Physalis coztomatl

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Ethnobotanical Use

General Uses

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Subtypes (subspecies, varieties, subvarieties, forms)

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Details Top

Internal ID	UUID6440416544c63359957393
Scientific name	Physalis coztomatl
Authority	Dunal
First published in	Prodr. [A. P. de Candolle] 13(2): 450. 1849 [5 May 1849]

Ethnobotanical Use Top

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General Uses Top

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Food and beverages (non-medicinal):
The mature, sweet-tart fruits are consumed fresh and used as an ingredient in culinary preparations such as jams, sauces, savory dishes, and traditional Mexican stews like moles. Their distinct balance of sugars and organic acids (notably citric and malic acids) enables them to retain texture during cooking while contributing acidity. The fruits are also processed into preserves, chutneys, and fermented beverages where their pectin content aids gel formation in jams. No specific commercial food standards apply beyond general Mexican or international fruit product regulations.

Synonyms Top

No known synonyms.

Common names Top

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Language	Common/alternative name
nah	cōztomatl

Subspecies (abbr. subsp./ssp.) Top

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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

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

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0001024646
Tropicos	29606756
KEW	urn:lsid:ipni.org:names:817373-1
The Plant List	tro-29606756
Open Tree Of Life	414766
NCBI Taxonomy	304143
IUCN Red List	105088464
IPNI	817373-1
iNaturalist	153383
GBIF	5581419
Freebase	/m/05zlj4g
USDA GRIN	102413
Wikipedia	Physalis_coztomatl

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

Taxonomic revision of Physalis in Mexico

Martínez M, Vargas-Ponce O, Zamora-Tavares P

Front Genet

14-Apr-2023

PMCID:	PMC10141326
doi:	10.3389/fgene.2023.1080176
PMID:	37124620

Production and Structural Diversification of Withanolides by Aeroponic Cultivation of Plants of Solanaceae: Cytotoxic and Other Withanolides from Aeroponically Grown Physalis coztomatl

Xu YM, Wijeratne EM, Liu MX, Xuan L, Wang W, Gunatilaka AA

Molecules

28-Jan-2022

PMCID:	PMC8838488
doi:	10.3390/molecules27030909
PMID:	35164184

Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids

Dembitsky VM, Gloriozova TA, Poroikov VV

Mar Drugs

03-Jun-2021

PMCID:	PMC8228860
doi:	10.3390/md19060324
PMID:	34205074

Sucrose esters from the fruits of Physalis nicandroides var. attenuata.

Maldonado E, Torres FR, Martínez M, Pérez-Castorena AL

J Nat Prod

01-Oct-2006

doi:	10.1021/NP060274L
PMID:	17067174

Labdanes and withanolides from Physalis coztomatl.

Pérez-Castorena AL, Oropeza RF, Vazquez AR, Martínez M, Maldonado E

J Nat Prod

01-Jul-2006

doi:	10.1021/NP0601354
PMID:	16872139

Bioactive metabolites from Sicilian marine fennel, Crithmum maritimum.

Cunsolo F, Ruberto G, Amico V, Piattelli M

J Nat Prod

01-Sep-1993

doi:	10.1021/NP50099A022
PMID:	8254353

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(E,4R)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-ene-1,4-diol	162987779	Click to see CC1=CCC2C(CCCC2(C1CC(C(=CCO)C)O)C)(C)C	306.50	unknown	https://doi.org/10.1021/NP0601354
1-(5-hydroxy-3-methylpent-3-enyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	3758943	Click to see CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C	308.50	unknown	https://doi.org/10.1021/NP060274L
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-ene-1,4-diol	76389631	Click to see CC1=CCC2C(CCCC2(C1CC(C(=CCO)C)O)C)(C)C	306.50	unknown	https://doi.org/10.1021/NP060274L
Labd-13-ene-8,15-diol	5471228	Click to see	308.50	unknown	https://doi.org/10.1021/NP060274L
Physacoztomatin	49799161	Click to see	306.50	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(2R)-2-[(1R)-1-[(5R,6R,8R,9S,10R,13S,14S,17S)-5,6-dihydroxy-13-(hydroxymethyl)-10,14-dimethyl-1-oxo-4,6,7,8,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-4,5-dimethyl-2,5-dihydropyran-6-one	101403752	Click to see	502.60	unknown	https://doi.org/10.1021/NP0601354
(2R)-2-[(1R)-1-[(5R,6R,8S,9S,10R,13R,14S,17S)-5,6-dihydroxy-13-(hydroxymethyl)-10-methyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-4,5-dimethyl-2,3-dihydropyran-6-one	11844625	Click to see	488.60	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
[(1S,2R,7S,9R,11R,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-16-yl]methyl acetate	101403753	Click to see CC1C(=CC(OC1=O)C(C)(C2CCC3(C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)COC(=O)C)C)O)C	526.70	unknown	https://doi.org/10.1021/NP0601354
[(1S,2R,7S,9R,11S,12S,15S,16R)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-2-methyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-16-yl]methyl acetate	11844626	Click to see	512.60	unknown	https://doi.org/10.1021/NP0601354 https://doi.org/10.1021/NP060274L
[(5R,6R,8R,9S,10R,13S,14S,17S)-17-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-5,6-dihydroxy-10,14-dimethyl-1-oxo-4,6,7,8,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	101403751	Click to see CC1C(=CC(OC1=O)C(C)(C2CCC3(C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)COC(=O)C)C)O)C	544.70	unknown	https://doi.org/10.1021/NP0601354
[(5R,6R,8S,9S,10R,13R,14S,17S)-17-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-5,6-dihydroxy-10-methyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-13-yl]methyl acetate	11844624	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC(C5(C4(C(=O)C=CC5)C)O)O)COC(=O)C)O)C	530.60	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
[(6R,8R,9S,10R,13R,14R,17S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-6,14,17-trihydroxy-10-methyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	11844627	Click to see	544.60	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
[(6R,8R,9S,10R,13R,14R,17S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-6,14,17-trihydroxy-10-methyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	101403754	Click to see	544.60	unknown	https://doi.org/10.1021/NP0601354
[(8R,9S,10R,13R,14R,17R)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-6,14,17-trihydroxy-10-methyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	101403755	Click to see	544.60	unknown	https://doi.org/10.1021/NP0601354
[(8R,9S,10R,13R,14R,17S)-17-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-14-hydroxy-10-methyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-4H-cyclopenta[a]phenanthren-13-yl]methyl acetate	11844628	Click to see	512.60	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
[(8R,9S,10R,13R,14R,17S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-14,17-dihydroxy-10-methyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	101883242	Click to see	528.60	unknown	https://doi.org/10.1021/NP060274L https://doi.org/10.1021/NP0601354
[15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-2-methyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-16-yl]methyl acetate	73123620	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)COC(=O)C)O)C	512.60	unknown	https://doi.org/10.1021/NP060274L
[15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6-hydroxy-2-methyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-16-yl]methyl acetate	73197334	Click to see	528.60	unknown	https://doi.org/10.1021/NP060274L
[17-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-14-hydroxy-10-methyl-1-oxo-7,8,9,11,12,15,16,17-octahydro-4H-cyclopenta[a]phenanthren-13-yl]methyl acetate	73123622	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3(C2(CCC4C3CC=C5C4(C(=O)C=CC5)C)COC(=O)C)O)O)C	512.60	unknown	https://doi.org/10.1021/NP060274L
[17-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-14,17-dihydroxy-10-methyl-1-oxo-4,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	162964125	Click to see	528.60	unknown	https://doi.org/10.1021/NP060274L
[17-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-5,6-dihydroxy-10-methyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-13-yl]methyl acetate	73123618	Click to see	530.60	unknown	https://doi.org/10.1021/NP060274L
[17-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6,14,17-trihydroxy-10-methyl-1-oxo-6,7,8,9,11,12,15,16-octahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	73123621	Click to see	544.60	unknown	https://doi.org/10.1021/NP060274L
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6-hydroxy-16-(hydroxymethyl)-2-methyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	73800274	Click to see	486.60	unknown	https://doi.org/10.1021/NP060274L
18-acetoxywithanolide D	15519705	Click to see	528.60	unknown	https://doi.org/10.1021/NP0601354 https://doi.org/10.1021/NP060274L
18-Hydroxywithanolide D	21606687	Click to see	486.60	unknown	https://doi.org/10.1021/NP0601354 https://doi.org/10.1021/NP060274L
2-[1-[5,6-dihydroxy-13-(hydroxymethyl)-10-methyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-4,5-dimethyl-2,3-dihydropyran-6-one	73123619	Click to see	488.60	unknown	https://doi.org/10.1021/NP060274L
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1021/NP0601354
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1021/NP0601354
> Organoheterocyclic compounds / Pyrrolizidines
6-Hydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadecane-3,7-dione	12314909	Click to see	311.37	unknown	https://doi.org/10.1021/NP060274L
Retusine	3083583	Click to see CC1C(C(C(=O)OCC2CCN3C2C(CC3)OC1=O)(C)O)C	311.37	unknown	https://doi.org/10.1021/NP060274L
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethylchromen-4-one	162978833	Click to see CC1=CC(=C2C(=C1)OC(=C(C2=O)C)C3=CC(=C(C=C3)O)OC)O	312.30	unknown	https://doi.org/10.1021/NP060274L
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pachypodol	5281677	Click to see	344.30	unknown	https://doi.org/10.1021/NP0601354
Retusin	5352005	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC	358.30	unknown	https://doi.org/10.1021/NP0601354

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Physalis coztomatl

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top