Aglaia silvestris - Unknown
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Details Top

Internal ID UUID64400818e89d3989317538
Scientific name Aglaia silvestris
Authority (M.Roem.) Merr.
First published in Interpr. Herb. Amboin. : 310 (1917)

Description Top

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Aglaia silvestris is a plant species belonging to the Meliaceae family and is native to several countries in Southeast Asia and the Pacific. It is known for its role in the discovery and naming of the Rocaglamide derivatives silvestrol and episilvestrol, which were derived from the fruits and twigs of a related species, Aglaia foveolata. This plant has significant medicinal properties and has been used in traditional medicine for centuries.

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

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

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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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
    • 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

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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
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
Discovery of anticancer agents of diverse natural origin Kinghorn AD, Carcache de Blanco EJ, Chai HB, Orjala J, Farnsworth NR, Soejarto DD, Oberlies NH, Wani MC, Kroll DJ, Pearce CJ, Swanson SM, Kramer RA, Rose WC, Fairchild CR, Vite GD, Emanuel S, Jarjoura D, Cope FO Pure Appl Chem 01-Jan-2009
PMCID:PMC2765058
doi:10.1351/PAC-CON-08-10-16
PMID:20046887

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 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
2'-Episimulanoquinoline 102236946 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)CC4C5=C(C=CC(=C5OC)OC)C6=C(N4C)C7=CC8=C(C=C7C=C6)OCO8 618.70 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Simulansamide 5321312 Click to see CN(C=O)C1=C(C=CC2=CC(=C(C=C21)OC)OC)C3=C(C(=C(C=C3)OC)OC)O 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 COC1=CC(=CC(=C1O)OC)C(=O)O 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
5-(Hydroxymethyl)-1-[2-(4-hydroxyphenyl)ethyl]pyrrole-2-carbaldehyde 636825 Click to see C1=CC(=CC=C1CCN2C(=CC=C2C=O)CO)O 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 CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalyl acetate, (-)- 442474 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-alpha-Bulgarene 12306053 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
(+)-alpha-Muurolene 12306049 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid 5280896 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 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 CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.025
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 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 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,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 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
(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 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
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 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
> 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 CC12CCC(C1CCC3C2(CCC(C3(C)CC(OC)OC)C(C)(C)C(=O)O)C)C4(CCC(O4)C(C)(C)O)C 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 CC12CCC(C1CCC3C2(CCC(C3(C)CC(OC)OC)C(C)(C)C(=O)O)C)C4(CCC(O4)C(C)(C)O)C 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 CC12CCC(C1CCC3C2(CCC(C3(C)CC(OC)OC)C(C)(C)C(=O)O)C)C4(CCC(O4)C(C)(C)O)C 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 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
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 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
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 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
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 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
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.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
Methyl isoeichlerianate 101859479 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 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
> 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 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-[(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 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 foveolate A 70698185 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
> 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 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 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
Episilvestrol 11467934 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
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
Silvestrol 11787114 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
3,5-Dimethoxy-2-methyl-pyran-4-one 10419590 Click to see CC1=C(C(=O)C(=CO1)OC)OC 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 CC1=C2C(=C3C=CC4=CC5=C(C=C4C3=N1)OCO5)C=CC(=C2OC)OC 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
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Robustine 164950 Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O 215.20 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 CN1C2=CC=CC=C2C(=C(C1=O)CC3=C(C4=CC=CC=C4N(C3=O)C)O)O 362.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
4-Methoxy-1H-quinolin-2-one 600167 Click to see COC1=CC(=O)NC2=CC=CC=C21 175.18 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
6,6,12-Trimethylisochromeno[4,3-c]quinolin-11-one 10017165 Click to see CC1(C2=CC=CC=C2C3=C(O1)C4=CC=CC=C4N(C3=O)C)C 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 CC1=CC2=C(C=C1)C(OC3=C2C(=O)N(C4=CC=CC=C43)C)(C)C 305.40 unknown via CMAUP database
Flindersine 68230 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C 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
Ribalinine 932818 Click to see CC1(C(CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C 259.30 unknown via CMAUP database
Zanthobungeanine 5315422 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-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
(+)-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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-[4-[[(E)-3-phenylprop-2-enoyl]amino]butyl]benzamide 1755965 Click to see C1=CC=C(C=C1)C=CC(=O)NCCCCNC(=O)C2=CC=CC=C2 322.40 unknown https://doi.org/10.1021/NP50094A004
> 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 / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown via CMAUP database
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database

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