Scientific name	Authority	First published in
Parmentiera balduini	Raf.	Autik. Bot. 109. 1840
Parmentiera balduini	Raf.	Autik. Bot. 109. 1840
Solanum arnezii	Cárdenas	Bol. Soc. Peruana Bot. 5: 37. 1956.
Solanum bitteri	Hassl.	Repert. Spec. Nov. Regni Veg. 11: 190. 1912.
Solanum boergeri	Bukasov	Revista Argent. Agron. 4: 239. 1937.
Solanum caipipendense	Cárdenas	Bol. Soc. Peruana Bot. 5: 35. 1956.
Solanum calvescens	Bitter	Repert. Spec. Nov. Regni Veg. 11: 436. 1912.
Solanum chacoense subsp. muelleri	(Bitter) Hawkes & Hjert.	Rep. (Annual) Scott. Pl. Breed. Sta. 1956: 61. 1956.
Solanum chacoense subsp. subtilius	(Bitter) Hawkes	Rep. (Annual) Scott. Pl. Breed. Sta. 1956: 61. 1956.
Solanum chacoense var. angustisectum	(Hassl.) Hassl.	Annuaire Conserv. Jard. Bot. Genève 20: 187. 1917.
Solanum chacoense var. latisectum	(Hassl.) Hassl.	Annuaire Conserv. Jard. Bot. Genève 20: 187. 1917.
Solanum commersonii var. glabriusculum	J.Rémy	Fl. Chil. [Gay] 5: 75. 1849.
Solanum cuevoanum	Cárdenas	Bol. Soc. Peruana Bot. 5: 36. 1956.
Solanum dolichostigma	Bukasov	Theor. Pl. Breed. (Vavilov) 3: 72. 1937.
Solanum emmeae	Juz. & Bukasov	Izv. Akad. Nauk SSSR, Ser. Biol. 2: 321. 1937.
Solanum garciae	Juz. & Bukasov	Revista Argent. Agron. 3: 227. 1936.
Solanum gibberulosum	Juz. & Bukasov	Revista Argent. Agron. 3: 225. 1936.
Solanum guaraniticum var. angustisectum	Hassl.	Repert. Spec. Nov. Regni Veg. 9: 115. 1911.
Solanum guaraniticum var. latisectum	Hassl.	Repert. Spec. Nov. Regni Veg. 9: 115. 1911.
Solanum horovitzii var. glabristylum	Hawkes	Potato Collect. Exped. Mexico & S. Amer., 2, Syst. Classific. Collect. 19. 1944
Solanum horovitzii var. multijugum	Hawkes	Potato Collect. Exped. Mexico & S. Amer., 2, Syst. Classific. Collect. 19, 114. 1944.
Solanum jamesii var. grandifrons	Bitter	Repert. Spec. Nov. Regni Veg. 12: 151. 1913.
Solanum jujuyense	Hawkes	Potato Collect. Exped. Mexico & S. Amer., 2, Syst. Classific. Collect. 19, 114. 1944.
Solanum knappei	Juz. & Bukasov	Izv. Akad. Nauk SSSR, Ser. Biol. 2: 322. 1937.
Solanum laplaticum	Bukasov	Revista Argent. Agron. 4: 238. 1937.
Solanum limense	Correll	Wrightia 2: 188. 1961.
Solanum parodii	Juz. & Bukasov	Revista Argent. Agron. 3: 226. 1936.
Solanum pseudomaglia	L.Planch.	Ann. Fac. Sci. Marseille 18: 205. 1909
Solanum saltense	Hawkes	Potato Collect. Exped. Mexico & S. Amer., 2, Syst. Classific. Collect. 19, 113. 1944.
Solanum schickii	Juz. & Bukasov	Izv. Akad. Nauk SSSR, Ser. Biol. 2: 324. 1937.
Solanum subtilius	Bitter	Repert. Spec. Nov. Regni Veg. 12: 6. 1913.
Solanum tuberosum subsp. yanacochense	Ochoa	Arnaldoa 8(2): 59. 2001 [2002].
Solanum tuberosum var. glabriusculum	Dunal	Prodr. [A. P. de Candolle] 13(1): 32. 1852
Solanum yanacochense	(Ochoa) Gorbat.	Potato Sp. S. Amer. 396. 2006
Solanum yungasense	Hawkes	Ann. Mag. Nat. Hist., ser. 12, 7: 697. 1954.
Solanum chacoense f. caipipendense	(Cárdenas) Correll	Wrightia 2: 172. 1961
Solanum chacoense f. gibberulosum	(Juz. & Bukasov) Correll	Wrightia 2: 172. 1961
Solanum muelleri f. densipilum	Correll	Wrightia 2: 173. 1961.
Solanum chacoense f. plurijugum	Hassl.	Annuaire Conserv. Jard. Bot. Genève 20: 187. 1917.
Solanum chacoense f. glabrescens	(Hassl.) Hassl.	Annuaire Conserv. Jard. Bot. Genève 20: 186. 1917.
Solanum chacoense f. puberulum	Hassl.	Annuaire Conserv. Jard. Bot. Genève 20: 187. 1917.
Solanum guaraniticum f. glabrescens	Hassl.	Repert. Spec. Nov. Regni Veg. 9: 115. 1911.

Common names Top

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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 South
  - Brazil Southeast
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001026946
Tropicos	29600227
INPN	717553
KEW	urn:lsid:ipni.org:names:238539-2
The Plant List	tro-29600227
Open Tree Of Life	1020653
NCBI Taxonomy	4108
IUCN Red List	62758331
IPNI	238539-2
iNaturalist	702537
GBIF	2932643
Freebase	/m/0kv4_xs
EPPO	SOLCH
USDA GRIN	100940
Wikipedia	Solanum_chacoense
CMAUP	NPO25843

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_029582705.1	chc0917	Contig	McGill University	2023-04-04	100.0x	729.91 Mb

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 transcriptional analysis of Persea americana MYB, WRKY and AP2/ERF transcription factors following Phytophthora cinnamomi infection

Fick A, Swart V, Bombarely A, van den Berg N

Mol Plant Pathol

08-Apr-2024

PMCID:	PMC11002358
doi:	10.1111/mpp.13453
PMID:	38590150

Chromosomal dynamics in Senna: comparative PLOP–FISH analysis of tandem repeats and flow cytometric nuclear genome size estimations

Nguyen TH, Kang BY, Kim HH

Front Plant Sci

14-Dec-2023

PMCID:	PMC10762312
doi:	10.3389/fpls.2023.1288220
PMID:	38173930

Carboxypeptidase inhibitors from Solanaceae as a new subclass of pathogenesis related peptide aiming biotechnological targets for plant defense

Gomes GD, Espósito PC, Baracat-Pereira MC

Front Mol Biosci

16-Nov-2023

PMCID:	PMC10687636
doi:	10.3389/fmolb.2023.1259026
PMID:	38033385

Tetraose steroidal glycoalkaloids from potato provide resistance against Alternaria solani and Colorado potato beetle

Wolters PJ, Wouters D, Tikunov YM, Ayilalath S, Kodde LP, Strijker MF, Caarls L, Visser RG, Vleeshouwers VG

eLife

26-Sep-2023

PMCID:	PMC10522338
doi:	10.7554/eLife.87135
PMID:	37751372

Solanum americanum genome-assisted discovery of immune receptors that detect potato late blight pathogen effectors

Lin X, Jia Y, Heal R, Prokchorchik M, Sindalovskaya M, Olave-Achury A, Makechemu M, Fairhead S, Noureen A, Heo J, Witek K, Smoker M, Taylor J, Shrestha RK, Lee Y, Zhang C, Park SJ, Sohn KH, Huang S, Jones JD

Nat Genet

28-Aug-2023

PMCID:	PMC10484786
doi:	10.1038/s41588-023-01486-9
PMID:	37640880

A Review of Potato Salt Tolerance

Han X, Yang R, Zhang L, Wei Q, Zhang Y, Wang Y, Shi Y

Int J Mol Sci

27-Jun-2023

PMCID:	PMC10341983
doi:	10.3390/ijms241310726
PMID:	37445900

Rapid alkalinization factor: function, regulation, and potential applications in agriculture

Zhang R, Shi PT, Zhou M, Liu HZ, Xu XJ, Liu WT, Chen KM

Stress Biol

29-May-2023

PMCID:	PMC10442051
doi:	10.1007/s44154-023-00093-2
PMID:	37676530

GASA Proteins: Review of Their Functions in Plant Environmental Stress Tolerance

Bouteraa MT, Ben Romdhane W, Baazaoui N, Alfaifi MY, Chouaibi Y, Ben Akacha B, Ben Hsouna A, Kačániová M, Ćavar Zeljković S, Garzoli S, Ben Saad R

Plants (Basel)

21-May-2023

PMCID:	PMC10223810
doi:	10.3390/plants12102045
PMID:	37653962

Lateral Root Initiation in Cucumber (Cucumis sativus): What Does the Expression Pattern of Rapid Alkalinization Factor 34 (RALF34) Tell Us?

Kiryushkin AS, Ilina EL, Guseva ED, Pawlowski K, Demchenko KN

Int J Mol Sci

08-May-2023

PMCID:	PMC10179419
doi:	10.3390/ijms24098440
PMID:	37176146

A novel effector RipBT contributes to Ralstonia solanacearum virulence on potato

Qiu H, Wang B, Huang M, Sun X, Yu L, Cheng D, He W, Zhou D, Wu X, Song B, Tang N, Chen H

Mol Plant Pathol

08-May-2023

PMCID:	PMC10346376
doi:	10.1111/mpp.13342
PMID:	37154802

De novo genome assembly of the partial homozygous dihaploid potato identified PVY resistance gene (Rychc) derived from Solanum chacoense

Akai K, Asano K, Suzuki C, Shimosaka E, Tamiya S, Suzuki T, Takeuchi T, Ohki T

Breed Sci

13-Apr-2023

PMCID:	PMC10316315
doi:	10.1270/jsbbs.22078
PMID:	37404346

The RNA-binding protein MdHYL1 modulates cold tolerance and disease resistance in apple

Shen X, Song Y, Ping Y, He J, Xie Y, Ma F, Li X, Guan Q

Plant Physiol

27-Mar-2023

PMCID:	PMC10315269
doi:	10.1093/plphys/kiad187
PMID:	36970784

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

MAPKKKs in Plants: Multidimensional Regulators of Plant Growth and Stress Responses

Xie C, Yang L, Gai Y

Int J Mol Sci

18-Feb-2023

PMCID:	PMC9963060
doi:	10.3390/ijms24044117
PMID:	36835531

Genome-wide identification and expression analysis of the HD2 protein family and its response to drought and salt stress in Gossypium species

Bano N, Fakhrah S, Lone RA, Mohanty CS, Bag SK

Front Plant Sci

13-Feb-2023

PMCID:	PMC9968887
doi:	10.3389/fpls.2023.1109031
PMID:	36860898

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	https://doi.org/10.1002/CHIN.197139400
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1002/CHIN.197139400
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1002/CHIN.197139400
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1002/CHIN.197139400
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
7-hydroxy-3,8a-dimethyl-5-methylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one	5316022	Click to see CC1=C2CC3C(=C)CC(CC3(CC2OC1=O)C)O	248.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3alpha-Hydroxyfriedelane-2-one	14465808	Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	442.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Neoruscogenin	9910474	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6	428.60	unknown	via CMAUP database
Ruscogenin	441893	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1	430.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol	13754059	Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O	402.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1R,3S,6S,8S,11S,12R,15S,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	162953300	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1002/CHIN.197139400
9,19-Cyclo-9beta-lanost-24-en-3beta-ol	500213	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1002/CHIN.197139400
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2S,7S,10R,11R,14S,15R,16S,17S,20S,23R)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol	162994426	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	https://doi.org/10.1016/S0031-9422(00)97267-4
(7-Hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-18-yl) acetate	14455251	Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC(=O)C	455.70	unknown	https://doi.org/10.1021/JF9702914
[(1S,2S,7S,10R,11S,14S,15R,16S,17S,18S,20S,23S)-7-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-18-yl] acetate	101699424	Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC(=O)C	455.70	unknown	https://doi.org/10.1021/JF9702914
Solanid-5-en-3-ol	522740	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	https://doi.org/10.1021/JF9702914 https://doi.org/10.1016/S0031-9422(00)97267-4
Solanidine	65727	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	https://doi.org/10.1021/JF9702914
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(23S,25R)-23-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]spirosta-5-ene-3beta-ol	100982641	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O	754.90	unknown	via CMAUP database
(23S)-1beta-[[2-O-[3-O-(beta-D-Glucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyl]oxy]-23-(beta-D-glucopyranosyloxy)spirosta-5,25(27)-diene-3beta-ol	10581939	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19C(CC(=C)CO9)OC1C(C(C(C(O1)CO)O)O)O	1047.10	unknown	via CMAUP database
(25R)-1beta-(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyloxy)spirosta-5-ene-3beta-ol	44575746	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	708.90	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23R)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-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	134688107	Click to see CC1CCC2C(C3C(N2C1)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	868.10	unknown	https://doi.org/10.1021/JF00068A056
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(1S,2R,5S,7S,10S,11S,14S,15R,17S,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-yl]oxy]oxan-2-yl]methoxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11968403	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)C)C)C	1018.20	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-yl]oxy]oxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163189904	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C	1046.20	unknown	https://doi.org/10.1016/0304-4211(77)90140-7
(2S,3R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-yl]oxy]-5-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	129627776	Click to see CC1CCC2C(C3C(N2C1)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	852.10	unknown	https://doi.org/10.1021/JF00068A056
[(1S,2S,7S,10R,11S,14S,15R,16S,17S,18S,20S,23S)-7-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-18-yl] acetate	101699887	Click to see CC1CC(C2C(C3C(N2C1)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)OC(=O)C	910.10	unknown	https://doi.org/10.1021/JF00108A028 https://doi.org/10.1021/JF00068A056
[(1S,2S,7S,10R,11S,14S,15R,16S,17S,18S,20S,23S)-7-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-18-yl] acetate	101699888	Click to see CC1CC(C2C(C3C(N2C1)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)OC(=O)C	926.10	unknown	https://doi.org/10.1021/JF00108A028 https://doi.org/10.1021/JF00068A056
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate	21590070	Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O	1139.20	unknown	via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol	44567205	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O	869.00	unknown	via CMAUP database
1beta-[2-O-(3-O-beta-D-Glucopyranosyl-alpha-L-rhamnopyranosyl)-4-O-acetyl-alpha-L-arabinopyranosyloxy]spirosta-5,25(27)-dien-3beta-ol	101937241	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9	911.00	unknown	via CMAUP database
Aculeoside B	154169	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O	1205.30	unknown	via CMAUP database
alpha-Chaconine	442971	Click to see CC1CCC2C(C3C(N2C1)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	852.10	unknown	https://doi.org/10.1021/JF00068A056
alpha-Solanine	9549171	Click to see CC1CCC2C(C3C(N2C1)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	868.10	unknown	https://doi.org/10.1021/JF00068A056
beta-Chaconine	119393	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C	705.90	unknown	https://doi.org/10.1021/JF00068A056
CID 10462472	10462472	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8	706.90	unknown	via CMAUP database
Commersonine	185997	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C	1048.20	unknown	via CMAUP database
Dehydrocommersonine	101699426	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C	1046.20	unknown	https://doi.org/10.1016/0304-4211(77)90140-7
Leptinine I	101699423	Click to see CC1CC(C2C(C3C(N2C1)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)O	868.10	unknown	https://doi.org/10.1021/JF00108A028 https://doi.org/10.1021/JF00068A056
Leptinine II	101699425	Click to see CC1CC(C2C(C3C(N2C1)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)O	884.10	unknown	https://doi.org/10.1021/JF00068A056 https://doi.org/10.1021/JF00108A028
Ruscin(P)	13935613	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9	869.00	unknown	via CMAUP database
Ruscoside [WHO-DD]	91936850	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC1(CCC(=C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/CHIN.197139400
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/10.1002/CHIN.197139400
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Euparone	104654	Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C	218.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran	323624	Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C	254.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
7-Hydroxy-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one	5316531	Click to see CC(C)C1C2C3C4(C(CCC4(C1C(=O)O2)O)CN3C)C	279.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	via CMAUP database

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Solanum chacoense

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