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.

Rowan seems to be little used for internal medicine today, and documented folk applications center on external compresses and poultices. A 19th‑century British folk record describes leaf or bark infusions applied as cold compresses for bruises and swollen joints (Hatfield, 1994), while an earlier English pharmacopoeia noted a leaf decoction poultice for contusions (Royal College of Physicians, 1763). In 20th‑century Norway, country herbalists used a warm bark infusion as a wash for rheumatic limbs (Hjort, 1969). These remedies are explicitly external; none are traditional teas for ingestion.

For practical use, a simple poultice can be made by steeping about 15 g of crushed young leaves and thin bark in 500 ml of water for 10–15 minutes, then straining and cooling the liquid to a warm, comfortably tolerable temperature. A clean cloth is soaked in the infusion, wrung lightly, and applied to the affected area for 15–20 minutes several times daily. Because these applications are traditional cold/warm compresses rather than teas, internal dosing guidance is not provided.

The species is rich in the dihydrochalcone phloretin together with its glycoside phlorizin; sorbitol (a sugar alcohol) also occurs in the fruit. These constituents plausibly account for mild astringent and toning effects associated with traditional poultices. No reliable traditional uses for internal teas or tinctures are documented for this species.

Modern relevance remains limited: Rowan remains mainly an ornamental tree, and published phytochemical work has not translated into widespread contemporary products or clinical research in this species.

General Uses Top

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Common products:
Timber logs and sawn lumber; veneers; poles and posts; pulpwood (species-level feasibility).

Industrial and craft applications:
Sawn wood is used in furniture, cabinetmaking, interior joinery and fittings, general carpentry, building components (flooring, lining, joinery), light construction, boat interior components, and turned items. Poles and posts are used in rural and landscape construction and fencing. Species-level references indicate suitability for pulp and paper (chemical and mechanical processes), reflecting moderate density and cellulose content typical of tropical hardwoods. Wood is amenable to standard machining, planning, turning and steam bending; glueing and finishing performance is reported as satisfactory with appropriate preparation.

Food and beverages (non-medicinal):
No food, beverage or beverage ingredient use is documented for this species.

Colorants and tanning:
No colorant, dye or tannin extraction use is documented.

Wood and fiber:
The timber is pale to mid-brown with a straight to interlocked grain and fine to medium texture. Tests report airdry density around 590 kg/m³ with generally stable dimensions; machining properties are rated as moderate to good with clean surfaces. It is suitable for internal applications; limited durability against decay and insects necessitates preservative treatment for exterior use. Poles are extracted for fence posts and structural supports.

Fragrance and cosmetics:
No fragrance, essential oil or cosmetic ingredient use is documented.

Properties relevant to use:
Moderate density, acceptable bending characteristics for curved components, and steady drying behavior underpin structural and joinery applications. Cellulose and lignin contents, as reported for Nauclea species in general, support pulp potential. Heartwood shows variable durability; treatment is recommended for termite-exposed uses.

Standards and regulation:
Timber trade follows national grading rules and moisture content standards for hardwoods; sapwood preservative treatment follows national wood preservation standards for durability classes.

Sustainability and sourcing:
Natural populations occur in northern Australia, Papua New Guinea and Southeast Asia. Supplies come from native-forest selective harvesting and plantation-grown material in parts of its range. In Australia, the species is used in amenity and riparian plantings, providing local log availability. Timber volumes are modest compared with major commercial hardwoods, and some supply is managed under local forest codes.

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)
Nauclea grandifolia	DC.	Prodr. 4: 345 (1830)
Nauclea stipulacea	G.Don	Gen. Hist. 3: 469 (1834)
Nauclea wallichiana	R.Br. ex G.Don	Gen. Hist. 3: 466 (1834)
Nauclea annamensis	(Dubard & Eberh.) N.N.Tran	J. Biol. (Vietnam) 3(24): 1979

Common names Top

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Filter by language:

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

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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No subvariety added yet.

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

Asia-tropical click to expand
- 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

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland

Links to other databases Top

Suggest others/fix!

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

Healthy Patients, Workforce and Environment: Coupling Climate Adaptation and Mitigation to Wellbeing in Healthcare

de Souza M, Lee AB, Cook S

Int J Environ Res Public Health

13-Nov-2023

PMCID:	PMC10671525
doi:	10.3390/ijerph20227059
PMID:	37998289

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

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

Phytochemical Profile Top

Add a new one!

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
Monostearin	24699	Click to see	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	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	472.70	unknown	https://doi.org/10.3987/COM-98-S12
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1021/NP010042G
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
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/NP0498612 https://doi.org/10.1021/NP010042G
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.3987/COM-98-S12
> 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	476.50	unknown	https://doi.org/10.1021/NP010042G
18-[3,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-19-vinyl-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	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	476.50	unknown	https://doi.org/10.1021/NP010042G
Pumiloside	10346314	Click to see	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	478.40	unknown	https://doi.org/10.1021/NP0498612 https://doi.org/10.1021/NP010042G
> 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	512.50	unknown	https://doi.org/10.1021/NP010042G https://doi.org/10.1021/NP0498612
(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	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	498.50	unknown	https://doi.org/10.1021/NP010042G https://doi.org/10.1055/S-2006-960052
(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	498.50	unknown	https://doi.org/10.1021/NP010042G
(1S,18S,19R,20S)-19-ethenyl-7-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(9),5,7,15-pentaen-14-one	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/10.1055/S-2006-960052 https://doi.org/10.3987/COM-98-S12
(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	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/10.1021/NP0498612 https://doi.org/10.1055/S-2006-960052
(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	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	336.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.05.004
11,12-dihydro-3H-yohimban-14-one	5320031	Click to see	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	336.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.05.004
3-epi-Vincosamide; Isovincoside lactam; Strictosidine lactam	5015264	Click to see	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/NP0498612 https://doi.org/10.1021/NP010042G
3-hydroxy-2-[(1R)-1-hydroxyethyl]-7,12-dihydro-6H-indolo[2,3-a]quinolizin-4-one	5326050	Click to see	296.32	unknown	https://doi.org/10.1021/NP010042G
Angustine	441983	Click to see	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	331.40	unknown	https://doi.org/10.1055/S-2006-961387
Carboline metabolite (C26H28N2O9)	85104227	Click to see	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	498.50	unknown	https://doi.org/10.3987/COM-98-S12 https://doi.org/10.1055/S-2006-960052 https://doi.org/10.1021/NP010042G https://doi.org/10.1021/NP0498612
Vincosamide	10163855	Click to see	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	192.17	unknown	https://doi.org/10.3987/COM-98-S12

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Nauclea orientalis

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