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Mimusops laurifolia

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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 UUID643fe3840efa8358556165
Scientific name Mimusops laurifolia
Authority (Forssk.) Friis
First published in Kew Bull. 35: 787 (1981)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mimusops schimperi Hochst. Tent. Fl. Abyss. 2: 22 (1850)
Binectaria laurifolia Forssk. Fl. Aegypt.-Arab. : cx (1775)

Common names Top

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Language Common/alternative name
Arabic نبخ غاري الأوراق
Arabic برساء
Arabic لبخ

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000244634
Tropicos 50305169
KEW urn:lsid:ipni.org:names:909101-1
The Plant List kew-128512
Open Tree Of Life 421748
NCBI Taxonomy 1227943
IPNI 909101-1
GBIF 2883821
EOL 1154214
Wikipedia Mimusops_laurifolia
CMAUP NPO27880

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
Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia Al-Ghamdi AA, Al-Sagheer NA Plants (Basel) 22-Mar-2023
PMCID:PMC10058344
doi:10.3390/plants12061402
PMID:36987090
Phenolic compounds versus SARS-CoV-2: An update on the main findings against COVID-19 Tirado-Kulieva VA, Hernández-Martínez E, Choque-Rivera TJ Heliyon 20-Sep-2022
PMCID:PMC9484857
doi:10.1016/j.heliyon.2022.e10702
PMID:36157310
Predicting potential distribution of Ziziphus spinosa (Bunge) H.H. Hu ex F.H. Chen in China under climate change scenarios Zhao Q, Mi Z, Lu C, Zhang X, Chen L, Wang S, Niu J, Wang Z Ecol Evol 17-Feb-2022
PMCID:PMC8855015
doi:10.1002/ece3.8629
PMID:35222979
Inhibition of SARS-CoV-2 main protease by phenolic compounds from Manilkara hexandra (Roxb.) Dubard assisted by metabolite profiling and in silico virtual screening Abd El-Mordy FM, El-Hamouly MM, Ibrahim MT, El-Rheem GA, Aly OM, Abd El-kader AM, Youssif KA, Abdelmohsen UR RSC Adv 28-Aug-2020
PMCID:PMC9056568
doi:10.1039/d0ra05679k
PMID:35518160
Influence of gold and silver nanoparticles on the germination and growth of Mimusops laurifolia seeds in the South-Western regions in Saudi Arabia Abdulla Abdulaziz Alshehddi L, Bokhari N Saudi J Biol Sci 21-Nov-2019
PMCID:PMC6933259
doi:10.1016/j.sjbs.2019.11.013
PMID:31889884
Application of metabolomics and molecular networking in investigating the chemical profile and antitrypanosomal activity of British bluebells (Hyacinthoides non-scripta) Raheem DJ, Tawfike AF, Abdelmohsen UR, Edrada-Ebel R, Fitzsimmons-Thoss V Sci Rep 22-Feb-2019
PMCID:PMC6385288
doi:10.1038/s41598-019-38940-w
PMID:30796274
Antioxidant potential of phenolic extracts of Mimusops elengi Shahwar D, Raza MA Asian Pac J Trop Biomed 01-Jul-2012
PMCID:PMC3609342
doi:10.1016/S2221-1691(12)60094-X
PMID:23569968
Comparison of the Selected Secondary Metabolite Content Present in the Cancer-Bush Lessertia (Sutherlandia) Frutescens L. Extracts Shaik S, Singh N, Nicholas A Afr J Tradit Complement Altern Med 01-Jun-2011
PMCID:PMC3218450
doi:10.4314/ajtcam.v8i4.14
PMID:22654222
Saponins from the seeds of Mimusops laurifolia. Eskander J, Lavaud C, Pouny I, Soliman HS, Abdel-Khalik SM, Mahmoud II Phytochemistry 01-Aug-2006
doi:10.1016/J.PHYTOCHEM.2005.11.008
PMID:16376393

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene 44268166 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C 254.40 unknown via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol 101586702 Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C 286.50 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 300.40 unknown via CMAUP database
Abietatriene 6432211 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C 272.50 unknown via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 11290126 Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C 318.50 unknown via CMAUP database
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4R,4aR,5R,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5-dihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 101691097 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1237.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4R,4aR,5R,6aR,6bS,8R,8aR,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid 101409947 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)OC1C(C(CO1)(CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1385.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] 5,8,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 14707463 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1239.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] 8,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 75110929 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1223.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5-dihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 156602834 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1237.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 74203438 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1253.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid 162910535 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)OC1C(C(CO1)(CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1385.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Arganine C 21603545 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1239.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Mi-saponin A 179637 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1223.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Tieghemelin 11051494 Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O 1253.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown via CMAUP database
16-Oxo-21-episerratenediol 101280208 Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown via CMAUP database
Serratenediol 3-methyl ether 21672660 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C 456.70 unknown via CMAUP database
Serratenediol dimethyl ether 101280202 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C 470.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene 102594798 Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C 276.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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