PlantaeDB Logo
Login Sign-up

Aglaia foveolata

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

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400810e610a149976872
Scientific name Aglaia foveolata
Authority Pannell
First published in Kew Bull., Addit. Ser. 16: 211 (1992)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000524080
Tropicos 50162160
KEW urn:lsid:ipni.org:names:968391-1
The Plant List kew-2626313
Open Tree Of Life 5516770
NCBI Taxonomy 1475093
IUCN Red List 34910
IPNI 968391-1
iNaturalist 189033
GBIF 5597693
Freebase /m/02x7pyy
USDA GRIN 448902
Wikipedia Aglaia_foveolata
CMAUP NPO8087

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
Anticancer Drug Discovery Based on Natural Products: From Computational Approaches to Clinical Studies Chunarkar-Patil P, Kaleem M, Mishra R, Ray S, Ahmad A, Verma D, Bhayye S, Dubey R, Singh HN, Kumar S Biomedicines 16-Jan-2024
PMCID:PMC10813144
doi:10.3390/biomedicines12010201
PMID:38255306
MicroRNAs Associated with a Bad Prognosis in Acute Myeloid Leukemia and Their Impact on Macrophage Polarization Jimbu L, Mesaros O, Joldes C, Neaga A, Zaharie L, Zdrenghea M Biomedicines 07-Jan-2024
PMCID:PMC10813737
doi:10.3390/biomedicines12010121
PMID:38255226
Tracing down the updates on Ebola virus surges: An update on anti-ebola therapeutic strategies Malik S, Waheed Y J Transl Int Med 02-Sep-2023
PMCID:PMC10474883
doi:10.2478/jtim-2023-0100
PMID:37662888
Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study de Blanco EJ, Addo EM, Rakotondraibe HL, Soejarto DD, Kinghorn AD Nat Prod Rep 19-Jul-2023
PMCID:PMC10524867
doi:10.1039/d2np00080f
PMID:37194649
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
An overview on medicinal plants used for combating coronavirus: Current potentials and challenges Abou Baker DH, Hassan EM, El Gengaihi S J Agric Food Res 20-May-2023
PMCID:PMC10198795
doi:10.1016/j.jafr.2023.100632
PMID:37251276
Phytochemicals and bioactive compounds effective against acute myeloid leukemia: A systematic review Egbuna C, Patrick‐Iwuanyanwu KC, Onyeike EN, Khan J, Palai S, Patel SB, Parmar VK, Kushwaha G, Singh O, Jeevanandam J, Kumarasamy S, Uche CZ, Narayanan M, Rudrapal M, Odoh U, Chikeokwu I, Găman M, Saravanan K, Ifemeje JC, Ezzat SM, Olisah MC, Chikwendu CJ, Adedokun KA, Imodoye SO, Bello IO, Twinomuhwezi H, Awuchi CG Food Sci Nutr 15-May-2023
PMCID:PMC10345688
doi:10.1002/fsn3.3420
PMID:37457145
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Virtual and In Vitro Screening of Natural Products Identifies Indole and Benzene Derivatives as Inhibitors of SARS-CoV-2 Main Protease (Mpro) Ang D, Kendall R, Atamian HS Biology (Basel) 29-Mar-2023
PMCID:PMC10135783
doi:10.3390/biology12040519
PMID:37106720
Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L Phytochem Rev 12-Mar-2023
PMCID:PMC10008214
doi:10.1007/s11101-023-09855-2
PMID:37359711
Strategies to target the cancer driver MYC in tumor cells Weber LI, Hartl M Front Oncol 08-Mar-2023
PMCID:PMC10032378
doi:10.3389/fonc.2023.1142111
PMID:36969025
Role of bioactive compounds in the treatment of hepatitis: A review Roy A, Roy M, Gacem A, Datta S, Zeyaullah M, Muzammil K, Farghaly TA, Abdellattif MH, Yadav KK, Simal-Gandara J Front Pharmacol 21-Dec-2022
PMCID:PMC9810990
doi:10.3389/fphar.2022.1051751
PMID:36618936
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
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
Virtual screening and molecular dynamics simulation analysis of Forsythoside A as a plant-derived inhibitor of SARS-CoV-2 3CLpro Bibi S, Khan MS, El-Kafrawy SA, Alandijany TA, El-Daly MM, Yousafi Q, Fatima D, Faizo AA, Bajrai LH, Azhar EI Saudi Pharm J 25-May-2022
PMCID:PMC9132386
doi:10.1016/j.jsps.2022.05.003
PMID:35637849

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
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1002/CHIN.200438214
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
N-[4-[[2-(2-hydroxy-4,6-dimethoxybenzoyl)-4-(4-methoxyphenyl)-4-oxo-3-phenylbutanoyl]amino]butyl]benzamide 162938714 Click to see COC1=CC=C(C=C1)C(=O)C(C2=CC=CC=C2)C(C(=O)C3=C(C=C(C=C3OC)OC)O)C(=O)NCCCCNC(=O)C4=CC=CC=C4 638.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4R,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 91752279 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
alpha-Muurolol 91753440 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown via CMAUP database
Grasshopper ketone 13922639 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)O)(C)C 224.30 unknown https://doi.org/10.1002/CHIN.200438214
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Ledol 6431133 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
(1aR,4R,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 162940153 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
(1aS,4S,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 25089154 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
4-Hydroxy-1-(hydroxymethyl)-4a-methyl-7-propan-2-yl-3,4,5,6-tetrahydronaphthalen-2-one 75576990 Click to see CC(C)C1=CC2=C(C(=O)CC(C2(CC1)C)O)CO 250.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
4,6-Diene-1beta,14-dihydroxyeudesma-3-one 50901153 Click to see CC(C)C1=CC2=C(C(=O)CC(C2(CC1)C)O)CO 250.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-Germacrene D 24771782 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
3-[(3aS,5aR,6S,9aR,9bR)-3-[(2S)-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 138113877 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/S0031-9422(98)00305-7
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/S0031-9422(98)00305-7
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
https://doi.org/10.1016/S0031-9422(98)00305-7
Eichlerianic acid 12315516 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/S0031-9422(98)00305-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
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/S0031-9422(98)00305-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(20R,24S)-20,24-Epoxy-25-hydroxydammaran-3-one 4357290 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
(8R,9R,10R,14S,17S)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 91884737 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1002/CHIN.200438214
15-[5-(2-Hydroxypropan-2-yl)-2-methyloxolan-2-yl]-2,7,7,11,12-pentamethyl-6-oxatetracyclo[9.7.0.02,8.012,16]octadecan-5-one 75576947 Click to see CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 474.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
20S,24S-epoxy-25-hydroxy-A-homo-4-oxadammaran-3-one 53318969 Click to see CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 474.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
3-[(3S,3aR,5aR,6R,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]propanoic acid 100927655 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
3-[(3S,3aR,5aR,6S,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]propanoic acid 162867736 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
3-[(3S,3aR,5aR,6S,7R,9aR,9bR)-7-(2-hydroxypropan-2-yl)-3-[(2S,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]propanoic acid 162867735 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
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]propanoic acid 77916115 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
3-epiocotillol II 12313664 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 460.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
Cabraleone 21625900 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
https://doi.org/10.1002/CHIN.200438214
Foveolin A 70698208 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
https://doi.org/10.1016/S0031-9422(98)00305-7
methyl 3-[(3S,3aR,5aR,6R,7R,9aR,9bR)-7-(2-hydroxypropan-2-yl)-3-[(2S,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 100927656 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
Ocotillol 3850493 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 460.70 unknown https://doi.org/10.1016/S0031-9422(98)00305-7
Ocotillone 12313665 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 458.70 unknown https://doi.org/10.1002/CHIN.200438214
rel-20R,24S-epoxy-25-hydroxy-A-homo-4-oxadammaran-3-one 53323547 Click to see CC1(C2CCC3(C(C2(CCC(=O)O1)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 474.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Eremanthin 100572 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18alpha,19alpha)-5alpha-Urs-20(30)-en-3-one 14485466 Click to see CC1C2C3CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)C 424.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
2-(12a-methoxy-7,10a,10b-trimethyl-8-propan-2-yl-7-propyl-2,3,4a,4b,5,6,6a,8,9,10,11,12-dodecahydro-1H-naphtho[1,2-h]chromen-3-yl)propan-2-ol 162851275 Click to see CCCC1(C(CCC2(C1CCC3C2(CCC4(C3OC(CC4)C(C)(C)O)OC)C)C)C(C)C)C 462.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
2-[(3S,4aR,4bS,6aR,7S,8R,10aR,10bR,12aS)-12a-methoxy-7,10a,10b-trimethyl-8-propan-2-yl-7-propyl-2,3,4a,4b,5,6,6a,8,9,10,11,12-dodecahydro-1H-naphtho[1,2-h]chromen-3-yl]propan-2-ol 162851276 Click to see CCCC1(C(CCC2(C1CCC3C2(CCC4(C3OC(CC4)C(C)(C)O)OC)C)C)C(C)C)C 462.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CHIN.200438214
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CHIN.200438214
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1002/CHIN.200438214
> Organoheterocyclic compounds / Benzofurans / Flavaglines
2'''-Episilvestrol 11679084 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 via CMAUP database
2''',5'''-Diepisilvestrol 11607102 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 via CMAUP database
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/10.1002/CHIN.200438214
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
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/10.1002/CHIN.200438214
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
> Organoheterocyclic compounds / Naphthopyrans
(1R,2R,5R,8S,10R,11S,14R,15R,20S)-8-(2-hydroxypropan-2-yl)-1,2,5,15,19,19-hexamethyl-9-oxapentacyclo[12.8.0.02,11.05,10.015,20]docosan-18-one 163194478 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4OC(CC5)C(C)(C)O)C)C)C)C 458.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
17,24-Epoxy-20alpha,25-dihydroxy-21-norbaccharan-3-one 50901039 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4OC(CC5)C(C)(C)O)O)C)C)C 460.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
5-Hydroxy-8-(2-hydroxypropan-2-yl)-1,2,15,19,19-pentamethyl-9-oxapentacyclo[12.8.0.02,11.05,10.015,20]docosan-18-one 75576946 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4OC(CC5)C(C)(C)O)O)C)C)C 460.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
8-(2-Hydroxypropan-2-yl)-1,2,5,15,19,19-hexamethyl-9-oxapentacyclo[12.8.0.02,11.05,10.015,20]docosan-18-one 72807847 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CCC5(C4OC(CC5)C(C)(C)O)C)C)C)C 458.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
(+)-Dehydrodiconiferyl alcohol 11824478 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
5-O-Methylhierochin D 188976 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993763/
> 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://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1002/CHIN.200438214
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1002/CHIN.200438214
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1002/CHIN.200438214
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
N-(4-benzamidobutyl)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-11-carboxamide 162925644 Click to see COC1=CC=C(C=C1)C23C(C(C(C2O)(C4=C(O3)C=C(C=C4OC)OC)O)C(=O)NCCCCNC(=O)C5=CC=CC=C5)C6=CC=CC=C6 652.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
N-(4-benzamidobutyl)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-10-carboxamide 162948843 Click to see COC1=CC=C(C=C1)C23C(C(C(C2O)(C4=C(O3)C=C(C=C4OC)OC)O)C5=CC=CC=C5)C(=O)NCCCCNC(=O)C6=CC=CC=C6 652.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/
N-[4-[2,3-dihydroxy-12,14-dimethoxy-8-(4-methoxyphenyl)-5-oxo-7-phenyl-9-oxa-4-azatetracyclo[8.4.0.02,6.03,8]tetradeca-1(10),11,13-trien-4-yl]butyl]benzamide 162945046 Click to see COC1=CC=C(C=C1)C23C(C4C(=O)N(C2(C4(C5=C(O3)C=C(C=C5OC)OC)O)O)CCCCNC(=O)C6=CC=CC=C6)C7=CC=CC=C7 650.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034361/

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.