Scientific name	Authority	First published in
Theobroma guazuma	L.	Sp. Pl. : 782 (1753)
Theobroma tomentosum	(Kunth) M.Gómez	Anales Soc. Esp. Hist. Nat. 19: 217 (1890)
Bubroma guasuma	Willd.	Sp. Pl., ed. 4 , 3: 1423 (1802)
Bubroma polybotryum	(Cav.) Willd.	Enum. Pl. : 806 (1809)
Bubroma tomentosum	(Kunth) Spreng.	Syst. Veg. 3: 332 (1826)
Bubroma ulmifolia	(Lam.) Oken	Allg. Naturgesch. 3(2): 1204 (1841)
Diuroglossum rufescens	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 25(II): 157 (1852)
Guazuma blumei	G.Don	Gen. Hist. 1: 523 (1831)
Guazuma burbroma	Tussac	Fl. Antill. 4: 69 (1827)
Guazuma coriacea	Rusby	Bull. New York Bot. Gard. 4: 332 (1907)
Guazuma guazuma	(L.) Cockerell	Bull. Torrey Bot. Club 19(3): 95. 1892
Guazuma guazuma var. ulmifolia	(Lam.) Kuntze	Revis. Gen. Pl. 3(2): 24 (1898)
Guazuma parvifolia	A.Rich.	Hist. Phys. Cuba, Pl. Vasc. 190.
Guazuma polybotrya	Cav.	Icon. 3: 51 (1795)
Guazuma tomentosa	Kunth	Nov. Gen. Sp. 5: 32 (1821)
Guazuma tomentosa var. parvifolia	Kitan.	Fitologiya 11: 48 (1979)
Guazuma ulmifolia var. glabra	K.Schum.	Fl. Bras. 12(3): 81 (1886)
Guazuma ulmifolia var. tomentosa	(Kunth) K.Schum.	Fl. Bras. 12(3): 81 (1886)
Guazuma ulmifolia var. trianae	K.Schum.	Fl. Bras. 12(3): 82 (1886)
Guazuma ulmifolia var. velutina	K.Schum.	Fl. Bras. 12(3): 81 (1886)
Guazuma utilis	Poepp.	Nov. Gen. Sp. Pl. 3: 72 (1845)
Guazuma tomentosa var. cumanensis	G.Don	Gen. Hist. 1: 523 1831
Guazuma tomentosa var. monpoxensis	G.Don	Gen. Hist. 1: 523 1831
Guazuma guazuma var. tomentosa	(Kunth) Kuntze	Revis. Gen. Pl. 3(2): 24 (1898)
Bubroma guazuma	(L.) Willd.	Sp. Pl. 3(2): 1423 1802
Theobroma celtifolium	Salisb.	Prodr. Stirp. Chap. Allerton : 387 (1796)

Common names Top

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Filter by language:

Language	Common/alternative name
English	bastardcedar
Spanish	theobroma guazuma
Spanish	guazuma utilis
Spanish	guazuma polybotrya
Spanish	guazuma parvifolia
Spanish	guazuma invira
Spanish	guazuma grandiflora
Spanish	guazuma blumei
Spanish	guásima
Spanish	guasima
Spanish	guacima
Spanish	bubroma tomentosum
Spanish	bubroma polybotryum
Spanish	bubroma invira
Spanish	bubroma grandiflorum
Spanish	guacimo
Spanish	guácimo
Spanish	guácima
jv	jati walanda
Malayalam	കാട്ടുരുദ്രാക്ഷം
Chinese	瘤果麻
Chinese	毛可可

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

Africa click to expand
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan
  - Sri Lanka
- Indo-China
  - Vietnam

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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Venezuelan Antilles
  - 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
  - Galápagos
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000711645
UNII	L4W707YWSL
USDA Plants	GUUL
Tropicos	30400486
INPN	447624
KEW	urn:lsid:ipni.org:names:823393-1
The Plant List	kew-2834705
Missouri Botanical Garden	287260
Open Tree Of Life	526994
Observations.org	209557
NCBI Taxonomy	93772
IUCN Red List	61785778
IPNI	823393-1
iNaturalist	154538
GBIF	3152195
Freebase	/m/0bwgq4t
EPPO	GUZUL
EOL	584815
Elurikkus	365975
USDA GRIN	312760
Wikipedia	Guazuma_ulmifolia

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

Immunomodulatory potential of Sarcophaga argyostoma larval hemolymph as a natural alternative to berenil in treating Trypanosoma evansi in vivo

Sadek AS, Farghaly DS, Kadada H, Mashaal A

Sci Rep

23-Mar-2024

PMCID:	PMC10960805
doi:	10.1038/s41598-024-57113-y
PMID:	38521853

Effect of intraspecific seed trait variation on the germination of eight tropical dry forest species

Villa-Rivera N, Castellanos-Barliza J, Mondragón-Botero A, Barranco-Pérez W

Naturwissenschaften

22-Mar-2024

PMCID:	PMC10959815
doi:	10.1007/s00114-024-01898-5
PMID:	38517488

Ubenimex combined with Albendazole for the treatment of Echinococcus multilocularis-induced alveolar echinococcosis in mice

Zhou Z, Huayu M, Mu Y, Tang F, Ge RL

Front Vet Sci

15-Mar-2024

PMCID:	PMC10995866
doi:	10.3389/fvets.2024.1320308
PMID:	38585297

Harnessing Natural Antioxidants for Enhancing Food Shelf Life: Exploring Sources and Applications in the Food Industry

Petcu CD, Tăpăloagă D, Mihai OD, Gheorghe-Irimia RA, Negoiță C, Georgescu IM, Tăpăloagă PR, Borda C, Ghimpețeanu OM

Foods

23-Aug-2023

PMCID:	PMC10486681
doi:	10.3390/foods12173176
PMID:	37685108

Transcriptomic, Physiological, and Metabolomic Response of an Alpine Plant, Rhododendron delavayi, to Waterlogging Stress and Post-Waterlogging Recovery

Zhang XM, Duan SG, Xia Y, Li JT, Liu LX, Tang M, Tang J, Sun W, Yi Y

Int J Mol Sci

22-Jun-2023

PMCID:	PMC10341954
doi:	10.3390/ijms241310509
PMID:	37445685

Preliminary Evaluation of Lablab purpureus Phytochemicals for Anti-BoHV-1 Activity Using In Vitro and In Silico Approaches

Bhat SS, Pradeep S, Patil SS, Flores-Holguín N, Glossman-Mitnik D, Frau J, Sommano SR, Ali N, Mohany M, Shivamallu C, Prasad SK, Kollur SP

ACS Omega

14-Jun-2023

PMCID:	PMC10308559
doi:	10.1021/acsomega.3c01478
PMID:	37396248

Potential use of saline resources for biofuel production using halophytes and marine algae: prospects and pitfalls

Abideen Z, Ansari R, Hasnain M, Flowers TJ, Koyro HW, El-Keblawy A, Abouleish M, Khan MA

Front Plant Sci

02-Jun-2023

PMCID:	PMC10272829
doi:	10.3389/fpls.2023.1026063
PMID:	37332715

Patterns of shade plant diversity in four agroforestry systems across Central America: a meta-analysis

Esquivel MJ, Vilchez-Mendoza S, Harvey CA, Ospina MA, Somarriba E, Deheuvels O, de M. Virginio Filho E, Haggar J, Detlefsen G, Cerdan C, Casanoves F, Ordoñez JC

Sci Rep

26-May-2023

PMCID:	PMC10219940
doi:	10.1038/s41598-023-35578-7
PMID:	37237175

Potential plant leaves as sustainable green coagulant for turbidity removal

Khalid Salem A, Fadhile Almansoory A, Al-Baldawi IA

Heliyon

15-May-2023

PMCID:	PMC10213182
doi:	10.1016/j.heliyon.2023.e16278
PMID:	37251892

Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach

De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K

In Silico Pharmacol

28-Apr-2023

PMCID:	PMC10141836
doi:	10.1007/s40203-023-00143-7
PMID:	37131867

Indirect Methods to Determine the Risk of Damage to the Health of Firefighters and Children Due to Exposure to Smoke Emission from Burning Wood/Coal in a Controlled Environment

Ocampos MS, Leite LC, de Pádua Melo ES, de Cássia Avellaneda Guimarães R, Oliveira RJ, de Cássia Freitas K, Hiane PA, Karuppusamy A, do Nascimento VA

Int J Environ Res Public Health

21-Apr-2023

PMCID:	PMC10139234
doi:	10.3390/ijerph20085607
PMID:	37107889

Pest categorisation of Paracoccus marginatus

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

31-Mar-2023

PMCID:	PMC10064853
doi:	10.2903/j.efsa.2023.7899
PMID:	37009439

Neurobiological effects of gallic acid: current perspectives

Bhuia MS, Rahaman MM, Islam T, Bappi MH, Sikder MI, Hossain KN, Akter F, Al Shamsh Prottay A, Rokonuzzman M, Gürer ES, Calina D, Islam MT, Sharifi-Rad J

Chin Med

15-Mar-2023

PMCID:	PMC10015939
doi:	10.1186/s13020-023-00735-7
PMID:	36918923

Magnetic sodium alginate grafted with waste carbonaceous material for diclofenac sodium removal: optimization of operational parameters and process mechanism

Al-Qahtani SD, Ibarhiam S, Sallam S, Almotairy AR, Al-bonayan AM, Munshi AM, El-Metwaly NM

RSC Adv

27-Feb-2023

PMCID:	PMC9969960
doi:	10.1039/d3ra00495c
PMID:	36860528

Current Status of Phytoseiid Mites as Biological Control Agents in Latin America and Experiences from Argentina Using Neoseiulus californicus

Vásquez C, Colmenárez YC, Greco N, Ramos M

Neotrop Entomol

22-Feb-2023

PMCID:	PMC10997537
doi:	10.1007/s13744-023-01026-4
PMID:	36811713

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 / Very long-chain fatty acids
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	https://doi.org/10.1007/S10600-010-9722-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aR,6aS,6aS,6bS,8aS,12aR,14aR,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	162968765	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1055/S-0028-1097596
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	619165	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
3-O-Acetyloleanolic acid	151202	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C	498.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-4H-picen-3-one	23222909	Click to see CC1C(=O)C=CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	424.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1055/S-0028-1097596
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://doi.org/10.1007/S10600-010-9722-2 https://doi.org/10.1055/S-0028-1097596
Friedelane-1-ene-3-one	11384730	Click to see CC1C(=O)C=CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	424.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
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://doi.org/10.1007/S10600-010-9722-2
Lup-20(29)-ene-3beta,28-diol	221023	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1055/S-0028-1097596
Methyl oleanolate acetate	10255859	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C	512.80	unknown	https://doi.org/10.1007/S10600-010-9722-2
Olean-12-en-28-oic acid, 3beta-hydroxy-, methyl ester, acetate	609115	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C	512.80	unknown	https://doi.org/10.1007/S10600-010-9722-2
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1007/S10600-010-9722-2
Stigmast-5-en-3-ol, octadecanoate, (3beta)-	13828710	Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C	681.20	unknown	https://doi.org/10.1007/S10600-010-9722-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9S,10R,13R,14R,17S)-17-[(2R,5R)-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	162965368	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1055/S-0028-1097596
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/10.1055/S-0028-1097596 https://doi.org/10.1007/S10600-010-9722-2
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/10.1055/S-0028-1097596 https://doi.org/10.1007/S10600-010-9722-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Gerontoxanthone C	14259059	Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)CC=C(C)C)(C)C	396.40	unknown	https://doi.org/10.1007/S10600-010-9722-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
7,8-Methylenedioxy-6-methoxycoumarin	5319474	Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2	220.18	unknown	https://doi.org/10.1007/S10600-010-9722-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
3,3'-Methylenebis(4,6-dihydroxycoumarin)	129881889	Click to see C1=CC2=C(C=C1O)C(=C(C(=O)O2)CC3=C(C4=C(C=CC(=C4)O)OC3=O)O)O	368.30	unknown	https://doi.org/10.1007/S10600-010-9722-2
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol	5320711	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	16163749	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1155.00	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	14309768	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=C(C(=C4)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	14237654	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Cinnamtannin A2	16130899	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O	1155.00	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Endotelon	130556	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
ent-Epicatechin-(4alpha->6)-ent-epicatechin	13990892	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Epicatechin-(4beta->6)-epicatechin-(4beta->8)-epicatechin	10865804	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=C(C(=C4)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Epicatechin-(4beta-8)-epicatechin-(4beta-6)-epicatechin	14237653	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Procyanidin B5	124017	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Procyanidin C1	169853	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
Procyanidin trimer T2	13751990	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	https://doi.org/10.1016/0031-9422(95)00855-1
> 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/10.1016/0031-9422(95)00855-1
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/10.1016/0031-9422(95)00855-1

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Guazuma ulmifolia

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