Scientific name	Authority	First published in
Physalis angulata var. philadelphica	(Lam.) A.Gray	Manual (Gray), ed. 2. 340. 1856
Physalis cavaleriei	H.Lév.	Repert. Spec. Nov. Regni Veg. 11: 295. 1912
Physalis laevigata	M.Martens & Galeotti	Bull. Acad. Roy. Soc. Bruxelles 12(1): 131. 1845.
Physalis philadelphica var. minor	Dunal	Prodr. [A. P. de Candolle] 13(1): 450. 1852 [10 May 1852]
Physalis philadelphica f. pilosa	Waterf.	Rhodora 69: 214. 1969

Common names Top

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Filter by language:

Language	Common/alternative name
English	mexican groundcherry
English	physalis ixocarpa
English	tomatillo
Spanish	tomate milpero
Spanish	physalis ixocarpa
Spanish	tomate verde
Spanish	tomate de fresadilla
Spanish	tomate de cascara
Spanish	miltomate
Spanish	physalis aequata
Spanish	tomate de cáscara
Arabic	التوماتيلو
Azerbaijani	physalis ixocarpa
Belarusian	Мексіканскі тамат
Catalan	tomatillo
Catalan	physalis ixocarpa
Czech	mochyně dužnoplodá
Czech	tomatillo
German	physalis
Estonian	physalis ixocarpa
Estonian	mehhiko füüsal
Estonian	tomatillofüüsal
Estonian	physalis laevigata
Estonian	physalis cavaleriei
Estonian	physalis aequata
Persian	فیسالیس
Persian	فیسالیس بنفش
Finnish	physalis ixocarpa
Finnish	tomatillo
French	physalis ixocarpa
French	tomatille
Hebrew	טומטילו
Hungarian	mexikói földicseresznye
Italian	physalis ixocarpa
Japanese	トマティーヨ
Kazakh	Физалис жаңғағы
Korean	토마티요
nah	mīltomātl
nah	tomate
nah	tomatl
Dutch	physalis ixocarpa
Dutch	tomatillo
Dutch	mexicaanse aardkers
Polish	physalis ixocarpa
Polish	miechunka pomidorowa
Portuguese	physalis ixocarpa
Russian	Физалис овощной
Russian	Овощной физалис
Russian	Мексиканский физалис
Russian	Мексиканский томат
Russian	Земляничный томат
Russian	physalis ixocarpa
Slovak	tomatillo
Swedish	tomatillo
Tamil	சிறு தக்காளி
yi	טאמאטיאו
Chinese	黏果酸浆
Chinese	黏果酸漿
Chinese	綠番茄
Chinese	樹蕃茄
Chinese	费城酸浆
Chinese	毛酸浆

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
- East Tropical Africa
  - Kenya
- Northeast Tropical Africa
  - Sudan
- Northern Africa
  - Morocco
- South Tropical Africa
  - Angola
  - Zambia
  - Zimbabwe
- Southern Africa
  - Kwazulu-Natal

Asia-temperate click to expand
- China
  - Manchuria
- Western Asia
  - Turkey

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - Victoria
  - Western Australia

Europe click to expand
- Eastern Europe
  - Central European Russia
  - Ukraine
- Middle Europe
  - Belgium
  - Czechoslovakia
- Southeastern Europe
  - Bulgaria
  - Greece
  - Yugoslavia
- Southwestern Europe
  - Portugal
  - Spain

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Wisconsin
- Northeastern U.S.A.
  - New York
  - Vermont
- Southeastern U.S.A.
  - Kentucky
  - Maryland
- Southwestern U.S.A.
  - Arizona

Southern America click to expand
- Caribbean
  - Cuba
  - Haiti
  - Leeward Islands
- Central America
  - Belize
  - El Salvador
  - Guatemala
  - Honduras
  - Panamá

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001024903
UNII	Z8IR1JJJ9B
Canadensys	9371
USDA Plants	PHPH2
Tropicos	29603031
INPN	161577
KEW	urn:lsid:ipni.org:names:817532-1
The Plant List	kew-2549657
Open Tree Of Life	788338
NCBI Taxonomy	304130
NBN Atlas	NBNSYS0000014906
Nature Serve	2.141177
IUCN Red List	109716592
IPNI	817532-1
iNaturalist	51734
GBIF	5341801
Freebase	/m/02l9bx
WisFlora	9102
EPPO	PHYIX
EOL	486222
Elurikkus	521409
Calflora (Californian flora)	6483
USDA GRIN	102411
Wikipedia	Tomatillo

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

Knowledge, Attitudes, and Practices of Parents in the Use of Antibiotics: A Case Study in a Mexican Indigenous Community

González-Villoria AM, García Quiroz AD, Osorio Guzmán EU, Suarez-Herrera JC, Abeldaño Zuñiga RA

Healthcare (Basel)

24-Jan-2024

PMCID:	PMC10855187
doi:	10.3390/healthcare12030294
PMID:	38338179

Biocultural diversity and crop improvement

Gepts P

Emerg Top Life Sci

12-Dec-2023

PMCID:	PMC10754339
doi:	10.1042/ETLS20230067
PMID:	38084755

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

Antioxidant and Anti-Inflammatory Compounds from Edible Plants with Anti-Cancer Activity and Their Potential Use as Drugs

Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Juárez ZN, Hernández LR

Molecules

03-Feb-2023

PMCID:	PMC9920972
doi:	10.3390/molecules28031488
PMID:	36771154

Emerging Issues on Tropane Alkaloid Contamination of Food in Europe

de Nijs M, Crews C, Dorgelo F, MacDonald S, Mulder PP

Toxins (Basel)

19-Jan-2023

PMCID:	PMC9961018
doi:	10.3390/toxins15020098
PMID:	36828413

Complete Plastome of Physalis angulata var. villosa, Gene Organization, Comparative Genomics and Phylogenetic Relationships among Solanaceae

Zhan X, Zhang Z, Zhang Y, Gao Y, Jin Y, Shen C, Wang H, Feng S

Genes (Basel)

05-Dec-2022

PMCID:	PMC9778145
doi:	10.3390/genes13122291
PMID:	36553558

Germination Response of Datura stramonium L. to Different pH and Salinity Levels under Different Temperature Conditions

Nikolić N, Šoštarčić V, Pismarović L, Šćepanović M, Masin R

Plants (Basel)

27-Nov-2022

PMCID:	PMC9736371
doi:	10.3390/plants11233259
PMID:	36501298

Interspecific variation in resistance and tolerance to herbicide drift reveals potential consequences for plant community co-flowering interactions and structure at the agro-eco interface

Iriart V, Baucom RS, Ashman TL

Ann Bot

23-Nov-2022

PMCID:	PMC9851304
doi:	10.1093/aob/mcac137
PMID:	36415945

Mexico: A Landscape of Viroid Origin and Epidemiological Relevance of Endemic Species

Aviña-Padilla K, Zamora-Macorra EJ, Ochoa-Martínez DL, Alcántar-Aguirre FC, Hernández-Rosales M, Calderón-Zamora L, Hammond RW

Cells

03-Nov-2022

PMCID:	PMC9653797
doi:	10.3390/cells11213487
PMID:	36359881

Michael acceptor molecules in natural products and their mechanism of action

Liang ST, Chen C, Chen RX, Li R, Chen WL, Jiang GH, Du LL

Front Pharmacol

02-Nov-2022

PMCID:	PMC9666775
doi:	10.3389/fphar.2022.1033003
PMID:	36408214

Physalis: A new model crop to understand plant diversity

Lopez-Gomollon S

Plant Cell

25-Oct-2022

PMCID:	PMC9806580
doi:	10.1093/plcell/koac315
PMID:	36350573

Establishing Physalis as a Solanaceae model system enables genetic reevaluation of the inflated calyx syndrome

He J, Alonge M, Ramakrishnan S, Benoit M, Soyk S, Reem NT, Hendelman A, Van Eck J, Schatz MC, Lippman ZB

Plant Cell

21-Oct-2022

PMCID:	PMC9806562
doi:	10.1093/plcell/koac305
PMID:	36268892

Testing the effectiveness of rbcLa DNA-barcoding for species discrimination in tropical montane cloud forest vascular plants (Oaxaca, Mexico) using BLAST, genetic distance, and tree-based methods

Trujillo-Argueta S, del Castillo RF, Velasco-Murguía A

PeerJ

16-Aug-2022

PMCID:	PMC9390329
doi:	10.7717/peerj.13771
PMID:	35990900

Research Status and Hotspots of Anticancer Natural Products Based on the Patent Literature and Scientific Articles

Shen J, Li J, Yu P, Du G

Front Pharmacol

17-Jun-2022

PMCID:	PMC9247190
doi:	10.3389/fphar.2022.903239
PMID:	35784720

Hidden in Plants—A Review of the Anticancer Potential of the Solanaceae Family in In Vitro and In Vivo Studies

Kowalczyk T, Merecz-Sadowska A, Rijo P, Mori M, Hatziantoniou S, Górski K, Szemraj J, Piekarski J, Śliwiński T, Bijak M, Sitarek P

Cancers (Basel)

11-Mar-2022

PMCID:	PMC8946528
doi:	10.3390/cancers14061455
PMID:	35326606

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 / Sphingolipids / Ceramides / Phytoceramides
(2S,3S,4R,9E)-1,3,4-trihydroxyl-2-[(2'R)-2'-hydroxytetracosanoylamino]-9-octadecene	11765141	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCC=CCCCCCCCC)O)O)O	682.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
2-(2'-Hydroxytetracosanoylamino)-octadecane-1,3,4-triol, (2S,3S,4R,2'R)-	10212035	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCCCCCCCCCCC)O)O)O	684.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
2-Hydroxy-N-(1,3,4-trihydroxyoctadecan-2-yl)tetracosanamide	25203220	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCCCCCCCCCCC)O)O)O	684.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
C24 Phytoceramide (t18:0/24:0)	14653935	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)NC(CO)C(C(CCCCCCCCCCCCCC)O)O	668.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
N-tetracosanoylphytosphingosine	10462091	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)NC(CO)C(C(CCCCCCCCCCCCCC)O)O	668.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2R,5S,6S,7R,9R,11S,12S,14S,15R,16S)-15-[(1R,2R)-1-[(2R,3R,4R)-3,4-dimethyl-5-oxooxolan-2-yl]-1,2-dihydroxypropan-2-yl]-6,14-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one	101239132	Click to see CC1C(C(=O)OC1C(C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)O)O)C	536.70	unknown	https://doi.org/10.1248/CPB.51.530
(1S,2R,5S,6S,7R,9R,11S,12S,14S,15R,16S)-15-[(1R)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,14-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one	102330251	Click to see CC1CC(OC(=O)C1C)C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)O	520.70	unknown	https://doi.org/10.1021/JF970246W
(1S,2R,6S,7R,9R,11S,12S,14S,15R,16S)-15-[(1R,2R)-1-[(2R,3R,4R)-3,4-dimethyl-5-oxooxolan-2-yl]-1,2-dihydroxypropan-2-yl]-6,14-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	101316966	Click to see CC1C(C(=O)OC1C(C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C	504.60	unknown	https://doi.org/10.1248/CPB.51.530
(1S,2R,6S,7R,9R,11S,12S,14S,15R,16S)-15-[(1R,2R)-1-[(2S,3R,4R)-3,4-dimethyl-5-oxooxolan-2-yl]-1,2-dihydroxypropan-2-yl]-6,14-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	21673107	Click to see CC1C(C(=O)OC1C(C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C	504.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018 https://doi.org/10.1016/S0040-4020(02)00277-6
(1S,2R,6S,7R,9R,11S,12S,14S,15R,16S)-15-[(1R)-1-[(2R,4S)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,14-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	102330662	Click to see CC1CC(OC(=O)C1C)C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1021/JF970246W https://doi.org/10.1016/S0040-4020(02)00277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-6,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	12070588	Click to see CC1CC(OC(=O)C1C)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-6,15-dihydroxy-15-[(1S)-1-hydroxy-1-[(2R,4R,5R)-4-hydroxy-4,5-dimethyl-6-oxooxan-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	12070589	Click to see CC1C(=O)OC(CC1(C)O)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	504.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-6,15-dihydroxy-15-[(1S)-1-hydroxy-1-[(4R,5R)-4-hydroxy-4,5-dimethyl-6-oxooxan-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	11730849	Click to see CC1C(=O)OC(CC1(C)O)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	504.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
(1S,2S,3'R,4S,4'R,6S,7S,8R,9R,10S,13S,14R,17S,18S,19R,21R)-7,8,17,18-tetrahydroxy-3',4',8,10,14-pentamethylspiro[5,20-dioxahexacyclo[11.9.0.02,10.04,9.014,19.019,21]docosane-6,5'-oxolane]-2',15-dione	162871567	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)CC(C7O)O)C)O6)C)(C)O)O)OC1=O)C	520.60	unknown	https://doi.org/10.1248/CPB.51.530
(1S,2S,3'R,4S,4'R,6S,7S,8R,9R,10S,13S,14R,17S,18S,19R,21R)-7,8,18-trihydroxy-17-methoxy-3',4',8,10,14-pentamethylspiro[5,20-dioxahexacyclo[11.9.0.02,10.04,9.014,19.019,21]docosane-6,5'-oxolane]-2',15-dione	162984569	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)CC(C7O)OC)C)O6)C)(C)O)O)OC1=O)C	534.60	unknown	https://doi.org/10.1248/CPB.51.530
(1S,2S,4S,5R,10R,11S,14S,15S,18S)-15-[(1R)-1-[(2R,4S,5R)-4,5-dimethyl-6-oxooxan-2-yl]-1-hydroxyethyl]-5-hydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one	14605185	Click to see CC1CC(OC(=O)C1C)C(C)(C2CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O	472.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018
(3R,4S,6S)-6-[(1R)-1-[(4S,7R,8S,9S,10R,13S,14S,17S)-4,7-dihydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-3,4-dimethyloxan-2-one	162885618	Click to see CC1CC(OC(=O)C1C)C(C)(C2CCC3C2(CCC4C3C(C=C5C4(C(=O)C=CC5O)C)O)C)O	472.60	unknown	https://doi.org/10.1248/CPB.51.530
15-[1-(3,4-Dimethyl-5-oxooxolan-2-yl)-1,2-dihydroxypropan-2-yl]-6,14-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one	85306826	Click to see CC1C(C(=O)OC1C(C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)O)O)C	536.70	unknown	https://doi.org/10.1248/CPB.51.530
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 CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)CO)O)C	486.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
15-[1-(4,5-Dimethyl-6-oxooxan-2-yl)-1-hydroxyethyl]-6,14-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one	85285380	Click to see CC1CC(OC(=O)C1C)C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)O	520.70	unknown	https://doi.org/10.1021/JF970246W
15-[1-(4,5-Dimethyl-6-oxooxan-2-yl)-1-hydroxyethyl]-6,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	85123263	Click to see CC1CC(OC(=O)C1C)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018 https://doi.org/10.1016/S0040-4020(02)00277-6
16b,23S-Diepoxy-4b,20R,22S-trihydroxy-1-oxo-5b-ergost-2-eno-26,23S-lactone	74821938	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C)(C)O)O)OC1=O)C	502.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
18-hydroxywithanolide D	21606687	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)CO)O)C	486.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
24,25-dihydrowithanolide D	23266167	Click to see CC1CC(OC(=O)C1C)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O	472.60	unknown	https://doi.org/10.1021/JF970246W
5,6b-Epoxy-4b,16b,20R-trihydroxy-1-oxo-5b,22R,24R,25R-with-2-enolide	75072261	Click to see CC1CC(OC(=O)C1C)C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018 https://doi.org/10.1016/S0040-4020(02)00277-6 https://doi.org/10.1021/JF970246W
6-[1-(4,7-Dihydroxy-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-1-hydroxyethyl]-3,4-dimethyloxan-2-one	85116322	Click to see CC1CC(OC(=O)C1C)C(C)(C2CCC3C2(CCC4C3C(C=C5C4(C(=O)C=CC5O)C)O)C)O	472.60	unknown	https://doi.org/10.1248/CPB.51.530
6,15-Dihydroxy-15-[1-hydroxy-1-(4-hydroxy-4,5-dimethyl-6-oxooxan-2-yl)ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	73077149	Click to see CC1C(=O)OC(CC1(C)O)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	504.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
7,8,17,18-Tetrahydroxy-3',4',8,10,14-pentamethylspiro[5,20-dioxahexacyclo[11.9.0.02,10.04,9.014,19.019,21]docosane-6,5'-oxolane]-2',15-dione	162871566	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)CC(C7O)O)C)O6)C)(C)O)O)OC1=O)C	520.60	unknown	https://doi.org/10.1248/CPB.51.530
7,8,18-Trihydroxy-17-methoxy-3',4',8,10,14-pentamethylspiro[5,20-dioxahexacyclo[11.9.0.02,10.04,9.014,19.019,21]docosane-6,5'-oxolane]-2',15-dione	74822192	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)CC(C7O)OC)C)O6)C)(C)O)O)OC1=O)C	534.60	unknown	https://doi.org/10.1248/CPB.51.530
CID 301757	301757	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
Ixocarpalactone A	327287	Click to see CC1C(C(=O)OC1C(C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O)O)C	504.60	unknown	https://doi.org/10.1002/CHIN.200342192 https://doi.org/10.1248/CPB.51.530 https://doi.org/10.1016/S0040-4020(02)00277-6 https://doi.org/10.1016/J.STEROIDS.2011.03.018
Ixocarpalactone B	12070590	Click to see CC1C(C2(C(C(C3C(O2)CC4C3(CCC5C4CC6C7(C5(C(=O)C=CC7O)C)O6)C)(C)O)O)OC1=O)C	502.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
Ixocarpanolide	14605184	Click to see CC1CC(OC(=O)C1C)C(C)(C2CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O	472.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018
Philadelphicalactone A	11038269	Click to see CC1CC(OC(=O)C1C)C(C)(C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
Withanone	21679027	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
Withaphysacarpin	44567005	Click to see CC1CC(OC(=O)C1C)C(C)(C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)O	488.60	unknown	https://doi.org/10.1016/J.STEROIDS.2011.03.018 https://doi.org/10.1016/S0040-4020(02)00277-6 https://doi.org/10.1021/JF970246W
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-hydroxy-N-(1,3,4-trihydroxyoctadec-9-en-2-yl)tetracosanamide	73091963	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCC=CCCCCCCCC)O)O)O	682.10	unknown	https://doi.org/10.1016/S0040-4020(02)00277-6
> Organoheterocyclic compounds / Benzofurans / Flavaglines
Rocaglamide I	10626755	Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC(=C(C=C4)OC)O)C5=CC=CC=C5)C(=O)N(C)C	563.60	unknown	https://doi.org/10.1021/JF970246W

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Physalis philadelphica

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