Phaleria macrocarpa

Details Top

Internal ID UUID64405a0b25e91579096781
Scientific name Phaleria macrocarpa
Authority Boerl.
First published in Handl. Fl. Ned. Ind. 3: 111 (1900)

Ethnobotanical Use Top

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Important notice
  • 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 Uses

Among Javanese communities in Central and East Java, decoctions of Phaleria macrocarpa leaves and bark are taken for gastrointestinal discomfort and as a general tonic (Rohyani et al., 2015). In Bali, a poultice of macerated leaves is applied to swellings, with support for analgesic and anti-inflammatory actions (Rufi et al., 2013). In West Java’s traditional healers, infusions of the fruit are used for diabetes and hypertension, occasionally combined with other plants (Nurjanah et al., 2016). In Malaysia, tea-like infusions of dried fruits and leaves are drunk for hypertension and mild colds (Al-Snafi, 2015). Across Java, Malaysia, and southern Thailand, poultices of leaves or fruit are applied to wounds and burns, sometimes as a paste with other botanicals (Basir et al., 2014; Fard et al., 2017).

A practical tea preparation: rinse a half cup of dried young leaves, place in 1 liter of near-boiling water, simmer gently 10–15 minutes, then steep off-heat for another 10 minutes. Strain and drink warm in two divided doses in a day. A commonly used amount among Javanese folk healers is 6–12 g dried leaves per liter. Avoid in pregnancy; monitor blood sugar and blood pressure if used concurrently with standard medicines; start with smaller quantities and discontinue if GI upset occurs (Fard et al., 2017).

Well-established constituents include saponins, flavonoids such as quercetin and kaempferol, coumarins, phenolics such as gallic acid, lignans, and phalerin; the fruit skin is notably rich in saponins and phenolics. The decoctions and infusions used in Java and Malaysia leverage these antioxidant and anti-inflammatory compounds, aligning with the reported gastrointestinal, tonic, and blood-pressure applications (Rohyani et al., 2015; Al-Snafi, 2015; Fard et al., 2017). Contemporary work explores these extracts for antimicrobial and anti-diabetic activity, and in Indonesia they remain part of the local pharmacopoeia, with teas and tinctures widely available in urban markets and online (Al-Snafi, 2015; Fard et al., 2017).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Drimyspermum macrocarpum Scheff. Ann. Jard. Bot. Buitenzorg 1: 46 (1876)
Phaleria calantha Gilg Nova Guinea 8: 411 (1910)
Phaleria papuana Warb. ex K.Schum. & Lauterb. Fl. Schutzgeb. Südsee : 460 (1900)
Phaleria wichmannii Valeton Icon. Bogor. 4: t. 371 (1913)
Phaleria papuana var. wichmannii (Valeton) Backer Bekn. Fl. Java 4a(2, fam. 77): 2 1942

Common names Top

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Language Common/alternative name
bjn kamalaka
Indonesian mahkota dewa
jv mahkota dewa
Malayalam മക്കോട്ടദേവ
Malay pokok mahkota dewa
Malay mahkota dewa
su mahkota déwa
Chinese 皇冠果
Chinese 大皇冠果

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001281784
UNII O7QW247SCY
Tropicos 50315226
KEW urn:lsid:ipni.org:names:832478-1
The Plant List tro-50315226
Open Tree Of Life 428516
NCBI Taxonomy 223762
IUCN Red List 198841662
IPNI 832478-1
iNaturalist 345937
GBIF 5524327
Freebase /m/0dd99xd
EOL 5470270
USDA GRIN 468733
Wikipedia Phaleria_macrocarpa
CMAUP NPO25054

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
Premenstrual syndrome: new insights into etiology and review of treatment methods Modzelewski S, Oracz A, Żukow X, Iłendo K, Śledzikowka Z, Waszkiewicz N Front Psychiatry 23-Apr-2024
PMCID:PMC11075635
doi:10.3389/fpsyt.2024.1363875
PMID:38716118
Antidiabetic Property Optimization from Green Leafy Vegetables Using Ultrasound-Assisted Extraction to Improve Cracker Production Maser WH, Maiyah N, Karnjanapratum S, Nukthamna P, Thompson AK, Huda N, Moula Ali AM, Bavisetty SC Prev Nutr Food Sci 31-Mar-2024
PMCID:PMC10987381
doi:10.3746/pnf.2024.29.1.47
PMID:38576886
Mathematical Modeling Approach and Simulation in Food Drying Applications Lončar B, Pezo L Foods 24-Jan-2024
PMCID:PMC10855026
doi:10.3390/foods13030384
PMID:38338519
Nondestructive Metabolomic Fingerprinting: FTIR, NIR and Raman Spectroscopy in Food Screening Cebi N, Bekiroglu H, Erarslan A Molecules 04-Dec-2023
PMCID:PMC10707828
doi:10.3390/molecules28237933
PMID:38067662
Potential of electro-sprayed purified mangiferin nanoparticles for anti-aging cosmetic applications Chomchoei N, Leelapornpisid P, Tipduangta P, Sangthong P, Papan P, Sirithunyalug B, Samutrtai P RSC Adv 01-Dec-2023
PMCID:PMC10690135
doi:10.1039/d3ra06308a
PMID:38046636
Assessment of antibacterial activity and cytotoxic effects of in vitro and in vivo plant parts of a medicinal plant Gynura procumbens (Lour.) Merr. Saha S, Al Amin GM, Khan MS, Goswami B, Afroz F, Habib MA, Akter S, Banu TA Heliyon 28-Nov-2023
PMCID:PMC10731072
doi:10.1016/j.heliyon.2023.e22954
PMID:38125427
Improvement in Pharmacological Activity of Mahkota Dewa (Phaleria macrocarpa (Schef. Boerl)) Seed Extracts in Nanoemulsion Dosage Form: In vitro and In vivo Studies Agustin E, Insanu M, Mauludin R Pharm Nanotechnol 05-Oct-2023
PMCID:PMC10661950
doi:10.2174/2211738511666230602100045
PMID:37264623
Anti-inflammatory natural products modulate interleukins and their related signaling markers in inflammatory bowel disease: A systematic review Gandhi GR, Mohana T, Athesh K, Hillary VE, Vasconcelos AB, Farias de Franca MN, Montalvão MM, Ceasar SA, Jothi G, Sridharan G, Gurgel RQ, Xu B J Pharm Anal 22-Sep-2023
PMCID:PMC10785269
doi:10.1016/j.jpha.2023.09.012
PMID:38223446
Changes in the Physical Properties and Volatile Odor Characteristics of Shiitake Mushrooms (Lentinula edodes) in Far Infrared Radiation Drying Xie L, Jiang YS, Wang YB, Xiao HW, Liu W, Ma Y, Zhao XY Foods 25-Aug-2023
PMCID:PMC10486590
doi:10.3390/foods12173213
PMID:37685146
Antibacterial activity of hexane and methanol fractions of some selected plants against Klebsiella pneumoniae Andriani Y, Hanifah W, Kholieqoh AH, Abdul Majid FA, Hermansyah H, Amir H, Muhammad TS J Adv Pharm Technol Res 28-Jul-2023
PMCID:PMC10483901
doi:10.4103/JAPTR.JAPTR_183_23
PMID:37692002
Effect of Temperatures on Drying Kinetics, Extraction Yield, Phenolics, Flavonoids, and Antioxidant Activity of Phaleria macrocarpa (Scheff.) Boerl. (Mahkota Dewa) Fruits Stephenus FN, Benjamin MA, Anuar A, Awang MA Foods 27-Jul-2023
PMCID:PMC10417056
doi:10.3390/foods12152859
PMID:37569127
Phytochemicals: Alternative for Infertility Treatment and Associated Conditions Chorosho SH, Malik N, Panesar G, Kumari P, Jangra S, Kaur R, Al-Ghamdi MS, Albishi TS, Chopra H, Singh R, Murthy HC Oxid Med Cell Longev 11-May-2023
PMCID:PMC10195183
doi:10.1155/2023/1327562
PMID:37215366
Natural Gallic Acid and Methyl Gallate Induces Apoptosis in Hela Cells through Regulation of Intrinsic and Extrinsic Protein Expression Abdullah H, Ismail I, Suppian R, Zakaria NM Int J Mol Sci 09-May-2023
PMCID:PMC10218240
doi:10.3390/ijms24108495
PMID:37239840
Revealing the Second and the Third Causes of AgNPs Property to Restore the Bacterial Susceptibility to Antibiotics Bogdanchikova N, Maklakova M, Villarreal-Gómez LJ, Nefedova E, Shkil NN, Plotnikov E, Pestryakov A Int J Mol Sci 26-Apr-2023
PMCID:PMC10178359
doi:10.3390/ijms24097854
PMID:37175561
Phaleria macrocarpa (Scheff.) Boerl.: An updated review of pharmacological effects, toxicity studies, and separation techniques Ahmad R, Khairul Nizam Mazlan M, Firdaus Abdul Aziz A, Mohd Gazzali A, Amir Rawa MS, Wahab HA Saudi Pharm J 12-Apr-2023
PMCID:PMC10205762
doi:10.1016/j.jsps.2023.04.006
PMID:37234341

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 / Cytochalasans
[(1S,2R,3E,5R,7S,9E,11S,14S,15R,16S)-16-benzyl-5-hydroxy-13-(hydroxymethyl)-5,7,14-trimethyl-6,18-dioxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,12-trien-2-yl] acetate 102258993 Click to see 507.60 unknown via CMAUP database
Cytochalasin D 5458428 Click to see 507.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
7-Chloromellein-5-ol 102258989 Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1 228.63 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 25769005 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid 486250 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-[(8S)-1,8-dimethyl-7,8-dihydronaphthalen-2-yl]propane-1,2,3-triol 44555346 Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C 248.32 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S,4S)-6-(3-hydroxyprop-1-en-2-yl)-4,5-dimethyl-1,2,3,4-tetrahydronaphthalene-1,2-diol 44255026 Click to see 248.32 unknown via CMAUP database
7-Chloroscytalone 102258990 Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O 228.63 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol 91885030 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C 400.50 unknown via CMAUP database
Isotaxiresinol 9,9'-acetonide 102004573 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)O)O)OC)C 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101568249 Click to see 344.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-4-(ethoxymethyl)-5-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101936591 Click to see 404.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol 10022393 Click to see 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-hydroxy-4-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101369318 Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1S,3R,11S)-8,9-dimethoxy-15,15-dimethyl-4,14-dioxo-7-propan-2-yl-2-oxatetracyclo[9.4.0.01,3.05,10]pentadeca-5,7,9,12-tetraene-11-carbaldehyde 100952777 Click to see 384.40 unknown via CMAUP database
(2S,4aS,10aR)-2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101529198 Click to see 316.40 unknown via CMAUP database
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one 100952776 Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C 302.50 unknown via CMAUP database
Hinokiol 12310492 Click to see 302.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
Taxamairin A 130631 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC 338.40 unknown via CMAUP database
Taxamairin B 130632 Click to see 352.40 unknown via CMAUP database
Taxamairin H 100952784 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC 338.40 unknown via CMAUP database
Taxusabietane A 76330776 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5319245 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 769.90 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'R,9'R,10'R,13'S)-2',5',10',13'-tetraacetyloxy-1',9'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 21159040 Click to see 610.60 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',13'-diacetyloxy-1',7',9',10'-tetrahydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 102066555 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O 526.60 unknown via CMAUP database
[(1'S,2S,2'R,3'R,5'S,8'R,9'R,10'R,14'S)-9'-acetyloxy-2',5',14'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-10'-yl] acetate 11247972 Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C 452.50 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',10',13'-triacetyloxy-1',7',9'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5321726 Click to see 568.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321730 Click to see 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321728 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',9',10',13'-tetraacetyloxy-1',7'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5316776 Click to see 610.60 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 24862000 Click to see 450.50 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 101006401 Click to see 534.60 unknown via CMAUP database
[(1R,2S,3S,5S,8R,9R,10R,11S,13R,16S)-5,16-diacetyloxy-10-(acetyloxymethyl)-8,9,11-trihydroxy-3-(2-hydroxypropan-2-yl)-6-methyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-2-yl] benzoate 10886794 Click to see 646.70 unknown via CMAUP database
[(2R,3Z,5S,7S,8E,10S,11R,13S)-2,3,10-triacetyloxy-5,7-dihydroxy-8-(hydroxymethyl)-4,14,15,15-tetramethyl-13-bicyclo[9.3.1]pentadeca-1(14),3,8-trienyl] acetate 6325023 Click to see 552.60 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-2,5,6,8,10-pentaacetyloxy-4-hydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321724 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 654.70 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-5,6,8,10-tetraacetyloxy-2,4-dihydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321723 Click to see 612.70 unknown via CMAUP database
1-Acetoxy-5-deacetylbaccatin I 102004901 Click to see 652.70 unknown via CMAUP database
13-Deacetylcanadensene_758363543 6325022 Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
13-O-Deacetyltaxumairol Z 10864961 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 604.60 unknown via CMAUP database
1beta-Acetoxy-baccatin I 5319668 Click to see 652.70 unknown via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I 21159039 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
CID 5318150 5318150 Click to see 652.70 unknown via CMAUP database
Taxin B 5321699 Click to see 534.60 unknown via CMAUP database
Taxumairol B 10053709 Click to see 568.60 unknown via CMAUP database
Taxumairol D 102065502 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
taxumairol F 10651372 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
Taxumairol K 10769688 Click to see 588.60 unknown via CMAUP database
Taxumairol U 11124920 Click to see 612.70 unknown via CMAUP database
Taxumairol V 10875480 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1O)C(C)(C)O)O)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 570.60 unknown via CMAUP database
Taxumairol W 10918805 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10918656 Click to see 550.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10907330 Click to see 508.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-8-acetyloxy-4,7,12,13-tetrahydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 11733602 Click to see 484.50 unknown via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11814223 Click to see 630.70 unknown via CMAUP database
Sporogen-AO 1 177175 Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O 248.32 unknown via CMAUP database
Taxumairol Y 11005902 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 526.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D 100952779 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 762.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione 100952778 Click to see 384.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 11-oxosteroids
(8S,9R,13R,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,9,13,14-tetramethyl-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-11-one 101839558 Click to see CC1=C2CCC3C4(CC(C(C4(CC(=O)C3(C2=CC(=C1O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C 500.60 unknown https://doi.org/10.1271/BBB.70627
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(8S,9R,13R,14S,16R,17R)-2,3,16-trihydroxy-4,9,13,14-tetramethyl-11-oxo-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate 13819212 Click to see 542.70 unknown https://doi.org/10.1271/BBB.70627
[6-hydroxy-2-methyl-5-oxo-6-(2,3,16-trihydroxy-4,9,13,14-tetramethyl-11-oxo-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-17-yl)hept-3-en-2-yl] acetate 74822202 Click to see 542.70 unknown https://doi.org/10.1271/BBB.70627
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,3,16-trihydroxy-4,9,13,14-tetramethyl-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-11-one 163020822 Click to see 500.60 unknown https://doi.org/10.1271/BBB.70627
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(8S,9R,13R,14S,16R,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-3,16-dihydroxy-4,9,13,14-tetramethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-11-one 101641876 Click to see CC1=C2CCC3C4(CC(C(C4(CC(=O)C3(C2=CC(=C1O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CCC(C)(C)O)O)O)C 664.80 unknown https://doi.org/10.1271/BBB.70627
[(E,6R)-6-[(8S,9R,13R,14S,16R,17R)-3,16-dihydroxy-4,9,13,14-tetramethyl-11-oxo-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 101641878 Click to see CC1=C2CCC3C4(CC(C(C4(CC(=O)C3(C2=CC(=C1O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)OC(=O)C)O)O)C 704.80 unknown https://doi.org/10.1271/BBB.70627
[6-[3,16-dihydroxy-4,9,13,14-tetramethyl-11-oxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 74822915 Click to see CC1=C2CCC3C4(CC(C(C4(CC(=O)C3(C2=CC(=C1O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)OC(=O)C)O)O)C 704.80 unknown https://doi.org/10.1271/BBB.70627
17-(1,5-dihydroxy-1,5-dimethyl-2-oxo-hexyl)-3,16-dihydroxy-4,9,13,14-tetramethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-7,8,12,15,16,17-hexahydro-6H-cyclopenta[a]phenanthren-11-one 500268 Click to see 664.80 unknown https://doi.org/10.1271/BBB.70627
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11072583 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C 714.80 unknown via CMAUP database
Taxacin 15226199 Click to see 816.80 unknown via CMAUP database
Taxumairol R 21593833 Click to see 728.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1E,3S,4R,6S,9R,11S)-3,9-diacetyloxy-7,11,16,16-tetramethyl-10,14-dioxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7,12-trienyl] acetate 10027779 Click to see 472.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-Hydroxy-4-methoxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-(4-hydroxyphenyl)methanone 78071755 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)C3=CC=C(C=C3)O)O 422.40 unknown https://doi.org/10.1271/BBB.90242
Mahkoside A 71451475 Click to see 422.40 unknown https://doi.org/10.1271/BBB.90242
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
Cis-7-chloro-4-hydroxymellein 102258988 Click to see 228.63 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one 40468114 Click to see CC(=C)C1(C(=CC(=O)O1)OC)O 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione 639435 Click to see 154.12 unknown via CMAUP database
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2S,3S,4Z,6S,8S)-3,6,8-trihydroxy-2-nonyl-2,3,6,7,8,9-hexahydrooxecin-10-one 44632077 Click to see CCCCCCCCCC1C(C=CC(CC(CC(=O)O1)O)O)O 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid 3084064 Click to see 154.12 unknown via CMAUP database

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