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Scilla peruviana

Scilla peruviana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Scilla peruviana - 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 UUID64402271c614d755046338
Scientific name Scilla peruviana
Authority L.
First published in Sp. Pl. : 309 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Caloscilla clusii Jord. & Fourr. Icon. Fl. Eur. 2: 14 (1869)
Caloscilla elegans Jord. & Fourr. Icon. Fl. Eur. 2: 16 (1869)
Caloscilla flaveola Jord. & Fourr. Icon. Fl. Eur. 2: 17 (1869)
Caloscilla grandiflora Jord. & Fourr. Icon. Fl. Eur. 2: 16 (1869)
Caloscilla hughii Jord. & Fourr. Icon. Fl. Eur. 2: 15 (1869)
Caloscilla livida Jord. & Fourr. Icon. Fl. Eur. 2: 15 (1869)
Caloscilla pallidiflora Jord. & Fourr. Icon. Fl. Eur. 2: 15 (1869)
Caloscilla subalbida Jord. & Fourr. Icon. Fl. Eur. 2: 16 (1869)
Caloscilla subcarnea Jord. & Fourr. Icon. Fl. Eur. 2: 16 (1869)
Caloscilla venusta Jord. & Fourr. Icon. Fl. Eur. 2: 15 (1869)
Hyacinthus peruvianus (L.) Vilm. Fl. Pleine Terre : 795 (1863)
Loncomelos purpureum Raf. Fl. Tellur. 3: 62 (1837)
Melomphis peruviana (L.) Raf. Fl. Tellur. 2: 22 (1837)
Melomphis sicula Raf. Fl. Tellur. 2: 22 (1837)
Ornithogalum coeruleum Parl. Fl. Ital. 2: 467 (1857)
Ornithogalum ceruleum Raf. Caratt. Nuov. Gen. : 85 (1810)
Oncostema peruviana (L.) Speta Phyton (Horn) 26: 264 (1987)
Oncostema elongata (Parl.) Speta Phyton (Horn) 26: 265 (1987)
Oncostema hughii (Tineo ex Guss.) Speta Phyton (Horn) 26(2): 265. 1987
Oncostema cerulea (Raf.) Speta Phyton (Horn) 26: 265 (1987)
Oncostema sicula (Tineo ex Guss.) Speta Phyton (Horn) 26: 265 (1987)
Oncostema cupanii (Guss.) Speta Phyton (Horn) 38: 110 (1998)
Scilla comata Hoffmanns. Verz. Pfl.-Kult. (1824)
Scilla clusii Parl. Fl. Ital. 2: 462 (1857)
Scilla candida Guss. Fl. Sicul. Syn. 2: 814 (1845)
Scilla cupaniana Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 559 (1829)
Scilla cupanii Guss. Index Seminum (Boccadifalco) 1825: 10 (1825)
Scilla elongata Parl. Nuov. Gen. Sp. Monocot. : 24 (1854)
Scilla clusiana Endl. Cat. Horti Vindob. 1: 129 (1842)
Scilla cerulea (Raf.) Soldano Atti Soc. Ital. Sci. Nat. Mus. Civico Storia Nat. Milano 131: 253 (1991)
Scilla vivianii Bertol. Fl. Ital. 10: 517 (1857)
Scilla filangeri Tineo ex Lojac. Fl. Sicul. 3: 123 (1909)
Scilla fistulosa Raf. Précis Découv. Somiol. : 45 (1814)
Scilla hemisphaerica Boiss. Voy. Bot. Espagne : 613 (1842)
Scilla sicula Tineo ex Guss. in Guss. Fl. Sic. Syn. ii. 813.
Scilla ughii Tineo ex Guss. Fl. Sicul. Prodr. , Suppl.: 162 (1832)
Scilla speciosa Samp. Herb. Port. : 30 (1913)
Scilla stellaris Salisb. Prodr. Stirp. Chap. Allerton : 241 (1796)
Scilla pubens Welw. ex Lindl. Edwards's Bot. Reg. 31(Misc.): 40 (1845)
Scilla praebracteata Haw. ex G.Don Hort. Brit. , ed. 3: 697 (1839)
Scilla pseudoperuviana Tineo ex Lojac. Fl. Sicul. 3: 123 (1909)
Basaltogeton peruvianum (L.) Salisb. Gen. Pl. : 27 (1866)
Scilla hughii Tineo ex Guss. Fl. Sicul. Prodr. Suppl.: 162 1832
Scilla peruviana var. ifniensis Font Quer Mem. Real Acad. Ci. Barcelona ser. 3, 25(14): 16. 1936
Scilla peruviana subsp. elongata (Parl.) Maire Cat. Pl. Maroc 4: 958. 1941 (1941)
Scilla peruviana var. venusta (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 143. 1958
Scilla peruviana var. pallidiflora (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 143. 1958
Scilla peruviana var. grandiflora (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 143. 1958
Scilla peruviana var. subalbida (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 143. 1958
Scilla peruviana var. flaveola (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 143. 1958
Scilla peruviana var. livida (Jord. & Fourr.) Maire Bull. Soc. Hist. Nat. Afrique N. 30: 367. 1939
Scilla peruviana var. subcarnea (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 144. 1958
Scilla peruviana var. elegans (Jord. & Fourr.) Maire & Weiller Fl. Afrique N. 5: 144. 1958
Scilla peruviana var. killianii Maire Bull. Soc. Hist. Nat. Afrique N. 20: 39. 1929
Scilla peruviana var. sublivida Maire & Weiller Bull. Soc. Hist. Nat. Afrique N. 30: 367. 1939
Scilla peruviana var. stenopetala Maire Bull. Soc. Hist. Nat. Afrique N. 30: 367. 1939
Scilla peruviana var. gattefossei Maire Bull. Soc. Hist. Nat. Afrique N. 30: 367. 1939
Scilla peruviana var. diluta Maire Bull. Soc. Hist. Nat. Afrique N. 30: 367. 1939
Scilla clusii var. comata (Hoffmanns.) Nyman Consp. Fl. Eur. 729. 1882
Scilla clusii var. candida (Guss.) Nyman Consp. Fl. Eur. 729. 1882
Scilla peruviana subsp. glabra (Boiss.) K.Richt. Pl. Eur. 1: 220. 1890 (1890)
Scilla peruviana subsp. hughii (Tineo ex Guss.) K.Richt. Pl. Eur. 1: 220 1890
Scilla hemisphaerica var. glabra Boiss. Voy. Bot. Espagne 2: 613. 1842
Scilla peruviana var. zaborskiana Emb. Bull. Soc. Sci. Nat. Maroc 17: 223. 1937

Common names Top

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Language Common/alternative name
English portuguese squill
Spanish bartsia peruvianum
Spanish lirio cubano
Spanish jacinto peruano
Spanish esquila portuguesa
Spanish escila peruano
Spanish caloscilla hipponensis
Bulgarian перуански синчец
Catalan escil·la portuguesa
Welsh seren portiwgal
German peruanischer blaustern
Finnish isosinililja
French scille du perou
French scille du pérou
Japanese オオツルボ
Japanese シラー・ペルビアナ
Polish cebulica peruwiańska
Chinese 地中海绵枣儿
Chinese 地中海綿棗兒
Chinese 野風信子
Chinese 葡萄牙绵枣儿
Chinese 葡萄牙綿棗兒
Chinese 秘魯綿棗兒
Chinese 地中海藍鐘花
Chinese 葡萄牙蓝瑰花
Chinese 地中海蓝钟花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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germinates in 4 weeks outdoors in autumn, seedlings must remain at 4°C for full 3 months, then gradually raise temp t20°C

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Australasia
    • Australia
      • South Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Italy
      • Sicilia
    • Southwestern Europe
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000741698
Tropicos 18400328
KEW urn:lsid:ipni.org:names:540971-1
The Plant List kew-288872
Open Tree Of Life 803330
Observations.org 138366
NCBI Taxonomy 65771
NBN Atlas NBNSYS0000014706
IPNI 540971-1
iNaturalist 244096
GBIF 2767432
Freebase /m/08k9_r
EOL 1082630
USDA GRIN 33340
Wikipedia Scilla_peruviana

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
Nine new species of black lichenicolous fungi from the genus Cladophialophora (Chaetothyriales) from two different climatic zones of China Chang R, Wang Y, Liu Y, Wang Y, Li S, Zhao G, Zhang S, Dai M, Zheng X, Bose T, Si H Front Microbiol 16-Jun-2023
PMCID:PMC10312087
doi:10.3389/fmicb.2023.1191818
PMID:37396360
Fungal Planet description sheets: 1182–1283 Crous PW, Cowan DA, Maggs-Kölling G, Yilmaz N, Thangavel R, Wingfield MJ, Noordeloos ME, Dima B, Brandrud TE, Jansen GM, Morozova OV, Vila J, Shivas RG, Tan YP, Bishop-Hurley S, Lacey E, Marney TS, Larsson E, Le Floch G, Lombard L, Nodet P, Hubka V, Alvarado P, Berraf-Tebbal A, Reyes JD, Delgado G, Eichmeier A, Jordal JB, Kachalkin AV, Kubátová A, Maciá-Vicente JG, Malysheva EF, Papp V, Rajeshkumar KC, Sharma A, Spetik M, Szabóová D, Tomashevskaya MA, Abad JA, Abad ZG, Alexandrova AV, Anand G, Arenas F, Ashtekar N, Balashov S, Bañares Á, Baroncelli R, Bera I, Biketova AY, Blomquist CL, Boekhout T, Boertmann D, Bulyonkova TM, Burgess TI, Carnegie AJ, Cobo-Diaz JF, Corriol G, Cunnington JH, da Cruz MO, Damm U, Davoodian N, de A. Santiago AL, Dearnaley J, de Freitas LW, Dhileepan K, Dimitrov R, Di Piazza S, Fatima S, Fuljer F, Galera H, Ghosh A, Giraldo A, Glushakova AM, Gorczak M, Gouliamova DE, Gramaje D, Groenewald M, Gunsch CK, Gutiérrez A, Holdom D, Houbraken J, Ismailov AB, Istel Ł, Iturriaga T, Jeppson M, Jurjević Ž, Kalinina LB, Kapitonov VI, Kautmanová I, Khalid AN, Kiran M, Kiss L, Kovács Á, Kurose D, Kušan I, Lad S, Læssøe T, Lee HB, Luangsa-ard JJ, Lynch M, Mahamedi AE, Malysheva VF, Mateos A, Matočec N, Mešić A, Miller AN, Mongkolsamrit S, Moreno G, Morte A, Mostowfizadeh-Ghalamfarsa R, Naseer A, Navarro-Ródenas A, Nguyen TT, Noisripoom W, Ntandu JE, Nuytinck J, Ostrý V, Pankratov TA, Pawłowska J, Pecenka J, Pham TH, Polhorský A, Pošta A, Raudabaugh DB, Reschke K, Rodríguez A, Romero M, Rooney-Latham S, Roux J, Sandoval-Denis M, Smith MT, Steinrucken TV, Svetasheva TY, Tkalčec Z, van der Linde EJ, v.d. Vegte M, Vauras J, Verbeken A, Visagie CM, Vitelli JS, Volobuev SV, Weill A, Wrzosek M, Zmitrovich IV, Zvyagina EA, Groenewald JZ Persoonia 13-Jul-2021
PMCID:PMC9311394
doi:10.3767/persoonia.2021.46.11
PMID:35935893
Ovicidal, pupicidal, adulticidal, and repellent activity of Helicteres velutina K. Schum against Aedes aegypti L. (Diptera: Culicidae) Fernandes DA, Rique HL, de Oliveira LH, Santos WG, de Souza MD, Nunes FD Braz J Vet Med 26-Mar-2021
PMCID:PMC9179187
doi:10.29374/2527-2179.bjvm112120
PMID:35749063
Chemical Constituents of the Bulbs of Scilla peruviana and Their Pancreatic Lipase Inhibitory Activity Matsuo Y, Yamashiro A, Ootomo K, Nakagawa M, Tsuchihashi H, Inaba N, Mimaki Y Int J Mol Sci 27-Jan-2021
PMCID:PMC7865276
doi:10.3390/ijms22031262
PMID:33514028
Omics approaches in Allium research: Progress and way ahead Khandagale K, Krishna R, Roylawar P, Ade AB, Benke A, Shinde B, Singh M, Gawande SJ, Rai A PeerJ 09-Sep-2020
PMCID:PMC7486827
doi:10.7717/peerj.9824
PMID:32974094
Telomerase RNAs in land plants Fajkus P, Peška V, Závodník M, Fojtová M, Fulnečková J, Dobias Š, Kilar A, Dvořáčková M, Zachová D, Nečasová I, Sims J, Sýkorová E, Fajkus J Nucleic Acids Res 08-Aug-2019
PMCID:PMC6765143
doi:10.1093/nar/gkz695
PMID:31392988
The History of the Glycosidase Inhibiting Hyacinthacine C-type Alkaloids: From Discovery to Synthesis Carroll AW, Pyne SG Curr Org Synth 01-Jun-2019
PMCID:PMC7432187
doi:10.2174/1570179416666190126100312
PMID:31984928
Antiangiogenic Activity and Cytotoxicity of Triterpenoids and Homoisoflavonoids from Massonia pustulata and Massonia bifolia. Schwikkard SL, Whitmore H, Corson TW, Sishtla K, Langat MK, Carew M, Mulholland DA Planta Med 28-Feb-2018
PMCID:PMC6467464
doi:10.1055/a-0577-5322
PMID:29490386
Phytotherapy in diabetes: Review on potential mechanistic perspectives El-Abhar HS, Schaalan MF World J Diabetes 15-Apr-2014
PMCID:PMC3990312
doi:10.4239/wjd.v5.i2.176
PMID:24748931
Aphids (Hemiptera, Aphididae) on ornamental plants in greenhouses in Bulgaria Yovkova M, Petrović-Obradović O, Tasheva-Terzieva E, Pencheva A Zookeys 30-Jul-2013
PMCID:PMC3764532
doi:10.3897/zookeys.319.4318
PMID:24039530
The genus Cladosporium Bensch K, Braun U, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2012
PMCID:PMC3390897
doi:10.3114/sim0003
PMID:22815589
Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies) Ali SS, Yu Y, Pfosser M, Wetschnig W Ann Bot 27-Oct-2011
PMCID:PMC3241591
doi:10.1093/aob/mcr274
PMID:22039008
POT1-independent single-strand telomeric DNA binding activities in Brassicaceae Shakirov EV, McKnight TD, Shippen DE Plant J 18-Feb-2009
PMCID:PMC5880214
doi:10.1111/j.1365-313X.2009.03837.x
PMID:19228335
Analysis of Carica papaya Telomeres and Telomere-Associated Proteins: Insights into the Evolution of Telomere Maintenance in Brassicales Shakirov EV, Salzberg SL, Alam M, Shippen DE Trop Plant Biol 01-Dec-2008
PMCID:PMC2909770
doi:10.1007/s12042-008-9018-x
PMID:20664721
Biodiversity of the genus Cladophialophora Badali H, Gueidan C, Najafzadeh MJ, Bonifaz A, van den Ende AH, de Hoog GS Stud Mycol 01-Jan-2008
PMCID:PMC2610306
doi:10.3114/sim.2008.61.18
PMID:19287540

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
methyl (E)-3-[(2S,4S,6R,7R,8R,9S,10S,14S,17S,18S,19R)-17-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,9-dihydroxy-18-(hydroxymethyl)-2,8,10,14,18-pentamethyl-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-1(13)-en-7-yl]-2-methylprop-2-enoate 162971288 Click to see CC1C(C(OC2C1(C3(CCC4=C(C3(C2)C)CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)O)C=C(C)C(=O)OC 1003.10 unknown https://doi.org/10.1246/BCSJ.66.1182
methyl (E)-3-[(2S,4S,6R,7R,8R,9S,10S,14S,17S,19R)-17-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,9-dihydroxy-2,8,10,14,18,18-hexamethyl-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-1(13)-en-7-yl]-2-methylprop-2-enoate 162916137 Click to see CC1C(C(OC2C1(C3(CCC4=C(C3(C2)C)CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)O)C=C(C)C(=O)OC 987.10 unknown https://doi.org/10.1246/BCSJ.66.1182
Methyl 3-[17-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,9-dihydroxy-18-(hydroxymethyl)-2,8,10,14,18-pentamethyl-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-1(13)-en-7-yl]-2-methylprop-2-enoate 162971287 Click to see CC1C(C(OC2C1(C3(CCC4=C(C3(C2)C)CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)O)C=C(C)C(=O)OC 1003.10 unknown https://doi.org/10.1246/BCSJ.66.1182
Methyl 3-[17-[3-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,9-dihydroxy-2,8,10,14,18,18-hexamethyl-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-1(13)-en-7-yl]-2-methylprop-2-enoate 162916136 Click to see CC1C(C(OC2C1(C3(CCC4=C(C3(C2)C)CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)O)O)C=C(C)C(=O)OC 987.10 unknown https://doi.org/10.1246/BCSJ.66.1182
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
CID 11029658 11029658 Click to see CC1CC2(CC(C3(O2)CCC4(C3(CCC5=C4CCC6C5(CCC(C6(CO)CO)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC2C(C(C(C(O2)CO)O)O)O)OC2C(C(C(C(O2)C)O)O)O)O)O)O)C)C)C)C)OC1=O 1267.40 unknown https://doi.org/10.1246/CL.1992.1863
CID 85373277 85373277 Click to see CC1CC2(CC(C3(O2)CCC4(C3(CCC5=C4CCC6C5(CCC(C6(CO)CO)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC2C(C(C(C(O2)CO)O)O)O)OC2C(C(C(C(O2)C)O)O)O)O)O)O)C)C)C)C)OC1=O 1267.40 unknown https://doi.org/10.1246/CL.1992.1863
> Organoheterocyclic compounds / Pyrrolidines
(13R)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]tridecane-1,2,7,9,13-pentol 11773821 Click to see C(CCC(CO)O)CC(CC(CCCC(C1C(C(C(N1)CO)O)O)O)O)O 395.50 unknown https://doi.org/10.1021/NP0499721
(2R,3R,4R,5R)-2-(hydroxymethyl)-5-[(2S)-2-hydroxypropyl]pyrrolidine-3,4-diol 162880766 Click to see CC(CC1C(C(C(N1)CO)O)O)O 191.22 unknown https://doi.org/10.1021/NP0499721
(2R,3R,4R,5R)-2-[(1S,2S)-1,2-dihydroxypropyl]-5-(hydroxymethyl)pyrrolidine-3,4-diol 163046460 Click to see CC(C(C1C(C(C(N1)CO)O)O)O)O 207.22 unknown https://doi.org/10.1021/NP0499721
(2R,7S,9R,13R)-13-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]tridecane-1,2,7,9,13-pentol 162851931 Click to see C(CCC(CO)O)CC(CC(CCCC(C1C(C(C(N1)CO)O)O)O)O)O 395.50 unknown https://doi.org/10.1021/NP0499721
13-[3,4-Dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]tridecane-1,2,7,9,13-pentol 73095992 Click to see C(CCC(CO)O)CC(CC(CCCC(C1C(C(C(N1)CO)O)O)O)O)O 395.50 unknown https://doi.org/10.1021/NP0499721
2-(1,2-Dihydroxypropyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol 15953616 Click to see CC(C(C1C(C(C(N1)CO)O)O)O)O 207.22 unknown https://doi.org/10.1021/NP0499721
2-(Hydroxymethyl)-5-(2-hydroxypropyl)pyrrolidine-3,4-diol 85427488 Click to see CC(CC1C(C(C(N1)CO)O)O)O 191.22 unknown https://doi.org/10.1021/NP0499721
alpha-1-C-(1,2-Dihdroxypropyl)-1,4-dideoxy-1,4-imino-D-arabinitol 11183361 Click to see CC(C(C1C(C(C(N1)CO)O)O)O)O 207.22 unknown https://doi.org/10.1021/NP0499721
alpha-1-C-(2-Hydroxypropyl)-1,4-dideoxy-1,4-imino-D-arabinitol 11183118 Click to see CC(CC1C(C(C(N1)CO)O)O)O 191.22 unknown https://doi.org/10.1021/NP0499721
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2R,3R,5R,7R,8R)-5-[(3S)-3-hydroxybutyl]-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 163018419 Click to see CC(CCC1CC(C2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
(1R,2R,3R,5S,8R)-5-(3-hydroxybutyl)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 16737241 Click to see CC(CCC1CCC2N1C(C(C2O)O)CO)O 245.32 unknown https://doi.org/10.1021/NP0499721
(1S,2R,3R,5S,8R)-5-[(1R,3S)-1,3-dihydroxybutyl]-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 163185024 Click to see CC(CC(C1CCC2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
(1S,2R,3R,5S,8R)-5-[(3S)-3-hydroxybutyl]-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 163194900 Click to see CC(CCC1CCC2N1C(C(C2O)O)CO)O 245.32 unknown https://doi.org/10.1021/NP0499721
(2R,4R)-4-[(3S,5R,6R,7S,8R)-6,7-dihydroxy-5-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-3-yl]butane-1,2,4-triol 163044133 Click to see C1CC(N2C1C(C(C2CO)O)O)C(CC(CO)O)O 277.31 unknown https://doi.org/10.1021/NP0499721
3-(Hydroxymethyl)-1,2,7-trihydroxypyrrolizidine 72360 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown https://doi.org/10.1021/NP0499721
4-[6,7-dihydroxy-5-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-3-yl]butane-1,2,4-triol 72978987 Click to see C1CC(N2C1C(C(C2CO)O)O)C(CC(CO)O)O 277.31 unknown https://doi.org/10.1021/NP0499721
5-(1,3-dihydroxybutyl)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 73699058 Click to see CC(CC(C1CCC2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
5-(3-hydroxybutyl)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2-diol 72770762 Click to see CC(CCC1CCC2N1C(C(C2O)O)CO)O 245.32 unknown https://doi.org/10.1021/NP0499721
5-(3-hydroxybutyl)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 72770901 Click to see CC(CCC1CC(C2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
alpha-5-C-(1,3-Dihydroxybutyl)hyacinthacine A1 10355288 Click to see CC(CC(C1CCC2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
alpha-5-C-(1,3,4-Trihydroxybutyl)hyacinthacine A1 11482798 Click to see C1CC(N2C1C(C(C2CO)O)O)C(CC(CO)O)O 277.31 unknown https://doi.org/10.1021/NP0499721
alpha-5-C-(3-Hydroxybutyl)-7-epi-australine 11254004 Click to see CC(CCC1CC(C2N1C(C(C2O)O)CO)O)O 261.31 unknown https://doi.org/10.1021/NP0499721
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-[[3,4-Dihydroxy-5-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]oxolan-3-yl]methoxy]-8-methoxy-3-(4-methoxyphenyl)chromen-4-one 163012475 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3OC)OCC4(COC(C4O)OCC5C(C(C(C(O5)O)O)O)O)O 592.50 unknown https://doi.org/10.1246/BCSJ.66.1182
https://doi.org/10.1246/CL.1992.1999

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