Solanum lycocarpum, also known as wolf apple, is a plant commonly found in the Brazilian savanna, known as the Cerrado ecoregion. It is also called lobeira or fruta-do-lobo in Portuguese. The plant gets its name from its importance in the diet of the maned wolf, with its scientific name "lycocarpum" meaning "wolf fruit" in Latinized Greek. It grows in moist, clay soil and produces large, sweet and aromatic fruits that are consumed by humans and used as a food source for cattle. The plant has also been used in traditional medicine for various purposes, although there is no scientific evidence to support its medicinal uses. The fruits contain glycoalkaloids and phenolic compounds that have been shown to have anti-parasitic properties. The plant also plays a role in protecting the maned wolf from a fatal infection. However, the plant is also susceptible to pests, such as a butterfly larva and a weevil, which can cause damage to the plant and its fruit production.

Synonyms Top

Scientific name	Authority	First published in
Solanum grandiflorum var. angustifolium	Sendtn.	Fl. Bras. (Martius) 10: 87. 1846.
Solanum grandiflorum var. macrocarpum	Hassl.	Repert. Spec. Nov. Regni Veg. 9: 118. 1911.
Solanum grandiflorum var. pulverulentum	Sendtn.	Fl. Bras. (Martius) 10: 87. 1846.
Solanum lycocarpum subsp. macrophyllum	Hassl.	Repert. Spec. Nov. Regni Veg. 15: 232. 1918.
Solanum lycocarpum var. decalvatum	Witasek	Denkschr. Kaiserl. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 79: (advance separate) 46. 1910. (also in 79(2): 358. 1931)
Solanum lycocarpum var. genuinum	(A.St.-Hil.) Hassl.	Repert. Spec. Nov. Regni Veg. 15: 232. 1918.
Solanum lycocarpum var. macrocarpum	(Hassl.) Hassl.	Repert. Spec. Nov. Regni Veg. 15: 233. 1918.
Solanum lycocarpum var. paraguariense	(Chodat & Hassl.) Hassl.	Repert. Spec. Nov. Regni Veg. 15: 233. 1918.
Solanum rupincola var. macrocarpum	(Hassl.) Chodat	Bull. Soc. Bot. Genève sér. 2, 8: 54. 1916
Solanum grandiflorum f. apaense	Chodat & Hassl.	Bull. Herb. Boissier sér. 2, 4: 83. 1903.
Solanum grandiflorum f. paraguariensis	Chodat & Hassl.	Bull. Herb. Boissier sér. 2, 4: 83. 1903.

Common names Top

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Filter by language:

Language	Common/alternative name
Esperanto	agvaraofrukto
Esperanto	lupofrukto
Japanese	ウルフアップル
Portuguese	fruta-de-lobo
Portuguese	guarambá
Chinese	狼蘋果
Chinese	狼果

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

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Southern South America
  - Paraguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001029205
UNII	TB5Z48S32H
Tropicos	29600117
KEW	urn:lsid:ipni.org:names:239186-2
The Plant List	tro-29600117
Open Tree Of Life	691771
NCBI Taxonomy	329783
IUCN Red List	146113767
IPNI	239186-2
iNaturalist	347865
GBIF	2930421
Freebase	/m/06j_np
EPPO	SOLLY
EOL	5697161
USDA GRIN	438816
Wikipedia	Solanum_lycocarpum

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 and perception of milk producers about thermal stress in Brazilian dairy farms

Brettas PK, Nascimento FG, Guimarães EC, Faria PN, Ferreira AV, Nascimento MR

Heliyon

17-Feb-2024

PMCID:	PMC10884848
doi:	10.1016/j.heliyon.2024.e26115
PMID:	38404894

Recent Advances Regarding Polyphenol Oxidase in Camellia sinensis: Extraction, Purification, Characterization, and Application

Zou C, Zhang X, Xu Y, Yin J

Foods

09-Feb-2024

PMCID:	PMC10887689
doi:	10.3390/foods13040545
PMID:	38397522

Characterization of the Effect of N-(2-Methoxyphenyl)-1-methyl-1H-benzimidazol-2-amine, Compound 8, against Leishmania mexicana and Its In Vivo Leishmanicidal Activity

Nieto-Meneses R, Castillo R, Hernández-Campos A, Nogueda-Torres B, López-Villegas EO, Moreno-Rodríguez A, Matadamas-Martínez F, Yépez-Mulia L

Int J Mol Sci

04-Jan-2024

PMCID:	PMC10779428
doi:	10.3390/ijms25010659
PMID:	38203832

Influence of ripeness stage on the bioactive compounds’ contents and antioxidant activities of Solanum anguivi Lam. fruits accessions

Nakitto AM, Byaruhanga YB, Wagner AE, Muyonga JH

Heliyon

27-Oct-2023

PMCID:	PMC10651511
doi:	10.1016/j.heliyon.2023.e21614
PMID:	38027920

Meta-analysis of the responses of tree and herb to elevated CO2 in Brazil

da Silva Fortirer J, Grandis A, Pagliuso D, de Toledo Castanho C, Buckeridge MS

Sci Rep

22-Sep-2023

PMCID:	PMC10517018
doi:	10.1038/s41598-023-40783-5
PMID:	37739974

The Therapeutic Value of Solanum Steroidal (Glyco)Alkaloids: A 10-Year Comprehensive Review

Delbrouck JA, Desgagné M, Comeau C, Bouarab K, Malouin F, Boudreault PL

Molecules

23-Jun-2023

PMCID:	PMC10343844
doi:	10.3390/molecules28134957
PMID:	37446619

The Sarcoptic Mange in Maned Wolf (Chrysocyon brachyurus): Mapping an Emerging Disease in the Largest South American Canid

Fiori F, de Paula RC, Navas-Suárez PE, Boulhosa RL, Dias RA

Pathogens

15-Jun-2023

PMCID:	PMC10301014
doi:	10.3390/pathogens12060830
PMID:	37375520

Gel Formulations for Topical Treatment of Skin Cancer: A Review

Slavkova M, Tzankov B, Popova T, Voycheva C

Gels

22-Apr-2023

PMCID:	PMC10216957
doi:	10.3390/gels9050352
PMID:	37232944

Alkaloids in food: a review of toxicity, analytical methods, occurrence and risk assessments

Akinboye AJ, Kim K, Choi S, Yang I, Lee JG

Food Sci Biotechnol

05-Apr-2023

PMCID:	PMC10290023
doi:	10.1007/s10068-023-01295-0
PMID:	37362815

Natural Products as New Approaches for Treating Bladder Cancer: From Traditional Medicine to Novel Drug Discovery

Kang Y, Park C, Lee H, Kang S, Cheon C, Kim B

Pharmaceutics

31-Mar-2023

PMCID:	PMC10145408
doi:	10.3390/pharmaceutics15041117
PMID:	37111603

Development of a Halochromic, Antimicrobial, and Antioxidant Starch-Based Film Containing Phenolic Extract from Jaboticaba Peel

Luz RF, Ferreira RD, Silva CN, Miranda BM, Piccoli RH, Silva MS, Paula LC, Leles MI, Fernandes KF, Cruz MV, Batista KA

Foods

02-Feb-2023

PMCID:	PMC9914361
doi:	10.3390/foods12030653
PMID:	36766181

Solanum dulcamara L. Berries: A Convenient Model System to Study Redox Processes in Relation to Fruit Ripening

Milutinović M, Nakarada Đ, Božunović J, Todorović M, Gašić U, Živković S, Skorić M, Ivković Đ, Savić J, Devrnja N, Aničić N, Banjanac T, Mojović M, Mišić D

Antioxidants (Basel)

01-Feb-2023

PMCID:	PMC9952312
doi:	10.3390/antiox12020346
PMID:	36829905

Two-Phase Extraction Processes, Physicochemical Characteristics, and Autoxidation Inhibition of the Essential Oil Nanoemulsion of Citrus reticulata Blanco (Tangerine) Leaves

Rashed MM, You L, Ghaleb AD, Du Y

Foods

22-Dec-2022

PMCID:	PMC9818749
doi:	10.3390/foods12010057
PMID:	36613276

Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021

Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T

Molecules

04-Nov-2022

PMCID:	PMC9656935
doi:	10.3390/molecules27217579
PMID:	36364404

Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats

Satyanarayana N, Chinni SV, Gobinath R, Sunitha P, Uma Sankar A, Muthuvenkatachalam BS

Front Nutr

28-Oct-2022

PMCID:	PMC9650639
doi:	10.3389/fnut.2022.987552
PMID:	36386935

Phytochemical Profile Top

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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 / Steroidal alkaloids / Spirosolanes and derivatives
(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol	137704740	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	https://doi.org/10.1016/S0378-8741(00)00165-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[(1R,2S,4S,5'R,6S,6'R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-6'-methoxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447944	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1OC	931.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447949	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1	901.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447947	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1	885.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447948	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	884.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1R,2S,4S,5'R,6S,6'R,7S,8R,9S,10R,12S,13R,16S)-10-hydroxy-6'-methoxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447946	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1OC	915.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-6-[(1R,2S,4S,5'R,6S,6'R,7S,8R,9S,10R,12S,13R,16S)-6',10-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101447945	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1O	901.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
(2S,3R,4R,5R,6S)-2-[(2R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	146014454	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	884.10	unknown	https://doi.org/10.1021/NP0680580
12-Hydroxysolasonine	21573761	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	900.10	unknown	https://doi.org/10.1021/NP0680580 https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
2-[4-Hydroxy-2-(hydroxymethyl)-6-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	78153025	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1	885.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
2-[4-Hydroxy-2-(hydroxymethyl)-6-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162910844	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	884.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003 https://doi.org/10.1021/NP0680580
2-[4-Hydroxy-6-(10-hydroxy-6'-methoxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162879596	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1OC	915.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
2-[5-Hydroxy-2-(10-hydroxy-6'-methoxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162932465	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1OC	931.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
2-[5-Hydroxy-6-(hydroxymethyl)-2-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162899264	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1	901.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
alpha-Solasonine	537159	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	884.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003 https://doi.org/10.1021/NP0680580
Robeneoside A	16109797	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	884.10	unknown	https://doi.org/10.1021/NP0680580 https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
Robeneoside B	16109798	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)NC1	900.10	unknown	https://doi.org/10.1021/NP0680580 https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
Solamargine	73611	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	868.10	unknown	https://doi.org/10.1021/NP0680580 https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
Solamarin, beta	437080	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	868.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003 https://doi.org/10.1021/NP0680580
Solasonine	119247	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	884.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003 https://doi.org/10.1021/NP0680580
Spirostane + 2O,-2H, O-Hex-dHex-dHex	139291973	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1O	901.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
Methyl 3,5-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4-dihydroxycyclohexane-1-carboxylate	460893	Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	530.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003 https://doi.org/10.1021/NP0680580
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-Maltose	439341	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1590/S0100-879X2003000400017
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	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	594.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.02.003

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Solanum lycocarpum

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