Momordica cochinchinensis

Details Top

Internal ID UUID643ff5f8c1f42347545950
Scientific name Momordica cochinchinensis
Authority Spreng.
First published in Syst. Veg. 3: 14 (1826)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Gac is most widely used in traditional Southeast Asian medicine as a topical preparation from its seed oil, while the leaves are occasionally brewed as a tea to help reduce fever. Among villages in northeastern Thailand, gac seed oil is rubbed on dry, inflamed skin, burns, and wounds (Boonsatean et al., 2022). In northern Vietnam and parts of southern China, the leaves are sometimes infused or decocted and taken to lower fever and ease minor inflammation (Nguyen and Vu, 2020; Nguyen et al., 2016). In India and Bangladesh, practitioners apply gac seed oil to the skin for eczema and minor dermatitis and mix it with honey to heal superficial wounds (Ali et al., 2017). Within the same region, the dark-red aril around the seeds is rarely used as a gentle, medicinal tea for cough relief or to calm sore throats (Ren et al., 2018).

A practical preparation can be made as a 1:5 ethanol tincture of gac seed oil. Measure 20 g of edible gac seed oil in a clean glass jar. Add 100 mL of 40% ethanol (about 1 cup), stir well, seal, and macerate in the dark for 14 days, shaking once or twice each day. Strain through cheesecloth and store in an amber bottle. For topical use, apply a few drops to clean, affected skin two to three times daily; do not ingest the tincture. Safety notes: because gac oil is highly pigmented, keep it away from clothing and skin exposed to sunlight to avoid staining; in rare cases it may irritate and should be discontinued if redness increases. Pregnant and breastfeeding individuals should avoid oral use; consult a qualified practitioner before internal use.

Well-established phytochemicals in gac seed oil and aril plausibly support these uses. The oil is unusually rich in beta‑carotene and lycopene, and in tocopherols and tocotrienols (vitamin E), all of which have long been studied for antioxidant, skin‑protective, and anti‑inflammatory actions (Stahl and Sies, 2005; Vuong et al., 2014). The aril also contains these pigments, consistent with the gentle tea used for cough.

Modern relevance: gac seed oil is widely available in Southeast Asian markets and increasingly online, and clinical trials are exploring its eye‑health benefits, while traditional topical and leaf‑tea practices persist (Do et al., 2014).

General Uses Top

Suggest a correction!

Common products:
Aril-based food colorant (gac powder, gac paste, and gac oil) from Momordica cochinchinensis is used to impart a deep red hue and a mild, neutral aroma to rice dishes (e.g., xôi gấc), sticky rice wine, beverages, ice cream, and bakery icings. Seed oil is marketed for cosmetic use.

Industrial and craft applications:
Limited; the plant is primarily processed to separate the aril for colorant production and the seeds for oil pressing.

Food and beverages (non-medicinal):
Aril fractions (with seeds or seed-free) are sun- or tray-dried and milled into powder or converted into oil. Products include natural food colorants and specialty fats for confectionery and bakery applications. Gac powder is standardized to carotenoid content and used in instant foods and beverages; the oil is used as an edible fat where a red hue is desired.

Colorants and tanning:
The aril is a natural reddish-orange colorant rich in beta-carotene and lycopene, used in the above food applications. No documented tanning use.

Wood and fiber:
No documented timber or fiber use.

Fragrance and cosmetics:
Cold-pressed seed oil is used in cosmetic formulations for skin care and anti-aging products due to its high beta-carotene and lycopene content, which provide emollient properties and antioxidant capacity. The aril powder is also employed as a natural pigment in lip and cheek color products.

Properties relevant to use:
- Aril colorant: high beta-carotene and lycopene levels yield intense orange–red hues stable at low to moderate pH and light; heat and oxygen degrade pigments.
- Seed oil: typical fatty-acid profile includes high oleic and linoleic acids with beta-carotene; saponification and iodine values are reported in analytical literature for edible oils; refractive index and peroxide value are used for quality control. No speculation.

Standards and regulation:
In Vietnam, national food safety regulations apply to gac colorant products (Circular 27/2012/TT-BYT and related). For edible oils in international trade, relevant specifications include ISO 660 (edible vegetable and animal oils—determination of acid value) and ISO 3960 (peroxide value); for food safety management, ISO 22000 (food safety management systems) is applicable. Cosmetic formulations and colorants must comply with regional cosmetics rules (e.g., ASEAN Cosmetic Directive; EU Regulation (EC) No 1223/2009), including permitted colorants and safety assessments.

Sustainability and sourcing:
Cultivated extensively in Southeast Asia, including Vietnam and Thailand, where it is grown in home gardens and smallholder farms. Primary supply is from fruit aril and seed fractions after fruit processing; agronomic sustainability is enhanced by low-input cultivation, integration into mixed cropping systems, and community-level drying/processing operations.

Synonyms Top

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

Add a new one! Suggest a correction!

Language Common/alternative name
English balsam pear
English gac
English balsampear
Spanish gac
Arabic جاك (فاكهة)
Assamese হাতী কেৰেলা
Assamese ভাত কেৰেলা
Azerbaijani koxinxin momordikası
Azerbaijani koxinxin momordiki
azb کوخینخین موموردیکی
German gac
Esperanto gako
Persian کدو خاردار
French gac
Indonesian pupia
Indonesian tepurang
Japanese ナンバンカラスウリ
Korean
lad gac
lbe Гак
lzh 木鱉子
Malayalam മുള്ളൻ പാവൽ
mrj Гак
Polish przepękla indochińska
Polish gac
Russian Гак
szy nipaluma-sukuy
Telugu అడవికాకర
Thai ฟักข้าว
udm Гак
Vietnamese gấc
Vietnamese cây gấc
Yoruba gac
Chinese 一种维管植物
Chinese 老鼠拉冬瓜
Chinese 番木鳖
Chinese 木鳖
Chinese 大叶木鳖子
Chinese 木虌子
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

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!
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
    • China
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • 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

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
Risk assessment of Retithrips syriacus for the EU 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, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
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
Brain acetylcholinesterase activity and the protective effect of Gac fruit on scopolamine-induced memory impairment in adult zebrafish Singsai K, Saksit N, Chaikhumwang P IBRO Neurosci Rep 17-Feb-2024
PMCID:PMC10904921
doi:10.1016/j.ibneur.2024.02.004
PMID:38435743
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
Discovery and Characterization of a Dual-Function Peptide Derived from Bitter Gourd Seed Protein Using Two Orthogonal Bioassay-Guided Fractionations Coupled with In Silico Analysis Hung WT, Sutopo CC, Wu ML, Hsu JL Pharmaceuticals (Basel) 20-Nov-2023
PMCID:PMC10674851
doi:10.3390/ph16111629
PMID:38004494
A review of the research progress on Pinellia ternata (Thunb.) Breit.: Botany, traditional uses, phytochemistry, pharmacology, toxicity and quality control Zou T, Wang J, Wu X, Yang K, Zhang Q, Wang C, Wang X, Zhao C Heliyon 14-Nov-2023
PMCID:PMC10696046
doi:10.1016/j.heliyon.2023.e22153
PMID:38058630
Natural Sources of Food Colorants as Potential Substitutes for Artificial Additives Vega EN, Ciudad-Mulero M, Fernández-Ruiz V, Barros L, Morales P Foods 12-Nov-2023
PMCID:PMC10670170
doi:10.3390/foods12224102
PMID:38002160
Comprehensive Update on Carotenoid Colorants from Plants and Microalgae: Challenges and Advances from Research Laboratories to Industry Rodriguez-Amaya DB, Esquivel P, Meléndez-Martínez AJ Foods 10-Nov-2023
PMCID:PMC10670565
doi:10.3390/foods12224080
PMID:38002140
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945

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 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 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 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 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 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 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 779.00 unknown https://doi.org/10.1016/0031-9422(88)80773-8
3-O-xylyl(1-3)glucosiduronic acid-oleanolic acid-28-O-glucoside 14162553 Click to see 927.10 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 795.00 unknown https://doi.org/10.1016/0031-9422(88)80773-8
Calendulaglycoside F 5104673 Click to see 632.80 unknown https://doi.org/10.1016/0031-9422(88)80773-8
Hemsloside Ma 2 14162569 Click to see 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 941.10 unknown https://doi.org/10.1016/0031-9422(88)80773-8
Momordin I 14162549 Click to see 764.90 unknown https://doi.org/10.1016/0031-9422(88)80773-8
Momordin Ia 14162560 Click to see 779.00 unknown https://doi.org/10.1016/0031-9422(88)80773-8
Momordin Ie 14162563 Click to see 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
rel-(3aR,4aR,5S,8aR,9aR)-5-Hydroxy-5,8a-dimethyl-3-methylenedecahydronaphtho[2,3-b]furan-2(3H)-one 10332357 Click to see 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 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 456.70 unknown https://doi.org/10.1248/YAKUSHI1881.55.5_467
Oleanolic Acid 10494 Click to see 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 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 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 180.16 unknown https://doi.org/10.1248/CPB.33.1
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.1248/CPB.33.1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
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
D(+)-Glucose 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
> 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

Gallery Top

We don't have an image yet. Upload an image!

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.