Scientific name	Authority	First published in
Solanum chloropetalon	Schltdl.	Linnaea 19: 291. 1847.
Solanum macranthum	M.Martens & Galeotti	Bull. Acad. Roy. Sci. Bruxelles12(1): 143. 1845.
Solanum porphyranthum	Dunal	Prodr. [A. P. de Candolle] 13(1): 244. 1852.
Solanum reflexum var. chloropetalon	(Schltdl.) Witasek	Denkschr. Kaiserl. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 79: (advance separate) 37. 1910. (also in 79(2): 349. 1931)

Common names Top

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Language	Common/alternative name
Chinese	喀西茄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Nepal
- Indo-China
  - Myanmar

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Caribbean
  - Cuba
- Central America
  - Belize
  - Costa Rica
  - Guatemala
  - Honduras
  - Nicaragua

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001029728
Tropicos	29601700
KEW	urn:lsid:ipni.org:names:820196-1
The Plant List	tro-29601700
Open Tree Of Life	877389
NCBI Taxonomy	267268
IPNI	820196-1
iNaturalist	280969
GBIF	2932223
EPPO	SOLMY
USDA GRIN	314197
Wikipedia	Solanum_myriacanthum

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

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

New Genera and Species Records of Nicaraguan Eumolpinae (Coleoptera: Chrysomelidae) Including a New Species in a New Generic Record for Central America

Gómez-Zurita J, Maes JM

Neotrop Entomol

19-Aug-2022

PMCID:	PMC9546993
doi:	10.1007/s13744-022-00987-2
PMID:	35984567

Pest categorisation of Leucinodes orbonalis

Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Gregoire J, Malumphy C, Czwienczek E, Maiorano A, MacLeod A

EFSA J

12-Nov-2021

PMCID:	PMC8586846
doi:	10.2903/j.efsa.2021.6890
PMID:	34804235

Anti-trypanosomal screening of Salvadoran flora

Castillo UG, Komatsu A, Martínez ML, Menjívar J, Núñez MJ, Uekusa Y, Narukawa Y, Kiuchi F, Nakajima-Shimada J

J Nat Med

16-Sep-2021

PMCID:	PMC8732892
doi:	10.1007/s11418-021-01562-6
PMID:	34529189

The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis

Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E

Front Pharmacol

08-Jun-2021

PMCID:	PMC8248671
doi:	10.3389/fphar.2021.690432
PMID:	34220515

Top-down and bottom-up controls on an herbivore on a native and introduced plant in a tropical agricultural landscape

Despland E, Santacruz PG

PeerJ

13-Mar-2020

PMCID:	PMC7075360
doi:	10.7717/peerj.8782
PMID:	32206453

Efficacy of Four Solanum spp. Extracts in an Animal Model of Cutaneous Leishmaniasis

Cos P, Janssens J, Piñón A, Cuesta-Rubio O, Yglesias-Rivera A, Díaz-García A, Vilegas W, Monzote L

Medicines (Basel)

05-Jun-2018

PMCID:	PMC6023388
doi:	10.3390/medicines5020049
PMID:	29874837

Genistein: is the multifarious botanical a natural anthelmintic too?

Tandon V, Das B

J Parasit Dis

05-Mar-2018

PMCID:	PMC5962493
doi:	10.1007/s12639-018-0984-0
PMID:	29844617

Anthelmintic activity of a standardized extract from the rhizomes of Acorus calamus Linn. (Acoraceae) against experimentally induced cestodiasis in rats

Nath P, Yadav AK

J Intercult Ethnopharmacol

14-Jun-2016

PMCID:	PMC5061482
doi:	10.5455/jice.20160521124439
PMID:	27757269

Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods

Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP

J Ethnobiol Ethnomed

03-May-2016

PMCID:	PMC4855762
doi:	10.1186/s13002-016-0089-8
PMID:	27142597

Steroidal glycosides from the fruits of Solanum viarum.

Ono M, Kakiuchi T, Ebisawa H, Shiono Y, Nakamura T, Kai T, Ikeda T, Miyashita H, Yoshimitsu H, Nohara T

Chem Pharm Bull (Tokyo)

01-Jun-2009

doi:	10.1248/CPB.57.632
PMID:	19483350

Steroidal Alkaloids and Sapogenins from Roots of SomeSolanumSpecies1

Helmut Ripperger

Georg Thieme Verlag KG

13-Jan-2009

doi:	10.1055/S-2006-958081

Antifilarial Effect of Solamargine Isolated from Solatium khasianum

M. Ghosh, S. P. Sinhababu, N. C. Sukul, N. P. Sahu, S. B. Mahato

Informa UK Limited

25-Nov-2007

doi:	10.3109/13880209409082991

Chemical Examination of Leaves ofSolanum khasianum

Amin Uddin, A. R. Chowdhury

Informa UK Limited

19-Nov-2007

doi:	10.3109/13880208209055189

Ethnomedicinal botany of the Apatani in the Eastern Himalayan region of India

Kala CP

J Ethnobiol Ethnomed

16-Nov-2005

PMCID:	PMC1315349
doi:	10.1186/1746-4269-1-11
PMID:	16288657

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
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1016/0031-9422(96)00173-2 https://doi.org/10.1021/NP010186V
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
Solanesol	5477212	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C	631.10	unknown	https://doi.org/10.3109/13880208209055189
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	https://doi.org/10.3109/13880208209055189
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,3'R,4S,6R,7S,8R,9S,12S,13R,16S)-3',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3',16-diol	162930998	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(CO6)(C)O	430.60	unknown	https://doi.org/10.1016/0031-9422(80)83101-3
3',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,6'-oxane]-3',16-diol	12311128	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(CO6)(C)O	430.60	unknown	https://doi.org/10.1016/0031-9422(80)83101-3
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/10.1016/0003-2697(84)90319-1
Isonuatigenin	12311129	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(CO6)(C)O	430.60	unknown	https://doi.org/10.1055/S-2006-958081
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
5'-(Hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxolane]-16-ol	4483042	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(O6)(C)CO	430.60	unknown	https://doi.org/10.1016/0031-9422(80)83101-3
Nuatigenin	440453	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(O6)(C)CO	430.60	unknown	https://doi.org/10.1016/0031-9422(80)83101-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1R,2R,4R,5'S,6R,7S,8R,9R,12S,13S,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol	162857933	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	https://doi.org/10.1055/S-0028-1099541
(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/10.1055/S-2006-958081 https://doi.org/10.1055/S-2007-969895 https://doi.org/10.3109/13880209409082991 https://doi.org/10.1055/S-2007-969622
Purapuridine	5250	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	https://doi.org/10.1055/S-0028-1099541
Solasodine	442985	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/S0031-9422(01)00185-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-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,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162980351	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(01)00185-6
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[(2S,3'S,4S,5'S,6S,7S,8S,9S,12S,13R,16S)-3',8-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	163189918	Click to see CC1CC(C2(C(C3(C(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)O)C)OC1)O	887.00	unknown	https://doi.org/10.1021/NP980301A
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-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	102445416	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)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	1035.20	unknown	https://doi.org/10.1248/CPB.57.632
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(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-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163075706	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(01)00185-6
(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/NP980301A https://doi.org/10.3109/13880209409082991 https://doi.org/10.1248/CPB.57.632
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4-hydroxy-2-(hydroxymethyl)-6-[(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-5-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163075701	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(01)00185-6
(2S,3R,4R,5R,6S)-2-[(2S,3S,4S,5S,6R)-2-[(1R,2S,3'S,4S,5'S,6S,7S,8S,9S,12S,13R,16S)-3',8-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]-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	100933836	Click to see CC1CC(C2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)C7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)O)C)OC1)O	871.00	unknown	https://doi.org/10.1021/NP980301A
(2S,3R,4S,5R,6S)-2-[(2S,3S,4S,5S,6S)-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,3S,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162980342	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(01)00185-6
2-[2-(3',8-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	73820914	Click to see CC1CC(C2(C(C3(C(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)O)C)OC1)O	887.00	unknown	https://doi.org/10.1021/NP980301A
2-[4,5-dihydroxy-2-(hydroxymethyl)-6-[(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-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	138114744	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)O)C)C)C)NC1	721.90	unknown	https://doi.org/10.3109/13880209409082991
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/S0031-9422(01)00185-6 https://doi.org/10.1016/0031-9422(80)83026-3
CID 21573759	21573759	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)O)C)C)C)NC1	721.90	unknown	https://doi.org/10.1016/0031-9422(80)83026-3
Khasianine	3479482	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)O)C)C)C)NC1	721.90	unknown	https://doi.org/10.1016/0031-9422(80)83026-3
L-Rhamnopyranosyl-14-D-glucopyranose solasodine	73606	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)O)C)C)C)NC1	721.90	unknown	https://doi.org/10.3109/13880209409082991
Ninxzccvhcvbgb-fxzpvaojsa-	21672264	Click to see CC1CC(C2(C(C3(C(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)O)C)OC1)O	887.00	unknown	https://doi.org/10.1021/NP980301A
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/10.1248/CPB.57.632
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(01)00185-6 https://doi.org/10.1021/NP980301A https://doi.org/10.3109/13880209409082991 https://doi.org/10.1016/0031-9422(80)83026-3 https://doi.org/10.1248/CPB.57.632
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/S0031-9422(01)00185-6 https://doi.org/10.1016/0031-9422(80)83026-3
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(01)00185-6 https://doi.org/10.1021/NP980301A https://doi.org/10.3109/13880209409082991 https://doi.org/10.1016/0031-9422(80)83026-3 https://doi.org/10.1248/CPB.57.632
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(e)-N-(2-hydroxy-2-(4-hydroxyphenyl) ethyl)-3-(3-hydroxy-4-methoxyphenyl)acrylamide	70681748	Click to see COC1=C(C=C(C=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	https://doi.org/10.1016/0031-9422(96)00173-2
n-cis-Feruloyltyramine	6440659	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1016/0031-9422(96)00173-2
N-feruloyltyramine; Moupinamide	125213	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1021/NP010186V

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Solanum myriacanthum

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