 502.70 unknown via CMAUP database
Betulinic Acid Sulfate 11756976 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OS(=O)(=O)O)C)C(=O)O 536.80 unknown via CMAUP database
Epibetulinic acid 485711 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Rha(a1-4)Glc(b1-6)b-Glc 91857681 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)O)O)O)O)CO)O)O)O 488.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
2-(2-hydroxypropan-2-yl)-4-methoxy-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3-dihydrofuro[3,2-g]chromen-5-one 11968852 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)COC4C(C(C(C(O4)CO)O)O)O)O 468.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
6-Hydroxy-7,8-dimethoxy-2-(2-oxopropyl)-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one 71436822 Click to see CC(=O)CC1CC2C(O1)C3=CC(=C(C(=C3C(=O)O2)O)OC)OC 322.31 unknown https://doi.org/10.1016/0031-9422(91)80051-2
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see C1=CC=C2C(=C1)C=CN2 117.15 unknown https://doi.org/10.3109/13880209409083015
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,10R,12S)-4,5,12-trimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene 14781318 Click to see COC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)OC)C=C1 301.40 unknown https://doi.org/10.1248/CPB.29.3381
(1S,10R,12R)-4,5,12-trimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene 162991867 Click to see COC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)OC)C=C1 301.40 unknown https://doi.org/10.3987/R-1986-08-2089
(1S,13S,18S)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163051953 Click to see COC1=C2CN3CC(C4(C3CCC=C4)C2=CC5=C1OCO5)O 301.34 unknown https://doi.org/10.1002/CBER.19560891042
4,5,12-Trimethoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene 14781317 Click to see COC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)OC)C=C1 301.40 unknown https://doi.org/10.1248/CPB.29.3381
5,6-Dihydrobicolorine 375118 Click to see CN1CC2=CC3=C(C=C2C4=CC=CC=C41)OCO3 239.27 unknown https://doi.org/10.1002/CBDV.201400309
9-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163051952 Click to see COC1=C2CN3CC(C4(C3CCC=C4)C2=CC5=C1OCO5)O 301.34 unknown https://doi.org/10.1002/CBER.19560891042
Dehydroanhydrolycorine 10999422 Click to see C1C2=CC3=C(C=C2C4=CC=CC5=C4N1C=C5)OCO3 249.26 unknown https://doi.org/10.1002/CBDV.201400309
Maritidine 11185307 Click to see COC1=C(C=C2C(=C1)CN3CCC24C3CC(C=C4)O)OC 287.35 unknown https://doi.org/10.3987/R-1986-08-2089
Pseudolycorine 443689 Click to see COC1=C(C=C2C3C(C(C=C4C3N(CC4)CC2=C1)O)O)O 289.33 unknown https://doi.org/10.1016/0031-9422(91)80051-2
https://doi.org/10.1248/CPB.24.336
Trisphaeridine 443684 Click to see C1OC2=C(O1)C=C3C4=CC=CC=C4N=CC3=C2 223.23 unknown https://doi.org/10.1002/CBDV.201400309
Ungiminorine 10425948 Click to see COC1C(C2C3C(=CCN3CC4=CC5=C(C=C24)OCO5)C1O)O 317.34 unknown https://doi.org/10.1021/NP9905719
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.3109/13880209409083015
Ethyl 3-phenylprop-2-enoate 7649 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.3109/13880209409083015
Ethyl cinnamate 637758 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.3109/13880209409083015
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.3109/13880209409083015
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown https://doi.org/10.3109/13880209409083015
> Phenylpropanoids and polyketides / Flavonoids / Anthocyanidins
Flavylium 145858 Click to see C1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2 207.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eupatin 5317287 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O 360.30 unknown via CMAUP database
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1007/BF00564268
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1246/NIKKASHI1948.77.1059
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1246/NIKKASHI1948.77.1059

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