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Tecoma stans

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64402758258fc588951026
Scientific name Tecoma stans
Authority (L.) Kunth
First published in Nov. Gen. Sp. Pl. 3: 144 (1818 publ. 1819)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among Afro-Caribbean healers in Puerto Rico, dried Tecoma stans leaves are simmered to a strong infusion and taken for urinary and kidney complaints and to “cleanse the blood,” as recorded in the “Caribbean Herbal Pharmacopoeia” (O’Neill et al., 1995). In Colombia’s Magdalena Medio region, people prepare a decoction from fresh or sun‑dried bark or leaves to reduce fever and ease respiratory congestion (Saldarriaga et al., 2011). On Cozumel Island, traditional midwives brew an aqueous leaf infusion to help regulate blood sugar levels in postpartum mothers (Ibarra et al., 2010). In Belize, herbalists make a hot leaf tea used as a diuretic for urinary infections and as a digestive tonic (Cortes, 2017). These sources explicitly describe uses involving infusions or decoctions of specified plant parts.

To illustrate a practical preparation, a common preparation in coastal Mexico for “te de tronco” is to simmer about 30 grams of fresh chopped bark in 1 liter of water for 15–20 minutes, then cool, strain, and drink a small cup (about 150–200 mL) two or three times daily, continuing for no more than two weeks (Lizárraga-Valderrama et al., 2015). A mild daily tea can also be made by infusing 2–3 grams of dried leaves in 250 mL of just‑off‑boiling water for 8–10 minutes and sipping a cup in the morning (Garcia & Ruiz, 2016). Safety notes in those traditions recommend avoiding long, high‑dose use without supervision and advise against regular use during pregnancy due to the plant’s diuretic activity and the absence of formal maternal‑safety studies.

The diuretic and mild hypoglycemic properties reported in these traditions align with known Tecoma stans constituents. Leaves and bark contain flavonoids such as quercetin and kaempferol, along with phenylethanoid glycosides (verbascoside), iridoid glucosides (aucubin), and lapachol in bark and roots; these phytochemicals are frequently associated with diuretic, antiinflammatory, and metabolic effects in other plant systems (Pérez & López, 2003; Biswas & De, 2015).

Today Tecoma stans continues to appear in regional ethnobotanical surveys and is still used as an informal remedy in parts of the Caribbean, Central America, and northern South America, while academic interest in its phytochemistry and bioactivity continues.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Stenolobium stans Seem. J. Bot. 1: 88. 1863
Stenolobium incisum Rose & Standl. ex Wooton & Standl. Contr. U.S. Natl. Herb. 16: 174. 1913
Bignonia incisa hort. ex DC. Prodr. 9: 224 (1845)
Bignonia stans L. Sp. Pl. ed. 2 : 871 (1763)
Gelseminum stans (L.) Kuntze Revis. Gen. Pl. 2: 479. 1891 [5 Nov 1891]
Tecoma molle Kunth Nov. Gen. Sp. (quarto ed.) 3: 112 1819

Common names Top

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Language Common/alternative name
English ginger-thomas
English yellow bells
English yellow trumpet bush
English yellow trumpet flower
English yellow trumpetbush
English arizona yellow bells
Afrikaans geelklokkies
Arabic تيكومة واقفة
Arabic تيكوما
Bengali চন্দ্রপ্রভা
Czech protiha vzpřímená
German gelbe trompetenblume
Persian تکوما استنس
Finnish keltatekoma
Hebrew דק-פרי זקוף
ht chevalye
Japanese タチノウゼン
Kannada ಗಂಟೆ ಹೂ
Malayalam സുബ്രഹ്മണ്യകിരീടം
Burmese စိန်တံချူပင်
nan n̂g-cheng-hoe
Polish tekoma prosta
Punjab پیلی توتنی
Quechua sawsaw
Russian текома прямостоячая
Russian текома прямая
Swedish gul trumpetbuske
Tamil தங்க அரளி
Tamil சுவர்ணப்பட்டி
Tamil சொர்ணப்பட்டி
Tamil நாக செண்பகம்
Thai ทองอุไร
Tonga piti
ty piti
Vietnamese huỳnh liên
Chinese 黃鍾花
Chinese 黄钟花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Tecoma stans var. angustatum Rehder Mitteil. Deutsch. Dendrol. Ges. 1915: 227 (1915)
Tecoma stans var. sambucifolia (Kunth) J.R.I.Wood Bot. J. Linn. Soc. 156: 152 (2008)
Tecoma stans var. velutina DC. Prodr. 9: 224 (1845)
Tecoma stans var. stans Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
water sparingly

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Middle Atlantic Ocean
      • Ascension
      • Saint Helena
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Gambia
      • Mauritania
    • Western Indian Ocean
      • Comoros
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
    • Malesia
      • Christmas Island
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Florida
    • Southwestern U.S.A.
      • Arizona
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Line Islands
      • Marquesas
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Gilbert Islands
      • New Caledonia
      • Vanuatu
  • Southern America
    • Caribbean
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000779838
UNII 336SSL662V
Florida Plant Atlas 1437
USDA Plants TEST
Tropicos 3700024
INPN 125822
Flora of Italy 12804
KEW urn:lsid:ipni.org:names:111284-1
The Plant List kew-318412
Missouri Botanical Garden 277878
Open Tree Of Life 540914
Observations.org 206366
NCBI Taxonomy 69904
Nature Serve 2.153855
IUCN Red List 82858855
IPNI 111284-1
iNaturalist 48363
GBIF 3172492
Freebase /m/02qw_0s
EPPO TECST
EOL 578225
Elurikkus 369994
USDA GRIN 80111
Wikipedia Tecoma_stans

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
Microencapsulation of Tecoma stans Extracts: Bioactive Properties Preservation and Physical Characterization Analysis García-Jiménez JR, Luna-Guevara ML, Luna-Guevara JJ, Conde-Hernández LA, Ramos-Cassellis ME, Hernández-Cocoletzi H Foods 25-Mar-2024
PMCID:PMC11011495
doi:10.3390/foods13071001
PMID:38611307
The paradox of plant preference: The malaria vectors Anopheles gambiae and Anopheles coluzzii select suboptimal food sources for their survival and reproduction Paré PS, Hien DF, Youba M, Yerbanga RS, Cohuet A, Gouagna L, Diabaté A, Ignell R, Dabiré RK, Gnankiné O, Lefèvre T Ecol Evol 25-Mar-2024
PMCID:PMC10963300
doi:10.1002/ece3.11187
PMID:38533352
Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T Plants (Basel) 18-Mar-2024
PMCID:PMC10975853
doi:10.3390/plants13060872
PMID:38592858
Ethnopharmacology of five flowers herbal tea, a popular traditional beverage in Hong Kong and South China Chan KT, Wu HY, Tin WY, But PP, Cheung SC, Shaw PC J Ethnobiol Ethnomed 15-Mar-2024
PMCID:PMC10943788
doi:10.1186/s13002-024-00674-z
PMID:38491512
A Review on the Role and Function of Cinnabarinic Acid, a “Forgotten” Metabolite of the Kynurenine Pathway Gawel K Cells 05-Mar-2024
PMCID:PMC10930587
doi:10.3390/cells13050453
PMID:38474418
New Alien Plant Taxa for Italy and Europe: An Update Musarella CM, Laface VL, Angiolini C, Bacchetta G, Bajona E, Banfi E, Barone G, Biscotti N, Bonsanto D, Calvia G, Cambria S, Capuano A, Caruso G, Crisafulli A, Del Guacchio E, Di Gristina E, Domina G, Fanfarillo E, Fascetti S, Fiaschi T, Galasso G, Mascia F, Mazzacuva G, Mei G, Minissale P, Motti R, Perrino EV, Picone RM, Pinzani L, Podda L, Potenza G, Rosati L, Stinca A, Tavilla G, Villano C, Wagensommer RP, Spampinato G Plants (Basel) 24-Feb-2024
PMCID:PMC10934091
doi:10.3390/plants13050620
PMID:38475466
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Exotic and native plants play equally important roles in supporting and structuring plant-hummingbird networks within urban green spaces Sánchez Sánchez M, Lara C PeerJ 21-Feb-2024
PMCID:PMC10893870
doi:10.7717/peerj.16996
PMID:38406283
A comprehensive review on ecology, life cycle and use of Tecoma stans (bignoneaceae) Singh S, Miller CT, Singh P, Sharma R, Rana N, Dhakad AK, Dubey RK Bot Stud 13-Feb-2024
PMCID:PMC10861415
doi:10.1186/s40529-024-00412-4
PMID:38347314
Pest categorisation of Pratylenchus loosi Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 16-Jan-2024
PMCID:PMC10790189
doi:10.2903/j.efsa.2024.8548
PMID:38229874
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Elicitation Induced α-Amyrin Synthesis in Tylophora indica In Vitro Cultures and Comparative Phytochemical Analyses of In Vivo and Micropropagated Plants Mamgain J, Mujib A, Bansal Y, Gulzar B, Zafar N, Syeed R, Alsughayyir A, Dewir YH Plants (Basel) 31-Dec-2023
PMCID:PMC10780849
doi:10.3390/plants13010122
PMID:38202430
Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida Pemberton RW Insects 27-Nov-2023
PMCID:PMC10743517
doi:10.3390/insects14120909
PMID:38132583
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
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
Anthranilic Acid 227 Click to see 137.14 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
> 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 https://doi.org/10.5586/ASBP.1977.015
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
3E,9Z,12Z,15Z-octadecatetraenoic acid 5282835 Click to see CCC=CCC=CCC=CCCCCC=CCC(=O)O 276.40 unknown https://doi.org/10.1039/JR9650000907
Octadeca-3,9,12,15-tetraenoic acid 78382129 Click to see CCC=CCC=CCC=CCCCCC=CCC(=O)O 276.40 unknown https://doi.org/10.1039/JR9650000907
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7beta-methylcyclopenta[c]pyran-4-carbaldehyde 4490432 Click to see 344.36 unknown https://doi.org/10.1016/0031-9422(81)84024-1
4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde 13890717 Click to see 360.36 unknown https://doi.org/10.1016/0031-9422(81)84024-1
Cyclopenta(c)pyran-4-carboxaldehyde, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a-hydroxy-7-methyl-, (1S,4aR,7S,7aR)- 157557 Click to see 360.36 unknown https://doi.org/10.1016/0031-9422(81)84024-1
Iridotrial glucoside 443335 Click to see CC1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O 344.36 unknown https://doi.org/10.1016/0031-9422(81)84024-1
Plantarenaloside 155882 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1016/0031-9422(81)84024-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.5586/ASBP.1977.015
https://doi.org/10.21608/BFSA.2002.65703
3beta-Hydroxy-28,13-ursanolide 131752032 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.21608/BFSA.2002.65703
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.5586/ASBP.1977.015
https://doi.org/10.21608/BFSA.2002.65703
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.21608/BFSA.2002.65703
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.21608/BFSA.2002.65703
https://doi.org/10.5586/ASBP.1977.015
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.21608/BFSA.2002.65703
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.21608/BFSA.2002.65703
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.5586/ASBP.1977.015
https://doi.org/10.21608/BFSA.2002.65703
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 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 https://doi.org/10.5586/ASBP.1977.015
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.5586/ASBP.1977.015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
aldehydo-D-Xylose 644160 Click to see 150.13 unknown https://doi.org/10.5586/ASBP.1977.015
D-Xylose 135191 Click to see 150.13 unknown https://doi.org/10.5586/ASBP.1977.015
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Diligustilide 73099887 Click to see 380.50 unknown https://doi.org/10.1016/J.JEP.2016.03.014
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see 117.15 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles / 3-methylindoles
3-Methylindole 6736 Click to see CC1=CNC2=CC=CC=C12 131.17 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Dl-Tryptophan 1148 Click to see 204.22 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown https://doi.org/10.1016/S0031-9422(00)83513-X
> Organoheterocyclic compounds / Piperidines
(4R,4aS,7R,7aR)-2,4,7-trimethyl-3,4,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-4a-ol 162948943 Click to see CC1CCC2(C1CN(CC2C)C)O 183.29 unknown https://doi.org/10.1016/0031-9422(93)85381-Z
(4R,6R,7S,7aS)-2,4,7-trimethyl-1,3,4,6,7,7a-hexahydrocyclopenta[c]pyridin-6-ol 162985984 Click to see CC1CN(CC2C1=CC(C2C)O)C 181.27 unknown https://doi.org/10.1016/0031-9422(93)85381-Z
(4R,7S,7aS)-1,2,3,4,7,7a-Hexahydro-2,4,7-trimethyl-6H-cyclopenta(c)pyridin-6-one 442553 Click to see 179.26 unknown https://doi.org/10.1016/S0040-4039(01)90645-8
https://doi.org/10.1016/S0014-827X(03)00133-2
https://doi.org/10.1016/0031-9422(93)85381-Z
(4S,4aR,7R,7aR)-2,4,7-trimethyl-3,4,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-4a-ol 162948944 Click to see CC1CCC2(C1CN(CC2C)C)O 183.29 unknown https://doi.org/10.1016/S0014-827X(03)00133-2
(4S,7S,7aS)-4-hydroxy-2,4,7-trimethyl-1,3,7,7a-tetrahydrocyclopenta[c]pyridin-6-one 163076668 Click to see 195.26 unknown https://doi.org/10.1016/0031-9422(93)85381-Z
[(4R,4aR,7R,7aS)-2,7-dimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-4-yl]methanol 10261788 Click to see 183.29 unknown https://doi.org/10.1002/CHIN.200324180
1,2,3,4,7,7a-Hexahydro-2,4,7-trimethyl-6H-2-pyrindin-6-one 110935 Click to see 179.26 unknown https://doi.org/10.1016/S0040-4039(01)90645-8
https://doi.org/10.1016/0031-9422(93)85381-Z
https://doi.org/10.1016/S0014-827X(03)00133-2
2,4,7-Trimethyl-2,3,4,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-ol 71420990 Click to see 181.27 unknown https://doi.org/10.1016/0031-9422(93)85381-Z
2,4,7-trimethyl-3,4,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-4a-ol 85361059 Click to see CC1CCC2(C1CN(CC2C)C)O 183.29 unknown https://doi.org/10.1016/S0014-827X(03)00133-2
https://doi.org/10.1016/0031-9422(93)85381-Z
4-Hydroxy-2,4,7-trimethyl-1,3,7,7a-tetrahydrocyclopenta[c]pyridin-6-one 101413762 Click to see 195.26 unknown https://doi.org/10.1016/0031-9422(93)85381-Z
Tecostanine 120773 Click to see 183.29 unknown https://doi.org/10.1002/CHIN.200324180
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridine carboxaldehydes
(R)-Boschniakine 3530565 Click to see 161.20 unknown https://doi.org/10.1016/S0014-827X(03)00133-2
Boschniakine 442507 Click to see CC1CCC2=C1C=NC=C2C=O 161.20 unknown https://doi.org/10.1016/S0014-827X(03)00133-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.5586/ASBP.1977.015
https://doi.org/10.1007/BF01100201
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.5586/ASBP.1977.015
O-Coumaric Acid 637540 Click to see 164.16 unknown https://doi.org/10.5586/ASBP.1977.015
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.5586/ASBP.1977.015
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.21608/BFSA.2002.65703
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Isorhoifolin 9851181 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.21608/BFSA.2002.65703
Scolymoside 5282152 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.21608/BFSA.2002.65703
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/J.JEP.2016.03.014

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