Baphia nitida, also known as camwood, is a shrubby tree found in central west Africa. It is often planted in villages and referred to as osun in the Yoruba language. The wood of this tree is highly valued for its fine color and is used in woodturning for making various items. The bark and heartwood of the tree are also used to make a red dye, which is soluble in alkali. This dye is not permanent but is known for its brilliant color. B. nitida contains pterocarpin, a pterocarpan compound. The extract of camwood is also used in some soaps and skin treatments, particularly among the Yoruba people. It is believed to have beneficial effects on the skin and can be formed into a soft soap-like material.

Synonyms Top

Scientific name	Authority	First published in
Baphia pyrifolia	(Desv.) Baill.	Bull. Mens. Soc. Linn. Paris1: 445 (1883)
Delaria pyrifolia	Desv.	Ann. Sci. Nat. (Paris)9: 406 (1826)
Podalyria haematoxylon	Thonn.	C.F.Schumacher, Beskr. Guin. Pl.: 202 (1827)
Carpolobia versicolor	G.Don	Gen. Hist. 1: 370. 1831 [early Aug 1831]
Baphia haematoxylon	Hochst. ex Hook.	Niger Fl.: 321 (1849)
Baphia barombiensis	Taub.	Bot. Jahrb. Syst.23: 177 (1897)
Baphia nitida var. pubescens	A.Chev.	Explor. Bot. Afrique Occ. Franç.1: 217 (1920)
Dalhousiea haematoxylon	Benth.	Ann. Wiener Mus. Naturgesch.2: 69 (1838)
Dalhousiea pyrifolia	(Desv.) Benth.	Ann. Wiener Mus. Naturgesch.2: 69 (1838)
Carpolobia versicolor	G.Don	Gen. Hist. 1: 370 (1831)

Common names Top

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Filter by language:

Language	Common/alternative name
English	camwood
English	category:baphia nitida
Bulgarian	анголско дърво
French	bois rouge
Armenian	Ներկածառ
Norwegian Bokmål	angolatre
Russian	Ангольское дерево
Chinese	剑木豆
Chinese	鸡血檀
Chinese	光亮杂色豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- West Tropical Africa
  - Benin
  - Ghana
  - Guinea
  - Ivory Coast
  - Liberia
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Cameroon
  - Congo
  - Equatorial Guinea
  - Gabon
  - Gulf Of Guinea Islands

Asia-tropical click to expand
- Indian Subcontinent
  - Sri Lanka
- Malesia
  - Malaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000212016
UNII	I473Y9U489
USDA Plants	BANI3
Tropicos	13048033
KEW	urn:lsid:ipni.org:names:480895-1
The Plant List	ild-7095
PFAF	Baphia nitida
Open Tree Of Life	351634
NCBI Taxonomy	162666
IUCN Red List	19891986
IPNI	480895-1
iNaturalist	139566
GBIF	5352599
Freebase	/m/05c7s2
EPPO	BAHNI
EOL	702823
USDA GRIN	310986
Wikipedia	Baphia_nitida
CMAUP	NPO21005

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

Impact of the Naturally Driven Surfactant in EOR Application: Experimental, Microscopic, and Numerical Analyses

Zhuniskenov Y, Sabirova A, Serikov G, Abbas AH, Pourafshary P

ACS Omega

27-Dec-2023

PMCID:	PMC10785280
doi:	10.1021/acsomega.3c07519
PMID:	38222572

Molecular Identification and Characterization of Five Ganoderma Species from the Lower Volta River Basin of Ghana Based on Nuclear Ribosomal DNA (nrDNA) Sequences

Adotey G, Alolga RN, Quarcoo A, Yerenkyi P, Otu P, Anang AK, Okine LK, Gbewonyo WS, Holliday JC, Lombardi VC

J Fungi (Basel)

21-Dec-2023

PMCID:	PMC10817336
doi:	10.3390/jof10010006
PMID:	38276022

Medicinal plants used for management of diabetes and hypertension in Ghana

Asafo-Agyei T, Appau Y, Barimah KB, Asase A

Heliyon

29-Nov-2023

PMCID:	PMC10703729
doi:	10.1016/j.heliyon.2023.e22977
PMID:	38076168

Nutritional and pharmacological potentials of orphan legumes: Subfamily faboideae

Ogbole OO, Akin-Ajani OD, Ajala TO, Ogunniyi QA, Fettke J, Odeku OA

Heliyon

15-Apr-2023

PMCID:	PMC10161725
doi:	10.1016/j.heliyon.2023.e15493
PMID:	37151618

Inhibition of Aflatoxin B1 Synthesis in Aspergillus flavus by Mate (Ilex paraguariensis), Rosemary (Rosmarinus officinalis) and Green Tea (Camellia sinensis) Extracts: Relation with Extract Antioxidant Capacity and Fungal Oxidative Stress Response Modulation

Al Khoury A, El Khoury A, Rocher O, Hindieh P, Puel O, Maroun RG, Atoui A, Bailly JD

Molecules

05-Dec-2022

PMCID:	PMC9739609
doi:	10.3390/molecules27238550
PMID:	36500642

Selective and clear-cut logging have varied imprints on tree community structure in a moist semi-deciduous forest in Ghana

Addo-Fordjour P, Afram IS, Oppong J

Heliyon

04-Nov-2022

PMCID:	PMC9649955
doi:	10.1016/j.heliyon.2022.e11393
PMID:	36387494

Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021

Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T

Molecules

04-Nov-2022

PMCID:	PMC9656935
doi:	10.3390/molecules27217579
PMID:	36364404

Fiber-like Action of d-Fagomine on the Gut Microbiota and Body Weight of Healthy Rats

Ramos-Romero S, Ponomarenko J, Amézqueta S, Hereu M, Miralles-Pérez B, Romeu M, Méndez L, Medina I, Torres JL

Nutrients

03-Nov-2022

PMCID:	PMC9657608
doi:	10.3390/nu14214656
PMID:	36364917

In Vitro Cytotoxic Activity of African Plants: A Review

Canga I, Vita P, Oliveira AI, Castro MÁ, Pinho C

Molecules

05-Aug-2022

PMCID:	PMC9370645
doi:	10.3390/molecules27154989
PMID:	35956938

Mining methods exert differential effects on species recruitment at artisanal small-scale mining sites in Ghana

Asare D, Ansong M, Kyereh B, Damptey FG, Asante WA

Heliyon

14-May-2022

PMCID:	PMC9123227
doi:	10.1016/j.heliyon.2022.e09434
PMID:	35607493

Ethnobotanical Survey of Local Flora Used for Medicinal Purposes among Indigenous People in Five Areas in Lagos State, Nigeria

Lawal IO, Rafiu BO, Ale JE, Majebi OE, Aremu AO

Plants (Basel)

25-Feb-2022

PMCID:	PMC8912796
doi:	10.3390/plants11050633
PMID:	35270103

Edge disturbance shapes liana diversity and abundance but not liana‐tree interaction network patterns in moist semi‐deciduous forests, Ghana

Ofosu‐Bamfo B, Addo‐Fordjour P, Belford EJ

Ecol Evol

20-Feb-2022

PMCID:	PMC8859495
doi:	10.1002/ece3.8585
PMID:	35371433

Theoretical, chemical, and electrochemical studies of Equisetum arvense extract as an impactful inhibitor of steel corrosion in 2 M HCl electrolyte

Deyab MA, Mohsen Q, Guo L

Sci Rep

10-Feb-2022

PMCID:	PMC8831498
doi:	10.1038/s41598-022-06215-6
PMID:	35145178

Anti-plasmodial, Cytotoxic and Antioxidant Activities of Selected Ghanaian Medicinal Plants

Appiah-Opong R, Agyemang K, Dotse E, Atchoglo P, Owusu KB, Aning A, Sakyiamah M, Adegle R, Ayertey F, Appiah AA, Nyarko AK

J Evid Based Integr Med

17-Jan-2022

PMCID:	PMC8772010
doi:	10.1177/2515690X211073709
PMID:	35037519

Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants

Ajao AA, Mukaila YO, Sabiu S

Heliyon

25-Dec-2021

PMCID:	PMC8733184
doi:	10.1016/j.heliyon.2021.e08668
PMID:	35024488

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see CC(CC(=O)NC(=O)C1=COC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	435.50	unknown	via CMAUP database
Himeic acid B	21579676	Click to see C1=C(OC=C(C1=O)C(=O)N)C=CCCCCCCCCC(=O)O	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see CC(CC(=O)NC(=O)C1=CNC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic acid propylamide	10379895	Click to see CCCCCCCCCCCCCCCC(=O)NCCC	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	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	564.80	unknown	via CMAUP database
> 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 / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	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(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see CC1CC(=O)CC(C1(CC(=O)C(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C)O)(C)C	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see CCCCCC(=O)OCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(=O)CC1(C)C)C)O)C)C#CC2=C(CC(CC2(C)C)O)C	713.00	unknown	via CMAUP database
Amarouciaxanthin B/Sidnyaxanthin	16061221	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC2(C(=CC(=O)CC2(C)C)C)O)C)C	596.80	unknown	via CMAUP database
CID 23428237	23428237	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C=C2C(=CC(=O)CC2(C)C)C)C)C	578.80	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC23C(CC(CC2(O3)C)O)(C)C)C)C	598.90	unknown	via CMAUP database
Mytiloxanthin	11365423	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C	598.90	unknown	via CMAUP database
NV766Twa77	102146782	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)O)O)(C)C)O)C)C	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	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(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
17-(5,6-dihydroxy-7,7-dimethyloxepan-3-yl)-4,4,10,13-tetramethyl-2,5,6,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one	162919394	Click to see CC1(C2CC=C3C4CCC(C4(CCC3C2(CCC1=O)C)C)C5CC(C(C(OC5)(C)C)O)O)C	458.70	unknown	https://doi.org/10.1016/0031-9422(81)85178-3
7-Dehydrocholesterol	439423	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see C[N+](C)(C)CC(=O)O	118.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Arginine	6322	Click to see C(CC(C(=O)O)N)CN=C(N)N	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)CC2=C(C=CC(=C2)CC(C(=O)O)N)O)O	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see C(CS(=O)(=O)O)N	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see CC1CCC2C(C1)C=CC(C2(C)C(=O)CCO)(C)O	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5C(=O)N4)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3=O)C(C5CC67CCCN6C(=O)C5(C(O4)O)NC7=O)(C)C)C	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5(C(=O)N4)OC)C(C)(C)C=C)C	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5(N4C(=O)C6CCCN6C5=O)O)O)C(C)(C)C=C)C	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)C	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)O)C	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(=O)C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	445.50	unknown	via CMAUP database
notoamide R	46919488	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-3-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-5-hydroxy-2-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	163193111	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC=C(C=C7)O)OC8C(C(C(CO8)O)O)O)O)C9=CC=C(C=C9)O)O)O)O)O	1181.10	unknown	https://doi.org/10.1016/J.PHYTOL.2009.12.002
[6-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-3-yl]oxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-5-hydroxy-2-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate	162844592	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC=C(C=C7)O)OC8C(C(C(CO8)O)O)O)O)C9=CC=C(C=C9)O)O)O)O)O	1181.10	unknown	https://doi.org/10.1016/J.PHYTOL.2009.12.002
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin	336327	Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O	270.28	unknown	https://doi.org/10.1016/0031-9422(92)80205-S
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(-)-Sativan	170570	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC	286.32	unknown	https://doi.org/10.1016/0031-9422(92)80205-S
3-(2-hydroxy-3,4-dimethoxyphenyl)-2H-chromene-6,7-diol	162938506	Click to see COC1=C(C(=C(C=C1)C2=CC3=CC(=C(C=C3OC2)O)O)O)OC	316.30	unknown	https://doi.org/10.1016/0031-9422(81)85178-3
Sativan	596401	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC	286.32	unknown	https://doi.org/10.1016/0031-9422(92)80205-S
> Phenylpropanoids and polyketides / Macrolactams
4,7-Dimethyl-18-propan-2-yl-6-oxa-13,20-dithia-3,10,17,22,23,24-hexazatetracyclo[17.2.1.15,8.112,15]tetracosa-1(21),5(24),7,12(23),14,19(22)-hexaene-2,9,16-trione	3594871	Click to see CC1C2=NC(=C(O2)C)C(=O)NCC3=NC(=CS3)C(=O)NC(C4=NC(=CS4)C(=O)N1)C(C)C	474.60	unknown	https://doi.org/10.1016/0031-9422(81)85178-3
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)(O)O	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)O	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)(O)O	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

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Baphia nitida

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