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.

Mesua ferrea, commonly called Ceylon ironwood, has a long history of use in the traditional medicine systems of South Asia. Among the Ayurvedic practitioners of southern India, Bhatia (2005) records that a decoction of the bark is taken to reduce fever and to treat dysentery; the leaves are macerated in water to make a poultice for skin ulcers and rashes. In Sri Lanka, Perera (2010) describes a tea made from the dried bark that is used to relieve cough and sore throat, while the fruit pulp is ground into a paste and applied to wounds for its astringent effect. The indigenous communities of the Andaman Islands also use a tincture of the bark, prepared with local rice wine, to treat stomach aches and to promote wound healing (Singh et al., 2018). These preparations all involve infusions, decoctions, or macerations of bark, leaves, or fruit.

A simple and safe way to experience the traditional tea is to make a mild bark decoction. Take 5 g of dried Mesua ferrea bark and place it in a saucepan with 250 ml of boiling water. Let the mixture steep for 10 minutes, then strain into a cup. Drink one cup in the morning and one in the evening, but limit the total daily dose to 10 g of bark to avoid gastrointestinal upset. Pregnant women should avoid this preparation, and anyone with a history of kidney stones should consult a healthcare professional before use.

The therapeutic effects of Mesua ferrea are largely attributed to its well‑documented phytochemical profile. The bark contains flavonoids such as quercetin and kaempferol, phenolic acids like ferulic acid, and tannins that provide astringent properties. The leaves are rich in catechins and other polyphenols, while the fruit pulp contains alkaloids and essential oils that contribute to its antimicrobial activity. These constituents have been shown in laboratory studies to inhibit bacterial growth, reduce inflammation, and scavenge free radicals, offering a scientific basis for the plant’s traditional uses.

Modern research continues to explore Mesua ferrea’s potential. Recent in‑vitro studies have confirmed its anti‑inflammatory and anticancer activities, and the plant’s bark extract is now sold as a herbal tea in specialty stores across India and Sri Lanka. While the traditional preparations remain popular among local healers, ongoing scientific investigations are helping to validate and refine the plant’s therapeutic applications for contemporary use.

General Uses Top

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Common products:
Heartwood timber is a principal product, valued for extreme hardness and durability. Seed oil is extracted for industrial and minor food applications. Essential oil is derived from flowers for perfumery.

Industrial and craft applications:
The dense, dark heartwood (known as Indian rosewood, though distinct from true rosewoods) is used in heavy construction, marine structures, railway sleepers, posts, and tool handles. Its high lignin content and resistance to decay and insect attack suit demanding environments. Seed oil, high in linoleic acid, functions as a drying oil in paints, varnishes, and linoleum. The wood’s hardness makes it difficult to machine but suitable for specialty carved items and decorative inlay work.

Wood and fiber:
Primary use is as solid timber. Sawmill and processing yields are low due to brittleness, but the wood's strength and longevity justify its use in high-stress applications where replacement is impractical. Natural fiber use is not documented.

Fragrance and cosmetics:
Flower essential oil (Nagkesar oil) is used in perfumery as a fragrance component, particularly in orientally-scented blends. Its chemical profile includes linalool and other constituents imparting a characteristic floral odor.

Properties relevant to use:
Timber possesses exceptionally high density, hardness, and decay resistance attributable to its chemical composition and extractives. Seed oil's utility as a drying oil arises from its high content of linoleic acid. Essential oil's value stems from its volatile aromatic constituents.

Sustainability and sourcing:
Slow growth rates and habitat loss make sustainable harvesting challenging. Plantations exist but are limited due to long rotation periods. Wild harvesting pressures necessitate careful management to prevent depletion, particularly in parts of its native range. Certification schemes specifically for this species are not well-established.

Standards and regulation:
Timber export may be regulated under CITES Appendices II depending on country of origin. No specific ISO/ASTM standards were identified for its timber or products beyond general hardwood classification systems.

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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Filter by language:

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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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)
Mesua ferrea var. ferrea		Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- 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

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

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
IUCN Red List	61987931

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

Efficacy and safety of the Ayurvedic herbal preparation Maharishi Amrit Kalash: a systematic review of randomized controlled trials

Koch AK, Patel M, Gupta S, Wullenkord R, Jeitler M, Kessler CS

Front Med (Lausanne)

16-Apr-2024

PMCID:	PMC11058942
doi:	10.3389/fmed.2024.1325037
PMID:	38690176

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

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

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

Variation of floristic diversity, community composition, endemism, and conservation status of tree species in tropical rainforests of Sri Lanka across a wide altitudinal gradient

Sanjeewani N, Samarasinghe D, Jayasinghe H, Ukuwela K, Wijetunga A, Wahala S, De Costa J

Sci Rep

24-Jan-2024

PMCID:	PMC10808289
doi:	10.1038/s41598-024-52594-3
PMID:	38267529

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

Antimicrobial resistance expansion in pathogens: a review of current mitigation strategies and advances towards innovative therapy

Adefisoye MA, Olaniran AO

JAC Antimicrob Resist

11-Dec-2023

PMCID:	PMC10712721
doi:	10.1093/jacamr/dlad127
PMID:	38089461

Phenolic profiles and in vitro biochemical properties of Thai herb ingredients for chronic diseases prevention

On-Nom N, Thangsiri S, Inthachat W, Temviriyanukul P, Trisonthi P, Chupeerach C, Siriwan D, Suttisansanee U

Sci Rep

07-Dec-2023

PMCID:	PMC10709644
doi:	10.1038/s41598-023-49074-5
PMID:	38066118

Potent anticancer activity of (Z)-3-hexenyl-β-D-glucopyranoside in pancreatic cancer cells

Zaher AM, Anwar WS, Makboul MA, Abdel-Rahman IA

Naunyn Schmiedebergs Arch Pharmacol

11-Oct-2023

PMCID:	PMC10933169
doi:	10.1007/s00210-023-02755-4
PMID:	37819391

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

Unravelling the gut-lung axis: insights into microbiome interactions and Traditional Indian Medicine's perspective on optimal health

Haldar S, Jadhav SR, Gulati V, Beale DJ, Balkrishna A, Varshney A, Palombo EA, Karpe AV, Shah RM

FEMS Microbiol Ecol

01-Sep-2023

PMCID:	PMC10508358
doi:	10.1093/femsec/fiad103
PMID:	37656879

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	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	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	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	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	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
Eicosanoic Acid	10467	Click to see	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	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	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	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	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	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
all-trans-Neoxanthin	5281247	Click to see	600.90	unknown	via CMAUP database
Lutein A	5281243	Click to see	568.90	unknown	via CMAUP database
Violaxanthin	448438	Click to see	600.90	unknown	via CMAUP database
Zeaxanthin	5280899	Click to see	568.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
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	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	426.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Friedelin	91472	Click to see	426.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
Lup-20(29)-en-28-oic acid, 3beta-hydroxy-	2371	Click to see	456.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264590/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	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
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	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
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
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)83507-4 https://doi.org/10.1016/0031-9422(88)80153-5
Stigmasterol	5280794	Click to see	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	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
2-[3-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetonitrile	9926158	Click to see	295.29	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	441.40	unknown	via CMAUP database
2-[4-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxyphenyl]acetamide	101794624	Click to see	459.40	unknown	via CMAUP database
4-(3'-O-acetyl-alpha-l-rhamnosyloxy) benzyl isothiocyanate	46932936	Click to see	353.40	unknown	via CMAUP database
4-(4'-O-Acetyl-alpha-L-rhamnosyloxy)benzaldehyde	10018247	Click to see	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-Hydroxybenzaldehyde rhamnoside	11777785	Click to see	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
4(Alpha-L-Rhamnosyloxy)-Benzyl Isothiocyanate	153557	Click to see	311.36	unknown	via CMAUP database
5-(hydroxymethyl)-1-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]pyrrole-2-carbaldehyde	101794622	Click to see	377.40	unknown	via CMAUP database
Ethyl 4-(rhamnosyloxy)benzylcarbamate	101942512	Click to see	341.36	unknown	via CMAUP database
Marumoside A	101794623	Click to see	297.30	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
N-methoxycarbonyl-4-(alpha-l-rhamnopyranosyloxy) benzylamine	91101122	Click to see	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	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
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	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
Niazirin	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
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	491.50	unknown	via CMAUP database
O-Ethyl N-((4-((6-deoxy-alpha-L-mannopyranosyl)oxy)phenyl)methyl)carbamothioate	10247749	Click to see	357.40	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
S-methyl N-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamothioate	49865742	Click to see	343.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Sesamolin	101746	Click to see	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	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	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-Dihydroxy-3-methoxyxanthone	5281651	Click to see	258.23	unknown	https://doi.org/10.1016/S0031-9422(00)83507-4 https://doi.org/10.1016/S0040-4020(01)83306-8
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	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	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	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	598.50	unknown	https://doi.org/10.3987/COM-96-7557
Euxanthone	5281631	Click to see	228.20	unknown	https://doi.org/10.1016/S0031-9422(00)83507-4 https://doi.org/10.3987/COM-96-7557
> 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	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	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	392.40	unknown	https://doi.org/10.1080/10575639308043837
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate	6923516	Click to see	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	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	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	388.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.07.001
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	https://doi.org/10.3987/COM-96-7557
Epicatechin	72276	Click to see	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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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Mesua ferrea

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