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.

Acronychia pedunculata has been used in a range of traditional preparations that involve infusions, decoctions, tinctures, macerations, and poultices. In the Malay Peninsula, hot bark decoctions were taken for dysentery and fevers, while cold macerations of the bark were used as stomachic tonics (Burkill, 1935). In Vietnam, infusions of the leaves or bark were employed as antidiarrheal and antipyretic remedies (Perry, 1980), and in Northeast India among Assamese communities, leaf infusions were prepared for gastrointestinal complaints and as a mild febrifuge (Shukla et al., 1989). Across this region the most frequent preparations are bark infusions/decoctions, often drank in small cups, and fresh leaf poultices applied to wounds or sore joints (Bennett, 2021).

A practical and gentle preparation is a bark tincture suitable for preserving the plant’s constituents. Roughly chop 1 part dried bark and macerate it in 5 parts 45–50% ethanol, keeping the container sealed and dark for 4–6 weeks with occasional agitation. This yields a hydroalcoholic extract that captures both alkaloids and volatile constituents. Because A. pedunculata contains acronycine and related alkaloids with cytotoxic potential, limit to very small doses of 1–2 drops once daily in water, avoid use during pregnancy and breastfeeding, and do not exceed short courses without qualified supervision (Heinrich, 2019; van Valkenburg, 2001). Store finished tincture away from light and reach out to a qualified practitioner before combining with other medicines.

The plant is notable for quinolone alkaloids such as acronycine, evodiamine, and related tetranortriterpenoids (limonoids), along with flavonoids and essential oils dominated by monoterpenes. These constituents plausibly account for the observed antimicrobial, anti-inflammatory, and antispasmodic activities reported in folk use (Perry, 1980; Heinrich, 2019).

Modern relevance: the quinolone alkaloid acronycine has been studied for antitumor properties and remains a point of interest for pharmacology and drug discovery; standardized essential oil is commercially available, and locally prepared leaf infusions or poultices continue to be used in parts of Southeast Asia and Northeast India (van Valkenburg, 2001; Bennett, 2021).

General Uses Top

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Common products:
Timber (sawn wood, rough planks) for construction and general carpentry; locally also used for flooring, joinery, and light furniture.

Industrial and craft applications:
Processed into solid wood components for interior framing, beams, rafters, and posts; used for flooring and joinery where a moderately heavy hardwood with straight grain is acceptable.

Food and beverages (non-medicinal):
No reported non-medicinal food or beverage uses in reliable sources.

Colorants and tanning:
No documented dye, ink, or tannin uses.

Wood and fiber:
A moderately heavy hardwood with straight to slightly interlocked grain and coarse texture. Used in heavy construction (posts, beams, rafters, planks), flooring, joinery, and furniture where durability and strength are required. Wood is moderately durable under dry conditions.

Fragrance and cosmetics:
No documented essential oil, perfume, or cosmetic applications in reliable sources.

Properties relevant to use:
High density (specific gravity approx. 0.75) and strength; coarse texture; typically straight grain; moderate durability under dry conditions. These properties enable use in structural applications and flooring.

Standards and regulation:
No plant-specific standards or regulatory frameworks identified in reliable sources.

Sustainability and sourcing:
Widely distributed in South and Southeast Asia; often sourced from secondary forest and mixed hardwood stands. No species-specific conservation concerns noted in standard regional timber references.

Synonyms Top

Scientific name	Authority	First published in
Acronychia apiculata	Miq.	Fl. Ned. Ind., Eerste Bijv. : 532 (1861)
Acronychia arborea	Blume	Bijdr. Fl. Ned. Ind. : 244 (1825)
Acronychia barberi	Gamble	Bull. Misc. Inform. Kew 1915: 245 (1915)
Acronychia elliptica	Merr. & L.M.Perry	J. Arnold Arbor. 22: 56 (1941)
Acronychia laurifolia	Blume	Catalogus : 27 (1823)
Acronychia resinosa	Forst. ex Crevost & Lemarié	Cat. Prod. Indochine : 173 (1917)
Clausena simplicifolia	Dalzell	Hooker's J. Bot. Kew Gard. Misc. 3: 180 (1851)
Cyminosma ankenda	Gaertn.	Fruct. Sem. Pl. 1: 280 (1788)
Cyminosma chinensis	G.Don	Gen. Hist. 1: 781 (1831)
Cyminosma pedunculata	(L.) Roxb.	Hort. Bengal. 88 1814
Cyminosma resinosa	DC.	Prodr. 1: 722 (1824)
Doerrienia malabarica	Dennst.	Schlüssel Hortus Malab. : 31 (1818)
Gela lanceolata	Lour.	Fl. Cochinch. : 232 (1790)
Jambolifera pedunculata	L.	Sp. Pl. : 349 (1753)
Cyminosma pedunculata	Roxb.	Prodr. 1: 722 (1824)
Jambolifera rezinosa	Lour.	Fl. Cochinch. 2: 231 1790
Ximenia lanceolata	DC.	Prodr. 1: 533 (1824)
Selas lanceolatum	Spreng.	Syst. Veg. 2: 216 (1825)
Jambolifera arborea	Zoll. & Moritzi	Syst. Verz. Java : 14 (1846)
Laxmannia ankenda	Raeusch.	Nomencl. Bot. [Raeusch.] ed. 3, 99. 1797
Melicope conferta	Blanco
Jambolifera odorata	Lour.	Fl. Cochinch. 231 1790
Acronychia odorata	(Lour.) Baill. ex Crevost & Lemari	Cat. Proc. Indo-Chine 172 1917
Cyminosma odorata	(Lour.) DC.	Prodr. 1: 722 1824
Jambolifera resinosa	Lour.	Fl. Cochinch. : 231 (1790)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	selas lanceolatum
Spanish	acronychia laurifolia
Spanish	acronychia barberi
Spanish	acronychia arborea
Spanish	clausena simplicifolia
Spanish	acronychia elliptica
Spanish	cyminosma ankenda
Spanish	cyminosma chinensis
Spanish	cyminosma pedunculata
Spanish	cyminosma resinosa
Spanish	jambolifera arborea
Spanish	jambolifera resinosa
Spanish	jambolifera rezinosa
Spanish	melicope conferta
Malayalam	വിടുകനലി
Malayalam	വെട്ടുകനല
Malayalam	വെരുകുതീനി
Malayalam	മുട്ടനാറി
Sinhala	අංකෙන්ද
Thai	พูมารี
Chinese	山油柑
Chinese	砂糖木
Chinese	石苓舅
Chinese	山柑
Chinese	降真香
Chinese	沙糖木
Chinese	山油柑果实
Chinese	山油柑叶
Chinese	山油柑（降真香）

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-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000518861
UNII	0X81369L7G
Tropicos	28100015
KEW	urn:lsid:ipni.org:names:770718-1
The Plant List	kew-2620314
Open Tree Of Life	891870
NCBI Taxonomy	354485
IUCN Red List	147652658
IPNI	770718-1
iNaturalist	556222
GBIF	3836457
Freebase	/m/0cz9340
USDA GRIN	456877
Wikipedia	Acronychia_pedunculata
CMAUP	NPO1267

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

Natural-derived acetophenones: chemistry and pharmacological activities

Ahmadpourmir H, Attar H, Asili J, Soheili V, Taghizadeh SF, Shakeri A

Nat Prod Bioprospect

10-May-2024

PMCID:	PMC11087454
doi:	10.1007/s13659-024-00447-x
PMID:	38727781

Spatial habitat suitability prediction of essential oil wild plants on Indonesia’s degraded lands

Renjana E, Firdiana ER, Angio MH, Ningrum LW, Lailaty IQ, Rahadiantoro A, Martiansyah I, Zulkarnaen R, Rahayu A, Raharjo PD, Abywijaya IK, Usmadi D, Risna RA, Cropper, Jr WP, Yudaputra A

PeerJ

01-Apr-2024

PMCID:	PMC10993885
doi:	10.7717/peerj.17210
PMID:	38577415

Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India

Ralte L, Sailo H, Singh YT

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765666
doi:	10.1186/s13002-023-00642-z
PMID:	38172927

Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus

Moreno Cardenas C, Çiçek SS

Front Microbiol

15-Aug-2023

PMCID:	PMC10463185
doi:	10.3389/fmicb.2023.1234115
PMID:	37649631

Choice Modeling for the Commercial Cultivation of Underutilized Aromatic Plants for Producing Mosquito Repellents: Targeting Rural Sector Income Generation

Munugoda KD, Talagala TS, Subasinghe SM, Hettiarachchi DS, Cooray AT

Econ Bot

25-May-2023

PMCID:	PMC10211285
doi:	10.1007/s12231-023-09573-y
PMID:	37359047

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Successful identification of the species of the semipetrified amber medicinal resin benzoin using molecular diagnostic technology

Feng J, He Q, Xie A, Liu Y

Sci Rep

20-Feb-2023

PMCID:	PMC9941088
doi:	10.1038/s41598-023-30034-y
PMID:	36808137

Effects of Geographical and Climatic Factors on the Intrinsic Water Use Efficiency of Tropical Plants: Evidence from Leaf 13C

Lin X, Wu B, Wang J, Wang G, Chen Z, Liang Y, Liu J, Wang H

Plants (Basel)

20-Feb-2023

PMCID:	PMC9962877
doi:	10.3390/plants12040951
PMID:	36840299

Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae)

Liu Q, Gao Y, Dong W, Zhao L

Ecol Evol

09-Feb-2023

PMCID:	PMC9911629
doi:	10.1002/ece3.9821
PMID:	36789335

Three New Eriophyid Mite Species from China (Acari: Eriophyidae)

Hao KX, Lotfollahi P, Xue XF

Insects

05-Feb-2023

PMCID:	PMC9967555
doi:	10.3390/insects14020159
PMID:	36835728

Antimicrobial Secondary Metabolites from the Mangrove Plants of Asia and the Pacific

Sulaiman M, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Rusdi NA, Seelan JS, Suleiman M, Zakaria ZA, Wiart C

Mar Drugs

15-Oct-2022

PMCID:	PMC9605323
doi:	10.3390/md20100643
PMID:	36286466

Potential Therapeutic Applications of Plant-Derived Alkaloids against Inflammatory and Neurodegenerative Diseases

Aryal B, Raut BK, Bhattarai S, Bhandari S, Tandan P, Gyawali K, Sharma K, Ranabhat D, Thapa R, Aryal D, Ojha A, Devkota HP, Parajuli N

Evid Based Complement Alternat Med

09-Mar-2022

PMCID:	PMC8926539
doi:	10.1155/2022/7299778
PMID:	35310033

Global Perspective of Plant-Based Cosmetic Industry and Possible Contribution of Sri Lanka to the Development of Herbal Cosmetics

Nadeeshani Dilhara Gamage DG, Dharmadasa RM, Chandana Abeysinghe D, Saman Wijesekara RG, Prathapasinghe GA, Someya T

Evid Based Complement Alternat Med

04-Mar-2022

PMCID:	PMC8916882
doi:	10.1155/2022/9940548
PMID:	35280508

Tree regeneration characteristics in limestone forests of the Cat Ba National Park, Vietnam

Pham VV, Ammer C, Annighöfer P, Heinrichs S

BMC Ecol Evol

15-Jan-2022

PMCID:	PMC8761296
doi:	10.1186/s12862-021-01957-9
PMID:	35033001

Ethnopharmacological Survey on Medicinal Plants Used for Cosmetic Treatments in Traditional and Ayurveda Systems of Medicine in Sri Lanka

Gamage DG, Dharmadasa RM, Abeysinghe DC, Wijesekara RG, Prathapasinghe GA, Someya T

Evid Based Complement Alternat Med

26-Jun-2021

PMCID:	PMC8257331
doi:	10.1155/2021/5599654
PMID:	34257686

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
> Alkaloids and derivatives / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone	6453733	Click to see	307.30	unknown	via CMAUP database
N-Acetyldehydroanonaine	5315739	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3	305.30	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(2S)-2-[[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]methyl]-7-methoxy-2,6-dimethylpyrano[3,2-c]quinolin-5-one	102236946	Click to see	618.70	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine	2703	Click to see	348.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Simulansamide	5321312	Click to see	397.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Acetophenones
1-[4-Hydroxy-2-(2-hydroxypropan-2-yl)-6-methoxy-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]ethanone	21672085	Click to see	334.40	unknown	https://doi.org/10.1021/NP030054X
Acronyculatin B	11067612	Click to see	334.40	unknown	https://doi.org/10.1007/S11418-013-0803-Y https://doi.org/10.1021/NP030054X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid	10742	Click to see	198.17	unknown	via CMAUP database
> 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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-(3-(1-(3-Acetyl-2,6-dihydroxy-4-methoxy-5-(3-methyl-2-buten-1-yl)phenyl)-3-methylbutyl)-2,4,6-trihydroxy-5-(3-methyl-2-buten-1-yl)phenyl)ethanone	159969	Click to see	554.70	unknown	https://doi.org/10.1021/NP50066A014 https://doi.org/10.1007/S11418-013-0803-Y https://doi.org/10.1021/NP030054X https://doi.org/10.1016/0031-9422(89)80234-1
1-[3-[(1R)-1-[3-acetyl-2,6-dihydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-3-methylbutyl]-2,4,6-trihydroxy-5-(3-methylbut-2-enyl)phenyl]ethanone	44559660	Click to see	554.70	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Pyrrolezanthine	636825	Click to see	245.27	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Sinapaldehyde	5280802	Click to see COC1=CC(=CC(=C1O)OC)C=CC=O	208.21	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
Yangambin	443028	Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC	446.50	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2Z,6E,8E,10E)-N-(2-methylpropyl)dodeca-2,6,8,10-tetraenamide	5321101	Click to see	247.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalyl acetate, (-)-	442474	Click to see	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene oxide	1742210	Click to see	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic Acid	5280896	Click to see	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Amyrenol	225689	Click to see	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	via CMAUP database
beta-Sitosterone	9801811	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Ganodine	126543	Click to see C1=CC=C(C=C1)CCN2C(=CC=C2C=O)CO	229.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
[4-Acetyl-3-acetyloxy-5-hydroxy-2,6-bis(3-methylbut-2-enyl)phenyl] acetate	162957514	Click to see	388.50	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
1-[4,6-Dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]ethanone	15558323	Click to see	250.29	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
1-[4,6-dihydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2-methoxyphenyl]ethanone	163042882	Click to see	266.29	unknown	https://doi.org/10.1021/NP030054X
1-[4,6-dihydroxy-3-[(2S)-2-hydroxy-3-methylbut-3-enyl]-2-methoxyphenyl]ethanone	163042881	Click to see	266.29	unknown	https://doi.org/10.1021/NP030054X
1-[5-(1-Ethoxy-3-methylbutyl)-2,4-dihydroxy-6-methoxy-3-(3-methylbut-2-enyl)phenyl]ethanone	100943939	Click to see	364.50	unknown	https://doi.org/10.1016/S0031-9422(99)00252-6
1-[5-[(1R)-1-ethoxy-3-methylbutyl]-2,4-dihydroxy-6-methoxy-3-(3-methylbut-2-enyl)phenyl]ethanone	163004607	Click to see	364.50	unknown	https://doi.org/10.1016/S0031-9422(99)00252-6
Acronyculatin A	11780847	Click to see	278.30	unknown	https://doi.org/10.1007/S11418-013-0803-Y https://doi.org/10.1021/NP030054X
Acronyculatin C	10914615	Click to see	334.40	unknown	https://doi.org/10.1007/S11418-013-0803-Y https://doi.org/10.1021/NP030054X
Acronyculatin D	11010921	Click to see	266.29	unknown	https://doi.org/10.1007/S11418-013-0803-Y https://doi.org/10.1021/NP030054X
> Organoheterocyclic compounds / Benzodioxoles
(+)-Sesamolin	585998	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
Sesamolin	101746	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Acronyculatin E	10892453	Click to see CC(=CCC1=C2C(=C(C(=C1OC)C(=O)C)O)C=CC(O2)(C)C)C	316.40	unknown	https://doi.org/10.1021/NP030054X https://doi.org/10.1007/S11418-013-0803-Y
Evodinnol	225062	Click to see	248.27	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Zanthopyranone	10419590	Click to see	170.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives
2,3-Methylenedioxy-4,7-dimethoxyquinoline	10775978	Click to see COC1=CC2=C(C=C1)C(=C3C(=N2)OCO3)OC	233.22	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1,2-Dimethoxy-13-methyl[1,3]benzodioxolo[5,6-c]phenanthridine	101673185	Click to see	347.40	unknown	via CMAUP database
Oxychelerythrine	147279	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC	363.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine	164950	Click to see	215.20	unknown	via CMAUP database
Dictamnine	68085	Click to see	199.20	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
Evolitrine	196980	Click to see	229.23	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4 https://doi.org/10.1016/0031-9422(79)80162-4
Gamma-Fagarine	107936	Click to see	229.23	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
Kokusaginine	10227	Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1016/0031-9422(79)80162-4 https://doi.org/10.1016/0031-9422(89)80234-1 https://doi.org/10.1016/S0031-9422(99)00039-4
Maculosidine	68222	Click to see COC1=CC2=C(C(=C1)OC)N=C3C(=C2OC)C=CO3	259.26	unknown	https://doi.org/10.1016/S0031-9422(99)00039-4
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1016/0031-9422(89)80234-1 https://doi.org/10.1016/S0031-9422(99)00039-4
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroxyquinolines
Zanthobisquinolone	54688597	Click to see	362.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1H-quinolin-2-one	600167	Click to see	175.18	unknown	via CMAUP database
4-methoxy-N-methyl-2-quinolone	182073	Click to see	189.21	unknown	via CMAUP database
N-Methylschinifoline	101652163	Click to see CC(=C)C=CC1=C(C2=CC=CC=C2N(C1=O)C)OC	255.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3S)-3-hydroxy-2,2,10-trimethyl-3,4-dihydropyrano[2,3-b]quinolin-5-one	932818	Click to see	259.30	unknown	via CMAUP database
6,6,12-Trimethylisochromeno[4,3-c]quinolin-11-one	10017165	Click to see	291.30	unknown	via CMAUP database
7-Methoxyflindersine	101995295	Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C	257.28	unknown	via CMAUP database
Benzosimuline	5321951	Click to see	305.40	unknown	via CMAUP database
Flindersine	68230	Click to see	227.26	unknown	via CMAUP database
N-Acetoxymethylflindersine	11289552	Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C	299.32	unknown	via CMAUP database
Rel-zanthodioline	5315424	Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C	305.32	unknown	via CMAUP database
Zanthobungeanine	5315422	Click to see	271.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Simulanol	52918181	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO	388.40	unknown	via CMAUP database
Balanophonin	23252258	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1016/0031-9422(89)80234-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin	5318565	Click to see	222.19	unknown	via CMAUP database
Scopoletin	5280460	Click to see	192.17	unknown	via CMAUP database

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Acronychia pedunculata

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