Solanum lasiocarpum, also known as Indian nightshade or hairy-fruited eggplant, is a plant with edible fruit. It is found in parts of Asia and is primarily known as a domesticated plant. The domesticated plants have larger fruits and lack the prickly skin found in wild plants. The fruit is light green in color and is used in food additives and as a folk medicine. In India, it is used as a sour-relish in curries and in Thailand, it is used to make a special sauce called nam prek. Botanists are interested in S. lasiocarpum because of its close relation to South American species, such as cocona, naranjilla, and pseudolulo. When grown outside of their native range, these plants can hybridize, potentially enhancing their commercial viability in other parts of the world.

Synonyms Top

Scientific name	Authority	First published in
Solanum ferox var. lasiocarpum	(Dunal) Miq.	Fl. Ned. Ind. 2: 647. 1861
Solanum hirsutum	Roxb.	Fl. Ind. (Carey & Wallich ed.) 2: 253. 1824.
Solanum lasiocarpum var. domesticum	Heiser	Solanaceae: Biol. & Syst. (ed. D'Arcy) 413. 1986.
Solanum lasiocarpum var. velutinum	Dunal	Prodr. [A. P. de Candolle] 13(1): 253. 1852
Solanum quadriloculare	Spreng.	Syst. Veg., ed. 16 [Sprengel] 4(2, Cur. Post.): 72. 1827.
Solanum zeylanicum	Blanco	Fl. Filip. [F.M. Blanco] 136. 1837.

Common names Top

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Filter by language:

Language	Common/alternative name
English	indian nightshade
iba	terung asam
mad	terrong perrat
Malay	pokok terung asam
Malay	pokok terung iban
Malay	pokok terung bulu
su	karundang
Chinese	羊不食
Chinese	毛茄

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sulawesi
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland

Pacific click to expand
- Southwestern Pacific
  - Vanuatu

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001028971
Tropicos	29600277
KEW	urn:lsid:ipni.org:names:819751-1
The Plant List	tro-29600277
Open Tree Of Life	835552
NCBI Taxonomy	227722
IPNI	819751-1
iNaturalist	426686
GBIF	2932691
Freebase	/m/09v1_nt
EOL	2894457
USDA GRIN	416240
Wikipedia	Solanum_lasiocarpum
CMAUP	NPO12170

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

Efficacy and safety of the Ayurvedic herbal preparation Maharishi Amrit Kalash: a systematic review of randomized controlled trials

Koch AK, Patel M, Gupta S, Wullenkord R, Jeitler M, Kessler CS

Front Med (Lausanne)

16-Apr-2024

PMCID:	PMC11058942
doi:	10.3389/fmed.2024.1325037
PMID:	38690176

Pest risk assessment of Leucinodes orbonalis for the European Union

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Vicent Civera A, Yuen J, Zappalà L, Mally R, Czwienczek E, Gobbi A, López Mercadal J, Maiorano A, Mosbach‐Schulz O, Pautasso M, Rossi E, Stancanelli G, Tramontini S, Van der Werf W

EFSA J

12-Mar-2024

PMCID:	PMC10928798
doi:	10.2903/j.efsa.2024.8498
PMID:	38476322

Unleashed Treasures of Solanaceae: Mechanistic Insights into Phytochemicals with Therapeutic Potential for Combatting Human Diseases

Jan S, Iram S, Bashir O, Shah SN, Kamal MA, Rahman S, Kim J, Jan AT

Plants (Basel)

04-Mar-2024

PMCID:	PMC10935155
doi:	10.3390/plants13050724
PMID:	38475570

A Case Study of Furunculosis following an Ayurvedic Oil Massage, Sudation Therapy, and Lessons to Learn

Kulkarni SP, Kulkarni PS, Kumar S

Case Rep Dermatol Med

08-Feb-2024

PMCID:	PMC10869181
doi:	10.1155/2024/3660064
PMID:	38361501

Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region

Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK

Sci Rep

03-Jan-2024

PMCID:	PMC10764828
doi:	10.1038/s41598-023-50287-x
PMID:	38172161

Solanum aethiopicum L. from the Basilicata region as a source of specialized metabolites with promising anti-obesity effects: phytochemical characterization and in vivo investigation in high fat diet-fed mice

Ponticelli M, Hidalgo-García L, Diez-Echave P, Vezza T, Romero M, Robles-Vera I, Duarte J, De Biasio F, Gorgoglione D, Lela L, Galvez J, Milella L

Front Pharmacol

22-Nov-2023

PMCID:	PMC10702577
doi:	10.3389/fphar.2023.1306135
PMID:	38074123

Morphometrics and Structural Changes of “Terung Asam” Sarawak (Solanum lasiocarpum Dunal) During Growth and Development

Soon AT, Ding P, Ramaiya SD

Trop Life Sci Res

30-Sep-2023

PMCID:	PMC10583847
doi:	10.21315/tlsr2023.34.3.2
PMID:	37860092

Floristic composition and plant community distribution along environmental gradients in Guard dry Afromontane forest of Northwestern Ethiopia

Dagne Y, Birhanu L

BMC Ecol Evol

28-Aug-2023

PMCID:	PMC10463663
doi:	10.1186/s12862-023-02154-6
PMID:	37635212

Effects of Ayurveda interventions on acute pain and quality of life of a trigeminal neuralgia patient - A case report

De Silva UM, Mangal G, Attanayake AM, Upadhyay A, Vedpathak SM

J Ayurveda Integr Med

25-Jul-2023

PMCID:	PMC10382661
doi:	10.1016/j.jaim.2023.100743
PMID:	37494834

Management of allergic rhinitis with Rajanyadi Churna and Guduchi Kwatha- A case report

Sharma R, Bhat P

J Ayurveda Integr Med

19-Jul-2023

PMCID:	PMC10371786
doi:	10.1016/j.jaim.2023.100740
PMID:	37478634

The Effect of Ripening Stages on the Accumulation of Polyphenols and Antioxidant Activity of the Fruit Extracts of Solanum Species

Staveckienė J, Kulaitienė J, Levickienė D, Vaitkevičienė N, Vaštakaitė-Kairienė V

Plants (Basel)

17-Jul-2023

PMCID:	PMC10385256
doi:	10.3390/plants12142672
PMID:	37514286

Integrative management of anaplastic astrocytoma through a combination of Ayurveda and conventional care: A case report

Gautama PA, Subramanian N, Varma RG, Gangadharan GG

J Ayurveda Integr Med

11-Jul-2023

PMCID:	PMC10692369
doi:	10.1016/j.jaim.2023.100748
PMID:	37442646

An Evaluation of the Anti-Inflammatory Effects of a Thai Traditional Polyherbal Recipe TPDM6315 in LPS-Induced RAW264.7 Macrophages and TNF-α-Induced 3T3-L1 Adipocytes

Subin P, Sabuhom P, Naladta A, Luecha P, Nualkaew S, Nualkaew N

Curr Issues Mol Biol

05-Jun-2023

PMCID:	PMC10296878
doi:	10.3390/cimb45060311
PMID:	37367060

Green Synthesis of Silver Nanoparticles Using Acacia ehrenbergiana Plant Cortex Extract for Efficient Removal of Rhodamine B Cationic Dye from Wastewater and the Evaluation of Antimicrobial Activity

Alamier WM, D Y Oteef M, Bakry AM, Hasan N, Ismail KS, Awad FS

ACS Omega

15-May-2023

PMCID:	PMC10233848
doi:	10.1021/acsomega.3c01292
PMID:	37273622

Antifungal Activity of Juglans-regia-Mediated Silver Nanoparticles (AgNPs) against Aspergillus-ochraceus-Induced Toxicity in In Vitro and In Vivo Settings

Naqvi SI, Kausar H, Afzal A, Hashim M, Mujahid H, Javed M, Hano C, Anjum S

J Funct Biomater

14-Apr-2023

PMCID:	PMC10141138
doi:	10.3390/jfb14040221
PMID:	37103312

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
> Alkaloids and derivatives / Aporphines
CID 12305611	12305611	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)C	342.40	unknown	via CMAUP database
O,O'-Dimethylmagnoflorine	182680	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)OC)OC)C	370.50	unknown	via CMAUP database
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
Cocculine	21769966	Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)O	271.35	unknown	via CMAUP database
Cocculitine	72945082	Click to see COC1CC=C2CCN3C2(C1)C4=C(CC3)C=CC(=C4)OC	285.40	unknown	via CMAUP database
Coccuvine	3085221	Click to see COC1CC23C(=CCN2CCC4=C3C=C(C=C4)O)C=C1	269.34	unknown	via CMAUP database
Dihydroerysodine	22295116	Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CC3)O)OC	301.40	unknown	via CMAUP database
Isococculidine	442300	Click to see COC1CC23C(CCN2CCC4=C3C=C(C=C4)OC)C=C1	285.40	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-Stepharine	193686	Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC	297.30	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
(4R)-4-[(2,6-dimethylphenyl)methyl]-5,5-dimethyloxolan-2-one	11107208	Click to see CC1=C(C(=CC=C1)C)CC2CC(=O)OC2(C)C	232.32	unknown	https://doi.org/10.1021/NP010186V
(4S)-4-[(2,6-dimethylphenyl)methyl]-5,5-dimethyloxolan-2-one	163193554	Click to see CC1=C(C(=CC=C1)C)CC2CC(=O)OC2(C)C	232.32	unknown	https://doi.org/10.1021/NP010186V
Solafuranone	11637219	Click to see CC1=C(C(=CC=C1)C)CC2CC(=O)OC2(C)C	232.32	unknown	https://doi.org/10.1021/NP010186V
> Benzenoids / Phenanthrenes and derivatives
O-Methylflavinantine	11724883	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)OC)OC	341.40	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
5,16-Dimethoxy-10-methyl-10-azatricyclo[11.4.0.02,7]heptadeca-1(13),2,4,6,14,16-hexaen-4-ol	21768993	Click to see CN1CCC2=C(C=C(C=C2)OC)C3=CC(=C(C=C3CC1)OC)O	313.40	unknown	via CMAUP database
Laurifine	442309	Click to see COC1=CC2=C(CCNCCC3=CC(=C(C=C32)OC)OC)C=C1	313.40	unknown	via CMAUP database
> 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	via CMAUP database
> Lignans, neolignans and related compounds
Oxyacanthan-12'-ol, 6',7-epoxy-6-methoxy-2,2'-dimethyl-, (1'alpha)-	21579625	Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC	562.70	unknown	via CMAUP database
Trilobine	169007	Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC(=C(C=C5)OC)OC6=CC=C(CC7C8=C(O4)C(=C(C=C8CCN7)OC)O3)C=C6	562.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,5S,6S)-6,10-dimethyl-3-prop-1-en-2-ylspiro[4.5]dec-9-en-8-one	11085279	Click to see CC1CC(=O)C=C(C12CCC(C2)C(=C)C)C	218.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10S,13R,14R)-4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	44135612	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
Solasod-5-en-3 beta-ol	44584207	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[4-[17-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,19-dihydroxy-7,13,18-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11968860	Click to see CC1C2C3CCC4C(C3CC2OC1(CCC(C)COC5C(C(C(C(O5)CO)O)O)O)O)CC(C6(C4(CCCC6OC7C(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)O	1261.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,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,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	9876101	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
(2R,3S,4S,5S,6R)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3S)-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]-5-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	53384936	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	via CMAUP database
(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/NP50091A003 https://doi.org/10.1248/CPB.57.747 https://doi.org/10.1016/S0031-9422(96)00395-0
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-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	102445415	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)OC	1049.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,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-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163085568	Click to see CC1CC(C2(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)O	887.00	unknown	https://doi.org/10.1248/CPB.57.747
(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,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	9942086	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	via CMAUP database
(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://doi.org/10.1016/S0031-9422(96)00395-0
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,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	163034177	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/10.1016/S0031-9422(96)00395-0
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,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,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	134715195	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)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	1065.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
(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/10.1016/S0031-9422(96)00395-0
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-6-[(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-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	101838956	Click to see CC1CC(C2(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)O	901.00	unknown	https://doi.org/10.1248/CPB.57.747
(2S,3R,4R,5S,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[6-methoxy-7,9,13-trimethyl-6-[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]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11968769	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)C)O)O)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)OC	1209.40	unknown	via CMAUP database
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-4-hydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163085567	Click to see CC1CC(C2(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)O	887.00	unknown	https://doi.org/10.1248/CPB.57.747
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/10.1016/S0031-9422(96)00395-0
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://doi.org/10.1016/S0031-9422(96)00395-0
2-[5-Hydroxy-6-(hydroxymethyl)-2-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[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-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163034176	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/10.1016/S0031-9422(96)00395-0
2-[5-Hydroxy-6-(hydroxymethyl)-2-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[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-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	85099255	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)OC	1049.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
2-[6-(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-4-hydroxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	74941366	Click to see CC1CC(C2(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)O	901.00	unknown	https://doi.org/10.1248/CPB.57.747
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(96)00395-0
CID 146014454	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/10.1016/S0031-9422(96)00395-0
Furostane base-2H + O-Hex, O-Hex-dHex-dHex	500375	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.57.747
indioside D	102445417	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)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	1065.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
Indioside E	11764387	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)OC1	855.00	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
Liriope muscari baily saponins C	14682468	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)OC1	855.00	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
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.57.747
Trigofoenoside D	496770	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)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	1065.20	unknown	https://doi.org/10.1016/S0031-9422(96)00395-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Carpesterol	21155918	Click to see CCC(CC(C(C)C1CCC2C1(CCC3C2=CC(=O)C4C3(CCC(C4C)OC(=O)C5=CC=CC=C5)C)C)O)C(C)C	562.80	unknown	https://doi.org/10.1021/NP50091A003
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	https://doi.org/10.1021/NP50091A003
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol	441437	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Coclaurine	440989	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	via CMAUP database
(R)-N-Methylcoclaurine	440595	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	via CMAUP database
(S)-Laudanine	821396	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC	343.40	unknown	via CMAUP database
(S)-N-Methylcoclaurine	440584	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	via CMAUP database
Coclaurine	160487	Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O	285.34	unknown	via CMAUP database
Reticuline	439653	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)-	89322	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	https://doi.org/10.1021/NP010186V
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	https://doi.org/10.1021/NP010186V
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1021/NP010186V

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Solanum lasiocarpum

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