Scientific name	Authority	First published in
Melongena esculenta	(Dunal) Grecescu	Consp. Fl. Romaniei 423. 1898
Melongena incurva	Mill.	Gard. Dict., ed. 8, no. 3. 1768
Melongena ovata	Mill.	Gard. Dict., ed. 8, no. 1. 1768
Melongena spinosa	Mill.	Gard. Dict., ed. 8, no. 4. 1768
Melongena teres	Mill.	Gard. Dict., ed. 8, no. 2. 1768
Solanum aethiopicum var. violaceum	Dunal	Prodr. [A. P. de Candolle] 13(1): 351. 1852
Solanum album	Noronha	Verh. Batav. Genootsch. Kunst. 5(Art. 4): 84. 1791.
Solanum album	Lour.	Fl. Cochinch. 129. 1790.
Solanum album var. richardii	Dunal	Prodr. [A. P. de Candolle] 13(1): 362. 1852
Solanum album var. rumphii	Dunal	Prodr. [A. P. de Candolle] 13(1): 361. 1852
Solanum edule var. multifidum	Dunal	Prodr. [A. P. de Candolle] 13(1): 357. 1852
Solanum esculentum var. aculeatum	Dunal	Prodr. [A. P. de Candolle] 13(1): 355. 1852
Solanum esculentum var. inerme	Dunal	Prodr. [A. P. de Candolle] 13(1): 355. 1852.
Solanum esculentum var. subinerme	Dunal	Prodr. [A. P. de Candolle] 13(1): 355. 1852
Solanum lagenarium	Dunal	Prodr. [A. P. de Candolle] 13(1): 368. 1852.
Solanum longum	Roxb.	Hort. Bengal. 16. 1814.
Solanum melanoxylon	Link	Enum. Hort. Berol. Alt. 1: 188. 1821.
Solanum melongena subsp. agreste	Dikii	Trudy Prikl. Bot. 88: 105. 1984.
Solanum melongena var. angustum	Dikii	Trudy Prikl. Bot. 88: 105. 1984.
Solanum melongena var. cylindricum	Dikii	Trudy Prikl. Bot. 88: 105. 1984.
Solanum melongena var. esculentum	(Dunal) Walp.	Repert. Bot. Syst. (Walpers) 3: 81. 1844
Solanum melongena var. giganteum	(Alef.) Dikii	Trudy Prikl. Bot. Genet. Selek. 88: 105. 1984.
Solanum melongena var. globosi	Dikii	Trudy Prikl. Bot. 88: 106. 1984.
Solanum melongena var. inerme	(Dunal) Hiern	Cat. Afr. Pl. (Hiern) 1(3): 748. 1898.
Solanum melongena var. leucoum	(Alef.) Dikii	Trudy Prikl. Bot. Genet. Selek. 88: 105. 1984.
Solanum melongena var. ovigera	Pers.	Syn. Pl. [Persoon] 1: 221. 1805
Solanum melongena var. racemiflorum	Dikii	Trudy Prikl. Bot. 88: 105. 1984.
Solanum melongena var. racemosum	Dikii	Trudy Prikl. Bot. 88: 105. 1984.
Solanum melongena var. stenoleucum	(Alef.) Dikii	Trudy Prikl. Bot. Genet. Selek. 88: 104. 1984.
Solanum melongena var. variegatum	(Alef.) Dikii	Trudy Prikl. Bot. Genet. Selek. 88: 105. 1984.
Solanum melongena var. violaceum	(Alef.) Dikii	Trudy Prikl. Bot. Genet. Selek. 88: 105. 1984.
Solanum melongena var. viride	Dikii	Trudy Prikl. Bot. 88: 104. 1984.
Solanum mexianum	Hill	Veg. Syst. 9: 39. 1765.
Solanum sinuatorepandum	Dunal	Prodr. 13(1): 358 (1852)
Solanum subrepandum	Dunal	Prodr. 13(1): 358 (1852)
Solanum ovigerum var. album	Sweet	Hort. Brit. [Sweet], ed. 2. 387. 1830
Solanum ovigerum var. insanum	Blume	Bijdr. Fl. Ned. Ind. 13: 698. 1825
Solanum ovigerum var. luteum	Sweet	Hort. Brit. [Sweet], ed. 2. 387. 1830
Solanum ovigerum var. oblongo-cylindricum	Dunal	Prodr. [A. P. de Candolle] 13(1): 358. 1852
Solanum ovigerum var. ruber	Sweet	Hort. Brit. [Sweet], ed. 2. 387. 1830
Solanum ovigerum var. violaceum	Sweet	Hort. Brit. [Sweet], ed. 2. 387. 1830
Solanum violaceum	Dunal	Prodr. 13(1): 358 (1852)
Solanum pressum	Dunal	Hist. Nat. Solanum 217. 1813.
Solanum pseudoundatum var. albiflorum	Blume	Bijdr. Fl. Ned. Ind. 13: 699. 1826
Solanum pseudoundatum var. atropurpurascens	Blume	Bijdr. Fl. Ned. Ind. 13: 699. 1826
Solanum pseudoundatum var. leucocarpon	Blume	Bijdr. Fl. Ned. Ind. 13: 700. 1826
Solanum requienii	Dunal	Prodr. [A. P. de Candolle] 13(1): 363. 1852.
Solanum sativum var. albiflorum	(Blume) Dunal	Prodr. [A. P. de Candolle] 13(1): 360. 1852
Solanum sativum var. atropurpurascens	(Blume) Dunal	Prodr. [A. P. de Candolle] 13(1): 360. 1852
Solanum sativum var. leucocarpon	(Blume) Dunal	Prodr. [A. P. de Candolle] 13(1): 361. 1852
Solanum serpentinum	Noronha	Verh. Batav. Genootsch. Kunst. 5(Art. 4): 84. 1791.
Solanum serpentinum	Desf.	Cat. Pl. Horti Paris 397. 1829.
Solanum zeylanicum	Scop.	Delic. Fl. Faun. Insubr. 1: 1. 1786.
Solanum melongena subsp. meridionale	Filov
Solanum melongena subsp. orientale	Filov
Solanum melongena subsp. subspontaneum	Filov
Solanum melongena var. americanum	Filov
Solanum melongena var. arabicum	Filov
Solanum melongena var. azerbaijanicum	Filov
Solanum melongena var. bulgaricum	Filov
Solanum melongena var. europaeum	Filov
Solanum melongena var. palestinicum	Filov
Solanum melongena var. pekinense	Filov
Solanum melongena var. stenoides	Alef.
Solanum melongena subsp. agrestis	Filov
Solanum melongena var. racemosum	Filov
Solanum oviferum	Nocca

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	brinjal
English	aubergine
English	eggplant
English	garden ebrinjalgg
English	guinea squash
English	melongene
English	purple cucumber
English	white eggplant
Spanish	berenjena
ab	Абаклаџьан
ace	truëng
Amharic	ባዚንጀን
ang	Ǣȝƿyrt
Arabic	باذنجان
Arabic	شبيط
Arabic	باذنجان بري
Arabic	خروع بري
Azerbaijani	badımcan
azb	بادیمجان
ba	Баклажан
ban	tuung
bcl	talong
Belarusian	Баклажан
Bulgarian	патладжан
bho	बैगन
bi	obesin
Bengali	বার্তাকু
Bengali	বেগুন
Tibetan	རྡོ་ལུ་མ།
br	berjinez
Bosnian	patlidžan
Catalan	albergínia
Catalan	alberginiera
cdo	giò
Cherokee	ᏕᎭᎷᎨ ᎠᏓᏛᏍᎩ
co	milanzana
Czech	lilek vejcoplodý
Czech	baklažán
cv	Баклажан
Welsh	wylys
Welsh	planhigyn ŵy
Danish	aubergine
dag	kamli
German	eierfrucht
German	eierpflanze
German	melanzani
German	aubergine
dv	ބަށި
Greek	Βαζάνι
Greek	Μελιτζάνα
Esperanto	melongeno
Estonian	baklažaan
Basque	alberjinia
Basque	berenjena
Basque	aberjinia
Persian	بادمجانبابب
Persian	بادنجان
Fulah	huytaare
Finnish	patamunakoiso
Finnish	munakoiso
French	aubergine
frr	aubergine
Irish	ubhthoradh
Galician	berenxena
gom	vaingim
gor	ihu
got	𐌰𐌳𐌳𐌾𐌰𐌺𐍂𐌰𐌽
Gujarati	રીંગણ
Manx	lus ny h-oohyn
hak	khiô
Hebrew	חציל
Hindi	बैंगन
Croatian	patlidžan
Upper Sorbian	oberžina
ht	berejèn
Hungarian	tojásgyümölcs
Hungarian	padlizsán
Armenian	բադրիջան
Armenian	մանծակ
Armenian	պորինջան
Armenian	Սմբուկ
Indonesian	terung
ilo	tarong
io	berenjeno
Icelandic	eggaldin
Italian	melanzana
Japanese	茄子
Japanese	ナス
jv	térong
Georgian	ბადრიჯანი
kaa	baklajan
kbp	kela
kg	kitsukulu
Kazakh	баклажан
Kazakh	жертатақ
Kazakh	баялды
Kannada	ಬದನೆ
Korean	가지
ks	وانٛگُن
ku	balîcan
la	melongena
lad	berendjena
lb	aubergine
lbe	Бадуржан
ln	sóló
Lithuanian	baklažanas
Latvian	baklažāns
lzh	茄
mcn	kùytàsínà
Malagasy	baranjely
Macedonian	Модар патлиџан
Malayalam	എഗ്ഗ് പ്ലാന്റ്
Malayalam	ബ്രിഞ്ജാൾ
Malayalam	വഴുതന
Marathi	वांगे
Malay	terung
Malay	terung biru
Malay	terung cina
Malay	terung hijau
Malay	terung manis
Malay	terung ungu
mt	brunġiel
Burmese	ခရမ်းပင်
mzn	وینگوم
nan	kiô-á
nap	mulignana
Norwegian Bokmål	aubergine
Nepali	भान्टा
nia	toru
Dutch	white eggplant
Dutch	aubergine
Norwegian Nynorsk	eggfrukt
Norwegian Nynorsk	eggplante
Norwegian Nynorsk	aubergine
nv	ayęęzhii yiltʼąąʼí
oc	aubergina
Oriya	ବାଇଗଣ
os	Бадырджан
os	бадырджан
Punjabi	ਬੈਂਗਨ
pam	balasenas
pcd	oubàrjine
Polish	bakłażan
Polish	bakman
Polish	gruszka miłosna
Polish	jajko krzewiaste
Polish	oberżyna
Polish	psianka podłużna
Punjab	بتاؤں
Punjab	بینگن
Punjab	بینگݨ
Pashto	بانجان
Portuguese	beringela
Romanian	vânătă
Russian	бадриджан
Russian	бубриджан
Russian	паслён тёмноплодный
Russian	баклажан
rup	vinitâ
Kinyarwanda	urutoryi
sa	वृन्ताकः
sat	ᱵᱮᱸᱜᱟᱲ
scn	milinciana
sd	واڱڻ
Serbo-Croatian	patlidžan
Slovak	Ľuľok baklažánový
Slovenian	jajčevec
Slovenian	melancan
Slovenian	melancana
Albanian	patëllxhani
Serbian	Плави патлиџан
su	térong
Swedish	aubergine
Swahili	mbiringani
Tamil	கத்தரி
tcy	ಗುಳ್ಳ
Telugu	వంకాయ
tg	Боқлаҷон
Thai	มะเขือยาว
Tigrinya	ባዚንጀን
Tigrinya	መለንዛና
Tonga	paingani
Turkish	patlıcan
tt	битенгән
ug	Çeyze
Ukrainian	баклажан
Urdu	بینگن
Uzbek	baqlajon
Vietnamese	cà tím
vls	aubergine
Walloon	Åberdjene
war	tarong
xmf	ბადრიჯანი
yi	פאטלעזשאן
za	lwggwz
Chinese	茄子
Chinese	茄
Chinese	茄（白茄、大圆茄）
Chinese	茄叶
Chinese	茄子根
Chinese	茄根
Chinese	茄花
Chinese	茄蒂
Chinese	吊菜子
Chinese	白茄
Chinese	矮瓜
Chinese	紫茄
Chinese	落苏

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- West-central Tropical Africa
  - Zaïre
- Western Indian Ocean
  - Madagascar
  - Mauritius
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Laccadive Islands
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - South China Sea
  - Thailand
  - Vietnam
- Malesia
  - Malaya
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001029464
UNII	5DS5EE0N93
Florida Plant Atlas	1759
USDA Plants	SOME
Tropicos	29600121
INPN	124075
KEW	urn:lsid:ipni.org:names:820053-1
The Plant List	tro-29600121
Missouri Botanical Garden	287158
Open Tree Of Life	494843
Observations.org	133954
NCBI Taxonomy	4111
NBN Atlas	NBNSYS0200003200
Nature Serve	2.144588
IPNI	820053-1
iNaturalist	63190
iNaturalist	63192
GBIF	2930617
Freebase	/m/0cdk2
EPPO	SOLME
EOL	581188
Elurikkus	7298
US Library of Congress	sh85041224
USDA GRIN	101312
Wikipedia	Eggplant

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_000787875.1	SME_r2.5.1	Scaffold	Kazusa DNA Research Institute	2014-09-30	112.0x	794.49 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

Do biological control agents adapt to local pest genotypes? A multiyear test across geographic scales

Gibson AK, Mundim FM, Ramirez AL, Timper P

Evol Appl

11-Apr-2024

PMCID:	PMC11009426
doi:	10.1111/eva.13682
PMID:	38617827

Comparative physiology and transcriptome response patterns in cold-tolerant and cold-sensitive varieties of Solanum melongena

cai P, lan Y, Gong F, Li C, Xia F, Li Y, Fang C

BMC Plant Biol

09-Apr-2024

PMCID:	PMC11003173
doi:	10.1186/s12870-024-04922-y
PMID:	38594627

Physiological and transcriptomic comparisons shed light on the cold stress response mechanisms of Dendrobium spp

Li Z, Lu S, Yi S, Mo S, Yu X, Yin J, Zhang C

BMC Plant Biol

01-Apr-2024

PMCID:	PMC10985946
doi:	10.1186/s12870-024-04903-1
PMID:	38561687

Assembly and comparative analysis of the initial complete mitochondrial genome of Primulina hunanensis (Gesneriaceae): a cave-dwelling endangered plant

Chen L, Dong X, Huang H, Xu H, Rono PC, Cai X, Hu G

BMC Genomics

01-Apr-2024

PMCID:	PMC10983754
doi:	10.1186/s12864-024-10247-9
PMID:	38561677

Agriculture along the upper part of the Middle Zarafshan River during the first millennium AD: A multi-site archaeobotanical analysis

Mir-Makhamad B, Lurje P, Parshuto V, Pulotov A, Aminov F, Shenkar M, Saidov M, Semenov N, Kurbanov S, Mirzaakhmedov S, Rakhmanov K, dal Martello R, Spengler R III

PLoS One

28-Mar-2024

PMCID:	PMC10977675
doi:	10.1371/journal.pone.0297896
PMID:	38547085

Effects of nitrate- and ammonium- nitrogen on anatomical and physiological responses of Catalpa bungei under full and partial root-zone drought

Xu T, Wang Z, Wang Z, Guo M, Wang X, He X, Wang J, Rahman SU, Bourhia M, Alsahli AA, Zhang Y

BMC Plant Biol

26-Mar-2024

PMCID:	PMC10964640
doi:	10.1186/s12870-024-04874-3
PMID:	38532319

A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

Discontinuous Translocation of a Luciferase Protein beyond Graft Junction in Tobacco

Miyahara T, Ohkubo H, Umeyama Y, Oguchi T, Ogawa T, Ohta D, Mochizuki T, Kodama H

Food Saf (Tokyo)

22-Mar-2024

PMCID:	PMC10961615
doi:	10.14252/foodsafetyfscj.D-23-00010
PMID:	38532775

Discontinuous Translocation of a Luciferase Protein beyond Graft Junction in Tobacco

Miyahara T, Ohkubo H, Umeyama Y, Oguchi T, Ogawa T, Ohta D, Mochizuki T, Kodama H

Food Saf (Tokyo)

22-Mar-2024

PMCID:	PMC10961611
doi:	10.14252/foodsafetyfscj.D-23-00010
PMID:	38532772

Transcriptome sequencing and expression analysis in peanut reveal the potential mechanism response to Ralstonia solanacearum infection

Wang X, Qi F, Sun Z, Liu H, Wu Y, Wu X, Xu J, Liu H, Qin L, Wang Z, Sang S, Dong W, Huang B, Zheng Z, Zhang X

BMC Plant Biol

21-Mar-2024

PMCID:	PMC10956345
doi:	10.1186/s12870-024-04877-0
PMID:	38515036

Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon

Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M

Heliyon

21-Mar-2024

PMCID:	PMC10999872
doi:	10.1016/j.heliyon.2024.e28247
PMID:	38590891

Trading acyls and swapping sugars: metabolic innovations in Solanum trichomes

Fiesel PD, Kerwin RE, Daniel Jones A, Last RL

bioRxiv

19-Mar-2024

PMCID:	PMC10274652
doi:	10.1101/2023.06.05.542877
PMID:	37333341

Serratia spp. as plant growth-promoting bacteria alleviating salinity, drought, and nutrient imbalance stresses

Kulkova I, Wróbel B, Dobrzyński J

Front Microbiol

18-Mar-2024

PMCID:	PMC10982427
doi:	10.3389/fmicb.2024.1342331
PMID:	38562478

Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China

Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T

J Ethnobiol Ethnomed

18-Mar-2024

PMCID:	PMC10946099
doi:	10.1186/s13002-024-00676-x
PMID:	38500123

Recent advances in the biosynthesis and industrial biotechnology of Gamma-amino butyric acid

Milon RB, Hu P, Zhang X, Hu X, Ren L

Bioresour Bioprocess

16-Mar-2024

PMCID:	PMC10992975
doi:	10.1186/s40643-024-00747-7

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Aminobenzaldehyde	11158	Click to see C1=CC(=CC=C1C=O)N	121.14	unknown	https://doi.org/10.1080/00021369.1978.10863028
> Benzenoids / Benzene and substituted derivatives / Styrenes
N-[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxyphenyl)prop-2-enamide	72957130	Click to see C1=CC(=CC=C1C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	299.32	unknown	https://doi.org/10.1080/00021369.1978.10863028
> 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/10.1080/00021369.1978.10863028
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453 https://doi.org/10.1080/00021369.1978.10863028
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3S,8R)-heptadeca-1,9-dien-4,6-diyne-3,8-diol	131954651	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1054450/
Falcarindiol	5281148	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1054450/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,4aS,7R,8aR)-7-(2-hydroxypropan-2-yl)-4a,8a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-2-ol	162946613	Click to see CC12CCC(CC1(CC(CC2)O)C)C(C)(C)O	240.38	unknown	https://doi.org/10.1139/V86-001
(3E,6E,10R)-2,6,10-trimethyldodeca-3,6,11-triene-2,10-diol	14414307	Click to see CC(=CCCC(C)(C=C)O)CC=CC(C)(C)O	238.37	unknown	https://doi.org/10.1139/V75-478
(3E,6E,10S)-2,6,10-Trimethyl-3,6,11-dodecatriene-2,10-diol	162975988	Click to see CC(=CCCC(C)(C=C)O)CC=CC(C)(C)O	238.37	unknown	https://doi.org/10.1139/V86-001
(3S,5R,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde	162916893	Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O	236.35	unknown	https://doi.org/10.1139/V86-001
(3S,6E,9R)-3,7,11-trimethyldodeca-1,6,10-triene-3,9-diol	163069129	Click to see CC(=CC(CC(=CCCC(C)(C=C)O)C)O)C	238.37	unknown	https://doi.org/10.1139/V86-001
[(Z,6R)-2-methyl-6-(4-methylcyclohexa-1,3-dien-1-yl)hept-2-enyl] 4-methylpentanoate	162905707	Click to see CC1=CC=C(CC1)C(C)CCC=C(C)COC(=O)CCC(C)C	318.50	unknown	https://doi.org/10.1007/BF00580069
10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-one	71364441	Click to see CC(=CC(=O)CC(=CCCC(C)(C=C)O)C)C	236.35	unknown	https://doi.org/10.1139/V86-001
2,6,10-Trimethyldodeca-3,6,11-triene-2,10-diol	78409367	Click to see CC(=CCCC(C)(C=C)O)CC=CC(C)(C)O	238.37	unknown	https://doi.org/10.1139/V86-001
3,7,11-Trimethyldodeca-1,6,10-triene-3,9-diol	71360372	Click to see CC(=CC(CC(=CCCC(C)(C=C)O)C)O)C	238.37	unknown	https://doi.org/10.1139/V86-001
7-(2-Hydroxypropan-2-yl)-4a,8a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-2-ol	162946612	Click to see CC12CCC(CC1(CC(CC2)O)C)C(C)(C)O	240.38	unknown	https://doi.org/10.1139/V86-001
8-Hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde	3504626	Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O	236.35	unknown	https://doi.org/10.1139/V86-001
CID 73331190	73331190	Click to see CC(=CC(=O)CC(=CCCC(C)(C=C)O)C)C	236.35	unknown	https://doi.org/10.1139/V86-001
Epilubimin	21594965	Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O	236.35	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
Lubimin	442383	Click to see CC1CC(CC(C12CCC(C2)C(=C)C)C=O)O	236.35	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
Solavetivone	442399	Click to see CC1CC(=O)C=C(C12CCC(C2)C(=C)C)C	218.33	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,5,6,7,8,8a-hexahydronaphthalen-2-one	162974264	Click to see CC1C2CC(CCC2(C=CC1=O)C)C(C)(C)O	236.35	unknown	https://doi.org/10.1139/V75-478
[1R-(1alpha,4aalpha,7alpha,8abeta)]-4a,5,6,7,8,8a-Hexahydro-7-(1-hydroxy-1-methylethyl)-1,4a-dimethyl-2(1H)-naphthalenone	15601417	Click to see CC1C2CC(CCC2(C=CC1=O)C)C(C)(C)O	236.35	unknown	https://doi.org/10.1139/V86-001
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol	521215	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1139/V86-001
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol	521216	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1139/V86-001
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1139/V86-001
Auberganol	85157952	Click to see CC1C(CCC2(C1CC(CC2)C(C)(C)O)C)O	240.38	unknown	https://doi.org/10.1139/V86-001
Aubergenone	15601418	Click to see CC1C2CC(CCC2(C=CC1=O)C)C(C)(C)O	236.35	unknown	https://doi.org/10.1139/V86-001
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1139/V86-001
beta-Eudesmol cis epimer	12309818	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1139/V86-001
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
24,25-Dihydrolanosterol	440560	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	428.70	unknown	https://doi.org/10.1007/BF02537347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol	5997	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1007/BF02537347
Lophenol	160482	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O	400.70	unknown	https://doi.org/10.1007/BF02537347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3S,8R,9S,13R)-9-ethyl-4,4,13,14-tetramethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,10,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	5316233	Click to see CCC12CCC3(C(CCC3(C1CCC4C2CCC(C4(C)C)O)C)C(C)CCCC(C)C)C	444.80	unknown	https://doi.org/10.1007/BF02537347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	145925700	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/10.1007/BF02537347
24-Methylene-cycloartanol	9547213	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1007/BF02537347
24-Methylenecycloartanol	94204	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1007/BF02537347
Cycloartanol	12760132	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	428.70	unknown	https://doi.org/10.1007/BF02537347
Cycloartenol	92110	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/10.1007/BF02537347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/BF02537347
24-Methylenecholesterol	92113	Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.1007/BF02537347
24-Methylenelophenol	5283640	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O	412.70	unknown	https://doi.org/10.1007/BF02537347
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/BF02537347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
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/10.1051/AGRO:19890701 https://doi.org/10.1016/S0031-9422(97)00323-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1S,2R,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'-oxane]-16-yl]oxyoxane-3,4,5-triol	162909232	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	https://doi.org/10.1007/BF00580069
(2R)-2-[(6S)-4-hydroxy-2-(hydroxymethyl)-6-[[(1R,2R,4R,6R,8S,9S,12R,13R)-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]-5-[(2R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	137704870	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)OC	1063.20	unknown	https://doi.org/10.3109/14756369309040765
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1S,2R,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'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	124867337	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1007/BF00580069
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18S)-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]methoxy]butyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	162996106	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1(CCC(C)COCC9C(C(C(C(O9)CO)O)O)O)O	1081.20	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-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'-oxane]-16-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	162933680	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1047.20	unknown	https://doi.org/10.1007/BF00580099
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163022502	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	740.90	unknown	https://doi.org/10.1007/BF00580069
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-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'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44452707	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	738.90	unknown	https://doi.org/10.1007/BF00580069
(2S,3R,4S,5S,6R)-2-[[(2R)-4-[(1R,2S,4S,6R,7S,8R,9S,12S,13S,16S,18S)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]methyl]-6-(hydroxymethyl)oxane-3,4,5-triol	163062825	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(C)COCC8C(C(C(C(O8)CO)O)O)O)O	935.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
(2S,3R,4S,5S,6R)-2-[[(2R)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-16-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]methyl]-6-(hydroxymethyl)oxane-3,4,5-triol	163028309	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(C)COCC8C(C(C(C(O8)CO)O)O)O)O	933.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
2-[[4-[16-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]methyl]-6-(hydroxymethyl)oxane-3,4,5-triol	163028308	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(C)COCC8C(C(C(C(O8)CO)O)O)O)O	933.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
2-[[4-[16-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]methyl]-6-(hydroxymethyl)oxane-3,4,5-triol	163062824	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(C)COCC8C(C(C(C(O8)CO)O)O)O)O	935.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
2-[3-Hydroxy-2-(hydroxymethyl)-6-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]butyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-16-yl]oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	162996105	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1(CCC(C)COCC9C(C(C(C(O9)CO)O)O)O)O	1081.20	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	73092197	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	738.90	unknown	https://doi.org/10.1007/BF00580069 https://doi.org/10.18388/ABP.1993_4873
Collettiside I	12314556	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	https://doi.org/10.1007/BF00580069
Dioscin	119245	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)OC1	869.00	unknown	https://doi.org/10.3109/14756369309040765
Disogluside	11827970	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	https://doi.org/10.18388/ABP.1993_4873 https://doi.org/10.1007/BF00580069
Melongoside F	192242	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	738.90	unknown	https://doi.org/10.1007/BF00580069 https://doi.org/10.18388/ABP.1993_4873
Melongoside G	131752997	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	887.10	unknown	https://doi.org/10.1007/BF00580069
Melongoside H	3826176	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1007/BF00580069
Melongoside K	131752992	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1047.20	unknown	https://doi.org/10.1007/BF00580099
Melongoside L	131752998	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)OC2C(C(C(C(O2)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1211.30	unknown	https://doi.org/10.1016/S0031-9422(00)80843-2
Melongoside M	131752991	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)OC2C(C(C(C(O2)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1	1209.30	unknown	https://doi.org/10.1016/S0031-9422(00)80843-2
Melongoside O	131750948	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)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	919.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
Melongoside P	131750951	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1067.20	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
Officinalisinin I	4483043	Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O	921.10	unknown	https://doi.org/10.1016/S0031-9422(00)81067-5
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/10.3109/14756369309040765
Schidigerasaponin D5	3272925	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1	740.90	unknown	https://doi.org/10.1007/BF00580069
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(97)00323-3
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/10.1051/AGRO:19890701
tigogenin 3-O-beta-D-glucopyranoside	22880514	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	578.80	unknown	https://doi.org/10.1007/BF00580069
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/BF02537347
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF02537347
24-Ethyllophenol	541368	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.1007/BF02537347
alpha1-Sitosterol	9548595	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C	426.70	unknown	https://doi.org/10.1007/BF02537347
Fucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/BF02537347
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/10.3109/14756369309040765
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/BF02537347 https://doi.org/10.3109/14756369309040765
Stigmasterol glucoside	6602508	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.3109/14756369309040765
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Vitamin D and derivatives
Cholecalciferol	5280795	Click to see CC(C)CCCC(C)C1CCC2C1(CCCC2=CC=C3CC(CCC3=C)O)C	384.60	unknown	https://doi.org/10.1016/S0031-9422(98)00246-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-(2-carboxyacetyl)oxy-4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,5-dihydroxycyclohexane-1-carboxylic acid	53496122	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)CC(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O	440.40	unknown	https://doi.org/10.1021/JF102963F
(1S,3R,4R,5R)-3-(2-carboxyacetyl)oxy-4-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid	162973772	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)CC(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O	440.40	unknown	https://doi.org/10.1021/JF102963F
(1S,3R,4R,5R)-3-(2-carboxyacetyl)oxy-5-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4-dihydroxycyclohexane-1-carboxylic acid	53495987	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)CC(=O)O	440.40	unknown	https://doi.org/10.1021/JF102963F
(1S,3R,4R,5R)-3-(2-carboxyacetyl)oxy-5-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4-dihydroxycyclohexane-1-carboxylic acid	163038885	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)CC(=O)O	440.40	unknown	https://doi.org/10.1021/JF102963F
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid	7067333	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1271/BBB1961.27.121
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1271/BBB1961.27.121
Chlorogensaure	12310830	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1271/BBB1961.27.121
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol	162890773	Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O	404.40	unknown	https://doi.org/10.1055/S-2006-957412
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone	75142	Click to see COC1=C(C=CC(=C1)C(=O)CCO)O	196.20	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[9-[2-(Furan-3-yl)-2-hydroxyethyl]-11-hydroxy-9,10,12-trimethyl-3-oxo-2-oxatricyclo[6.3.1.04,12]dodec-4-en-7-yl] acetate	162893641	Click to see CC1C(C2C3(C(C1(C)CC(C4=COC=C4)O)C(CC=C3C(=O)O2)OC(=O)C)C)O	404.50	unknown	https://doi.org/10.1016/S0300-483X(00)00202-X https://doi.org/10.1271/BBB.58.570
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Bilirubins
4E,15Z-Bilirubin IXa	21252250	Click to see CC1=C(NC(=C1CCC(=O)O)CC2=C(C(=C(N2)C=C3C(=C(C(=O)N3)C)C=C)C)CCC(=O)O)C=C4C(=C(C(=O)N4)C=C)C	584.70	unknown	https://doi.org/10.3358/SHOKUEISHI.37.5_295
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(R)-N-trans-Feruloyloctopamine	11151622	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	https://doi.org/10.1080/00021369.1978.10863028
N-[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide	74178121	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	329.30	unknown	https://doi.org/10.1080/00021369.1978.10863028
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/10.1080/00021369.1978.10863028
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-p-Coumaroyloctopamine	11185637	Click to see C1=CC(=CC=C1C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O	299.32	unknown	https://doi.org/10.1080/00021369.1978.10863028
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester	66883	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1080/00021369.1978.10863028
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/10.1080/00021369.1978.10863028
Ethyl caffeate	5317238	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1080/00021369.1978.10863028 https://doi.org/10.3186/JJPHYTOPATH.54.453
Ethyl ferulate	736681	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)OC	222.24	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	https://doi.org/10.1080/00021369.1978.10863028 https://doi.org/10.1271/BBB1961.42.623
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1271/BBB1961.27.121
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1080/00021369.1978.10863028
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1271/BBB1961.27.121
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1080/00021369.1978.10863028
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.3186/JJPHYTOPATH.54.453
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O	192.17	unknown	https://doi.org/10.1080/00021369.1978.10863028
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B4	147299	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/JF000549H
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,3',4',5,5',7-Hexahydroxyflavylium	128853	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	303.24	unknown	https://doi.org/10.1055/S-2006-957412

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Solanum melongena

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top