Nauclea orientalis - Unknown
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Internal ID UUID643fe419e74d4275680413
Scientific name Nauclea orientalis
Authority L.
First published in Sp. Pl. ed. 2 : 243 (1762)

Description Top

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Nauclea orientalis is a species of tree in the family Rubiaceae, native to Southeast Asia, New Guinea, and Australia. It has many common names, including bur tree, canary wood, Leichhardt pine and yellow cheesewood. It grows to a maximum of around 30 m (98 ft) in height and has large glossy leaves. It bears spherical clusters of fragrant flowers that develop into golf ball-sized edible but bitter fruits. The yellowish to orange soft wood is also used for timber and in woodcarving and folk medicine. It is known by many common names, including Leichhardt tree, cheesewood, yellow cheesewood, and canary cheesewood. It is also sometimes known as the Leichhardt pine due to the overall shape of the tree, though it is not a conifer. It is closely related and sometimes confused with the bongkol or bulubangkal tree (Nauclea subdita). The bark surface of Liechhardt trees are grayish to reddish brown and may be smooth or fissured and flaky. The small fragrant flowers are tubular and are yellowish to orange with white stamens. They are grouped into

Synonyms Top

Scientific name Authority First published in
Nauclea annamensis Merr. J. Washington Acad. Sci. 5: 535 (1915)
Nauclea coadunata Roxb. ex Sm. Cycl. 24: n.º 6 (1813)
Nauclea cordata Roxb. Fl. Ind. 2: 118 (1824)
Nauclea elmeri Merr. J. Washington Acad. Sci. 5: 535 (1915)
Nauclea glaberrima Bartl. ex DC. Prodr. 4: 344 (1830)
Nauclea leichhardtii F.Muell. Essay Pl. Burdekin 12. 1860 (1860)
Nauclea lutea Blanco Fl. Filip. : 141 (1837)
Nauclea macrophylla Blume Bijdr. Fl. Ned. Ind. 16: 1010. [Oct 1826-Nov 1827]
Nauclea ovoidea (Pierre ex Pit.) N.N.Tran J. Biol. (Vietnam) 1(3): 24 (1979)
Nauclea roxburghii G.Don Gen. Hist. 3: 469 (1834)
Nauclea undulata Roxb. Fl. Ind. 2: 117 (1824)
Platanocarpum cordatum Korth. Observ. Naucl. Indic. : 19 (1839)
Sarcocephalus annamensis Dubard & Eberhardt Bull. Mus. Natl. Hist. Nat. 15: 493 (1909)
Sarcocephalus buruensis Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 179 (1869)
Sarcocephalus coadunatus Druce Bot. Soc. Exch. Club Brit. Isles 4: 644 (1917)
Sarcocephalus cordatus Miq. Fl. Ned. Ind. 2: 133 (1856)
Sarcocephalus glaberrimus Miq. Fl. Ned. Ind. 2: 134 (1856)
Sarcocephalus orientalis Merr. Philipp. J. Sci., C 3: 436 (1909)
Sarcocephalus ovatus Elmer Leafl. Philipp. Bot. 1: 33 (1906)
Sarcocephalus ovatus var. mollis Koord. & Valeton Atlas Baumart. Java 8: 15. 1906
Sarcocephalus ovoideus Pierre ex Pit. Fl. Indo-Chine 3: 28 (1922)
Sarcocephalus papagola Domin Biblioth. Bot. 22(89): 614 (1929)
Sarcocephalus undulatus Miq. Fl. Ned. Ind. 2: 133 (1856)
Sarcocephalus undulatus var. buruensis (Miq.) Havil. J. Linn. Soc., Bot. 33: 29. 1897
Bancalus grandifolius Kuntze Revis. Gen. Pl. 1: 276 (1891)
Bancalus orientalis Kuntze Revis. Gen. Pl. 1: 276 (1891)
Sarcocephalus cordatus var. pubescens Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 46: 125. 1877
Sarcocephalus cordatus var. glabra Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 46: 125. 1877
Nauclea orientalis var. pubescens (Kurz) Craib Fl. Siam. 2: 7 1932
Cadamba nocturna Buch.-Ham. Trans. Linn. Soc. London 15: 93 (1827)
Adina orientalis Lindm. ex Bakh.f. Taxon 19: 476 (1970)
Cephalanthus orientalis L. Sp. Pl. : 95 (1753)

Common names Top

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Language Common/alternative name
English canary cheesewood
English leichhardt tree
English yellow cheesewood
bcl mambog(kahoy)
Japanese バンカル
jv gempol
Malayalam റോസ്കടമ്പ്
Malayalam leichhardt tree
Malayalam yellow cheesewood
Malayalam കതമമരം
Malayalam നൗക്ലിയ ഓറിയെന്റലിസ്
Malayalam യെല്ലോ ചീസ്വുഡ്
Malayalam നീർക്കടമ്പ്
Burmese မအူပင်
Russian Науклея восточная
su gempol
Vietnamese gáo vàng
Vietnamese sarcocephalus papagola
Vietnamese sarcocephalus ovoideus
Vietnamese sarcocephalus ovatus var. mollis
Vietnamese sarcocephalus ovatus
Vietnamese sarcocephalus cordatus var.pubescens
Vietnamese sarcocephalus cordatus
Vietnamese sarcocephalus buruensis
Vietnamese sarcocephalus annamensis
Vietnamese nauclea macrophylla
Vietnamese nauclea elmeri
Vietnamese nauclea cordata
Vietnamese mitragyna parvifolia var.microphylla
Vietnamese bancalus orientalis
Vietnamese sarcocephalus glaberrimus
Vietnamese nauclea roxburghii

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000249611
Tropicos 27900130
KEW urn:lsid:ipni.org:names:757181-1
The Plant List kew-133249
Open Tree Of Life 559729
NCBI Taxonomy 43526
IUCN Red List 61958275
IPNI 757181-1
iNaturalist 370103
GBIF 5339133
Freebase /m/0gmchlb
EOL 1104522
USDA GRIN 25081
Wikipedia Nauclea_orientalis

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
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
Laboratory simulation of the swampy forest system for the passive treatment of acid mine drainage in coal mine reclamation areas Noor I, Arifin YF, Priatmadi BJ, Saidy AR Sci Rep 13-Apr-2023
PMCID:PMC10102076
doi:10.1038/s41598-023-32990-x
PMID:37055534
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Yellow Twig (Nauclea orientalis) from Thailand: Strictosamide as the Key Alkaloid of This Plant Species Songoen W, Brunmair J, Traxler F, Wieser VC, Phanchai W, Pluempanupat W, Brecker L, Schinnerl J Molecules 14-Aug-2022
PMCID:PMC9414341
doi:10.3390/molecules27165176
PMID:36014416
Aboriginal medicinal plants of Queensland: ethnopharmacological uses, species diversity, and biodiscovery pathways Turpin G, Ritmejerytė E, Jamie J, Crayn D, Wangchuk P J Ethnobiol Ethnomed 10-Aug-2022
PMCID:PMC9364609
doi:10.1186/s13002-022-00552-6
PMID:35948982
Indigenous Uses, Phytochemical Analysis, and Anti-Inflammatory Properties of Australian Tropical Medicinal Plants Yeshi K, Turpin G, Jamtsho T, Wangchuk P Molecules 15-Jun-2022
PMCID:PMC9231311
doi:10.3390/molecules27123849
PMID:35744969
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Nauclea orientalis (L.) Bark Extract Protects Rat Cardiomyocytes from Doxorubicin-Induced Oxidative Stress, Inflammation, Apoptosis, and DNA Fragmentation Sandamali JA, Hewawasam RP, Jayatilaka KA, Mudduwa LK Oxid Med Cell Longev 14-Feb-2022
PMCID:PMC8860544
doi:10.1155/2022/1714841
PMID:35198093
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Ethnobotanical Documentation of Medicinal Plants Used by the Indigenous Panay Bukidnon in Lambunao, Iloilo, Philippines Cordero CS, Meve U, Alejandro GJ Front Pharmacol 10-Jan-2022
PMCID:PMC8784692
doi:10.3389/fphar.2021.790567
PMID:35082673
Bioactive small-molecule constituents of Lao plants Ren Y, Elkington BG, Henkin JM, Sydara K, Kinghorn AD, Soejarto DD J Med Plant Res 31-Dec-2021
PMCID:PMC8849567
doi:10.5897/jmpr2021.7137
PMID:35178192
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Which Plants for What Ailments: A Quantitative Analysis of Medicinal Ethnobotany of Ile-Ife, Osun State, Southwestern Nigeria Mukaila YO, Oladipo OT, Ogunlowo I, Ajao AA, Sabiu S Evid Based Complement Alternat Med 03-Aug-2021
PMCID:PMC8355999
doi:10.1155/2021/5711547
PMID:34394387
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective Omar F, Tareq AM, Alqahtani AM, Dhama K, Sayeed MA, Emran TB, Simal-Gandara J Molecules 15-Apr-2021
PMCID:PMC8071433
doi:10.3390/molecules26082297
PMID:33921093
The use of antimalarial plants as traditional treatment in Papua Island, Indonesia Budiarti M, Maruzy A, Mujahid R, Sari AN, Jokopriyambodo W, Widayat T, Wahyono S Heliyon 14-Dec-2020
PMCID:PMC7736719
doi:10.1016/j.heliyon.2020.e05562
PMID:33344788

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 / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
Glyceryl Monostearate 24699 Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(CO)O 358.60 unknown https://doi.org/10.3987/COM-98-S12
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.3987/COM-98-S12
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.3987/COM-98-S12
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.3987/COM-98-S12
> 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/10.1021/NP0498612
https://doi.org/10.1021/NP010042G
https://doi.org/10.3987/COM-98-S12
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3987/COM-98-S12
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP010042G
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/10.1021/NP010042G
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/10.1021/NP010042G
https://doi.org/10.1021/NP0498612
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4R,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(3,4,5-trimethoxyphenyl)methyl]oxane-3,4,5-triol 163053204 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 476.50 unknown https://doi.org/10.1021/NP010042G
19-Ethenyl-18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),4,6,8,15-pentaene-10,14-dione 14440700 Click to see C=CC1C2CC3C4=C(CN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP0498612
https://doi.org/10.1021/NP010042G
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(3,4,5-trimethoxyphenyl)methyl]oxane-3,4,5-triol 163053203 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 476.50 unknown https://doi.org/10.1021/NP010042G
Pumiloside 10346314 Click to see C=CC1C2CC3C4=C(CN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP010042G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Kelampayoside A 10552637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1021/NP010042G
https://doi.org/10.1021/NP0498612
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(18R,19R,20S)-19-ethenyl-16-hydroxy-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15-hexaen-14-one 10052120 Click to see C=CC1C2C=C3C4=C(CCN3C(=O)C2=C(OC1OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP0498612
https://doi.org/10.1021/NP010042G
(18R,19S,20S)-19-ethenyl-16-hydroxy-18-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15-hexaen-14-one 162949796 Click to see C=CC1C2C=C3C4=C(CCN3C(=O)C2=C(OC1OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP010042G
(19E)-19-ethylidene-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 5315222 Click to see CC=C1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1055/S-2006-960052
https://doi.org/10.1021/NP010042G
(1R,18S,19S,20S)-19-ethenyl-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 159304056 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP010042G
(1S,18S,19S,20S)-19-ethenyl-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 159304057 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP010042G
(1S,18S,19S)-19-ethenyl-16-hydroxy-18-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,20-hexaen-14-one 163100069 Click to see C=CC1C(OC(=C2C1=CC3C4=C(CCN3C2=O)C5=CC=CC=C5N4)O)OC6C(C(C(C(O6)CO)O)O)O 512.50 unknown https://doi.org/10.1021/NP010042G
(1S,20S)-19-ethenyl-18-[(2S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15-pentaen-14-one 137795339 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1055/S-2006-960052
https://doi.org/10.1021/NP0498612
(E)-2-[(2R,3Z,12bR)-3-(hydroxymethylidene)-4-oxo-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizin-2-yl]but-2-enal 163193685 Click to see CC=C(C=O)C1CC2C3=C(CCN2C(=O)C1=CO)C4=CC=CC=C4N3 336.40 unknown https://doi.org/10.1016/J.FITOTE.2010.05.004
(Z)-2-[(2R,3Z,12bR)-3-(hydroxymethylidene)-4-oxo-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizin-2-yl]but-2-enal 163193684 Click to see CC=C(C=O)C1CC2C3=C(CCN2C(=O)C1=CO)C4=CC=CC=C4N3 336.40 unknown https://doi.org/10.1016/J.FITOTE.2010.05.004
10-Hydroxystrictosamide 70675008 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=C(N4)C=CC(=C6)O 514.50 unknown https://doi.org/10.3987/COM-98-S12
https://doi.org/10.1055/S-2006-960052
11,12-dihydro-3H-yohimban-14-one 5320031 Click to see C1CN2C(=CC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4 286.30 unknown https://doi.org/10.1055/S-2006-961387
19-Ethenyl-7-hydroxy-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15(20),16,18-octaen-14-one 5318147 Click to see C=CC1=CN=CC2=C1C=C3C4=C(CCN3C2=O)C5=C(N4)C=CC(=C5)O 329.40 unknown https://doi.org/10.1055/S-2006-961387
2-[3-(Hydroxymethylidene)-4-oxo-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizin-2-yl]but-2-enal 162914631 Click to see CC=C(C=O)C1CC2C3=C(CCN2C(=O)C1=CO)C4=CC=CC=C4N3 336.40 unknown https://doi.org/10.1016/J.FITOTE.2010.05.004
3-epi-Vincosamide; Isovincoside lactam; Strictosidine lactam 5015264 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP010042G
3-hydroxy-2-(1-hydroxyethyl)-7,12-dihydro-6H-indolo[2,3-a]quinolizin-4-one 10379817 Click to see CC(C1=C(C(=O)N2CCC3=C(C2=C1)NC4=CC=CC=C34)O)O 296.32 unknown https://doi.org/10.1021/NP010042G
https://doi.org/10.1021/NP0498612
3-hydroxy-2-[(1R)-1-hydroxyethyl]-7,12-dihydro-6H-indolo[2,3-a]quinolizin-4-one 5326050 Click to see CC(C1=C(C(=O)N2CCC3=C(C2=C1)NC4=CC=CC=C34)O)O 296.32 unknown https://doi.org/10.1021/NP010042G
Angustine 441983 Click to see C=CC1=CN=CC2=C1C=C3C4=C(CCN3C2=O)C5=CC=CC=C5N4 313.40 unknown https://doi.org/10.1055/S-2006-961387
https://doi.org/10.1016/S0031-9422(00)91432-8
Angustoline 3084765 Click to see CC(C1=C2C=C3C4=C(CCN3C(=O)C2=CN=C1)C5=CC=CC=C5N4)O 331.40 unknown https://doi.org/10.1055/S-2006-961387
Carboline metabolite (C26H28N2O9) 85104227 Click to see C=CC1C2C=C3C4=C(CCN3C(=O)C2=C(OC1OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP010042G
nauclealine A 5324480 Click to see C=CC1=COC(=O)C2=C1C=C3C4=C(CCN3C2=O)C5=CC=CC=C5N4 330.30 unknown https://doi.org/10.1021/NP0498612
https://doi.org/10.1021/NP010042G
Naucleoside B 10369140 Click to see C=CC1C(OC(=C2C1=CC3C4=C(CCN3C2=O)C5=CC=CC=C5N4)O)OC6C(C(C(C(O6)CO)O)O)O 512.50 unknown https://doi.org/10.1021/NP0498612
Parvine 320217 Click to see C1CN2C(=CC3=C(C2=O)C=NC=C3)C4=C1C5=CC=CC=C5N4 287.30 unknown https://doi.org/10.1055/S-2006-961387
Strictosamide 10345799 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP0498612
https://doi.org/10.1055/S-2006-960052
https://doi.org/10.1021/NP010042G
https://doi.org/10.3987/COM-98-S12
Vincosamide 10163855 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP010042G
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(1S,18S,19S,20S)-19-ethenyl-18-[(2S,3R,4S,5S,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),4,6,8,15-pentaene-10,14-dione 161074405 Click to see C=CC1C2CC3C4=C(CN3C(=O)C2=COC1OC5C(C(C(C(O5)O)O)O)O)C(=O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP010042G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.3987/COM-98-S12

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