Common products:
Aglaia silvestris is used primarily as a timber species.Sa‑sa timber is employed in construction, joinery, furniture, interior trim, and specialty items such as tool handles and carving.

Industrial and craft applications:
The wood is suitable for flooring, paneling, and turned articles where dimensional stability and fine finishing are desirable. It is also used for small civil‑engineering elements and general carpentry.

Wood and fiber:
Sa‑sa yields a dense, hard, fine‑grained hardwood suitable for structural and decorative applications. The bark yields fiber used for cordage and binding.

Fragrance and cosmetics:
The wood is reported to possess a fragrant, camphor‑like scent and is used for incense and aromatic articles.

Properties relevant to use:
Timber density and hardness contribute to durability and finish quality; extractives associated with the wood’s limonoid constituents impart resistance to insects and fungi and contribute to aromatic properties. The fibrous bark’s long fibers facilitate rope and twine production.

Scientific/model use:
Aglaia silvestris is cited in studies of limonoid biosynthesis and chemotaxonomy within Meliaceae and serves as a reference species in pharmacognosy and ecology literature that investigates these bioactive natural products.

Synonyms Top

Scientific name	Authority	First published in
Lansium silvestre	M.Roem.	Fam. Nat. Syn. Monogr. 1: 99 (1846)
Lepidaglaia baillonii	Pierre	Fl. Forest. Cochinch. : t. 352B (1897)
Aglaia acuminata	Merr.	Philipp. J. Sci., C 9: 531 (1914 publ. 1915)
Aglaia baillonii	Pierre ex Pellegr.	Fl. Indo-Chine 1: 774 (1911)
Aglaia cedreloides	Harms	Bot. Jahrb. Syst. 72: 164 (1942)
Aglaia cochinchensis	Pierre	Fl. Forest. Cochinch. t. 334A 1895
Aglaia copelandii	Elmer	Leafl. Philipp. Bot. 9(128): 3286. 1937 [1 May 1937] , anglice
Aglaia forstenii	Miq.	Ann. Mus. Bot. Lugduno-Batavi 4: 46 (1868)
Aglaia ganggo	Miq.	Fl. Ned. Ind., Eerste Bijv. : 506 (1861)
Aglaia mannii	(King ex Brandis) S.S.Jain & R.C.Gaur	J. Econ. Taxon. Bot. 7: 466 (1985 publ. 1986)
Aglaia micropora	Merr.	Univ. Calif. Publ. Bot. 15: 129 (1929)
Aglaia multiflora	Merr.	Philipp. J. Sci. 1(Suppl.): 73 (1906)
Aglaia obliqua	C.T.White & W.D.Francis	Proc. Roy. Soc. Queensland 38: 236 (1926 publ. 1927)
Aglaia pyramidata	Hance	J. Bot. 15: 331 (1877)
Aglaia pyrrholepis	Miq.	Ann. Mus. Bot. Lugduno-Batavi 4: 47 (1868)
Amoora ganggo	Kurz	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 45: 123 (1876)
Dysoxylum baillonii	Pierre ex Laness.	Pl. Util. Col. Franç. : 309 (1886)
Epicharis baillonii	Pierre	Bull. Mens. Soc. Linn. Paris 1: 292 (1881)
Amoora mannii	King ex Brandis	Indian Trees 142 1906
Lepiaglaia pyramidata	Pierre	Fl. Forest. Cochinch. : t. 334 (1897)
Lepiaglaia baillonii	Pierre	Fl. Forest. Cochinch. : t. 352 (1896)
Lepidaglaia pyramidata	Pierre	Fl. Forest. Cochinch. : t. 334A (1897)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Hebrew	אגליה סילבסטריס
su	culan
Thai	จันทน์ชะมด
Vietnamese	gội hang

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000524354
Tropicos	50094823
KEW	urn:lsid:ipni.org:names:577321-1
The Plant List	kew-2626567
Open Tree Of Life	353178
NCBI Taxonomy	306516
IUCN Red List	34763
IPNI	577321-1
iNaturalist	189079
GBIF	5597971
Freebase	/m/02x7qxw
USDA GRIN	448903
Wikipedia	Aglaia_silvestris
CMAUP	NPO25201

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

Sesquiterpenoids from Meliaceae Family and Their Biological Activities

Riyadi SA, Naini AA, Supratman U

Molecules

20-Jun-2023

PMCID:	PMC10302239
doi:	10.3390/molecules28124874
PMID:	37375428

The dark side of mRNA translation and the translation machinery in glioblastoma

Montiel-Dávalos A, Ayala Y, Hernández G

Front Cell Dev Biol

13-Mar-2023

PMCID:	PMC10042294
doi:	10.3389/fcell.2023.1086964
PMID:	36994107

Antiplasmodial Properties of Aqueous and Ethanolic Extracts of Ten Herbal Traditional Recipes Used in Thailand against Plasmodium falciparum

Phuwajaroanpong A, Chaniad P, Plirat W, Phoopha S, Septama AW, Chukaew A, Punsawad C

Trop Med Infect Dis

04-Dec-2022

PMCID:	PMC9786625
doi:	10.3390/tropicalmed7120417
PMID:	36548672

Some natural compounds and their analogues having potent anti- SARS-CoV-2 and anti-proteases activities as lead molecules in drug discovery for COVID-19

Dinda B, Dinda M, Dinda S, Chakraborty M

Eur J Med Chem Rep

28-Aug-2022

PMCID:	PMC9420082
doi:	10.1016/j.ejmcr.2022.100079
PMID:	36060987

Update on Phytochemical and Biological Studies on Rocaglate Derivatives from Aglaia Species

Agarwal G, Chang LS, Soejarto DD, Kinghorn AD

Planta Med

30-Mar-2021

PMCID:	PMC8481333
doi:	10.1055/a-1401-9562
PMID:	33784769

Natural Products with Potential to Treat RNA Virus Pathogens Including SARS-CoV-2

Christy MP, Uekusa Y, Gerwick L, Gerwick WH

J Nat Prod

22-Dec-2020

PMCID:	PMC7771248
doi:	10.1021/acs.jnatprod.0c00968
PMID:	33352046

Promising Terpenes as Natural Antagonists of Cancer: An In-Silico Approach

Muhseen ZT, Li G

Molecules

30-Dec-2019

PMCID:	PMC6983034
doi:	10.3390/molecules25010155
PMID:	31906032

TARGETING THE eIF4A RNA HELICASE BLOCKS TRANSLATION OF THE MUC1-C ONCOPROTEIN

Jin C, Rajabi H, Rodrigo CM, Porco JA Jr, Kufe D

Oncogene

11-Jun-2012

PMCID:	PMC3443512
doi:	10.1038/onc.2012.236
PMID:	22689062

Targeted cancer therapy: What if the driver is just a messenger?

Schatz JH, Wendel HG

Cell Cycle

15-Nov-2011

PMCID:	PMC3266113
doi:	10.4161/cc.10.22.18288
PMID:	22064518

The Relevance of Higher Plants in Lead Compound Discovery Programs

Kinghorn AD, Pan L, Fletcher JN, Chai H

J Nat Prod

08-Jun-2011

PMCID:	PMC3158731
doi:	10.1021/np200391c
PMID:	21650152

Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae)

Ebada SS, Lajkiewicz N, Porco JA Jr, Li-Weber M, Proksch P

Prog Chem Org Nat Prod

01-Jan-2011

PMCID:	PMC4157394
doi:	10.1007/978-3-7091-0748-5_1
PMID:	21833837

Potential of Plant-Derived Natural Products in the Treatment of Leukemia and Lymphoma

Lucas DM, Still PC, Pérez LB, Grever MR, Kinghorn AD

Curr Drug Targets

01-Jul-2010

PMCID:	PMC2892601
doi:	10.2174/138945010791320809
PMID:	20370646

The continuing search for antitumor agents from higher plants

Pan L, Chai H, Kinghorn AD

Phytochem Lett

12-Mar-2010

PMCID:	PMC2836022
doi:	10.1016/j.phytol.2009.11.005
PMID:	20228943

The novel plant-derived agent silvestrol has B-cell selective activity in chronic lymphocytic leukemia and acute lymphoblastic leukemia in vitro and in vivo

Lucas DM, Edwards RB, Lozanski G, West DA, Shin JD, Vargo MA, Davis ME, Rozewski DM, Johnson AJ, Su BN, Goettl VM, Heerema NA, Lin TS, Lehman A, Zhang X, Jarjoura D, Newman DJ, Byrd JC, Kinghorn AD, Grever MR

Blood

07-May-2009

PMCID:	PMC2680369
doi:	10.1182/blood-2008-09-175430
PMID:	19190247

Discovery of Natural Product Anticancer Agents from Biodiverse Organisms

Kinghorn AD, Chin YW, Swanson SM

Curr Opin Drug Discov Devel

01-Mar-2009

PMCID:	PMC2877274
PMID:	19333864

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 / 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 / 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
> 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
(+)-alpha-Bulgarene	12306053	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
(+)-alpha-Muurolene	12306049	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene	101708	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
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 / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4S,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	131705161	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
Npc239037	101716	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
Viridiflorol	11996452	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(3R,3aR,3bR,5aR,6S,8aR,8bR,10aR)-6-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydro-3H-indeno[6,7-e]indene-3-carbaldehyde	163083423	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
(3R,3aR,3bR,5aR,6S,8aR,8bR,10aR)-6-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydro-3H-indeno[6,7-e]indene-3-carbaldehyde	163083424	Click to see CC1(C2CCC3(C(C2(C(C1=O)C=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
(3R,3aR,3bS,5aR,6S,8aR,8bR,10aR)-6-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydro-3H-indeno[6,7-e]indene-3-carbaldehyde	163083422	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
(3Z,3aR,3bS,5aR,6S,8aR,8bR,10aR)-3-[[[(Z)-[(3aR,3bS,5aR,6S,8aR,8bR,10aR)-6-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydroindeno[6,7-e]inden-3-ylidene]methyl]amino]methylidene]-6-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-3b,4,5,5a,6,7,8,9,10,10a-decahydroindeno[5,4-e]inden-2-one	102034507	Click to see CC1(C2CCC3(C(C2(C(=CNC=C4C(=O)C(C5C4(C6CCC7C(CCC7(C6(CC5)C)C)C8(CCC(O8)C(C)(C)O)C)C)(C)C)C1=O)C)CCC9C3(CCC9C1(CCC(O1)C(C)(C)O)C)C)C)C	926.40	unknown	https://doi.org/10.1016/J.TETLET.2008.11.048
6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydro-3H-indeno[6,7-e]indene-3-carbaldehyde	163083421	Click to see	472.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
6-[5-(2-Hydroxypropan-2-yl)-2-methyloxolan-2-yl]-3-[[[6-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-1,1,3a,8a,8b-pentamethyl-2-oxo-3b,4,5,5a,6,7,8,9,10,10a-decahydroindeno[6,7-e]inden-3-ylidene]methylamino]methylidene]-1,1,3a,8a,8b-pentamethyl-3b,4,5,5a,6,7,8,9,10,10a-decahydroindeno[5,4-e]inden-2-one	163005930	Click to see	926.40	unknown	https://doi.org/10.1016/J.TETLET.2008.11.048
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
2-[(3S,3aR,5aR,6R,7R,9aR,9bR)-6-(2,2-dimethoxyethyl)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-7-yl]-2-methylpropanoic acid	102026324	Click to see	536.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
2-[(3S,3aR,5aR,6S,7R,9aR,9bR)-6-(2,2-dimethoxyethyl)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-7-yl]-2-methylpropanoic acid	163001859	Click to see	536.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
2-[6-(2,2-Dimethoxyethyl)-3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-7-yl]-2-methylpropanoic acid	163001858	Click to see	536.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
3-[(3S,3aR,5aR,6R,7S,9aR,9bR)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid	162944570	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
3-[(3S,3aR,5aR,6R,7S,9aR,9bR)-3-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid	162142114	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
3-[(3S,3aR,5aR,6R,7S,9bR)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid	163187377	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
3-[(3S,3aR,5aR,6S,7S,9aR,9bR)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid	101859478	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025 https://doi.org/10.1016/J.TETLET.2008.04.109
3,4-Secodammar-4(28)-en-3-oic acid, 20,24-epoxy-25-hydroxy-, (24S)-	588519	Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC3C4(CCC(O4)C(C)(C)O)C)C)C	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025 https://doi.org/10.1016/J.TETLET.2008.04.109
methyl 3-[(3S,3aR,5aR,6S,7S,9aR,9bR)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate	101859479	Click to see	488.70	unknown	https://doi.org/10.1016/J.TETLET.2008.04.109 https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
Methyl 3-[3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate	124222314	Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)OC)CCC3C2(CCC3C4(CCC(O4)C(C)(C)O)C)C)C	488.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025 https://doi.org/10.1016/J.TETLET.2008.04.109
Shoreic Acid	12315515	Click to see	474.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl 3-[(3S,3aR,5aR,6R,7R,9aR,9bR)-7-(2-hydroxypropan-2-yl)-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate	102026322	Click to see	506.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
methyl 3-[(3S,3aR,5aR,6S,7R,9aR,9bR)-7-(2-hydroxypropan-2-yl)-3-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate	162897110	Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)OC)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C	506.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
Methyl 3-[7-(2-hydroxypropan-2-yl)-3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate	77916107	Click to see	506.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
methyl foveolate A	70698185	Click to see	506.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(5S,8R,9S,10S,13S,14S,17R)-17-hydroxy-17-[(1R)-1-hydroxyethyl]-3,3-dimethoxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15-dodecahydrocyclopenta[a]phenanthren-16-one	102026325	Click to see CC(C1(C(=O)CC2C1(CCC3C2CCC4C3(CCC(C4)(OC)OC)C)C)O)O	394.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
17-Hydroxy-17-(1-hydroxyethyl)-3,3-dimethoxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15-dodecahydrocyclopenta[a]phenanthren-16-one	162865954	Click to see	394.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
> 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
> Organoheterocyclic compounds / Benzofurans / Flavaglines
(-)-Silvestrol	11787114	Click to see	654.70	unknown	https://doi.org/10.1021/JO040120F
Episilvestrol	11467934	Click to see	654.70	unknown	https://doi.org/10.1021/JO040120F
methyl 6-[[6-(1,2-dihydroxyethyl)-3-methoxy-1,4-dioxan-2-yl]oxy]-1,8b-dihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	21301152	Click to see COC1C(OC(CO1)C(CO)O)OC2=CC3=C(C(=C2)OC)C4(C(C(C(C4(O3)C5=CC=C(C=C5)OC)C6=CC=CC=C6)C(=O)OC)O)O	654.70	unknown	https://doi.org/10.1021/JO040120F
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Zanthopyranone	10419590	Click to see	170.16	unknown	via CMAUP database
> 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	via CMAUP database
Gamma-Fagarine	107936	Click to see	229.23	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
> 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 / Cinnamic acids and derivatives / Cinnamic acid amides
Pyramidatine	1755965	Click to see	322.40	unknown	https://doi.org/10.1021/NP50094A004
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see	206.19	unknown	via CMAUP database
> 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

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Aglaia silvestris

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top