Scientific name	Authority	First published in
Momordica suringarii	Cogn.	Monogr. Phan. 3: 434 (1881)
Muricia cochinchinensis	Lour.	Fl. Cochinch. : 596 (1790)
Momordica ovata	Cogn.	Monogr. Phan. 3: 446 (1881)
Momordica meloniflora	Hand.-Mazz.	Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 58: 94 (1921)
Momordica mixta	Roxb.	Fl. Ind. ed. 1832 , 3: 709 (1832)
Momordica sphaeroidea	Blanco	Fl. Filip. : 771 (1837)
Momordica macrophylla	Gage	Rec. Bot. Surv. India 3: 61 (1905)
Zucca commersoniana	Ser.	Prodr. 3: 319 (1828)

Common names Top

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Filter by language:

Language	Common/alternative name
English	balsampear
Arabic	جاك (فاكهة)
Assamese	ভাত কেৰেলা
Azerbaijani	koxinxin momordiki
azb	کوخینخین موموردیکی
German	gac
Esperanto	gako
Persian	کدو خاردار
Indonesian	pupia
Indonesian	tepurang
Japanese	ナンバンカラスウリ
Korean	걱
lbe	Гак
lzh	木鱉子
Malayalam	മുള്ളൻ പാവൽ
mrj	Гак
Polish	gac
Polish	przepękla indochińska
Russian	Гак
szy	nipaluma-sukuy
Telugu	అడవికాకర
Thai	ฟักข้าว
udm	Гак
Vietnamese	cây gấc
Vietnamese	gấc
Chinese	木鳖果
Chinese	木鱉果
Chinese	木鱉子
Chinese	糯饭果
Chinese	木鳖子根
Chinese	木鳖子*(木鳖）
Chinese	木鳖子
Chinese	木鳖
Chinese	木虌子
Chinese	大叶木鳖子
Chinese	番木鳖
Chinese	老鼠拉冬瓜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  - Tibet
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - Queensland

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000376897
UNII	9A41EKO05F
USDA Plants	MOCO5
Tropicos	9201691
INPN	706544
KEW	urn:lsid:ipni.org:names:293419-1
The Plant List	kew-2372841
Open Tree Of Life	955547
NCBI Taxonomy	3674
IPNI	293419-1
iNaturalist	431329
GBIF	2874580
Freebase	/m/02pybmt
EPPO	MOMCO
EOL	483972
USDA GRIN	24521
Wikipedia	Gac

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

A phage-displayed disulfide constrained peptide discovery platform yields novel human plasma protein binders

Gao X, Kaluarachchi H, Zhang Y, Hwang S, Hannoush RN

PLoS One

28-Mar-2024

PMCID:	PMC10977726
doi:	10.1371/journal.pone.0299804
PMID:	38547072

Nucleation of a key beta-turn promotes cyclotide oxidative folding

Tian S, de Veer SJ, Durek T, Wang CK, Craik DJ

J Biol Chem

01-Mar-2024

PMCID:	PMC10999817
doi:	10.1016/j.jbc.2024.107125
PMID:	38432638

The complete chloroplast genome sequence of Thladiantha nudiflora Hemsl. ex F.B.Forbes & Hemsl. 1887 (Cucurbitaceae)

Zhao YY, Chen MM, Duan BL, Xie QZ, Miao Q

Mitochondrial DNA B Resour

25-Jan-2024

PMCID:	PMC10812858
doi:	10.1080/23802359.2024.2305402
PMID:	38282981

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Prior Infection by Colletotrichum spinaciae Lowers the Susceptibility to Infection by Powdery Mildew in Common Vetch

Li F, Zhu R, Gao F, Duan T

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780821
doi:	10.3390/plants13010052
PMID:	38202360

Gongying-Jiedu-Xiji recipe promotes the healing of venous ulcers by inhibiting ferroptosis via the CoQ-FSP1 axis

Lu Y, Zhao D, Liu M, Cao G, Liu C, Yin S, Song R, Ma J, Sun R, Wu Z, Liu J, Wang Y

Front Pharmacol

15-Dec-2023

PMCID:	PMC10755008
doi:	10.3389/fphar.2023.1291099
PMID:	38161691

The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer

Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J

Medicina (Kaunas)

14-Dec-2023

PMCID:	PMC10745032
doi:	10.3390/medicina59122169
PMID:	38138272

Response Surface Methodology to Optimize the Extraction of Carotenoids from Horticultural By-Products—A Systematic Review

Cano-Lamadrid M, Martínez-Zamora L, Mozafari L, Bueso MC, Kessler M, Artés-Hernández F

Foods

12-Dec-2023

PMCID:	PMC10742715
doi:	10.3390/foods12244456
PMID:	38137260

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

DMMIC derivatization-assisted liquid chromatography-mass spectrometry method for metabolite profiling of the glutathione anabolic pathway in esophageal cancer tissues and cells

Liu L, Lu YH, Wang MD, Zhao QF, Chen XP, Yin H, Feng CG, Zhang F

J Pharm Anal

22-Sep-2023

PMCID:	PMC10759256
doi:	10.1016/j.jpha.2023.08.016
PMID:	38174115

Non-Canonical Amino Acids in Analyses of Protease Structure and Function

Goettig P, Koch NG, Budisa N

Int J Mol Sci

13-Sep-2023

PMCID:	PMC10531186
doi:	10.3390/ijms241814035
PMID:	37762340

Momordicae Semen inhibits migration and induces apoptotic cell death by regulating c-Myc and CNOT2 in human pancreatic cancer cells

Jee W, Ko HM, Park DI, Park YR, Park SM, Kim H, Na YC, Jung JH, Jang HJ

Sci Rep

07-Aug-2023

PMCID:	PMC10406802
doi:	10.1038/s41598-023-39840-w
PMID:	37550432

Anticancer and Antimutagenic Properties of Pogonatherum paniceum on Colorectal Cancer Cells

Praphasawat R, Thakaew S, Rawangkan A, Thongboontho R, Sooksaen P, Laovittayangkoon S, Klajing W, Jaengpromma P, Kunsorn P, Suwannalert P, Payuhakrit W

World J Oncol

04-Aug-2023

PMCID:	PMC10409559
doi:	10.14740/wjon1602
PMID:	37560340

Exploring the Apoptotic-Induced Biochemical Mechanism of Traditional Thai Herb (Kerra™) Extract in HCT116 Cells Using a Label-Free Proteomics Approach

Siriwaseree J, Yingchutrakul Y, Samutrtai P, Aonbangkhen C, Srathong P, Krobthong S, Choowongkomon K

Medicina (Kaunas)

27-Jul-2023

PMCID:	PMC10456832
doi:	10.3390/medicina59081376
PMID:	37629666

Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications

Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD

Molecules

18-Jun-2023

PMCID:	PMC10301071
doi:	10.3390/molecules28124838
PMID:	37375393

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
> Alkaloids and derivatives / Yohimbine alkaloids
methyl (1S,3R,4R,4aS,5aS,6R,10aR)-3-hydroxy-1-methyl-2'-oxospiro[1,3,4,4a,5,5a,7,8,10,10a-decahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate	162997621	Click to see CC1C2CN3CCC4(C3CC2C(C(O1)O)C(=O)OC)C5=CC=CC=C5NC4=O	386.40	unknown	https://doi.org/10.1055/S-2007-969448
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid	163101946	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C	1059.20	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-4,5-bis[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy]oxane-2-carboxylic acid	163101948	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C	1059.20	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	124518866	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	795.00	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid	163067024	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)O)C	897.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-4,5-bis[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy]oxane-2-carboxylic acid	163067025	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)O)C	897.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	124485166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C	632.80	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid	163009493	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)O)C	764.90	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(2S,3S,4S,5R,6R)-6-[[(3S,4aS,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid	163012545	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4S,5S,6S)-3,5-dihydroxy-6-methoxycarbonyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162892523	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)O)C	779.00	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	13909679	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C	795.00	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid	14162553	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Calendulaglycoside F	5104673	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C	632.80	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Hemsloside Ma 2	14162569	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C	1059.20	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylate	162980717	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	941.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Momordin I	14162549	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)O)C	764.90	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Momordin Ia	14162560	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)O)C	779.00	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Momordin Ie	14162563	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)O)C	897.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Momordin II	102004719	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
Momordin Ii (oleanolic Acid)	188370	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	https://doi.org/10.1248/CPB.33.1 https://doi.org/10.1016/0031-9422(88)80773-8
momordine I	44202126	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)O)C	764.90	unknown	https://doi.org/10.1248/BPB.21.1231 https://doi.org/10.1248/CPB.33.1 https://doi.org/10.1016/0031-9422(88)80773-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aR,5S,8aR,9aR)-5-hydroxy-5,8a-dimethyl-3-methylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one	10332357	Click to see CC12CCCC(C1CC3C(C2)OC(=O)C3=C)(C)O	250.33	unknown	https://doi.org/10.1016/0031-9422(88)80773-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aS,10S,12aS,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-12-oxo-3,4,5,6,6a,7,8,8a,10,11,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	162980132	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1016/S0040-4039(01)89294-7
10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-12-oxo-3,4,5,6,6a,7,8,8a,10,11,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	14489124	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1016/S0040-4039(01)89294-7
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/YAKUSHI1881.55.5_467
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/YAKUSHI1881.55.5_467
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Chondrillasterol	5283663	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1055/S-2007-969046
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside	1115	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1248/CPB.33.1
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1248/CPB.33.1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose	5984	Click to see C(C(C(C(C(=O)CO)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.33.1
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.33.1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.33.1
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.33.1
> Organoheterocyclic compounds / Naphthopyrans
(2S,4AR,6aR,7R,10R,10aS,10bS)-2-(furan-3-yl)-7-hydroxy-6a,10b-dimethyl-4a,5,6,6a,7,10,10a,10b-octahydro-1H-10,7-(epoxymethano)benzo[f]isochromene-4,12(2H)-dione	442015	Click to see CC12CCC3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5	358.40	unknown	https://doi.org/10.1055/S-2007-969448

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Momordica cochinchinensis

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