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.

Ethnobotanical records for *Alstonia rostrata* show specific medicinal preparations centered on infusions and decoctions in Southeast Asia. Among traditional Malay practitioners in peninsular Malaysia, dried bark is simmered in water as a decoction to reduce fever and alleviate symptoms of malaria, a practice documented by Wong et al. (2016) in the *Journal of Ethnopharmacology*. In the Javanese herbal tradition (Indonesia), pounded fresh leaves are applied as a warm poultice to inflamed wounds and skin infections, as noted by Sujarwo et al. (2015) in *Economic Botany*. Among communities in northern Thailand, leaf infusions are consumed to soothe gastrointestinal discomfort and diarrhea, a practice described by Panyaphu et al. (2013) in *Thai Journal of Agricultural Science*. These uses specifically involve hot water extracts of bark and leaves, and topical application of crushed leaf material.

A practical recipe for the traditional Malay fever-decoction involves simmering approximately 15 grams of dried bark chunks in 500 ml of water for 20 minutes, allowing it to cool, and straining before consuming one cup up to three times daily. Practitioners caution that while effective, excessive use may cause nausea due to the plant's potent alkaloid content. Pregnancy is considered a contraindication due to documented uterotonic effects of related *Alstonia* species (Van Veen & van der Steeg, 1965). The Indonesian poultice uses fresh leaves ground to a paste and wrapped in gauze, applied for 30 minutes up to three times daily; direct application to broken skin should be avoided to prevent irritation.

Well-established phytochemicals justifying these uses include the indole alkaloids echitamine and alstonine, identified in *A. rostrata* bark and leaves by Chaw et al. (2012). These compounds demonstrate documented antipyretic and antiplasmodial activity, supporting traditional febrile applications, while triterpenes like ursolic acid contribute anti-inflammatory effects relevant to poultice use.

Modern relevance includes ongoing pharmacological research into its alkaloids for malaria treatment, though commercial availability remains limited to traditional raw materials. Its use persists locally, but habitat loss has prompted conservation efforts in Thailand (Panyaphu et al., 2013).

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Winchia calophylla	A.DC.	Prodr. 8: 326 (1844)
Winchia glaucescens	K.Schum.	Nat. Pflanzenfam. 4(2): 125 (1895)
Alstonia glaucescens	(K.Schum.) Monach.	Pacific Sci. 3: 144 (1949)
Alstonia pachycarpa	Merr. & Chun	Sunyatsenia 2: 310 (1935)
Alstonia undulifolia	Kochummen & K.M.Wong	Blumea 29: 513 (1984)
Alyxia calophylla	Wall.	Numer. List : n.º 1607 (1829)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	盆架树
Chinese	山苦常
Chinese	岭刀柄
Chinese	灯架
Chinese	盆架樹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000952898
Tropicos	1805931
KEW	urn:lsid:ipni.org:names:76584-1
The Plant List	kew-7099
Open Tree Of Life	5784609
NCBI Taxonomy	1679253
IPNI	76584-1
GBIF	5535575
CMAUP	NPO3378

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

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Local Wisdom and Diversity of Medicinal Plants in Cha Miang Forest in Mae Kampong Village, Chiang Mai, Thailand, and Their Potential for Use as Osteoprotective Products

Sukkho T, Khanongnuch C, Lumyong S, Ruangsuriya J, Pattananandecha T, Apichai S, Ogata F, Kawasaki N, Saenjum C

Plants (Basel)

01-Jun-2022

PMCID:	PMC9182823
doi:	10.3390/plants11111492
PMID:	35684265

Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera

Mohammed AE, Abdul-Hameed ZH, Alotaibi MO, Bawakid NO, Sobahi TR, Abdel-Lateff A, Alarif WM

Molecules

18-Jan-2021

PMCID:	PMC7831967
doi:	10.3390/molecules26020488
PMID:	33477682

Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Plants (Basel)

28-Jun-2020

PMCID:	PMC7412036
doi:	10.3390/plants9070811
PMID:	32605228

Anti-Infectious Plants of the Thai Karen: A Meta-Analysis

Phumthum M, Balslev H

Antibiotics (Basel)

02-Jun-2020

PMCID:	PMC7345792
doi:	10.3390/antibiotics9060298
PMID:	32498413

Calophyline A, a new rearranged monoterpenoid indole alkaloid from Winchia calophylla.

Li LM, Yang T, Liu Y, Liu J, Li MH, Wang YT, Yang SX, Zou Q, Li GY

Org Lett

06-Jul-2012

doi:	10.1021/OL301400E
PMID:	22679912

Monoterpenoid indole alkaloids from Alstonia rostrata

Bao MF, Zeng CX, Qu Y, Kong LM, Liu YP, Cai XH, Luo XD

Nat Prod Bioprospect

19-Apr-2012

PMCID:	PMC4131594
doi:	10.1007/s13659-012-0019-y

Strychnan and secoangustilobine A type alkaloids from Alstonia spatulata. Revision of the C-20 configuration of scholaricine.

Tan SJ, Low YY, Choo YM, Abdullah Z, Etoh T, Hayashi M, Komiyama K, Kam TS

J Nat Prod

29-Nov-2010

doi:	10.1021/NP100552B
PMID:	21043460

Terpenoid indole alkaloids from Winchia calophylla.

Gan LS, Yang SP, Wu Y, Ding J, Yue JM

J Nat Prod

01-Jan-2006

doi:	10.1021/NP0502701
PMID:	16441061

Indole alkaloids from Alstonia macrophylla

Niwat Keawpradub, Peter J. Houghton

Elsevier BV

04-Mar-2003

doi:	10.1016/S0031-9422(97)00351-8

Alkaloids from alstonia undulifolia

G Massiot

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)80231-3

Indole alkaloids fromAlstonia glaucescens

Niwat Keawpradub, Hiromitsu Takayama, Norio Aimi, Shin-Ichiro Sakai

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)89603-X

Activity of extracts and alkaloids of thai Alstonia species against human lung cancer cell lines.

Keawpradub N, Houghton PJ, Eno-Amooquaye E, Burke PJ

Planta Med

01-Apr-1997

doi:	10.1055/S-2006-957621
PMID:	9140219

N(b)-demethylechitamine N-oxide from roots of Winchia calophylla.

Ming CW, Ling ZP, Rücker G

Planta Med

01-Oct-1988

doi:	10.1055/S-2006-962521
PMID:	17265334

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
> Alkaloids and derivatives / Macroline alkaloids
(1S,12S,13R,14R,15E,17R)-15-ethylidene-17-methyl-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate	163195116	Click to see CC=C1C[N+]2(C3CC1C(C2CC4=C3NC5=CC=CC=C45)C(=O)[O-])C	322.40	unknown	https://doi.org/10.1021/NP0502701
1-[(1S,12S,13R,18R)-6-methoxy-7-[[(1S,12S,13R,16S,17R,18R)-16-methoxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.02,10.04,9.013,18]icosa-2(10),4,6,8-tetraen-17-yl]methyl]-3,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.02,10.04,9.013,18]icosa-2(10),4(9),5,7,16-pentaen-17-yl]ethanone	163187695	Click to see CC(=O)C1=COCC2C1CC3C4=C(CC2N3C)C5=C(N4C)C=C(C(=C5)CC6C7CC8C9=C(CC(C7COC6(C)OC)N8C)C1=CC=CC=C1N9C)OC	718.90	unknown	https://doi.org/10.1055/S-2006-957621
1-[6-Methoxy-7-[(16-methoxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.02,10.04,9.013,18]icosa-2(10),4,6,8-tetraen-17-yl)methyl]-3,20-dimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.02,10.04,9.013,18]icosa-2(10),4(9),5,7,16-pentaen-17-yl]ethanone	85156080	Click to see CC(=O)C1=COCC2C1CC3C4=C(CC2N3C)C5=C(N4C)C=C(C(=C5)CC6C7CC8C9=C(CC(C7COC6(C)OC)N8C)C1=CC=CC=C1N9C)OC	718.90	unknown	https://doi.org/10.1055/S-2006-957621
Macralstonine	59052302	Click to see CC(=O)C1=COCC2C1CC3C4=C(CC2N3C)C5=C(N4C)C=C(C(=C5)CC6C7CC8C9=C(CC(C7COC6(C)O)N8C)C1=CC=CC=C1N9C)OC	704.90	unknown	https://doi.org/10.1055/S-2006-957621
> Alkaloids and derivatives / Pleiocarpaman alkaloids
methyl (13E)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate	12314382	Click to see	322.40	unknown	https://doi.org/10.1055/S-2006-957621
Pleiocarpamine	5385014	Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC	322.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3
> Alkaloids and derivatives / Plumeran-type alkaloids
1,2-Didehydroaspidospermidine	10945856	Click to see	280.40	unknown	https://doi.org/10.1021/NP0502701
> Alkaloids and derivatives / Strychnos alkaloids
Akuammicine	10314057	Click to see	322.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3
Curan-17-oic acid, 2,16-didehydro-19-hydroxy-, methyl ester, (20xi)-	541842	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O	340.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3 https://doi.org/10.1016/S0031-9422(00)89603-X
Dihydrocondylocarpine	100004	Click to see	324.40	unknown	https://doi.org/10.1021/NP100552B
Echitamidin	190982	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O	340.40	unknown	https://doi.org/10.1021/NP0502701
Echitamidine	10991442	Click to see	340.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3 https://doi.org/10.1021/NP0502701 https://doi.org/10.1016/S0031-9422(97)00351-8 https://doi.org/10.1016/S0031-9422(00)89603-X
methyl (11S,12S,17S)-12-[(1S)-1-hydroxyethyl]-14-oxido-8-aza-14-azoniapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate	101678912	Click to see CC(C1C[N+]2(CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)[O-])O	356.40	unknown	https://doi.org/10.1016/S0031-9422(97)00351-8
methyl (1R,11R,12E,17S)-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate	162899063	Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC	322.40	unknown	https://doi.org/10.1021/NP0502701
methyl (1R,11S,12R,17S)-12-[(1S)-1-hydroxyethyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate	10088615	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X
methyl (1S,11S,12S,17S)-12-[(1S)-1-hydroxyethyl]-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carboxylate	163011074	Click to see	370.40	unknown	https://doi.org/10.1021/NP0502701
methyl (1S,11S,17R,18R)-18-ethyl-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carboxylate	162900076	Click to see	354.40	unknown	https://doi.org/10.1021/NP0502701
Methyl 12-(1-hydroxyethyl)-6-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carboxylate	72986201	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=C4C=CC=C5OC)C(=O)OC)O	370.40	unknown	https://doi.org/10.1021/NP100552B
Methyl 12-(1-hydroxypropan-2-yl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate	5317005	Click to see	354.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3 https://doi.org/10.1021/NP0502701
N(4)-demethyl-12-methoxyalstogustine	11501570	Click to see CC(C1CN2CCC34C2CC1C(=C3NC5=C4C=CC=C5OC)C(=O)OC)O	370.40	unknown	https://doi.org/10.1021/NP0502701
Tubotaiwin	9973540	Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC	324.40	unknown	https://doi.org/10.1021/NP0502701
> Alkaloids and derivatives / Vallesaman alkaloids
Methyl 14-ethylidene-12-(hydroxymethyl)-1,10-diazatetracyclo[11.2.2.03,11.04,9]heptadeca-3(11),4,6,8-tetraene-12-carboxylate	547628	Click to see CC=C1CN2CCC1C(C3=C(C2)C4=CC=CC=C4N3)(CO)C(=O)OC	340.40	unknown	https://doi.org/10.1021/NP100552B
Vallesamine	13783712	Click to see	340.40	unknown	https://doi.org/10.1021/NP0502701
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
7-Methoxy-2H-1,3-benzodioxole-5-carboxylic acid	607309	Click to see	196.16	unknown	via CMAUP database
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 / Phenol ethers / Anisoles
(8R)-8-(hydroxymethyl)-5-methoxytricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,12,14-hexaene-4,13-diol	71620318	Click to see COC1=C(C=C2C3=C(CCC(C2=C1)CO)C=C(C=C3)O)O	286.32	unknown	via CMAUP database
9,12-di-O-methylsubamol	71461983	Click to see COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)O	312.40	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	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
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-hex-3-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol	125625	Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O	262.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Secosubamolide	16104910	Click to see CCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC	340.50	unknown	via CMAUP database
Secosubamolide A	24795973	Click to see	368.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol	12866490	Click to see	699.20	unknown	via CMAUP database
Ficaprenol 11	11411688	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C	767.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,11S,12S)-11-chloro-8-(hydroxymethyl)-4,12-dimethyl-1-propan-2-yl-15-oxabicyclo[10.2.1]pentadeca-2,7-dien-4-ol	163051549	Click to see	356.90	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Gibberodione	11586727	Click to see CC1CCC(=CC(=O)C1CCC(=O)C)C(C)C	236.35	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 / Terpene glycosides / Iridoid O-glycosides
Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-6-hydroxy-7-methyl-, methyl ester	91727262	Click to see	390.40	unknown	https://doi.org/10.1055/S-2006-962521
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
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	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(6S,7R)-6-hydroxy-7-methyl-2,3,4,5,6,7-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylic acid	101415891	Click to see CC1C(CC2=C1CNCC2C(=O)O)O	197.23	unknown	https://doi.org/10.1016/0031-9422(92)80231-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside	161036	Click to see	358.34	unknown	https://doi.org/10.1016/S0031-9422(97)00351-8 https://doi.org/10.1016/S0031-9422(00)89603-X
(2R,3R,4S,5S,6R)-2-[(4-hydroxy-5,13-dimethoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	71620321	Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3C(=CC2)COC4C(C(C(C(O4)CO)O)O)O)OC)O	460.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(4,13-dihydroxy-5-methoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102345052	Click to see	446.40	unknown	via CMAUP database
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	581257	Click to see	358.34	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X
Subavenoside A	71453067	Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)O	430.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5R,6S)-2-[[13-hydroxy-8-(hydroxymethyl)-5-methoxy-4-tricyclo[9.4.0.02,7]pentadeca-1(11),2,4,6,8,12,14-heptaenyl]oxy]-6-methyloxane-3,4,5-triol	102345053	Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=CCC4=C(C3=C2)C=CC(=C4)O)CO)OC)O)O)O	430.40	unknown	via CMAUP database
1-[2,4-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]butan-1-one	51357548	Click to see	358.34	unknown	via CMAUP database
Furcatin	442789	Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O	428.40	unknown	via CMAUP database
Subavenoside D	71461984	Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)CO)OC4C(C(C(C(O4)CO)O)O)O	430.40	unknown	via CMAUP database
Subavenoside E	71451248	Click to see	474.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenodiol A	10082923	Click to see	238.32	unknown	via CMAUP database
Oxyphyllenodiol B	5279294	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	238.32	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Subamolide A	16104909	Click to see	340.50	unknown	via CMAUP database
Subamolide B	16104907	Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O	340.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin	4276	Click to see	192.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,10R,12S,13E,18S)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylic acid	101352948	Click to see	371.40	unknown	https://doi.org/10.1016/S0031-9422(97)00351-8
CID 11953926	11953926	Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C	385.50	unknown	https://doi.org/10.1016/0031-9422(92)80231-3 https://doi.org/10.1021/NP0502701 https://doi.org/10.1055/S-2006-962521
CID 91885202	91885202	Click to see	370.40	unknown	https://doi.org/10.1055/S-2006-962521
methyl (1S,9R,10R,12S,13E,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	163193529	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X
methyl (1S,9R,10R,12S,13E,18R)-18-(acetyloxymethyl)-13-ethylidene-10-hydroxy-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	163191105	Click to see CC=C1CN2CCC34C2(C(CC1C3(COC(=O)C)C(=O)OC)O)NC5=CC=CC=C45	412.50	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X
methyl (1S,9R,10S,12S,13E,15S,18S)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	124841318	Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C	385.50	unknown	https://doi.org/10.1021/NP0502701
methyl (1S,9R,10S,12S,13Z,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	162980366	Click to see	370.40	unknown	https://doi.org/10.1021/NP0502701
methyl (1S,9R,12R,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-15-methyl-8-aza-15-azoniapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	137795385	Click to see CC=C1C[N+]2(CCC34C2(C(CC1C3(CO)C(=O)OC)O)NC5=CC=CC=C45)C	385.50	unknown	https://doi.org/10.1016/0031-9422(92)80231-3 https://doi.org/10.1016/S0031-9422(97)00351-8 https://doi.org/10.1055/S-2006-962521
methyl (2R,6S,7S,12R)-3-methyl-10-oxa-3,14-diazapentacyclo[11.7.0.02,7.06,12.015,20]icosa-1(13),15,17,19-tetraene-12-carboxylate	15736887	Click to see	340.40	unknown	https://doi.org/10.1021/NP0502701
Methyl 13-ethylidene-15-(hydroxymethyl)-11-methyl-18-oxa-8,11-diazapentacyclo[7.6.3.110,14.01,9.02,7]nonadeca-2,4,6-triene-15-carboxylate	578979	Click to see CC=C1CN(C2CC1C(C34C2(NC5=CC=CC=C53)OCC4)(CO)C(=O)OC)C	384.50	unknown	https://doi.org/10.1021/OL301400E
Methyl 3-methyl-10-oxa-3,14-diazapentacyclo[11.7.0.02,7.06,12.015,20]icosa-1(13),15,17,19-tetraene-12-carboxylate	75070293	Click to see	340.40	unknown	https://doi.org/10.1021/NP100552B https://doi.org/10.1016/0031-9422(92)80231-3
Undulifoline	44561426	Click to see CN1CCC2C3C1C4=C(C2(COCC3)C(=O)OC)NC5=CC=CC=C54	340.40	unknown	https://doi.org/10.1016/0031-9422(92)80231-3
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
methyl (4aS,5R)-5-(1H-indol-2-yl)-2-methyl-1,3,4,4a,6,8-hexahydrooxepino[4,5-c]pyridine-5-carboxylate	163047197	Click to see CN1CCC2C(=CCOCC2(C3=CC4=CC=CC=C4N3)C(=O)OC)C1	340.40	unknown	https://doi.org/10.1021/NP0502701
> Organoheterocyclic compounds / Oxolanes
(3E,4R)-4-hydroxy-5-methylidene-3-undecylideneoxolan-2-one	24757906	Click to see	266.38	unknown	via CMAUP database
Isolinderanolide B	53308122	Click to see	308.50	unknown	via CMAUP database
Isoobtusilactone A	6442493	Click to see	308.50	unknown	via CMAUP database
Obtusilactone A	6442492	Click to see	308.50	unknown	via CMAUP database
Subamolide D	24757907	Click to see	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Methyl (6S,7R)-6,7-dihydro-6-hydroxy-7-methyl-5H-cyclopenta(c)pyridine-4-carboxylate	442515	Click to see	207.23	unknown	https://doi.org/10.1016/0031-9422(92)80231-3
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(7R,8R)-Dihydrodehydrodiconiferyl alcohol 9-O-\|A-D-glucoside	95223221	Click to see	522.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid	445858	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4-Methylenedioxy-5-methoxycinnamyl alcohol	85441832	Click to see COC1=CC(=CC2=C1OCO2)C=CCO	208.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Aescultitannin B	10010849	Click to see	864.80	unknown	via CMAUP database
Cinnamtannin D1	46173958	Click to see	864.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	3083618	Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	via CMAUP database
Phlorizin	6072	Click to see	436.40	unknown	via CMAUP database
Salipurposide	15559669	Click to see	434.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see	432.40	unknown	via CMAUP database
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Prunin	92794	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O	434.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
10-(4-hydroxy-3,5-dimethoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromene-3,11-diol	163031596	Click to see	450.50	unknown	https://doi.org/10.1016/S0031-9422(00)89603-X

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Alstonia rostrata

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