Genipa americana, also known as the genip tree, is a species of tree in the Rubiaceae family. It is found in the tropical forests of North and South America, as well as the Caribbean. The trees can grow up to 30 meters tall and have smooth bark and glossy dark green leaves. The flowers are white to yellowish and produce a thick-skinned edible fruit. This tree is native to the Americas and is used for various purposes such as dye for tattoos and skin painting, as well as for its edible fruits and strong wood.

Synonyms Top

Scientific name	Authority	First published in
Genipa americana var. riobranquensis	Kuhlm.	Publ. Inst. Nac. Pesq. Amazônia Bot. 5: 4 (1957)
Gardenia brasiliensis	Spreng.	Syst. Veg. 1: 763 (1824)
Gardenia genipa	Sw.	Prodr. Veg. Ind. Occ. : 51 (1788)
Gardenia hexandra	Willd.	Syst. Veg., ed. 15 bis [Roemer & Schultes] 5: 243. 1819 [Dec 1819]
Gardenia oblongifolia	Poir.	Encycl. , Suppl. 2: 708 (1812)
Genipa americana var. caruto	K.Schum.	Fl. Bras. 6(6): 352 (1889)
Genipa americana f. grandifolia	Chodat & Hassl.	Bull. Herb. Boissier , sér. 2, 4: 171 (1904)
Genipa americana f. jorgensenii	Steyerm.	Mem. New York Bot. Gard. 23: 353 (1972)
Genipa americana f. parvifolia	Chodat & Hassl.	Bull. Herb. Boissier , sér. 2, 4: 171 (1904)
Genipa barbata	C.Presl	Symb. Bot. 2: 13 (1832)
Genipa brasiliana	A.Rich.	Mém. Rubiac. : 164 (1830)
Genipa brasiliensis	Baill.	Hist. Pl. 7: 374 (1880)
Genipa caruto	Kunth	Nov. Gen. Sp. 3: 407 (1820)
Genipa codonocalyx	Standl.	Contr. U.S. Natl. Herb. 17: 446 (1914)
Genipa excelsa	K.Krause	Bot. Jahrb. Syst. 40: 327 (1908)
Genipa humilis	Vell.	Fl. Flumin. 2: t. 142 (1829)
Genipa oblongifolia	Ruiz & Pav.	Fl. Peruv. 2: 67 (1799)
Genipa oleosa	Rojas Acosta	Cat. Hist. Nat. Corrientes : 67, 166 (1897)
Genipa pubescens	DC.	Prodr. 4: 379 (1830)
Genipa venosa	Standl.	J. Washington Acad. Sci. 18: 168 (1928)

Common names Top

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Filter by language:

Language	Common/alternative name
English	jagua
Spanish	jagua
Spanish	maluco
Spanish	jagua azul
Spanish	lluale
Spanish	shagua
Spanish	tejoruco
Spanish	xagua
Catalan	huito
German	jenipapo
Persian	جنیپاپو
gn	Ñandypa
Hebrew	ג'ניפה אמריקנה
Korean	제니팝나무
koi	Генипа
kv	Генипа
lbe	Генипа
Lithuanian	amerikinė genipa
mrj	Генипа
Portuguese	jenipapeiro
Portuguese	bujê
Quechua	witu
Quechua	wituq
Quechua	jagua
Quechua	huito
Russian	Генипа
udm	Генипа
Chinese	靛欖
Chinese	靛榄
Chinese	大果茜

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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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

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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - 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-0000971808
UNII	C22I013G6O
USDA Plants	GEAM
Tropicos	27900116
INPN	629766
KEW	urn:lsid:ipni.org:names:751331-1
The Plant List	kew-89085
Open Tree Of Life	771037
Observations.org	357506
NCBI Taxonomy	58486
IUCN Red List	61958206
IPNI	751331-1
iNaturalist	118965
GBIF	2895593
Freebase	/m/01t5y0
EPPO	GEIAM
EOL	1096067
USDA GRIN	395
Wikipedia	Genipa_americana

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Comparative Analysis of Phytochemical Profiles and Selected Biological Activities of Various Morphological Parts of Ligustrum vulgare

Litewski S, Koss-Mikołajczyk I, Kusznierewicz B

Molecules

13-Jan-2024

PMCID:	PMC10819685
doi:	10.3390/molecules29020399
PMID:	38257312

Applications of Plant Bioactive Compounds as Replacers of Synthetic Additives in the Food Industry

Nieto G, Martínez-Zamora L, Peñalver R, Marín-Iniesta F, Taboada-Rodríguez A, López-Gómez A, Martínez-Hernández GB

Foods

21-Dec-2023

PMCID:	PMC10778451
doi:	10.3390/foods13010047
PMID:	38201075

Therapeutic potentials of iridoids derived from Rubiaceae against in vitro and in vivo inflammation: A scoping review

Jaafar A, Zulkipli MA, Mohd Hatta FH, Jahidin AH, Abdul Nasir NA, Hazizul Hasan M

Saudi Pharm J

16-Nov-2023

PMCID:	PMC10788517
doi:	10.1016/j.jsps.2023.101876
PMID:	38226349

Crypsis by background matching and disruptive coloration as drivers of substrate occupation in sympatric Amazonian bark praying mantises

de Alcantara Viana JV, Campos Duarte R, Vieira C, Augusto Poleto Antiqueira P, Bach A, de Mello G, Silva L, Rabelo Oliveira Leal C, Quevedo Romero G

Sci Rep

15-Nov-2023

PMCID:	PMC10652001
doi:	10.1038/s41598-023-46204-x
PMID:	37968331

Macro and trace element compositions and physicochemical parameters of guajiru fruits (Chrysobalanus icaco l.) from two Brazilian states

de Melo Rodrigues YJ, dos Santos NR, Lordelo Guimarães Tavares PP, Eugênia de Oliveira Mamede M, Menezes-Filho JA

Heliyon

22-Sep-2023

PMCID:	PMC10520804
doi:	10.1016/j.heliyon.2023.e20291
PMID:	37767506

An improved folate stable isotope dilution assay of unexploited food sources from Brazil

Obermaier L, da Mata BP, Perego CH, Sivieri K, Salgaço MK, dos Santos AG, Boehni R, Groehn V, Knapp JP, Rychlik M

Front Nutr

05-Sep-2023

PMCID:	PMC10508286
doi:	10.3389/fnut.2023.1252497
PMID:	37731402

Hunting practices in southwestern Amazonia: a comparative study of techniques, modalities, and baits among urban and rural hunters

Oliveira MA, Braga-Pereira F, El Bizri HR, Morcatty TQ, Doria CR, Messias MR

J Ethnobiol Ethnomed

03-Jul-2023

PMCID:	PMC10318826
doi:	10.1186/s13002-023-00599-z
PMID:	37400859

The oral repellent – science fiction or common sense? Insects, vector-borne diseases, failing strategies, and a bold proposition

Bauer IL

Trop Dis Travel Med Vaccines

28-Jun-2023

PMCID:	PMC10308739
doi:	10.1186/s40794-023-00195-9
PMID:	37381000

Re-Examination of Several Elsinoë Species Reported from Japan

Ujat AH, Ono T, Hattori Y, Nakashima C

Mycobiology

15-Jun-2023

PMCID:	PMC10288934
doi:	10.1080/12298093.2023.2219049
PMID:	37359956

New Trends in Supercritical Fluid Technology and Pressurized Liquids for the Extraction and Recovery of Bioactive Compounds from Agro-Industrial and Marine Food Waste

Fraguela-Meissimilly H, Bastías-Monte JM, Vergara C, Ortiz-Viedma J, Lemus-Mondaca R, Flores M, Toledo-Merma P, Alcázar-Alay S, Gallón-Bedoya M

Molecules

29-May-2023

PMCID:	PMC10254675
doi:	10.3390/molecules28114421
PMID:	37298897

Female naturalists and the patterns of suppression of women scientists in history: the example of Maria Sibylla Merian and her contributions about useful plants

Mariath F, Baratto LC

J Ethnobiol Ethnomed

12-May-2023

PMCID:	PMC10182609
doi:	10.1186/s13002-023-00589-1
PMID:	37173737

Ultrasound applications in drying of fruits from a sustainable development goals perspective

Fernandes FA, Rodrigues S

Ultrason Sonochem

04-May-2023

PMCID:	PMC10193121
doi:	10.1016/j.ultsonch.2023.106430
PMID:	37167783

Tissue engineering modalities in skeletal muscles: focus on angiogenesis and immunomodulation properties

Namjoo AR, Abrbekoh FN, Saghati S, Amini H, Saadatlou MA, Rahbarghazi R

Stem Cell Res Ther

15-Apr-2023

PMCID:	PMC10105969
doi:	10.1186/s13287-023-03310-x
PMID:	37061717

Genipin increases extracellular matrix synthesis preventing corneal perforation

Donovan C, Sun M, Cogswell D, Margo CE, Avila MY, Espana EM

Ocul Surf

03-Mar-2023

PMCID:	PMC10440284
doi:	10.1016/j.jtos.2023.02.003
PMID:	36871831

Effect of Antigen Structure in Subunit Vaccine Nanoparticles on Humoral Immune Responses

Park J, Champion JA

ACS Biomater Sci Eng

27-Feb-2023

PMCID:	PMC10015428
doi:	10.1021/acsbiomaterials.2c01516
PMID:	36848229

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
6,1'-O,O-dimethylaverantin	60199901	Click to see CCCCCC(C1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C=C(C=C3O)OC)O)OC	400.40	unknown	https://doi.org/10.1248/CPB.53.1342
> Benzenoids / Benzene and substituted derivatives / Terphenyls / P-terphenyls
Echoside E	76314408	Click to see CN1C2=C(C(=C(C(=C2SC1=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)C5=CC=CC=C5	525.50	unknown	https://doi.org/10.1248/CPB.53.1342
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (4aR,7aR)-7-(hydroxymethyl)-2-(4-methoxy-4-oxobutyl)-1-oxo-5,7a-dihydro-4aH-cyclopenta[c]pyridine-4-carboxylate	162860031	Click to see COC(=O)CCCN1C=C(C2CC=C(C2C1=O)CO)C(=O)OC	323.34	unknown	https://doi.org/10.1248/CPB.55.632
methyl 7-(hydroxymethyl)-2-(4-methoxy-4-oxobutyl)-1-oxo-5,7a-dihydro-4aH-cyclopenta[c]pyridine-4-carboxylate	73298976	Click to see COC(=O)CCCN1C=C(C2CC=C(C2C1=O)CO)C(=O)OC	323.34	unknown	https://doi.org/10.1248/CPB.55.632
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R)-1alpha,7aalpha-Dihydroxy-7-(hydroxymethyl)-1,4aalpha,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester	16655217	Click to see COC(=O)C1=COC(C2(C1CC=C2CO)O)O	242.22	unknown	https://doi.org/10.1248/CPB.55.632
Genipin	442424	Click to see COC(=O)C1=COC(C2C1CC=C2CO)O	226.23	unknown	https://doi.org/10.1248/CPB.55.632 https://doi.org/10.1016/S0040-4039(01)85186-8
Methyl 1-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate	23340	Click to see COC(=O)C1=COC(C2C1CC=C2CO)O	226.23	unknown	https://doi.org/10.1248/CPB.55.632
methyl 1,7a-dihydroxy-7-(hydroxymethyl)-4a,5-dihydro-1H-cyclopenta[c]pyran-4-carboxylate	73298977	Click to see COC(=O)C1=COC(C2(C1CC=C2CO)O)O	242.22	unknown	https://doi.org/10.1248/CPB.55.632
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	162985513	Click to see CC1(CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	392.35	unknown	https://doi.org/10.1248/CPB.55.632
(1S,4aS,7S,7aS)-7-hydroxy-7-methylol-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[d]pyran-4-carboxylic acid methyl ester	138113473	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1021/NP50078A032
5,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	14378605	Click to see CC1(CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	392.35	unknown	https://doi.org/10.1248/CPB.55.632
6alpha-Hydroxygeniposide; Deacetylasperulosidic acid methyl ester	3515876	Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1248/CPB.55.632
7-(Hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	323273	Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO	374.34	unknown	https://doi.org/10.1248/CPB.53.1342
Deacetyl asperulosidic acid methyl ester	6325021	Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1248/CPB.55.632
Gardenoside	442423	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1021/NP50078A032 https://doi.org/10.1248/CPB.53.1342
Genameside B	11495491	Click to see COC(=O)C1=COC(C2C1CC(C2(CO)O)O)OC3C(C(C(C(O3)CO)O)O)O	422.40	unknown	https://doi.org/10.1248/CPB.53.1342
Genameside C	11692460	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O	550.50	unknown	https://doi.org/10.1248/CPB.53.1342
Genameside D	11570273	Click to see COC(=O)C1=COC(C2C1CC=C2COC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	550.50	unknown	https://doi.org/10.1248/CPB.53.1342
Genipin 1-gentiobioside	3082301	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O	550.50	unknown	https://doi.org/10.1248/CPB.53.1342
Geniposide	107848	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O	388.40	unknown	https://doi.org/10.1021/NP50078A032 https://doi.org/10.1248/CPB.53.1342
Geniposidic acid	443354	Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO	374.34	unknown	https://doi.org/10.1021/NP50078A032 https://doi.org/10.1248/CPB.53.1342 https://doi.org/10.1016/S0040-4039(01)85186-8
methyl (1S,4aS,6R,7S,7aS)-6,7-dihydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	11690334	Click to see COC(=O)C1=COC(C2C1CC(C2(CO)O)O)OC3C(C(C(C(O3)CO)O)O)O	422.40	unknown	https://doi.org/10.1248/CPB.53.1342
methyl (4aR,7aS)-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate	137706142	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O	388.40	unknown	https://doi.org/10.1021/NP50078A032
Methyl 1-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate	73063764	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O	550.50	unknown	https://doi.org/10.1248/CPB.53.1342
Methyl 7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate	3515873	Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O	388.40	unknown	https://doi.org/10.1248/CPB.53.1342
methyl 7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate	100058	Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1248/CPB.53.1342
Scandoside methyl ester	442433	Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	404.40	unknown	https://doi.org/10.1248/CPB.55.632
Shanzhiside	11948668	Click to see CC1(CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	392.35	unknown	https://doi.org/10.1248/CPB.55.632
Tarennoside	182279	Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C=O)CO	358.34	unknown	https://doi.org/10.1021/NP50078A032
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4S,4aR,7aS)-4,7-bis(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one	160701616	Click to see C1C=C(C2C1C(C(=O)OC2)CO)CO	198.22	unknown	https://doi.org/10.1248/CPB.55.632
(4S,4aS,7aS)-4,7-bis(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one	101675239	Click to see C1C=C(C2C1C(C(=O)OC2)CO)CO	198.22	unknown	https://doi.org/10.1248/CPB.55.632
4,7-bis(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one	130146212	Click to see C1C=C(C2C1C(C(=O)OC2)CO)CO	198.22	unknown	https://doi.org/10.1248/CPB.55.632
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1R,3aS,4S,5aR,5bR,7aR,9S,11aR,11bR,13aS,13bR)-4-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] dodecanoate	163050706	Click to see CCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(C(CC4(C3(CCC2C1(C)C)C)C)O)CO)C(=C)C)C	641.00	unknown	https://doi.org/10.1248/CPB.53.1342
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
2-acetyloxy-2-[(3S,4R)-3-hydroxy-3,4,5,6-tetrahydro-1H-cyclopenta[c]furan-4-yl]acetic acid	5317551	Click to see CC(=O)OC(C1CCC2=C1C(OC2)O)C(=O)O	242.22	unknown	https://doi.org/10.1016/S0040-4020(01)99179-3
Genipinic acid	12310086	Click to see COC(=O)C(C1CCC2=C1C(OC2)O)C(=O)O	242.22	unknown	https://doi.org/10.1016/S0040-4020(01)99179-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1007/BF01185929
> Organoheterocyclic compounds / Dihydrofurans
2-[(3S,4S)-3-hydroxy-3,4,5,6-tetrahydro-1H-cyclopenta[c]furan-4-yl]acetic acid	5317549	Click to see C1CC2=C(C1CC(=O)O)C(OC2)O	184.19	unknown	https://doi.org/10.1016/S0040-4020(01)99179-3 https://doi.org/10.1021/JF60228A023
Genipic acid	78384968	Click to see C1CC2=C(C1CC(=O)O)C(OC2)O	184.19	unknown	https://doi.org/10.1021/JF60228A023 https://doi.org/10.1016/S0040-4020(01)99179-3

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Genipa americana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top