Physalis longifolia

Upload a new image!

Details

Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID64404167beafd038837919
Scientific name	Physalis longifolia
Authority	Nutt.
First published in	Trans. Amer. Philos. Soc. ser. 2, 5: 193. 1836 [early 1836]

Description Top

Suggest a correction or write a new one!

It is an attractive ornamental plant and is used in traditional medicine.

Physalis longifolia is a species of flowering plant in the nightshade family, native to North America. It has yellow bell-shaped flowers and yellow-green edible fruit that tastes like an effervescent, under-ripened strawberry. It has two varieties and is used for food, as an ornamental plant, and in traditional medicine. Native American groups used it for food, and the Zuni people used it in a sauce recipe. It is easy to grow and produces a flavorful fruit.

Synonyms Top

Scientific name	Authority	First published in
Physalis longifolia	Nutt.
Physalis polyphylla	Greene	Pittonia 4: 150. 1900
Physalis pumila var. sonorae	Torr.	Rep. U.S. Mex. Bound., Bot. 153. 1858 [Jul-Dec 1858]
Physalis rigida	Pollard & Ball	Proc. Biol. Soc. Wash. 13: 134. 1900
Physalis virginiana var. longiseta	Waterf.	Rhodora 69: 120. 1967
Physalis virginiana var. polyphylla	(Greene) Waterf.	Rhodora 60: 156. 1958
Physalis virginiana var. sonorae	(Torr.) Waterf.	Rhodora 60: 154. 1958

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	longleaf groundcherry
Swedish	smalbladig lyktört

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Physalis longifolia var. subglabrata	(Mack. & Bush) Cronquist	Vasc. Pl. Pacific NorthW. 4: 286. 1959
Physalis longifolia var. texana	(Rydb.) J.R.Sullivan	Rhodora 115: 291. 2013.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
- Eastern Canada
  - Ontario
  - Québec
- Mexico
  - Mexico Northeast
  - Mexico Northwest
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - New York
  - Vermont
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Wyoming
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Kentucky
  - Maryland
  - Tennessee
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001024806
Florida Plant Atlas	568
Canadensys	9368
USDA Plants	PHLO4
Tropicos	29600208
INPN	968807
Flora of Italy	12749
KEW	urn:lsid:ipni.org:names:817466-1
The Plant List	tro-29600208
Open Tree Of Life	179319
Observations.org	132417
NCBI Taxonomy	161495
Nature Serve	2.153744
IPNI	817466-1
iNaturalist	78569
GBIF	5341818
Freebase	/m/05bzp5f
WisFlora	8651
EPPO	PHYLF
EOL	581073
Calflora (Californian flora)	6482
USDA GRIN	316776
Wikipedia	Physalis_longifolia
CMAUP	NPO14874

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

The Whole Genome of Colletes collaris (Hymenoptera: Colletidae): An Important Step in Comparative Genomics of Cellophane Bees

Ferrari RR, Batista TM, Zhou QS, Hilário HO, Orr MC, Luo A, Zhu CD

Genome Biol Evol

19-Apr-2023

PMCID:	PMC10159585
doi:	10.1093/gbe/evad062
PMID:	37075227

Nuclear phylogeny and insights into whole-genome duplications and reproductive development of Solanaceae plants

Huang J, Xu W, Zhai J, Hu Y, Guo J, Zhang C, Zhao Y, Zhang L, Martine C, Ma H, Huang CH

Plant Commun

25-Mar-2023

PMCID:	PMC10363554
doi:	10.1016/j.xplc.2023.100595
PMID:	36966360

Combination Treatment of Withalongolide a Triacetate with Cisplatin Induces Apoptosis by Targeting Translational Initiation, Migration, and Epithelial to Mesenchymal Transition in Head and Neck Squamous Cell Carcinoma

Subramanian C, Spielbauer KK, Pearce R, Kovatch KJ, Prince ME, Timmermann BN, Cohen MS

Nutrients

19-Dec-2022

PMCID:	PMC9782118
doi:	10.3390/nu14245398
PMID:	36558560

Predicting potential global distribution and risk regions for potato cyst nematodes (Globodera rostochiensis and Globodera pallida)

He Y, Wang R, Zhao H, Ren Y, Agarwal M, Zheng D, Gao S, McKirdy SJ, Chu D

Sci Rep

17-Dec-2022

PMCID:	PMC9759053
doi:	10.1038/s41598-022-26443-0
PMID:	36528656

Natural products as a therapy to combat against SARS-CoV-2 virus infection

Malviya S, Parihar A, Parihar DS, Khan R

Computational Approaches for Novel Therapeutic and Diagnostic Designing to Mitigate SARS-CoV-2 Infection

15-Jul-2022

PMCID:	PMC9300459
doi:	10.1016/B978-0-323-91172-6.00017-0

Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change

Caven AJ, Wiese JD

Heliyon

03-Jun-2022

PMCID:	PMC9192816
doi:	10.1016/j.heliyon.2022.e09640
PMID:	35711997

Withaferin A: From Ancient Remedy to Potential Drug Candidate

Sultana T, Okla MK, Ahmed M, Akhtar N, Al-Hashimi A, Abdelgawad H, Haq IU

Molecules

20-Dec-2021

PMCID:	PMC8705790
doi:	10.3390/molecules26247696
PMID:	34946778

Characterization of the Exometabolome of Nitrosopumilus maritimus SCM1 by Liquid Chromatography–Ion Mobility Mass Spectrometry

Law KP, He W, Tao J, Zhang C

Front Microbiol

01-Jul-2021

PMCID:	PMC8281238
doi:	10.3389/fmicb.2021.658781
PMID:	34276593

Novel natural withanolides induce apoptosis and inhibit migration of neuroblastoma cells through down regulation of N-myc and suppression of Akt/mTOR/NF-κB activation

Subramanian C, Grogan PT, Opipari VP, Timmermann BN, Cohen MS

Oncotarget

07-Feb-2018

PMCID:	PMC5865686
doi:	10.18632/oncotarget.24429
PMID:	29581860

Synthetic high-density lipoprotein nanodisks for targeted withalongolide delivery to adrenocortical carcinoma

Kuai R, Subramanian C, White PT, Timmermann BN, Moon JJ, Cohen MS, Schwendeman A

Int J Nanomedicine

06-Sep-2017

PMCID:	PMC5593402
doi:	10.2147/IJN.S140591
PMID:	28919755

Allelic diversity of S-RNase alleles in diploid potato species

Dzidzienyo DK, Bryan GJ, Wilde G, Robbins TP

Theor Appl Genet

06-Aug-2016

PMCID:	PMC5025496
doi:	10.1007/s00122-016-2754-7
PMID:	27497984

Analysis of Major Withanolides in Physalis longifolia Nutt. by HPLC-PDA

Cao CM, Kindscher K, Gallagher RJ, Zhang H, Timmermann BN

J Chromatogr Sci

02-Dec-2014

PMCID:	PMC4592342
doi:	10.1093/chromsci/bmu162
PMID:	25466231

Antiproliferative withanolides from several Solanaceous species

Zhang H, Cao CM, Gallagher RJ, Timmermann BN

Nat Prod Res

28-May-2014

PMCID:	PMC4177291
doi:	10.1080/14786419.2014.919286
PMID:	24871278

Withanolides from Jaborosa caulescens var. bipinnatifida

Zhang H, Cao CM, Gallagher RJ, Day VW, Montenegro G, Timmermann BN

Phytochemistry

05-Dec-2013

PMCID:	PMC3947017
doi:	10.1016/j.phytochem.2013.11.005
PMID:	24314746

Identification and Analysis of Red Sea Mangrove (Avicennia marina) microRNAs by High-Throughput Sequencing and Their Association with Stress Responses

Khraiwesh B, Pugalenthi G, Fedoroff NV

PLoS One

08-Apr-2013

PMCID:	PMC3620391
doi:	10.1371/journal.pone.0060774
PMID:	23593307

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 / Steroids and steroid derivatives / Steroid lactones
withalongolide F	56926117	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)C=C5)C)C)CO	424.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-6-hydroxy-15-[(1S)-1-[(2S)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	49864510	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO	470.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
[6-Hydroxy-15-[1-[5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-5-yl] hydrogen sulfate	45359808	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OS(=O)(=O)O)C)O5)C)CO	568.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
11 Beta-Hydroxywithaferin A	56649372	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CC(C4C3CC5C6(C4(C(=O)C=CC6O)CO)O5)O)C)CO	502.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
16,17-Dihydroxy-7-[1-[5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-8,12-dimethyl-18-oxapentacyclo[13.2.1.03,11.04,8.012,17]octadecan-13-one	74021829	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O5)C)O)C)CO	488.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
2,3-dihydro-3beta-methoxy withaferin A	10767792	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)CO	502.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
2,3-dihydro-3beta-O-sulfate withaferin A	44581669	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OS(=O)(=O)O)C)O5)C)CO	568.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
2,3-Dihydrowithaferin A	15411208	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)CO	472.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
3-Methoxy-2,3-dihydrowithaferin-A	433363	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)CO	502.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
3alpha,6alpha-Epoxy-4beta,5beta,27-trihydroxy-1-oxowitha-24-enolide	11038270	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O5)C)O)C)CO	488.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
5,6-Dihydroxy-15-[1-[5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one	72835871	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O)C)O5)C)CO	488.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
6-Hydroxy-2,16-dimethyl-15-[1-[4-methyl-6-oxo-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3-dihydropyran-2-yl]ethyl]-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	78173488	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)COC7C(C(C(C(O7)CO)O)O)O	632.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Sitoindoside IX	189586	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)COC7C(C(C(C(O7)CO)O)O)O	632.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Viscosalactone B	57403080	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O)C)O5)C)CO	488.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withaferin A	265237	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO	470.60	unknown	https://doi.org/10.1055/S-0032-1320883 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withaferin A, dihydro-	418033	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CCC6O)C)O5)C)CO	472.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withaferine A	580064	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO	470.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide A	56649343	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)CO)O5)C)CO	486.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide B	56649344	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)CO)O5)C)C	470.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide D	56926115	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)CO)O5)C)CO	518.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide E	56926116	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CC(C4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)O)C)CO	518.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide G	56926118	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OS(=O)(=O)O)CO)O5)C)CO	584.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide H	56649370	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3=C(CC(OC3=O)C(C)C4CCC5C4(CCC6C5CC7C8(C6(C(=O)C=CC8O)C)O7)C)C)CO)O)O)O	778.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide J	56926206	Click to see CC1=C(CC(OC1=O)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)CO)C)COC6C(C(C(C(O6)CO)O)O)O	636.80	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives / Withanolide glycosides and derivatives
withalongolide I	56926205	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(=O)CC(C5)OC6C(C(C(C(O6)CO)O)O)O)CO)C)CO	634.80	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Withalongolide K	56926207	Click to see CC1=C(CC(OC1=O)C(C)C2CCC3C2(CCC4C3CC(C5=C4C(=CC=C5)O)O)C)COC6C(C(C(C(O6)CO)O)O)O	602.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
withalongolide L	56926208	Click to see CC1=C(CC(OC1=O)C(C)C2CCC3C2(CCC4C3CC(C5=C4C(=O)CC(C5)O)O)C)COC6C(C(C(C(O6)CO)O)O)O	620.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide M	56926294	Click to see CC1=C(CC(OC1=O)C(C)C2CCC3C2(CCC4C3CCC5=C4C(=O)CC(C5)O)C)COC6C(C(C(C(O6)CO)O)O)O	604.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Withalongolide N	56926295	Click to see CC1=C(CC(OC1=O)C(C)C2CCC3C2(CCC4C3CC(=O)C5=C4CCC(C5)O)C)COC6C(C(C(C(O6)CO)O)O)O	604.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
6,8-Di-C-methylmyricetin 4'-methyl ether	44259508	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)OC)O)O)C)O	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253737/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
5,7,4'-Trihydroxy-3,3'-dimethoxy-6,8-dimethylflavone	25059076	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)OC)OC)C)O	358.30	unknown	via CMAUP database
6,8-Di-C-methylmyricetin 3-methyl ether	44259708	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)C)O	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
6-C-Methylmyricetin 3,4'-dimethyl ether	44259716	Click to see CC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)O)OC)O)O	360.30	unknown	via CMAUP database
6,8-Di-C-methylmyricetin 3,4'-dimethyl ether	44259717	Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)OC)O)OC)C)O	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,4'-Dihydroxy-3,7,3'-trimethoxy-6,8-dimethylflavone	25059037	Click to see CC1=C(C2=C(C(=C1OC)C)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	372.40	unknown	via CMAUP database
6-C-Methylquercetin 3,7,3'-trimethyl ether	44259693	Click to see CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)OC)OC)OC	358.30	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Physalis longifolia

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