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Mesua ferrea

Mesua ferrea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64405b862bb44652222834
Scientific name Mesua ferrea
Authority L.
First published in Sp. Pl. : 515 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Mesua nagana Gardner Calcutta J. Nat. Hist. 8: 4 (1847)
Mesua roxburghii Wight Ill. Ind. Bot. 1: 127 (1838)
Mesua salicina Planch. & Triana Ann. Sci. Nat., Bot. , sér. 4, 15: 302 (1861)
Mesua sclerophylla Thwaites Enum. Pl. Zeyl. : 407 (1864)
Mesua speciosa Choisy Mém. Nouv. Gen. Guttif. 19. 1823
Mesua walkeriana Planch. & Triana Ann. Sci. Nat., Bot. , sér. 4, 15: 301 (1861)
Mesua pedunculata Wight Ill. Ind. Bot. 1: 127 (1838)
Calophyllum nagassarium Burm.f. Fl. Indica : 121 (1768)
Mesua nagassarium (Burm.f.) Kosterm. Ceylon J. Sci., Biol. Sci. 12: 71 (1976)

Common names Top

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Language Common/alternative name
Arabic نار مشك
Arabic نار هندي
Arabic رمان بري
Arabic مسك الرمان
Assamese নাহৰ
Bengali নাগেশ্বর
gom सुरंगा
Hindi नाग केसर
Indonesian nagasari
Indonesian dewadaru
Japanese セイロンテツボク
Kannada ನಾಗಸಂಪಿಗೆ
Malayalam നാഗകേസരം
Malayalam നാഗപ്പൂവ്
Marathi नागचाफा
mrj Мезуя
Malay penaga lilin
Malay matopus
Malay lenggapus
Malay penaga
Malay pokok penaga lilin
Burmese ကံ့ကော်ပင်
Punjabi ਨਾਗ ਕੇਸਰ
Russian Цейлонское железное дерево
Russian Мезуя железная
Russian Меза железная
sa नागकेसरः
Sinhala නා
Tamil நாகமரம்
Tamil நாகம் (மலர்)
Tamil நாகம் (மரம்)
Telugu నాగకేసరి
Telugu చంపేయ
Thai บุนนาค
Thai บุนนาค,ต้น
Chinese 莫拉
Chinese 铁棱
Chinese 铁力木
Chinese 铁力木花
Chinese 喃木波朗
Chinese 埋波朗
Chinese 鐵力木
Chinese 铁栗木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Mesua ferrea var. coromandeliana (Wight) N.P.Singh J. Econ. Taxon. Bot. 10: 203 (1987 publ. 1988)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001296121
UNII 03JD5N07WU
Tropicos 7801420
KEW urn:lsid:ipni.org:names:428832-1
The Plant List tro-7801420
Open Tree Of Life 531923
NCBI Taxonomy 210380
IPNI 428832-1
iNaturalist 354814
GBIF 7330039
Freebase /m/07fz1j
EPPO MSUFE
EOL 2889806
USDA GRIN 24194
Wikipedia Mesua_ferrea
CMAUP NPO681

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
Comparative discriminant analysis of Mesua ferrea L. and its adulterants Kuerban M, Ma F, Shan L, Wang Y, Zhou G Heliyon 01-Apr-2024
PMCID:PMC11004703
doi:10.1016/j.heliyon.2024.e28459
PMID:38601576
Management of Otitis externa with Ayurvedic formulation Gandhak Rasayana- A case report Patil S, Bhat P J Ayurveda Integr Med 01-Apr-2024
PMCID:PMC10999474
doi:10.1016/j.jaim.2024.100893
PMID:38564934
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
The interaction of Suk-Saiyasna remedy with GABAA and CB1 receptor-targeting drugs: Enhancing hypnotic and sedative effects in in vivo models Damjuti W, Thitikornpong W, Saengow S, Thanusuwannasak T, Fuangfoo T, Boonruab J J Adv Pharm Technol Res 15-Jan-2024
PMCID:PMC10880918
doi:10.4103/JAPTR.JAPTR_355_23
PMID:38389972
Assessment of antimalarial activity of crude extract of Chan-Ta-Lee-La and Pra-Sa-Chan-Dang formulations and their plant ingredients for new drug candidates of malaria treatment: In vitro and in vivo experiments Chaniad P, Phuwajaroanpong A, Plirat W, Konyanee A, Septama AW, Punsawad C PLoS One 11-Jan-2024
PMCID:PMC10783769
doi:10.1371/journal.pone.0296756
PMID:38206944
Accumulate and consolidate the traditional vernacular timber preservation technologies through a field survey Mendis MS, Abeyrathna W, Halwatura RU, Amarasekara HS, Somadewa R, Jayasinghe R Heliyon 20-Dec-2023
PMCID:PMC10787270
doi:10.1016/j.heliyon.2023.e23907
PMID:38223715
3-Substituted Coumarins Inhibit NorA and MepA Efflux Pumps of Staphylococcus aureus de Araújo-Neto JB, Oliveira-Tintino CD, de Araújo GA, Alves DS, Ribeiro FR, Brancaglion GA, Carvalho DT, Lima CM, Mohammed Ali HS, Rather IA, Wani MY, Emran TB, Coutinho HD, Balbino VD, Tintino SR Antibiotics (Basel) 15-Dec-2023
PMCID:PMC10741188
doi:10.3390/antibiotics12121739
PMID:38136773
Brazilin from Caesalpinia sappan L. as a Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitor: Pharmacophore-Based Virtual Screening, In Silico Molecular Docking, and In Vitro Studies Iqbal M, Hasanah N, Arianto AD, Aryati WD, Puteri MU, Saputri FC Adv Pharmacol Pharm Sci 11-Oct-2023
PMCID:PMC10584496
doi:10.1155/2023/5932315
PMID:37860715
Antibacterial Effect of Ethanolic Extracts of Dodonaea viscosa L. Jacq. and Mammea americana L. against Staphylococci Isolated from Skin Lesions Pérez-Narváez OA, Castillo Hernández S SL, Leos-Rivas C, Pérez-Hernández RA, Chávez-Montes A, Verduzco-Martínez JA, Sánchez-García E Biomed Res Int 04-Sep-2023
PMCID:PMC10495233
doi:10.1155/2023/5584412
PMID:37700878
Integrating traditional ecological knowledge into habitat restoration: implications for meeting forest restoration challenges Haq SM, Pieroni A, Bussmann RW, Abd-ElGawad AM, El-Ansary HO J Ethnobiol Ethnomed 10-Aug-2023
PMCID:PMC10413632
doi:10.1186/s13002-023-00606-3
PMID:37559120
Chromosome-scale genomes of commercial timber trees (Ochroma pyramidale, Mesua ferrea, and Tectona grandis) Sahu SK, Liu M, Chen Y, Gui J, Fang D, Chen X, Yang T, He C, Cheng L, Yang J, Sahu DN, Li L, Wang H, Mu W, Wei J, Liu J, Zhao Y, Zhang S, Lisby M, Liu X, Xu X, Li L, Wang S, Liu H Sci Data 03-Aug-2023
PMCID:PMC10400565
doi:10.1038/s41597-023-02420-8
PMID:37537171
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
A Narrative Review of the Herbal Preparation of Ayurvedic, Traditional Chinese, and Kampō Medicines Applied as Radioprotectors Ibáñez B, Melero A, Montoro A, Merino-Torres JF, Soriano JM, San Onofre N Antioxidants (Basel) 17-Jul-2023
PMCID:PMC10376155
doi:10.3390/antiox12071437
PMID:37507975
Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK Biomolecules 25-Jun-2023
PMCID:PMC10377637
doi:10.3390/biom13071038
PMID:37509074
Natural Ingredients of Transdermal Drug Delivery Systems as Permeation Enhancers of Active Substances through the Stratum Corneum Schafer N, Balwierz R, Biernat P, Ochędzan-Siodłak W, Lipok J Mol Pharm 06-Jun-2023
PMCID:PMC10324402
doi:10.1021/acs.molpharmaceut.3c00126
PMID:37279070

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
> Alkaloids and derivatives / Hasubanan alkaloids
(8S,11R)-11-hydroxy-3,4-dimethoxy-17-methyl-18-oxa-17-azapentacyclo[8.4.3.18,11.01,10.02,7]octadeca-2(7),3,5-trien-12-one 5319384 Click to see CN1CCC23C14CC(C5=C2C(=C(C=C5)OC)OC)OC4(C(=O)CC3)O 345.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
1,3-Dibenzylurea 72889 Click to see C1=CC=C(C=C1)CNC(=O)NCC2=CC=CC=C2 240.30 unknown via CMAUP database
Benzylcarbamic Acid 230054 Click to see C1=CC=C(C=C1)CNC(=O)O 151.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
4-Aminobenzoic acid 978 Click to see C1=CC(=CC=C1C(=O)O)N 137.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
Phenylacetonitrile 8794 Click to see C1=CC=C(C=C1)CC#N 117.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
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
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Octacosanoic acid 10470 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-dihydroxypropyl (9Z)-octadec-9-enoate 25021708 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)O 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Bornane-2,6-dione 382555 Click to see CC1(C2CC(=O)C1(C(=O)C2)C)C 166.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylated hydroquinones
2-[(3R)-3-hydroxy-3,7-dimethyloct-6-enyl]benzene-1,4-diol 162946344 Click to see CC(=CCCC(C)(CCC1=C(C=CC(=C1)O)O)O)C 264.36 unknown https://doi.org/10.3987/COM-96-7557
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
5,7-Dihydroxy-4-(1-hydroxypropyl)-8-(2-methylbutanoyl)-6-[3,7-dimeth ylocta-2,6-dienyl]-2h-chromen-2-one 5464895 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)O)O)CC=C(C)CCC=C(C)C)O 456.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-4-[(1R)-1-hydroxypropyl]-8-[(2R)-2-methylbutanoyl]chromen-2-one 163186708 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)O)O)CC=C(C)CCC=C(C)C)O 456.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5,8a,9',13'-tetramethyl-4'-methylidenespiro[5,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-3,15'-6-oxatetracyclo[9.2.2.01,10.03,7]pentadeca-9,12-diene]-2,5'-dione 163033077 Click to see CC1CCCC2(C1=CC3C(C2)OC(=O)C34CC56CC7C(CC(=C5C4C=C6C)C)OC(=O)C7=C)C 460.60 unknown https://doi.org/10.1016/0031-9422(88)80153-5
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
all-trans-Neoxanthin 5281247 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=C=C1C(CC(CC1(C)O)O)(C)C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C 600.90 unknown via CMAUP database
Lutein 5281243 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
Violaxanthin 448438 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
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 https://doi.org/10.1016/0031-9422(88)80153-5
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10575639308043837
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(88)80153-5
https://doi.org/10.1016/S0031-9422(00)83507-4
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
https://doi.org/10.1016/0031-9422(88)80153-5
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
CID 16058264 16058264 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 841.30 unknown via CMAUP database
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 via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 91492 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown via CMAUP database
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-methyl-6-phenoxyoxane-3,4,5-triol 11379460 Click to see CC1C(C(C(C(O1)OC2=CC=CC=C2)O)O)O 240.25 unknown via CMAUP database
(4-Methoxybenzyl)thiocarbamic acid 4'-O-(tri-O-acetyl-alpha-L-rhamnopyranoside) 10367398 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)OC(=O)C)OC(=O)C)OC(=O)C 469.50 unknown via CMAUP database
(Z)-N-[(4-hydroxyphenyl)methyl]ethoxycarbothioamide 4'-(tri-acetylrhamnoside) 10323025 Click to see CCOC(=S)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)OC(=O)C)OC(=O)C 483.50 unknown via CMAUP database
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-2-[4-(isothiocyanatomethyl)phenoxy]-6-methyloxan-3-yl] acetate 46933086 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)OC(=O)C)O)O 353.40 unknown via CMAUP database
[(2S,3R,4R,5S,6S)-3,5-dihydroxy-2-[4-(isothiocyanatomethyl)phenoxy]-6-methyloxan-4-yl] acetate 46932936 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)O)OC(=O)C)O 353.40 unknown via CMAUP database
2-[4-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxyphenyl]acetonitrile 11419325 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC#N)O)OC3C(C(C(C(O3)CO)O)O)O)O 441.40 unknown via CMAUP database
3-Hydroxy-4-[(6-deoxy-alpha-L-mannopyranosyl)oxy]benzeneacetonitrile 9926158 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)CC#N)O)O)O)O 295.29 unknown via CMAUP database
4-(4'-O-Acetyl-alpha-L-rhamnosyloxy)benzaldehyde 10018247 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=O)O)O)OC(=O)C 310.30 unknown via CMAUP database
4-(4'-O-Acetyl-alpha-L-rhamnosyloxy)benzyl isothiocyanate 10291650 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)O)O)OC(=O)C 353.40 unknown via CMAUP database
4-(Rhamnosyloxy)phenylacetonitrile 129556 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC#N)O)O)O 279.29 unknown via CMAUP database
4-Hydroxybenzaldehyde rhamnoside 11777785 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C=O)O)O)O 268.26 unknown via CMAUP database
4-Hydroxyphenylacetonitrile triacetylrhamnoside 101919835 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC#N)OC(=O)C)OC(=O)C)OC(=O)C 405.40 unknown via CMAUP database
Ethyl 4-(rhamnosyloxy)benzylcarbamate 101942512 Click to see CCOC(=O)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)O)O)O 341.36 unknown via CMAUP database
Marumoside A 101794623 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC(=O)N)O)O)O 297.30 unknown via CMAUP database
Marumoside B 101794624 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC(=O)N)O)OC3C(C(C(C(O3)CO)O)O)O)O 459.40 unknown via CMAUP database
methyl 2-[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetate 11220666 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC(=O)OC)O)O)O 312.31 unknown via CMAUP database
Moringin 153557 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)O)O)O 311.36 unknown via CMAUP database
N-methoxycarbonyl-4-(alpha-l-rhamnopyranosyloxy) benzylamine 91101122 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)OC)O)O)O 327.33 unknown via CMAUP database
Niazicin A 10068657 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)O)O)OC(=O)C 385.40 unknown via CMAUP database
Niazicinin A 101920262 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)OC)O)O)OC(=O)C 369.40 unknown via CMAUP database
Niazidin 11792427 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC#N)O)O)O 354.40 unknown via CMAUP database
Niazimicin A 10247749 Click to see CCOC(=S)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)O)O)O 357.40 unknown via CMAUP database
Niazimin A 10339912 Click to see CCOC(=O)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)O)O 383.40 unknown via CMAUP database
Niaziminin 10023860 Click to see CCOC(=S)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)O)O 399.50 unknown via CMAUP database
Niazinin 10088810 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)O)O)O 343.40 unknown via CMAUP database
O-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] N-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamothioate 11431835 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 491.50 unknown via CMAUP database
O-Ethyl-4-[(2',3',4'-tri-O-acetyl-alpha-L-rhamnosyloxy)benzyl]carbamate 10434741 Click to see CCOC(=O)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)OC(=O)C)OC(=O)C 467.50 unknown via CMAUP database
O-Methyl-4-[(2',3',4'-tri-O-acetyl-alpha-L-rhamnosyloxy)benzyl]carbamate 101919834 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)OC)OC(=O)C)OC(=O)C)OC(=O)C 453.40 unknown via CMAUP database
Pyrrolemarumine 4''-O-alpha-L-rhamnopyranoside 101794622 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN3C(=CC=C3C=O)CO)O)O)O 377.40 unknown via CMAUP database
S-methyl N-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamothioate 49865742 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)SC)O)O)O 343.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Sesamolin 101746 Click to see C1C2C(COC2OC3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 370.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(3S)-3-[(E)-2-(1,3-dihydroxy-5-methoxy-9-oxoxanthen-2-yl)ethenyl]-8,10-dihydroxy-5-methoxy-3-methyl-2H-[1,4]dioxino[2,3-c]xanthen-7-one 163193743 Click to see CC1(COC2=C3C(=CC(=C2O1)OC)C(=O)C4=C(C=C(C=C4O3)O)O)C=CC5=C(C6=C(C=C5O)OC7=C(C6=O)C=CC=C7OC)O 612.50 unknown https://doi.org/10.3987/COM-96-7557
(3S)-8,10-dihydroxy-5-methoxy-3-methyl-3-[(E)-2-(1,3,5-trihydroxy-9-oxoxanthen-2-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]xanthen-7-one 163189304 Click to see CC1(COC2=C3C(=CC(=C2O1)OC)C(=O)C4=C(C=C(C=C4O3)O)O)C=CC5=C(C6=C(C=C5O)OC7=C(C6=O)C=CC=C7O)O 598.50 unknown https://doi.org/10.3987/COM-96-7557
1-Hydroxy-7-methoxyxanthone 12214329 Click to see COC1=CC2=C(C=C1)OC3=CC=CC(=C3C2=O)O 242.23 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
https://doi.org/10.1016/S0040-4020(01)83306-8
1,5,6-Trihydroxyxanthone 5281652 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3O)O)O 244.20 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
2-Methoxy-9H-xanthen-9-one 71034 Click to see COC1=CC2=C(C=C1)OC3=CC=CC=C3C2=O 226.23 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
3-[2-(1,3-dihydroxy-5-methoxy-9-oxoxanthen-2-yl)ethenyl]-8,10-dihydroxy-5-methoxy-3-methyl-2H-[1,4]dioxino[2,3-c]xanthen-7-one 162945577 Click to see CC1(COC2=C3C(=CC(=C2O1)OC)C(=O)C4=C(C=C(C=C4O3)O)O)C=CC5=C(C6=C(C=C5O)OC7=C(C6=O)C=CC=C7OC)O 612.50 unknown https://doi.org/10.3987/COM-96-7557
5-Hydroxy-1-methoxyxanthone 479656 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O 242.23 unknown https://doi.org/10.3987/COM-96-7557
5,6-Dihydroxy-1,3-dimethoxy-9H-xanthen-9-one 53439039 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
6-hydroxy-1-methoxy-9H-xanthen-9-one 6260040 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C=C(C=C3)O 242.23 unknown https://doi.org/10.3987/COM-96-7557
8-hydroxy-5,10-dimethoxy-3-methyl-3-[(E)-2-(1,3,5-trihydroxy-9-oxoxanthen-2-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]xanthen-7-one 102149342 Click to see CC1(COC2=C3C(=CC(=C2O1)OC)C(=O)C4=C(C=C(C=C4O3)OC)O)C=CC5=C(C6=C(C=C5O)OC7=C(C6=O)C=CC=C7O)O 612.50 unknown https://doi.org/10.1080/10575639308043837
8,10-dihydroxy-5-methoxy-3-methyl-3-[2-(1,3,5-trihydroxy-9-oxoxanthen-2-yl)ethenyl]-2H-[1,4]dioxino[2,3-c]xanthen-7-one 162939928 Click to see CC1(COC2=C3C(=CC(=C2O1)OC)C(=O)C4=C(C=C(C=C4O3)O)O)C=CC5=C(C6=C(C=C5O)OC7=C(C6=O)C=CC=C7O)O 598.50 unknown https://doi.org/10.3987/COM-96-7557
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
https://doi.org/10.3987/COM-96-7557
Mesuaxanthone A 5281651 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(00)83507-4
https://doi.org/10.1016/S0040-4020(01)83306-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
22-Hydroxy-6,6,19,19-tetramethyl-2,5,20-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3(12),4(9),7,10,15,17,21-octaen-13-one 162909351 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=O)C4=C(O3)C(=C5C(=C4)C=CC(O5)(C)C)O)C 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
7,8,12-Trihydroxy-2,2-dimethyl-5-(2-methylbut-3-en-2-yl)pyrano[2,3-b]xanthen-11-one 162868753 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C(C)(C)C=C)C 394.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Blancoxanthone 11703574 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC=C4O)O)C 378.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Pyranojacareubin 15307925 Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C3=O)O)C 392.40 unknown https://doi.org/10.1080/10575639308043837
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-azaniumyl-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroxyquinolones
Hymoquinolone 5487041 Click to see COC1=C(C=CC2=C1NC=CC2=O)O 191.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
5,7-dihydroxy-4-[(1R)-1-hydroxypropyl]-8-[(2R)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)chromen-2-one 162917372 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)O)O)CC=C(C)C)O 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5,7-Dihydroxy-4-[1-(hydroxy)propyl]-6-(3-methyl-2-butenyl)-8-(2-methyl-1-oxobutyl)-2 h-1-benzopyran-2-one 10500479 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C(CC)O)O)CC=C(C)C)O 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.3987/COM-96-7557
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1080/10575639308043837
https://doi.org/10.3987/COM-96-7557
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Mesuein 42607965 Click to see CC1C(C(C(C(O1)OC2=C(C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-D-(6''-O-malonyl)-glucoside 14162699 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O 534.40 unknown via CMAUP database
Quercetin 3-o-beta-D-(6''-o-malonyl)-glucoside 5282159 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O 550.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Geraldone 5281618 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
Hygrocin C 139585109 Click to see CCC1CCC(=O)C2=C(C(=CC3=C2C(=O)C=C4C3(C(C=C(C(=O)OC(C=C1)C(C)O)C)C(=O)N4)O)C)O 509.50 unknown https://doi.org/10.1016/0031-9422(88)80153-5
> Phenylpropanoids and polyketides / Macrolides and analogues
Lasiodiplodin 14562696 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1 292.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
7,8-dihydroxy-4-phenyl-2H-chromen-2-one 5413034 Click to see C1=CC=C(C=C1)C2=CC(=O)OC3=C2C=CC(=C3O)O 254.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-6-(2-methylbutanoyl)-4-phenylchromen-2-one 72812795 Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(8R)-5-hydroxy-8-methyl-6-[(2R)-2-methylbutanoyl]-8-(4-methylpent-3-enyl)-4-phenylpyrano[2,3-h]chromen-2-one 162952483 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)CCC=C(C)C 472.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
(8R)-5-hydroxy-8-methyl-8-(4-methylpent-3-enyl)-6-(2-methylpropanoyl)-4-phenylpyrano[2,3-h]chromen-2-one 163073542 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)CCC=C(C)C 458.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
(8S)-5-hydroxy-6-(3-methylbutanoyl)-4-phenyl-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 11112232 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(=C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
(8S)-5-hydroxy-6-[(2R)-2-methylbutanoyl]-4-phenyl-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 163042058 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(=C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
(8S)-5-hydroxy-8-(1-hydroxy-1-methyl-ethyl)-6-(2-methylpropanoyl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 6483322 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
(8S)-5-hydroxy-8-(1-hydroxy-1-methyl-ethyl)-6-(3-methylbutanoyl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 6483323 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
1,2-Dihydro-5-hydroxy-2-(1-hydroxy-1-methylethyl)-4-(2-methylbutyryl)-6-phenylfurano[2,3-h][1]benzopyran-8-one 21579161 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5-Hydroxy-6'',6''-dimethyl-6-(2-methylbutyryl)-4-phenylpyrano[2'',3'':7,8]coumarin 15223665 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5-Hydroxy-8-methyl-6-(2-methylbutanoyl)-8-(4-methylpent-3-enyl)-4-phenyl-2h-pyrano[2,3-h]chromen-2-one 11167365 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)CCC=C(C)C 472.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5-Hydroxy-8-methyl-8-(4-methylpent-3-enyl)-6-(2-methylpropanoyl)-4-phenylpyrano[2,3-h]chromen-2-one 11178612 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)CCC=C(C)C 458.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5-hydroxy-8,8-dimethyl-6-[(2R)-2-methylbutanoyl]-4-phenylpyrano[2,3-h]chromen-2-one 26176279 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5-Methoxy-8,8-dimethyl-6-(2-methylpropanoyl)-4-phenylpyrano[2,3-h]chromen-2-one 5319382 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1OC)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 404.50 unknown via CMAUP database
5,7-Dihydroxy-6-(3-methylbutanoyl)-8-[(e)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2h-chromen-2-one 21579160 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5,7-dihydroxy-6-[(2R)-2-methylbutanoyl]-8-(3-methylbut-2-enyl)-4-phenylchromen-2-one 162892135 Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
5,7-dihydroxy-8-[(2R)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)-4-phenylchromen-2-one 162906900 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)C)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
6-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-8-(3-methylbutanoyl)-4-phenylchromen-2-one 74033414 Click to see CC(C)CC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)CCC=C(C)C)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-8-(3-methylbutanoyl)-4-phenylchromen-2-one 23250952 Click to see CC(C)CC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)CCC=C(C)C)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
6-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-8-[(2R)-2-methylbutanoyl]-4-phenylchromen-2-one 163190370 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)CCC=C(C)C)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8-(3,7-Dimethylocta-2,6-dienyl)-5,7-dihydroxy-6-(3-methylbutanoyl)-4-phenylchromen-2-one 73803900 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-6-[(2R)-2-methylbutanoyl]-4-phenylchromen-2-one 163032395 Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)CCC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 474.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8,9-Dihydro-5-hydroxy-6-(2-methylbutanoyl)-4-phenyl-8-(prop-1-en-2-yl)furo[2,3-h]chromen-2-one 11223422 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(=C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8,9-Dihydro-5-hydroxy-6-(3-methylbutanoyl)-4-phenyl-8-(prop-1-en-2-yl)furo[2,3-h]chrome n-2-one 11269696 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(=C)C 404.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
8,9-Dihydro-5-hydroxy-8-(1-hydroxy-1-methylethyl)-6-(2-methyl-1-oxopropyl)-4-phenyl-2H-furo[2,3-h]-1-benzopyran-2-one 44257538 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Cyclomammeisin 21592420 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 422.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mammea A/AB 6483317 Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mammea A/BA 5748555 Click to see CC(C)CC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)C)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mammea A/BB 11750116 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC=C(C)C)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mammeigin 5319255 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 404.50 unknown https://doi.org/10.1016/S0031-9422(00)89951-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mammeisin 5281419 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 406.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
Mesuagin 5319380 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
https://doi.org/10.1021/JO01264A009
Mesuol 5277586 Click to see CC(C)C(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 392.40 unknown https://doi.org/10.1016/S0031-9422(00)89951-3
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-[(2R,3S)-7-hydroxy-2,3-dimethyl-8-(3-methylbut-2-enyl)-8-(5-methyl-2-propan-2-ylidenehexyl)-4,5-dioxo-2,3,4a,8a-tetrahydrochromen-6-yl]-3-phenylpropanoic acid 5319381 Click to see CC1C(OC2C(C1=O)C(=O)C(=C(C2(CC=C(C)C)CC(=C(C)C)CCC(C)C)O)C(CC(=O)O)C3=CC=CC=C3)C 564.80 unknown via CMAUP database

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