Common products:
- Sawn timber and veneer from heartwood and sapwood are produced for construction and finishing applications.

Industrial and craft applications:
- Heartwood is used for heavy construction, exterior decking, flooring, marine pilings, and vehicle bodies due to decay and insect resistance attributed to natural extractives. The wood is workable with hand and machine tools and takes a fine polish, supporting cabinetry, turnery, and paneling.

Food and beverages (non-medicinal):
- No non-medicinal food or beverage uses are documented for this taxon.

Colorants and tanning:
- No tannin-based dye or leather tanning applications are documented for this taxon.

Wood and fiber:
- The species provides structural and decorative wood characterized by an interlocked to wavy grain and a uniform brown color. Specific gravity is approximately 0.65–0.85 and air-dry density about 700–950 kg/m³. Heartwood exhibits high natural durability with decay and termite resistance linked to extractives; sapwood is less durable and requires treatment.

Fragrance and cosmetics:
- No fragrance or cosmetic uses are documented for this taxon.

Properties relevant to use:
- The species contains extractives that contribute to resistance to decay fungi and wood-boring insects; these compounds also influence finishing and adhesive performance. Wood density and interlocked grain support structural applications while enabling a high-quality surface finish. Kiln drying is required to stabilize moisture and minimize warping.

Standards and regulation:
- Commercial timbers are graded under national or regional timber grading rules (for example, Brazil’s ABNT NBR standards and applicable export regulations). Structural uses must comply with local building codes and grade specifications.

Sustainability and sourcing:
- Timber is harvested from natural forests and plantations in Central and South America, including Brazil, Paraguay, and northern Argentina. For coastal and high-durability applications, sourcing from well-managed stands with chain-of-custody documentation is recommended to help mitigate habitat pressures.

Synonyms Top

Scientific name	Authority	First published in
Calophyllum brasiliense var. burchellii	Vesque	Monogr. Phan. 8: 592 (1893)
Calophyllum brasiliense var. elongatum	Engl.	Fl. Bras. 12(1): 399 (1888)
Calophyllum brasiliense var. gardneri	Vesque	Monogr. Phan. 8: 592 (1893)
Calophyllum brasiliense subsp. mariae	(Planch. & Triana) Vesque	Monogr. Phan. 8: 593 (1893)
Calophyllum brasiliense var. spruceana	Vesque	Monogr. Phan. 8: 592 (1893)
Calophyllum ellipticum	Rusby	Mem. New York Bot. Gard. 7: 303 (1927)
Calophyllum lucidum	Benth.	London J. Bot. 2: 370 (1843)
Calophyllum mariae	Planch. & Triana	Ann. Sci. Nat., Bot. , sér. 4, 15: 251 (1861)
Calophyllum piaroanum	A.Castillo & C.Gil	Ernstia 1(1): 41 (1991).
Calophyllum revolutum	Rich. ex Vesque	Monogr. Phan. 8: 596 (1893)
Calophyllum brasilinse subsp. wrightii	Vesque	Monogr. Phan. [A.DC. & C.DC.] 8: 594. 1893 [Dec 1893]
Calophyllum brasiliense subsp. verum	Vesque	Monogr. Phan. 8: 591 (1893)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	bonita hoja brasilena
Spanish	bonita hoja brasileña
Spanish	guanandi
Spanish	jacareuba
Spanish	jacareúba
Spanish	lantim
Spanish	olandi
Spanish	olandim
Spanish	lanti
Spanish	calophyllum lucidum
Azerbaijani	braziliya kalofillumu
Danish	santa maria
French	calophylle du brésil
French	calophyllum lucidum
Japanese	サンタマリア
Portuguese	arbol de santa maria
Portuguese	guanandi
Portuguese	jacareúba
Portuguese	jacareuba
Chinese	巴西红厚壳

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
Calophyllum brasiliense var. antillanum	(Britton) Standl.	Trop. Woods 30: 7 (1932)
Calophyllum brasiliense var. rekoi	(Standl.) Standl.	Trop. Woods 30: 7 (1932)
Calophyllum brasiliense var. brasiliense		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

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Bahamas
  - Bermuda
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Paraguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000581058
Tropicos	7800054
INPN	732993
KEW	urn:lsid:ipni.org:names:427115-1
The Plant List	kew-2693230
PFAF	Calophyllum brasiliense
Open Tree Of Life	576888
NCBI Taxonomy	280748
IUCN Red List	61988785
IPNI	427115-1
iNaturalist	83124
GBIF	5421069
Freebase	/m/025x__y
EPPO	CMUBR
EOL	488468
USDA GRIN	311269
Wikipedia	Calophyllum_brasiliense

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

Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family

Abdoul-Latif FM, Oumaskour K, Abdallah N, Ainane A, Houmed Aboubaker I, Merito A, Mohamed H, Ainane T

Pharmaceuticals (Basel)

18-Apr-2024

PMCID:	PMC11054980
doi:	10.3390/ph17040523
PMID:	38675483

Identification of Novel Flavonoids and Ansa-Macrolides with Activities against Leishmania donovani through Natural Product Library Screening

Phan TN, Lee H, Baek KH, No JH

Pathogens

28-Feb-2024

PMCID:	PMC10974828
doi:	10.3390/pathogens13030213
PMID:	38535556

Amazonian useful plants described in the book “Le Pays des Amazones” (1885) of the Brazilian propagandist Baron de Santa-Anna Nery: a historical and ethnobotanical perspective

Silva LN, Oliveira EC, Baratto LC

J Ethnobiol Ethnomed

26-Feb-2024

PMCID:	PMC10897987
doi:	10.1186/s13002-024-00663-2
PMID:	38409064

Yams (Dioscorea spp.) in shellmounds and swiddens: ancient history in Babitonga Bay, Santa Catarina State, southern Brazil

da Silva Souza DA, da Bandeira DR, Peroni N

J Ethnobiol Ethnomed

02-Feb-2024

PMCID:	PMC10836009
doi:	10.1186/s13002-024-00653-4
PMID:	38308263

Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact

Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH

Molecules

24-Nov-2023

PMCID:	PMC10707989
doi:	10.3390/molecules28237760
PMID:	38067489

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

Effects of Heavy Metals on Stomata in Plants: A Review

Guo Z, Gao Y, Yuan X, Yuan M, Huang L, Wang S, Liu C, Duan C

Int J Mol Sci

26-May-2023

PMCID:	PMC10252879
doi:	10.3390/ijms24119302
PMID:	37298252

Phenolic Compounds in Bacterial Inactivation: A Perspective from Brazil

Kauffmann AC, Castro VS

Antibiotics (Basel)

24-Mar-2023

PMCID:	PMC10135396
doi:	10.3390/antibiotics12040645
PMID:	37107007

Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action

Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV

Int J Mol Sci

02-Feb-2023

PMCID:	PMC9917851
doi:	10.3390/ijms24032839
PMID:	36769163

Artificial intelligence in microbial natural product drug discovery: current and emerging role

Sahayasheela VJ, Lankadasari MB, Dan VM, Dastager SG, Pandian GN, Sugiyama H

Nat Prod Rep

14-Dec-2022

PMCID:	PMC9931531
doi:	10.1039/d2np00035k
PMID:	36017693

Appearance of a population of the mangrove rail Rallus longirostris (Rallidae) in salt marshes invaded by the exotic tanner grass Urochloa arrecta (Poaceae) and its disappearance after plant management

Bornschein MR, Teixeira L, de Morais Guerra B, Melchiori BL, Reinert BL, Sandretti-Silva G

Wetlands (Wilmington)

08-Dec-2022

PMCID:	PMC9735195
doi:	10.1007/s13157-022-01642-7
PMID:	36530518

Plant Growth-Promoting Bacteria (PGPB) integrated phytotechnology: A sustainable approach for remediation of marginal lands

Poria V, Dębiec-Andrzejewska K, Fiodor A, Lyzohub M, Ajijah N, Singh S, Pranaw K

Front Plant Sci

21-Oct-2022

PMCID:	PMC9634634
doi:	10.3389/fpls.2022.999866
PMID:	36340355

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Jacareubin inhibits TLR4-induced lung inflammatory response caused by the RBD domain of SARS-CoV-2 Spike protein

Segura-Villalobos D, Roa-Velázquez D, Zavala-Vargas DI, Filisola-Villaseñor JG, Castillo Arellano JI, Morales Ríos E, Reyes-Chilpa R, González-Espinosa C

Pharmacol Rep

05-Aug-2022

PMCID:	PMC9362068
doi:	10.1007/s43440-022-00398-5
PMID:	35930194

Exploring the Immunotherapeutic Potential of Oleocanthal against Murine Cutaneous Leishmaniasis

Karampetsou K, Koutsoni OS, Badounas F, Angelis A, Gogou G, Skaltsounis LA, Halabalaki M, Dotsika E

Planta Med

08-Jul-2022

PMCID:	PMC9343937
doi:	10.1055/a-1843-9788
PMID:	35803258

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Tropane alkaloids
3alpha,6beta-Dihydroxytropane	13855897	Click to see	157.21	unknown	https://doi.org/10.1021/NP030438N
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
> Lignans, neolignans and related compounds / Lignan lactones
(3aR,9S,9aS)-3a,7-dihydroxy-9-(4-hydroxy-3-methoxyphenyl)-6-methoxy-1,4,9,9a-tetrahydrobenzo[f][2]benzofuran-3-one	163036100	Click to see	372.40	unknown	https://doi.org/10.1080/14786410701582282
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (2R,3S,4S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-3-(2-oxoethyl)-2-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	154496903	Click to see COC(=O)C1=COC(C(C1CC(=O)OCCC2=CC(=C(C=C2)O)O)CC=O)OC3C(C(C(C(O3)CO)O)O)O	556.50	unknown	https://doi.org/10.1021/NP030438N
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
6-[[8a-[3-[5-[3,4-Dihydroxy-6-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	162847943	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(COC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)CO)O)O)OC1C(C(C(CO1)O)O)O	1205.30	unknown	https://doi.org/10.1021/NP030438N
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2,12-Diacetyloxy-8-chloro-3-hydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadec-10-en-14-yl) acetate	162946113	Click to see CC1CCC(C2(C1C(C3(C(C(=O)OC3C(C(=C)C=CC2OC(=O)C)Cl)C)O)OC(=O)C)C)OC(=O)C	527.00	unknown	https://doi.org/10.1021/NP030438N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Canophyllic acid	596679	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C)O	458.70	unknown	https://doi.org/10.1016/S0031-9422(00)80326-X
Canophyllol	7330581	Click to see	442.70	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1016/J.LFS.2004.03.017
D:A-Friedooleanan-3-one, 28-hydroxy-	623591	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C	442.70	unknown	https://doi.org/10.1016/J.LFS.2004.03.017 https://doi.org/10.1248/BPB.27.1471
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1016/J.LFS.2004.03.017
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1016/J.LFS.2004.03.017 https://doi.org/10.1248/BPB.27.1471
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,11S)-6-(acetyloxymethyl)-11-methoxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-methylbut-2-enoate	138114059	Click to see	434.50	unknown	https://doi.org/10.1021/NP030438N
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Xentrivalpeptide N	139583857	Click to see CCC(C)C1C(=O)NC(C(=O)OC(C(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N1)C(C)C)CC3=CC=CC=C3)NC(=O)C(C(C)C)NC(=O)CC4=CC=CC=C4)C)C(C)C	874.10	unknown	https://doi.org/10.1021/NP030438N
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see	174.15	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
> Organoheterocyclic compounds / Benzopyrans
methyl 3-[(2R,3R)-5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	162820192	Click to see CCCC(CC(=O)OC)C1=C2C(=C(C(C1=O)(CC=C(C)C)CC(CC=C(C)C)C(=C)C)OC)C(=O)C(C(O2)C)C	554.80	unknown	https://doi.org/10.1080/14786410701582282
methyl 3-[(2R,3R)-5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-6-(5-methyl-2-prop-1-en-2-ylhex-5-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	163029978	Click to see CCCC(CC(=O)OC)C1=C2C(=C(C(C1=O)(CC=C(C)C)CC(CCC(=C)C)C(=C)C)OC)C(=O)C(C(O2)C)C	554.80	unknown	https://doi.org/10.1080/14786410701582282
methyl 3-[(2R,3R)-6-[(2,2-dimethyl-3-prop-1-en-2-ylcyclobutyl)methyl]-5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	162820211	Click to see	554.80	unknown	https://doi.org/10.1080/14786410701582282
methyl 3-[(2R,3R)-6-[(2,2-dimethyl-3-prop-1-en-2-ylcyclobutyl)methyl]-5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]nonanoate	162820179	Click to see	596.80	unknown	https://doi.org/10.1080/14786410701582282
Methyl 3-[5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	162820191	Click to see	554.80	unknown	https://doi.org/10.1080/14786410701582282
Methyl 3-[5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-6-(5-methyl-2-prop-1-en-2-ylhex-5-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	163029977	Click to see	554.80	unknown	https://doi.org/10.1080/14786410701582282
Methyl 3-[6-[(2,2-dimethyl-3-prop-1-en-2-ylcyclobutyl)methyl]-5-methoxy-2,3-dimethyl-6-(3-methylbut-2-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoate	162820209	Click to see	554.80	unknown	https://doi.org/10.1080/14786410701582282
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3R)-3-[(2S,3S)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]hexanoic acid	162932866	Click to see CCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C	388.50	unknown	https://doi.org/10.1248/BPB.27.1471
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid	23250748	Click to see	388.50	unknown	https://doi.org/10.1248/BPB.27.1471
(3R)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid	21577056	Click to see	388.50	unknown	https://doi.org/10.1248/BPB.27.1471
[Z,(-)]-3-(3,4-Dihydro-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,8H-benzo[1,2-b	54322117	Click to see	420.50	unknown	https://doi.org/10.1211/JPP.58.7.0013
3,4-Dihydro-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-beta-propyl-2H,8H-benzo[1,2-b	73081623	Click to see CCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C	388.50	unknown	https://doi.org/10.1248/BPB.27.1471
Isoapetalic acid	341189	Click to see	388.50	unknown	https://doi.org/10.1248/BPB.27.1471
Isocalophyllic acid	6473848	Click to see CC1C(OC2=C3C=CC(OC3=C(C(=C2C1=O)O)C(=CC(=O)O)C4=CC=CC=C4)(C)C)C	420.50	unknown	https://doi.org/10.1211/JPP.58.7.0013
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
2,2-dimethyl-6H-pyrano[3,2-b]xanthene-5,9,10-triol	14804159	Click to see	312.30	unknown	https://doi.org/10.1021/NP0203640
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3,8-Dihydroxy-1,2-dimethoxy-9H-xanthen-9-one	14630572	Click to see	288.25	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
4-Hydroxyxanthone	611428	Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O	212.20	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
Dimethoxyxanthone	14189053	Click to see COC1=C(C2=C(C=C1)OC3=CC=CC=C3C2=O)OC	256.25	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,6-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	21635678	Click to see	426.50	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
1,3,6-trihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	163039590	Click to see	426.50	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
1,3,6-Trihydroxy-5-methoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one	10024541	Click to see	410.50	unknown	https://doi.org/10.1021/NP010398S
1,3,8-Trihydroxy-5-methoxy-2,7-bis(3-methylbut-2-enyl)xanthen-9-one	163021413	Click to see CC(=CCC1=CC(=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)OC)C	410.50	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
2-(3-Hydroxy-3-methylbutyl)-1,3,5,6-tetrahydroxyxanthone	14804158	Click to see	346.30	unknown	https://doi.org/10.1248/BPB.27.141
5,9-Dihydroxy-10-methoxy-2,2-dimethyl-8-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	10364091	Click to see	408.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
9H-Xanthen-9-one, 1,3,5,6-tetrahydroxy-2-(3-methyl-2-butenyl)-	10404212	Click to see	328.30	unknown	https://doi.org/10.1248/BPB.27.141
Garcinone B	5495928	Click to see	394.40	unknown	https://doi.org/10.1021/NP0203640 https://doi.org/10.1021/NP010398S
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
12-[(2S)-2-hydroperoxy-3-methylbut-3-enyl]-5,8-dihydroxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	163190299	Click to see CC(=C)C(CC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)OO	410.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
5,9-Dihydroxy-8-methoxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	11015047	Click to see	408.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
Brasixanthone B	10362269	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)C	378.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
Brasixanthone C	10001590	Click to see	410.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
Latisxanthone C	10790224	Click to see	462.50	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
Trapezifolixanthone	188341	Click to see	378.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
12-[(3,3-Dimethyloxiran-2-yl)-hydroxymethyl]-5,8-dihydroxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	10341493	Click to see	410.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
12-[(R)-[(2S)-3,3-dimethyloxiran-2-yl]-hydroxymethyl]-5,8-dihydroxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	163048919	Click to see	410.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
5,9-Dihydroxy-8-methoxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	11035196	Click to see	340.30	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
6-Deoxyjacareubin	5281629	Click to see	310.30	unknown	https://doi.org/10.1078/S0944-7113(04)70070-7 https://doi.org/10.1021/NP010398S https://doi.org/10.1248/BPB.27.141
brasixanthone D	70678720	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)CC(C4C(O4)(C)C)O)OC5=C(C3=O)C=C(C=C5)O)O)C	424.40	unknown	https://doi.org/10.1021/NP010398S
Jacareubin	5281644	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C	326.30	unknown	https://doi.org/10.1078/S0944-7113(04)70070-7 https://doi.org/10.1248/BPB.27.141
Pyranojacareubin	15307925	Click to see	392.40	unknown	https://doi.org/10.1021/NP010398S https://doi.org/10.1021/NP0203640
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Stachybotrin C	10368882	Click to see	505.60	unknown	https://doi.org/10.1021/NP0203640 https://doi.org/10.1021/NP010398S
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbutanoyl)-9-propyl-2,3-dihydrofuro[2,3-f]chromen-7-one	163045574	Click to see CCCC1=CC(=O)OC2=C(C(=C3CC(OC3=C12)C(C)(C)O)O)C(=O)CC(C)C	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-[(2R)-2-methylbutanoyl]-9-propyl-2,3-dihydrofuro[2,3-f]chromen-7-one	162984734	Click to see	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
Cyclomammein	101967071	Click to see CCCC1=CC(=O)OC2=C(C(=C3CC(OC3=C12)C(C)(C)O)O)C(=O)CC(C)C	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
Cycloneomammein	90472430	Click to see	388.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
(S)-Neomammein	10339247	Click to see	372.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017 https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
5,7-Dihydroxy-8-(2-methylbutanoyl)-4-pentylchromen-2-one	129682011	Click to see	332.40	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
5,7-Dihydroxy-8-(3-methylbutanoyl)-4-pentylchromen-2-one	163020961	Click to see	332.40	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
5,7-dihydroxy-8-[(2R)-2-methylbutanoyl]-4-pentylchromen-2-one	162958238	Click to see	332.40	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
5,7-dihydroxy-8-[(2R)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)-4-propylchromen-2-one	163042714	Click to see	372.50	unknown	https://doi.org/10.1021/NP0203640
Mammea B/BA	5489487	Click to see	372.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
Mammea B/BB, (-)-	53320112	Click to see CCCC1=CC(=O)OC2=C1C(=C(C(=C2C(=O)C(C)CC)O)CC=C(C)C)O	372.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017 https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(+)-Calanolide A	64972	Click to see	370.40	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
(10R,11R,12S)-12-Benzoyl-6,6,10,11-tetramethyl-4-propyl-12-hydro-6H,10H-dipyrano[2,3-f	511360	Click to see	370.40	unknown	https://doi.org/10.1021/NP0203640
5-Methoxy-2,2-dimethyl-6-(2-methylbut-2-enoyl)-10-propylpyrano[2,3-f]chromen-8-one	155894564	Click to see	382.40	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
5-methoxy-2,2-dimethyl-6-[(E)-2-methylbut-2-enoyl]-10-propyl-pyrano[2,3-f]chromen-8-one	11100998	Click to see CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C(=C2C(=O)C(=CC)C)OC	382.40	unknown	https://doi.org/10.1021/NP0203640 https://doi.org/10.1211/JPP.58.7.0013
Brasimarin A	5323581	Click to see	390.40	unknown	https://doi.org/10.1021/NP0203640
Calanolide	1201	Click to see	370.40	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1021/NP0203640 https://doi.org/10.1211/JPP.58.7.0013
Calanolide C	454257	Click to see	370.40	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1021/NP0203640
Costatolide	461128	Click to see CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O	370.40	unknown	https://doi.org/10.1248/BPB.27.1471
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017 https://doi.org/10.1080/13880200802055818 https://doi.org/10.1248/BPB.27.1471
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one	162892327	Click to see CC(C)(C(CC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)O	358.40	unknown	https://doi.org/10.1021/NP030438N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	73032313	Click to see	612.50	unknown	https://doi.org/10.1021/NP030438N
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
[4,5-Diacetyloxy-6-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxyoxan-3-yl] acetate	74978532	Click to see	560.50	unknown	https://doi.org/10.1021/NP030438N
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(-)-Inophyllum P	72978	Click to see	404.50	unknown	https://doi.org/10.1248/BPB.27.1471
(16R,17S)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaene-4,18-dione	455251	Click to see	402.40	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
(16S,17S)-10,10,16,17-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1(14),2(7),5,8(13),11-pentaene-4,18-dione	5352084	Click to see	402.40	unknown	https://doi.org/10.1021/NP0203640
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-[(2R)-2-methylbutanoyl]-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one	163041954	Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)CC(O3)C(C)(C)O)C(=CC(=O)O2)C4=CC=CC=C4	422.50	unknown	https://doi.org/10.1021/NP0203640
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-[(2S)-2-methylbutanoyl]-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one	163041953	Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)CC(O3)C(C)(C)O)C(=CC(=O)O2)C4=CC=CC=C4	422.50	unknown	https://doi.org/10.1021/NP0203640
(8R,9S)-5-hydroxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione	11811548	Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C(=C2CC=C(C)C)O)C	404.50	unknown	https://doi.org/10.1021/NP0203640
(8S,9R)-5-hydroxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione	162936716	Click to see	404.50	unknown	https://doi.org/10.1021/NP0203640
5-Hydroxy-8,9-dimethyl-6-(3-methylbut-2-enyl)-4-phenyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione	73112696	Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C(=C2CC=C(C)C)O)C	404.50	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
5-Methoxy-2,2-dimethyl-6-(2-methylbut-2-enoyl)-10-phenylpyrano[2,3-f]chromen-8-one	196983	Click to see	416.50	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
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.LFS.2004.03.017
Brasimarin B	11015352	Click to see	422.50	unknown	https://doi.org/10.1021/NP0203640
Brasimarin C	10341168	Click to see CC1C(OC2=C(C1=O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C(=C2CC=C(C)C)O)C	404.50	unknown	https://doi.org/10.1021/NP0203640 https://doi.org/10.1211/JPP.58.7.0013
Calanone	5352087	Click to see	424.40	unknown	https://doi.org/10.1021/NP0203640
Calophyllolide	5281392	Click to see	416.50	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
cis-and-trans-Inophyllolide	5254	Click to see	402.40	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
Inophyllolide chromanol	15223670	Click to see CC1C(OC2=C(C1O)C3=C(C(=CC(=O)O3)C4=CC=CC=C4)C5=C2C=CC(O5)(C)C)C	404.50	unknown	https://doi.org/10.1248/BPB.27.1471 https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
Inophyllum A	455248	Click to see	404.50	unknown	https://doi.org/10.1021/NP0203640 https://doi.org/10.1211/JPP.58.7.0013
Inophyllum C	455252	Click to see	402.40	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
Inophyllum D	455250	Click to see	404.50	unknown	https://doi.org/10.1211/JPP.58.7.0013 https://doi.org/10.1021/NP0203640
Isomammeigin	52946774	Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C=CC(O3)(C)C)C(=CC(=O)O2)C4=CC=CC=C4	404.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
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.LFS.2004.03.017
Mammea A/BB	11750116	Click to see	406.50	unknown	https://doi.org/10.1016/J.LFS.2004.03.017
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Brasiliensophyllic acid A	10257238	Click to see	560.70	unknown	https://doi.org/10.1021/NP030438N
Brasiliensophyllic acid B	44566684	Click to see	560.70	unknown	https://doi.org/10.1021/NP030438N
Brasiliensophyllic acid C	44566694	Click to see	478.60	unknown	https://doi.org/10.1021/NP030438N
Isobrasiliensophyllic acid A	10030713	Click to see	560.70	unknown	https://doi.org/10.1021/NP030438N
Isobrasiliensophyllic acid B	44566693	Click to see	560.70	unknown	https://doi.org/10.1021/NP030438N
Isobrasiliensophyllic acid C	44566695	Click to see	478.60	unknown	https://doi.org/10.1021/NP030438N

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Calophyllum brasiliense

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