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Turnera ulmifolia

Turnera ulmifolia - 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 UUID643ffeef11c43398958258
Scientific name Turnera ulmifolia
Authority L.
First published in Sp. Pl. : 271 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Waltheria terminalis Vell. Fl. Flumin. : 275 (1829)
Turnera surinamensis Miq. Linnaea 18: 748 (1845)
Turnera corchoroides Klotzsch Reis. Br.-Guiana 3: 1166 (1849)
Turnera obtusifolia Sm. Cycl. 36: n.º 3 (1817)
Turnera alba Liebm. Ann. Sci. Nat., Bot. , sér. 3, 9: 318 (1848)
Turnera virgata Willd. ex Schult. Syst. Veg., ed. 15 bis 6: 678 (1820)
Turnera ulmifolia var. alba (Liebm.) Rose Contr. U.S. Natl. Herb. 5: 166. 1899

Common names Top

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Language Common/alternative name
English ramgoat dashalong
English yellow alder
Bengali বাসন্তী
Persian توسکای زرد
Indonesian bunga pukul delapan
Japanese ターネラ・ウルミフォリア
Malayalam ചെരവത്താലി
Malay lidah kucing
Vietnamese Đông hầu vàng
Chinese 时钟花
Chinese 黃時鐘花

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Western Indian Ocean
      • Aldabra
      • Chagos Archipelago
      • Comoros
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Malaya
      • Sumatera
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
      • Louisiana
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
    • South-central Pacific
      • Line Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
  • Southern America
    • Brazil
      • Brazil West-central
    • Caribbean
      • Bahamas
      • Bermuda
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Windward Islands
    • Central America
      • Belize
      • Central American Pacific
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000457708
Florida Plant Atlas 1809
USDA Plants TUUL
Tropicos 33100002
INPN 448524
KEW urn:lsid:ipni.org:names:836702-1
The Plant List kew-2518584
Open Tree Of Life 762467
Observations.org 198968
NCBI Taxonomy 45184
Nature Serve 2.139360
IUCN Red List 131292920
IPNI 836702-1
iNaturalist 170055
GBIF 2874852
Freebase /m/04f2b5m
EPPO TURUL
EOL 484396
Elurikkus 323030
USDA GRIN 40781
Wikipedia Turnera_ulmifolia
CMAUP NPO2339

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
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Seasonal dynamics of Amblyomma cajennense (Fabricius, 1787) sensu stricto in a degraded area of the Amazon biome, with notes on Rickettsia amblyommatis infection de Araújo FE, Martins TF, Ramos CC, Nogueira RM, Faccini JL, Tavares MA, de Lima NJ, de Almeida Júnior EB, de Sousa-Paula LC, Dantas-Torres F, da Silva Krawczak F, Costa-Junior LM, Labruna MB, Dall′Agnol LT, Luz HR Parasit Vectors 27-Oct-2023
PMCID:PMC10612284
doi:10.1186/s13071-023-05978-9
PMID:37891604
Seed morphology and germination of <Turnera diffusa> Willd. ex Schult. emulating environmental conditions within ant nest Puga-Guzmán PS, Magallán-Hernández F, Queijeiro-Bolaños M, Valencia-Hernández JA, Vergara-Pineda S PLoS One 20-Oct-2023
PMCID:PMC10588869
doi:10.1371/journal.pone.0292626
PMID:37862298
Assembly and Comparative Analysis of the Complete Mitochondrial Genome of Two Species of Calla Lilies (Zantedeschia, Araceae) Guo Y, Li Z, Jin S, Chen S, Li F, Wu H Int J Mol Sci 31-May-2023
PMCID:PMC10254018
doi:10.3390/ijms24119566
PMID:37298515
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
MRSA compendium of epidemiology, transmission, pathophysiology, treatment, and prevention within one health framework Shoaib M, Aqib AI, Muzammil I, Majeed N, Bhutta ZA, Kulyar MF, Fatima M, Zaheer CN, Muneer A, Murtaza M, Kashif M, Shafqat F, Pu W Front Microbiol 10-Jan-2023
PMCID:PMC9871788
doi:10.3389/fmicb.2022.1067284
PMID:36704547
Diverse mating consequences of the evolutionary breakdown of the sexual polymorphism heterostyly Yuan S, Zeng G, Zhang K, Wu M, Zhang D, Harder LD, Barrett SC Proc Natl Acad Sci U S A 03-Jan-2023
PMCID:PMC9926269
doi:10.1073/pnas.2214492120
PMID:36595698
Functional silver nanoparticles synthesis from sustainable point of view: 2000 to 2023 ‒ A review on game changing materials Hasan KM, Xiaoyi L, Shaoqin Z, Horváth PG, Bak M, Bejó L, Sipos G, Alpár T Heliyon 10-Dec-2022
PMCID:PMC9800342
doi:10.1016/j.heliyon.2022.e12322
PMID:36590481
Synergistic Role of Plant Extracts and Essential Oils against Multidrug Resistance and Gram-Negative Bacterial Strains Producing Extended-Spectrum β-Lactamases Alam M, Bano N, Ahmad T, Sharangi AB, Upadhyay TK, Alraey Y, Alabdallah NM, Rauf MA, Saeed M Antibiotics (Basel) 26-Jun-2022
PMCID:PMC9312036
doi:10.3390/antibiotics11070855
PMID:35884109
Report of Tuckerella pavoniformis (Acari: Tuckerellidae) on Mamey, Mammea americana (Calophyllaceae), in Northwestern Peru Escobar-Garcia HA, Beard JJ, Ochoa R Insects 18-May-2022
PMCID:PMC9146881
doi:10.3390/insects13050473
PMID:35621807
Emerging Anthelmintic Resistance in Poultry: Can Ethnopharmacological Approaches Offer a Solution? Zirintunda G, Biryomumaisho S, Kasozi KI, Batiha GE, Kateregga J, Vudriko P, Nalule S, Olila D, Kajoba M, Matama K, Kwizera MR, Ghoneim MM, Abdelhamid M, Zaghlool SS, Alshehri S, Abdelgawad MA, Acai-Okwee J Front Pharmacol 14-Feb-2022
PMCID:PMC8883056
doi:10.3389/fphar.2021.774896
PMID:35237147
Green Biosynthesis, Antioxidant, Antibacterial, and Anticancer Activities of Silver Nanoparticles of Luffa acutangula Leaf Extract Nallappan D, Fauzi AN, Krishna BS, Kumar BP, Reddy AV, Syed T, Reddy CS, Yaacob NS, Rao PV Biomed Res Int 29-Sep-2021
PMCID:PMC8494549
doi:10.1155/2021/5125681
PMID:34631882
The Use of SPME-GC-MS IR and Raman Techniques for Botanical and Geographical Authentication and Detection of Adulteration of Honey Sotiropoulou NS, Xagoraris M, Revelou PK, Kaparakou E, Kanakis C, Pappas C, Tarantilis P Foods 20-Jul-2021
PMCID:PMC8303172
doi:10.3390/foods10071671
PMID:34359541
The role of schools as an opportunity for transmission of local knowledge about useful Restinga plants: experiences in southeastern Brazil van Luijk N, Soldati GT, da Fonseca-Kruel VS J Ethnobiol Ethnomed 17-May-2021
PMCID:PMC8130333
doi:10.1186/s13002-021-00461-0
PMID:34001189
Ongoing ecological and evolutionary consequences by the presence of transgenes in a wild cotton population Vázquez-Barrios V, Boege K, Sosa-Fuentes TG, Rojas P, Wegier A Sci Rep 21-Jan-2021
PMCID:PMC7820435
doi:10.1038/s41598-021-81567-z
PMID:33479296

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
4-Amino-3-methoxyphenol 19818056 Click to see COC1=C(C=CC(=C1)O)N 139.15 unknown via CMAUP database
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(-)-leukotoxin B 5281128 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)80030-5
(9Z)-(12S,13R)-12,13-Epoxyoctadecenoic acid 6449780 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)80030-5
(Z)-11-[(2R,3R)-3-pentyloxiran-2-yl]undec-9-enoic acid 40491783 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)80030-5
11-(3-Pentyloxiran-2-yl)undec-9-enoic acid 1416 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Malvalic acid 10416 Click to see CCCCCCCCC1=C(C1)CCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/0031-9422(91)80030-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown https://doi.org/10.1016/0031-9422(91)80030-5
Sterculic acid 12921 Click to see CCCCCCCCC1=C(C1)CCCCCCCC(=O)O 294.50 unknown https://doi.org/10.1016/0031-9422(91)80030-5
> 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 https://doi.org/10.1016/0031-9422(91)80030-5
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
(6'S)-beta,epsilon-carotene 6419724 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Tigogenin 99516 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(1R,2S,4S,6R,7S,8R,9S,10R,12S,13R,16S)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-10,16-diol 46833330 Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCCCO6 416.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Physalins and derivatives
(1R,2R,4R,5R,8S,11R,13S,14S,15R,16S,19S,22S,23R,25S)-2,19-dihydroxy-13,16,23-trimethyl-6,10,17,26,27,30-hexaoxanonacyclo[23.2.2.15,14.15,15.01,23.04,22.08,13.011,16.015,19]hentriacont-28-ene-9,18,24,31-tetrone 21633629 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C89C=CC(C(=O)C8(C7CCC6(C(=O)O4)O)C)OO9)O)OCC2C(=O)O3)C 558.50 unknown via CMAUP database
(1R,2S,5S,8S,9R,15S,17R,18R,21S,24R,26S,27S)-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacosa-11,13-diene-4,10,22,29-tetrone 56683730 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C8=CC=CC(=O)C8(C7CCC6(C(=O)O4)O)C)O)OCC2C(=O)O3)C 526.50 unknown via CMAUP database
(1R,2S,5S,8S,9S,14R,15R,17R,18R,21S,24R,26S,27S)-14-chloro-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.118,27.01,5.02,24.08,17.09,14.021,26]nonacos-11-ene-4,10,22,29-tetrone 10769263 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC(C8(CC=CC(=O)C8(C7CCC6(C(=O)O4)O)C)Cl)O)OCC2C(=O)O3)C 563.00 unknown via CMAUP database
5,6-Epxoyphysalin B 49864133 Click to see CC12CC3C4(C56C1C(=O)C(O5)(C7CC8C9(O8)CC=CC(=O)C9(C7CCC6(C(=O)O4)O)C)OCC2C(=O)O3)C 526.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2S,3'R,4S,6R,7S,8R,9S,10R,12S,13R,16S)-10,16-dihydroxy-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-piperidine]-3'-carboxylic acid 21573758 Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCC(CN6)C(=O)O 459.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573757 Click to see CC1C2C(CC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C)OC16CCC(CN6)CO 445.60 unknown via CMAUP database
(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-10,16-diol 21573755 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C)NC1 429.60 unknown via CMAUP database
N-Methylsolasodine 21573751 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)N(C1)C 427.70 unknown via CMAUP database
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
12-Hydroxysolasonine 21573761 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1 900.10 unknown via CMAUP database
CID 21573759 21573759 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)NC1 721.90 unknown via CMAUP database
Degalactotigonin 162401 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1035.20 unknown via CMAUP database
Nigrumnin I 10820113 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1151.30 unknown via CMAUP database
Nigrumnin II 10630134 Click to see CC1CCC2(C(C3(C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1181.30 unknown via CMAUP database
Solamargine 73611 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 868.10 unknown via CMAUP database
Solanigroside C 16083118 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1=O)O 1111.20 unknown via CMAUP database
Solanigroside D 16083121 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1=O)O 1181.30 unknown via CMAUP database
Solanigroside E 16083119 Click to see CC1CC(C2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(CO2)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1=O)O 1197.30 unknown via CMAUP database
Solanigroside G 16083120 Click to see CC1CCC2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)O)C)OC1 1051.20 unknown via CMAUP database
Solanigroside H 16083123 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)O)C)OC1 1047.20 unknown via CMAUP database
Solasonine 119247 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 884.10 unknown via CMAUP database
Uttronin B 102058012 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Uttroside B 44566638 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1215.30 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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Azaniumylacetate 5257127 Click to see C(C(=O)[O-])[NH3+] 75.07 unknown via CMAUP database
Cyclopent-1-enylglycine 23288545 Click to see C1CC=C(C1)NCC(=O)O 141.17 unknown https://doi.org/10.1016/S0031-9422(00)81104-8
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(1S-trans)-1-(beta-D-Glucopyranosyloxy)-4-hydroxy-2-cyclopentene-1-carbonitrile 15596190 Click to see C1C(C=CC1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 287.27 unknown https://doi.org/10.1016/S0031-9422(00)81104-8
(1S)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclopent-2-ene-1-carbonitrile 15596187 Click to see C1CC(C=C1)(C#N)OC2C(C(C(C(O2)CO)O)O)O 271.27 unknown https://doi.org/10.1016/S0031-9422(00)83836-4
https://doi.org/10.1016/0031-9422(96)00065-9
(S)-1-(beta-D-Glucopyranosyloxy)-2-cyclopentene-1-carbonitrile 56842796 Click to see C1CC(C=C1)(C#N)OC2C(C(C(C(O2)CO)O)O)O 271.27 unknown https://doi.org/10.1016/S0031-9422(00)81104-8
2-(Hexopyranosyloxy)-2-methylpropanenitrile 4457489 Click to see CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 247.24 unknown https://doi.org/10.1016/0031-9422(96)00065-9
Deidaclin 73604 Click to see C1CC(C=C1)(C#N)OC2C(C(C(C(O2)CO)O)O)O 271.27 unknown https://doi.org/10.1016/0031-9422(92)80427-G
https://doi.org/10.1016/S0031-9422(00)81104-8
https://doi.org/10.1016/0031-9422(96)00065-9
Linamarin 11128 Click to see CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 247.24 unknown https://doi.org/10.1016/0031-9422(96)00065-9
Taraktophyllin 184167 Click to see C1C(C=CC1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 287.27 unknown https://doi.org/10.1016/0031-9422(96)00065-9
Tetraphyllin A 435459 Click to see C1CC(C=C1)(C#N)OC2C(C(C(C(O2)CO)O)O)O 271.27 unknown https://doi.org/10.1016/S0031-9422(00)83836-4
https://doi.org/10.1016/S0031-9422(00)81104-8
https://doi.org/10.1016/0031-9422(96)00065-9
Tetraphyllin B 115164 Click to see C1C(C=CC1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 287.27 unknown https://doi.org/10.1016/S0031-9422(00)81104-8
https://doi.org/10.1016/0031-9422(96)00065-9
Volkenin 181811 Click to see C1C(C=CC1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 287.27 unknown https://doi.org/10.1016/S0031-9422(00)81104-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Ethyl 4-O-(3-O-methyl-6-deoxy-beta-D-glucopyranosyl)-3-O-methyl-2,6-dideoxy-alpha-D-glucopyranoside 101490302 Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC 350.40 unknown via CMAUP database
Ethyl 4-O-(3-O-methyl-6-deoxy-beta-D-glucopyranosyl)-3-O-methyl-2,6-dideoxy-beta-D-glucopyranoside 101490301 Click to see CCOC1CC(C(C(O1)C)OC2C(C(C(C(O2)C)O)OC)O)OC 350.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
2-(1H-Indol-3-yl)ethyl acetate 588705 Click to see CC(=O)OCCC1=CNC2=CC=CC=C21 203.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
4-Hydroxy-3-methoxycinnamic Acid Ethyl Ester 65133 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)OC 222.24 unknown via CMAUP database
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
Methyl 4-hydroxy-3,5-dimethoxycinnamate; Sinapic acid methyl ester 159894 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Petunidin 3-(p-coumaroylrutinoside) 5-glucoside 101243377 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)OC)O)O)O)O)O)O)O)OC(=O)C=CC7=CC=C(C=C7)O 933.80 unknown via CMAUP database

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