Scientific name	Authority	First published in
Solanum albiflorum	De Wild.	Pl. Bequaert. 1: 422. 1922.
Solanum aurantiacobaccatum	De Wild.	Pl. Bequaert. 1: 421. 1922.
Solanum batangense	Dammer	Bot. Jahrb. Syst. 48: 239. 1912.
Solanum buettneri	Dammer	Bot. Jahrb. Syst. 38: 59. 1905.
Solanum carvalhoi	Dammer	Pflanzenw. Ost-Afrikas C (Engler): 355. 1895.
Solanum congense	Link	Enum. Hort. Berol. Alt. 1: 187. 1821.
Solanum cultum	De Wild.	Bull. Jard. Bot. État Bruxelles. 4: 406. 1914.
Solanum dichroanthum	Dammer	Bot. Jahrb. Syst. 53: 340. 1915.
Solanum dinklagei	Dammer	Bot. Jahrb. Syst. 48: 241. 1912.
Solanum distichum	Schumach. & Thonn.	Beskr. Guin. Pl. 122 [142]. 1827.
Solanum flamignii	De Wild.	Bull. Jard. Bot. État Bruxelles 4: 399. 1914.
Solanum grotei	Dammer	Bot. Jahrb. Syst. 53: 342. 1915.
Solanum halophilum	Pax	Bot. Jahrb. Syst. 39: 648. 1907.
Solanum indicum subsp. clinocarpum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 37. 1923.
Solanum indicum subsp. distichum	(Thonn.) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 13. 1923.
Solanum indicum subsp. grandifrons	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 29. 1923.
Solanum indicum subsp. newtonii	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 19. 1923.
Solanum indicum subsp. olivaceum	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 28. 1923.
Solanum indicum subsp. pervilleanum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 38. 1923.
Solanum indicum subsp. rohrii	(C.H.Wright) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 23. 1923.
Solanum indicum subsp. zechii	Dammer ex Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 36. 1923.
Solanum indicum var. arussorum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 35. 1923.
Solanum indicum var. breviaculeatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 25. 1923.
Solanum indicum var. brevipedicellatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 15. 1923
Solanum indicum var. brevistellatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 21. 1923.
Solanum indicum var. bukobense	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 24. 1923.
Solanum indicum var. busogae	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 37. 1923.
Solanum indicum var. carvalhoi	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 27. 1923.
Solanum indicum var. depauperatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 15. 1923.
Solanum indicum var. dichroanthum	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 18. 1923.
Solanum indicum var. eldamae	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 35. 1923.
Solanum indicum var. grandemunitum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 17. 1923
Solanum indicum var. grotei	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 22. 1923.
Solanum indicum var. halophilum	(Pax) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 18. 1923.
Solanum indicum var. immunitum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 14. 1923.
Solanum indicum var. jaegeri	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 27. 1923.
Solanum indicum var. kandtii	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 26. 1923.
Solanum indicum var. kiwuense	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 25. 1923.
Solanum indicum var. lividum	(Link) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 10. 1923.
Solanum indicum var. maroanum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 10. 1923.
Solanum indicum var. mesodolichum	Bitter	L., Repert. Spec. Nov. Regni Veg., Beih. 16: 34. 1923., 1923.
Solanum indicum var. micranthum	Hook.f.	J. Proc. Linn. Soc., Bot. 6: 18. 1861.
Solanum indicum var. modicearmatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 16. 1923.
Solanum indicum var. monbuttorum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 17. 1923.
Solanum indicum var. nguelense	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 25. 1923.
Solanum indicum var. profundelobatum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 26. 1923.
Solanum indicum var. pseudogeminifolium	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 22. 1923
Solanum indicum var. sakarense	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 25. 1923.
Solanum indicum var. spathotrichum	(Dammer) Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 24. 1923.
Solanum indicum var. subquercinum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 33. 1923.
Solanum indicum var. suprastrigulosum	Bitter	Repert. Spec. Nov. Regni Veg. Beih. 16: 28. 1923.
Solanum jaegeri	Dammer	Bot. Jahrb. Syst. 48: 256. 1912.
Solanum jespersenii	De Wild.	Bull. Jard. Bot. État Bruxelles 4: 407. 1914.
Solanum kandtii	Dammer	Bot. Jahrb. Syst. 48: 253. 1912.
Solanum keniense	Turrill	Bull. Misc. Inform. Kew 1915: 77. 1915.
Solanum lividum	Link	Enum. Hort. Berol. Alt. 1: 188. 1821.
Solanum mesodolichum	(Bitter) Pic.Serm.	Miss. Stud. Lago Tana, 7 Ricerche Bot., pt. 1: 133. 1951.
Solanum newtonii	Dammer	Bot. Jahrb. Syst. 48: 251. 1912.
Solanum nguelense	Dammer	Bot. Jahrb. Syst. 48: 252. 1912.
Solanum occidentale	Dunal	Prodr. [A. P. de Candolle] 13(1): 308. 1852.
Solanum olivaceum	Dammer	Bot. Jahrb. Syst. 53: 341. 1915.
Solanum orthocarpum	Pic.Serm.	Miss. Stud. Lago Tana, 7, Ricerche Bot., pt. 1: 129. 1951.
Solanum pseudogeminifolium	Dammer	Bot. Jahrb. Syst. 48: 249. 1912.
Solanum rederi	Dammer	Bot. Jahrb. Syst. 48: 251. 1912.
Solanum rohrii	C.H.Wright	Bull. Misc. Inform. Kew 1894: 128. 1894.
Solanum ruwenzoriense	De Wild.	Pl. Bequaert. 1: 435. 1922.
Solanum sakarense	Dammer	Bot. Jahrb. Syst. 48: 247. 1912.
Solanum scalare	C.H.Wright	J. Linn. Soc., Bot. 30: 93. 1894.
Solanum schroederi	Dammer	Bot. Jahrb. Syst. 48: 250. 1912.
Solanum senegambicum	Dunal	Prodr. [A. P. de Candolle] 13(1): 194. 1852.
Solanum spathotrichum	Dammer	Bot. Jahrb. Syst. 48: 238. 1912.
Solanum ueleense	De Wild.	Bull. Jard. Bot. État Bruxelles 4: 400. 1914.
Solanum wildemanii	Damm. ex De Wild. & T.Durand	Ann. Mus. Congo Belge, Bot., sér. 3, 1: 291. 1901.
Solanum yangambiense	De Wild.	Bull. Jard. Bot. État Bruxelles 4: 402. 1914.
Solanum aethiopicum var. anguivi	(Lam.) Banfi, Galasso & Bartolucci
Solanum indicum subsp. mesodolichum	Bitter

Common names Top

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Filter by language:

Language	Common/alternative name
English	african eggplant
English	forest bitterberry
Hausa	gautan tsuntsu
Quechua	indya t'ankar
Chinese	五宅茄
Chinese	印度茄

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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Benin
  - Gambia
  - Ghana
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Nigeria
  - Senegal
  - Sierra Leone
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Central African Republic
  - Congo
  - Equatorial Guinea
  - Gabon
  - Gulf Of Guinea Islands
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Comoros
  - Madagascar
  - Mauritius
  - Réunion

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - India

Australasia click to expand
- Australia
  - Queensland

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001026208
USDA Plants	SOAN8
Tropicos	29605616
INPN	706817
Flora of Italy	12640
KEW	urn:lsid:ipni.org:names:818243-1
The Plant List	tro-29605616
Open Tree Of Life	535397
NCBI Taxonomy	329760
IUCN Red List	101519334
IPNI	818243-1
iNaturalist	594566
GBIF	2931542
Freebase	/m/0z6v0k3
EPPO	SOLAG
USDA GRIN	310328
Wikipedia	Solanum_anguivi

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

Buffalo-bur (Solanum rostratum Dunal) invasiveness, bioactivities, and utilization: a review

Ozuzu SA, Hussain RS, Kuchkarova N, Fidelis GD, Zhou S, Habumugisha T, Shao H

PeerJ

27-Mar-2024

PMCID:	PMC10981417
doi:	10.7717/peerj.17112
PMID:	38560474

Dataset on the geographical distribution of species of the genus Solanum, subgenus Leptostemonum in Uganda

Kauma CM, Anywar G, Serunjogi D, Katuura E, Namaganda M

Data Brief

13-Feb-2024

PMCID:	PMC10881442
doi:	10.1016/j.dib.2024.110159
PMID:	38389959

An In Silico In Vitro and In Vivo Study on the Influence of an Eggplant Fruit (Solanum anguivi Lam) Diet on Metabolic Dysfunction in the Sucrose-Induced Diabetic-like Fruit Fly (Drosophila melanogaster)

Nwanna E, Ojo R, Shafiq N, Ali A, Okello E, Oboh G

Foods

12-Feb-2024

PMCID:	PMC10888091
doi:	10.3390/foods13040559
PMID:	38397536

Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia

Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E

J Ethnobiol Ethnomed

04-Jan-2024

PMCID:	PMC10768247
doi:	10.1186/s13002-023-00644-x
PMID:	38178202

Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India

Ralte L, Sailo H, Singh YT

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765666
doi:	10.1186/s13002-023-00642-z
PMID:	38172927

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

Targeting NF-κB pathway for the anti-inflammatory potential of Bhadradarvadi kashayam on stimulated RAW 264.7 macrophages

Ali A M MT, Narayana S DS, Lulu S S, Nag S, Sundararajan V

Heliyon

19-Aug-2023

PMCID:	PMC10469766
doi:	10.1016/j.heliyon.2023.e19270
PMID:	37664699

Therapeutic Candidates for Alzheimer’s Disease: Saponins

Zhang R, Zeng M, Zhang X, Zheng Y, Lv N, Wang L, Gan J, Li Y, Jiang X, Yang L

Int J Mol Sci

22-Jun-2023

PMCID:	PMC10341681
doi:	10.3390/ijms241310505
PMID:	37445682

Insects as food and medicine: a sustainable solution for global health and environmental challenges

Aidoo OF, Osei-Owusu J, Asante K, Dofuor AK, Boateng BO, Debrah SK, Ninsin KD, Siddiqui SA, Chia SY

Front Nutr

14-Jun-2023

PMCID:	PMC10303143
doi:	10.3389/fnut.2023.1113219
PMID:	37388630

Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau

Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P

Plants (Basel)

08-May-2023

PMCID:	PMC10181441
doi:	10.3390/plants12091909
PMID:	37176967

Characteristics, Comparative Analysis, and Phylogenetic Relationships of Chloroplast Genomes of Cultivars and Wild Relatives of Eggplant (Solanum melongena)

Yang Q, Li Y, Cai L, Gan G, Wang P, Li W, Li W, Jiang Y, Li D, Wang M, Xiong C, Chen R, Wang Y

Curr Issues Mol Biol

01-Apr-2023

PMCID:	PMC10136506
doi:	10.3390/cimb45040185
PMID:	37185709

Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches

Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005506
doi:	10.3390/plants12051145
PMID:	36904005

Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives

Dubey S, Dixit AK

J Ayurveda Integr Med

24-Feb-2023

PMCID:	PMC9988554
doi:	10.1016/j.jaim.2023.100688
PMID:	36841194

Community-Level Incentive Mechanisms for the Conservation of Crop Wild Relatives: A Malawi Case Study

Drucker AG, Mponya NK, Grazioli F, Maxted N, Brehm JM, Dulloo E

Plants (Basel)

24-Feb-2023

PMCID:	PMC10005345
doi:	10.3390/plants12051030
PMID:	36903889

Polygonatum sibiricum saponin Exerts Beneficial Hypoglycemic Effects in Type 2 Diabetes Mice by Improving Hepatic Insulin Resistance and Glycogen Synthesis-Related Proteins

Chen Z, Luo J, Jia M, Chai Y, Bao Y

Nutrients

08-Dec-2022

PMCID:	PMC9786127
doi:	10.3390/nu14245222
PMID:	36558381

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 / Prenol lipids / Triterpenoids
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	https://doi.org/10.1055/S-0028-1097583
Spirost-5-en-3-ol	234096	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	https://doi.org/10.1055/S-0028-1097583
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(2R,4R,5S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163021566	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C3(C(C4C(O3)CC5C4(CCC6C5CC=C7C6(CCC(C7)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)O	1049.20	unknown	https://doi.org/10.1021/NP020254T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(2S,4R,5S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11829165	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C3(C(C4C(O3)CC5C4(CCC6C5CC=C7C6(CCC(C7)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)O	1049.20	unknown	https://doi.org/10.1021/NP020254T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(2S,4R,5S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101222825	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C3(C(C4C(O3)CC5C4(CCC6C5CC=C7C6(CCC(C7)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)O	1049.20	unknown	https://doi.org/10.1021/NP020254T
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[[(3S,8S,9S,10R,13S,14S,16S,17R)-16-hydroxy-17-[(2S,3S,6R)-3-hydroxy-6-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-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	162912107	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC(C7C(C)C(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)CO)O)O)O	1051.20	unknown	https://doi.org/10.1016/S0040-4039(01)01711-7
(3S,8S,9S,10R,13S,14S,17R)-3-[(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-10,13-dimethyl-17-[(2S,6R)-6-methyl-3-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	10931132	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC(=O)C7C(C)C(=O)CCC(C)COC8C(C(C(C(O8)CO)O)O)O)C)C)CO)O)O)O	1047.20	unknown	https://doi.org/10.1021/NP020254T
(3S,8S,9S,10R,13S,14S,17R)-3-[(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-10,13-dimethyl-17-[(2S)-1-[(2R,4R,5S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-1-oxopropan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	162991156	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)C(C)C3C(=O)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	1061.20	unknown	https://doi.org/10.1021/NP020254T
(3S,8S,9S,10R,13S,14S,17R)-3-[(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-10,13-dimethyl-17-[(2S)-1-[(2S,4R,5S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-1-oxopropan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	11062115	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)C(C)C3C(=O)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	1061.20	unknown	https://doi.org/10.1021/NP020254T
(3S,8S,9S,10R,13S,14S,17R)-3-[(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-17-[(2S)-1-[(2R,4R,5R)-5-hydroxy-4-methyloxolan-2-yl]-1-oxopropan-2-yl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	162988443	Click to see CC1CC(OC1O)C(=O)C(C)C2C(=O)CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C	899.00	unknown	https://doi.org/10.1016/S0040-4039(01)01711-7
(3S,8S,9S,10R,13S,14S,17R)-3-[(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-17-[(2S)-1-[(2S,4R,5R)-5-hydroxy-4-methyloxolan-2-yl]-1-oxopropan-2-yl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	162988444	Click to see CC1CC(OC1O)C(=O)C(C)C2C(=O)CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C	899.00	unknown	https://doi.org/10.1016/S0040-4039(01)01711-7
2-[4-hydroxy-6-[[16-hydroxy-17-[3-hydroxy-6-methyl-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162912106	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC(C7C(C)C(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)CO)O)O)O	1051.20	unknown	https://doi.org/10.1016/S0040-4039(01)01711-7
2-[5-Hydroxy-6-(hydroxymethyl)-2-[[6-hydroxy-7,9,13-trimethyl-6-[4-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	73120581	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C3(C(C4C(O3)CC5C4(CCC6C5CC=C7C6(CCC(C7)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)O	1049.20	unknown	https://doi.org/10.1021/NP020254T
3-[4-Hydroxy-6-(hydroxymethyl)-3,5-bis[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy-10,13-dimethyl-17-[1-[4-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]-1-oxopropan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	85385167	Click to see CC1CC(OC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)C(C)C3C(=O)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	1061.20	unknown	https://doi.org/10.1021/NP020254T
3-[4-Hydroxy-6-(hydroxymethyl)-3,5-bis[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy-10,13-dimethyl-17-[6-methyl-3-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	85320529	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC(=O)C7C(C)C(=O)CCC(C)COC8C(C(C(C(O8)CO)O)O)O)C)C)CO)O)O)O	1047.20	unknown	https://doi.org/10.1021/NP020254T
3-[4-Hydroxy-6-(hydroxymethyl)-3,5-bis[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy-17-[1-(5-hydroxy-4-methyloxolan-2-yl)-1-oxopropan-2-yl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one	162988442	Click to see CC1CC(OC1O)C(=O)C(C)C2C(=O)CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C	899.00	unknown	https://doi.org/10.1016/S0040-4039(01)01711-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[(1S,2S,3'S,4S,5'R,6R,6'R,7S,8R,9S,12S,13R,16S)-3',6'-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-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	21603543	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1O)O	887.00	unknown	https://doi.org/10.1021/NP020254T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,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,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101678903	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	854.00	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766005/
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6S,6'R,7S,8R,9S,12S,13R,16S)-6'-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,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	10748197	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1O	871.00	unknown	https://doi.org/10.1248/CPB.48.568
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6S,6'R,7S,8R,9S,12S,13R,16S)-6'-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,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101017664	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(CO8)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1O	871.00	unknown	https://doi.org/10.1248/CPB.48.568
(2S,3R,4R,5R,6S)-2-[(2R,3R,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,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101678904	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	854.00	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766005/
2-[2-(3',6'-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-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	73798998	Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1O)O	887.00	unknown	https://doi.org/10.1021/NP020254T
2-[5-Hydroxy-6-(hydroxymethyl)-2-(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-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162938656	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1	854.00	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766005/
2-[5-Hydroxy-6-(hydroxymethyl)-2-(6'-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-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	85254827	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1O	871.00	unknown	https://doi.org/10.1248/CPB.48.568
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6S,6'R,7S,8R,9S,12S,13R,16S)-6'-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-2-methyloxan-3-yl]oxy-3-oxopropanoic acid	163032355	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)OC(=O)CC(=O)O)O)O)C)C)C)OC1O	971.10	unknown	https://doi.org/10.1248/CPB.48.568
3-[4,5-Dihydroxy-6-[4-hydroxy-6-(hydroxymethyl)-2-(6'-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-2-methyloxan-3-yl]oxy-3-oxopropanoic acid	85221211	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)OC(=O)CC(=O)O)O)O)C)C)C)OC1O	971.10	unknown	https://doi.org/10.1248/CPB.48.568
Anguivioside A	10795761	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)OC1O	885.00	unknown	https://doi.org/10.1248/CPB.48.568
Anguivioside B	10653503	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)OC(=O)CC(=O)O)O)O)C)C)C)OC1O	971.10	unknown	https://doi.org/10.1248/CPB.48.568
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
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/10.1016/S0031-9422(96)00395-0 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766005/
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/S0031-9422(96)00395-0
Spirostane + 1O,-2H, O-Hex-dHex-dHex	85271213	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)OC1O	885.00	unknown	https://doi.org/10.1248/CPB.48.568
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1021/NP50091A003

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Solanum anguivi

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