Momordica balsamina

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID643ff5f950379113485396
Scientific name	Momordica balsamina
Authority	L.
First published in	Sp. Pl. : 1009 (1753)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Momordica garriepensis	Arn.	J. Bot. (Hooker) 3: 277 (1841)
Momordica huberi	Tod.	Giorn. Reale Ist. Incoragg. Agric. Sicilia , ser. 3, 1: 165 (1863)
Nevrosperma cuspidata	Raf.	Amer. Monthly Mag. & Crit. Rev. 2: 40 (1818)
Momordica involucrata	E.Mey.	Fl. Cap. 2: 491 (1862)
Momordica schinzii	Cogn. ex Schinz	Verh. Bot. Vereins Prov. Brandenburg 30: 149 (1888)

Common names Top

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Filter by language:

Language	Common/alternative name
English	southern balsampear
Afrikaans	laloentjie
Arabic	مغض
Arabic	تفاح العجائب
Arabic	بيلسان
Arabic	مليح
Arabic	معضوضة بلسمية
ban	paya alas
Hausa	garafuni
Hebrew	לעוסית מטפסת
Malayalam	കാട്ടുപാവൽ
Polish	przepękla pospolita
Polish	balsamka pospolita
Portuguese	nkaka
Portuguese	cacana
Russian	Момордика бальзамическая
Chinese	胶苦瓜

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

Africa click to expand
- East Tropical Africa
  - Tanzania
- Northeast Tropical Africa
  - Chad
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- Northern Africa
  - Tunisia
- South Tropical Africa
  - Angola
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Caprivi Strip
  - Free State
  - Kwazulu-Natal
  - Namibia
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Benin
  - Burkina
  - Mali
  - Mauritania
  - Niger
  - Nigeria
  - Senegal
- West-central Tropical Africa
  - Cameroon

Asia-temperate click to expand
- Arabian Peninsula
  - Oman
  - Saudi Arabia
  - Yemen
- Western Asia
  - Palestine

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Nepal
  - Pakistan

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - South Australia
  - Western Australia

Northern America click to expand
- Mexico
  - Mexico Northwest
- North-central U.S.A.
  - Oklahoma
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Louisiana

Pacific click to expand
- South-central Pacific
  - Tuamotu

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Windward Islands
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000376910
UNII	P5JFB9U0GM
Florida Plant Atlas	1746
USDA Plants	MOBA
Tropicos	9200483
INPN	630179
KEW	urn:lsid:ipni.org:names:293397-1
The Plant List	kew-2372858
Open Tree Of Life	955518
Observations.org	119881
NCBI Taxonomy	3672
Nature Serve	2.129243
IPNI	293397-1
iNaturalist	165503
GBIF	2874582
Freebase	/m/025xlv4
EPPO	MOMBA
EOL	584305
Elurikkus	322953
USDA GRIN	24519
Wikipedia	Momordica_balsamina

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

Binding Pattern and Structural Interactome of the Anticancer Drug 5-Fluorouracil: A Critical Review

Lin ES, Huang CY

Int J Mol Sci

17-Mar-2024

PMCID:	PMC10970046
doi:	10.3390/ijms25063404
PMID:	38542377

Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan

Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW

Plants (Basel)

14-Mar-2024

PMCID:	PMC10974405
doi:	10.3390/plants13060832
PMID:	38592859

Tissue Inhibitor of Metalloproteinase 3: Unravelling Its Biological Function and Significance in Oncology

Lee WT, Wu PY, Cheng YM, Huang YF

Int J Mol Sci

10-Mar-2024

PMCID:	PMC10970424
doi:	10.3390/ijms25063191
PMID:	38542164

Investigation of phytochemicals isolated from selected Saudi medicinal plants as natural inhibitors of SARS CoV-2 main protease: In vitro, molecular docking and simulation analysis

Alharbi YT, Abdel-Mageed WM, Basudan OA, Mothana RA, Tabish Rehman M, ElGamal AA, Alqahtani AS, Fantoukh OI, AlAjmi MF

Saudi Pharm J

08-Mar-2024

PMCID:	PMC10973196
doi:	10.1016/j.jsps.2024.102023
PMID:	38550333

High-quality Momordica balsamina genome elucidates its potential use in improving stress resilience and therapeutic properties of bitter gourd

Vinay ND, Singh K, Ellur RK, Chinnusamy V, Jaiswal S, Iquebal MA, Munshi AD, Matsumura H, Boopalakrishnan G, Jat GS, Kole C, Gaikwad AB, Kumar D, Dey SS, Behera TK

Front Plant Sci

24-Jan-2024

PMCID:	PMC10851156
doi:	10.3389/fpls.2023.1258042
PMID:	38333042

Whitefly-Transmitted Viruses of Cucurbits in the Southern United States

Devendran R, Kavalappara SR, Simmons AM, Bag S

Viruses

20-Nov-2023

PMCID:	PMC10675411
doi:	10.3390/v15112278
PMID:	38005954

Exploring the Use of Indigenous Wild Vegetables by the Basotho People of Southern Africa: A Comprehensive Review of the Literature and Nutritional Analysis of Selected Species

Tshikororo RR, Ajao AA, Moteetee AN

Foods

20-Jul-2023

PMCID:	PMC10378859
doi:	10.3390/foods12142763
PMID:	37509855

Nutritional values of wild edible freshwater macrophytes

Zakaria MH, Ramaiya SD, Bidin N, Syed NN, Bujang JS

PeerJ

11-Jul-2023

PMCID:	PMC10348304
doi:	10.7717/peerj.15496
PMID:	37456903

Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens

Kernou ON, Azzouz Z, Madani K, Rijo P

Molecules

22-May-2023

PMCID:	PMC10220798
doi:	10.3390/molecules28104243
PMID:	37241981

Yarrowia lipolytica as a Platform for Punicic Acid Production

Urbanikova V, Park YK, Krajciova D, Tachekort M, Certik M, Grigoras I, Holic R, Nicaud JM, Gajdos P

Int J Mol Sci

16-May-2023

PMCID:	PMC10219088
doi:	10.3390/ijms24108823
PMID:	37240172

Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium

Almuzaini AM

Front Vet Sci

16-May-2023

PMCID:	PMC10228746
doi:	10.3389/fvets.2023.1188752
PMID:	37261108

Gummy stem blight: One disease, three pathogens

Seblani R, Keinath AP, Munkvold G

Mol Plant Pathol

02-May-2023

PMCID:	PMC10346371
doi:	10.1111/mpp.13339
PMID:	37129449

Anti-human immunodeficiency virus-1 activity of MoMo30 protein isolated from the traditional African medicinal plant Momordica balsamina

Khan M, Diop A, Gbodossou E, Xiao P, Coleman M, De Barros K, Duong H, Bond VC, Floyd V, Kondwani K, Rice VM, Harris-Hooker S, Villinger F, Powell MD

Virol J

22-Mar-2023

PMCID:	PMC10035133
doi:	10.1186/s12985-023-02010-5
PMID:	36949470

Carotenoid Content and Profiles of Pumpkin Products and By-Products

Ninčević Grassino A, Rimac Brnčić S, Badanjak Sabolović M, Šic Žlabur J, Marović R, Brnčić M

Molecules

15-Jan-2023

PMCID:	PMC9861221
doi:	10.3390/molecules28020858
PMID:	36677916

A systematic analysis of anti-diabetic medicinal plants from cells to clinical trials

Omale S, Amagon KI, Johnson TO, Bremner SK, Gould GW

PeerJ

05-Jan-2023

PMCID:	PMC9826616
doi:	10.7717/peerj.14639
PMID:	36627919

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(1R,4S,5S,8R,9R,12S,13S,16S)-8-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol	46882748	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)O)OC4)C)C	456.70	unknown	https://doi.org/10.1021/NP900457U https://doi.org/10.1016/J.BMC.2010.05.054
(1S,4S,5S,8R,9R,12S,13S,16S)-8-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol	163044502	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)O)OC4)C)C	456.70	unknown	https://doi.org/10.1021/NP900457U
(1S,4S,5S,8R,9R,13S,16S)-8-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol	163187649	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)O)OC4)C)C	456.70	unknown	https://doi.org/10.1021/NP900457U
(2R,3R,4R,5S,6R)-2-[[(3S,4S,7S,8R,9S,10S,13R,14S,17R)-3-hydroxy-4-(hydroxymethyl)-17-[(E,2R)-6-methoxy-6-methylhept-4-en-2-yl]-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163195247	Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C	650.90	unknown	https://doi.org/10.1055/S-0029-1234299
(3S,4S,7R,8R,9S,10S,13R,14S,17R)-17-[(2R,4R,5R)-4,5-dihydroxy-6-methylhept-6-en-2-yl]-4-(hydroxymethyl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	163086446	Click to see CC(CC(C(C(=C)C)O)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	490.70	unknown	https://doi.org/10.1021/NP900457U
(3S,4S,7R,8R,9S,10S,13R,14S,17R)-4-(hydroxymethyl)-17-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	163047238	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	474.70	unknown	https://doi.org/10.1021/NP900457U
(3S,4S,7R,8R,9S,10S,13R,14S,17R)-4-(hydroxymethyl)-17-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-7-methoxy-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	162965756	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)OC)C)C)C	488.70	unknown	https://doi.org/10.1021/NP900457U
(3S,7S,8R,9S,10S,13R,14S,17R)-17-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	25016665	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)O)O)C)C)C	458.70	unknown	https://doi.org/10.1021/NP900457U https://doi.org/10.1016/J.BMC.2010.05.054
17-(4-hydroxy-6-methylhept-5-en-2-yl)-7-methoxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	73241660	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)O)OC)C)C)C	472.70	unknown	https://doi.org/10.1055/S-0029-1234299
17-(4,5-dihydroxy-6-methylhept-6-en-2-yl)-4-(hydroxymethyl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	75080821	Click to see CC(CC(C(C(=C)C)O)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	490.70	unknown	https://doi.org/10.1021/NP900457U
17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	162988309	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)O)O)C)C)C	458.70	unknown	https://doi.org/10.1021/NP900457U
17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7,12-triol	75080824	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(C(CC3(C2C(C=C4C3CCC(C4(C)C)O)O)C)O)C)C	474.70	unknown	https://doi.org/10.1021/NP900457U
17-(6-hydroxy-6-methylhept-4-en-2-yl)-7-methoxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,12-diol	75080899	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(C(CC3(C2C(C=C4C3CCC(C4(C)C)O)OC)C)O)C)C	488.70	unknown	https://doi.org/10.1021/NP900457U
2-[[3-hydroxy-4-(hydroxymethyl)-17-(6-methoxy-6-methylhept-4-en-2-yl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163027899	Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C	650.90	unknown	https://doi.org/10.1055/S-0029-1234299
3-Hydroxy-17-(4-hydroxy-6-methylhept-5-en-2-yl)-4,4,9,13,14-pentamethyl-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	75251932	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)C)O)C)C)C	456.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
3-Hydroxy-4-(hydroxymethyl)-4,9,13,14-tetramethyl-17-(6-methyl-4-oxohept-5-en-2-yl)-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	75251931	Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)CO)O)C)C)C	470.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
4-(hydroxymethyl)-17-(4-hydroxy-6-methylhept-5-en-2-yl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	75080822	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	474.70	unknown	https://doi.org/10.1021/NP900457U
4-(hydroxymethyl)-17-(4-hydroxy-6-methylhept-5-en-2-yl)-7-methoxy-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol	75080823	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)OC)C)C)C	488.70	unknown	https://doi.org/10.1021/NP900457U
4-(hydroxymethyl)-17-(6-hydroxy-6-methylhept-4-en-2-yl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	75178498	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	474.70	unknown	https://doi.org/10.1055/S-0029-1234299
4-(hydroxymethyl)-17-(6-methoxy-6-methylhept-4-en-2-yl)-4,9,13,14-tetramethyl-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,7-diol	75068226	Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	488.70	unknown	https://doi.org/10.1055/S-0029-1234299
8-(4-Hydroxy-6-methylhept-5-en-2-yl)-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol	75225001	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)O)OC4)C)C	456.70	unknown	https://doi.org/10.1021/NP900457U
Balsaminagenin A	46226691	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	474.70	unknown	https://doi.org/10.1055/S-0029-1234299 https://doi.org/10.1016/J.BMC.2010.05.054
Balsaminagenin B	44555453	Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	488.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054 https://doi.org/10.1055/S-0029-1234299
Balsaminapentaol	44607275	Click to see CC(CC(C(C(=C)C)O)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	490.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054 https://doi.org/10.1021/NP900457U
Balsaminol A	44607276	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)O)C)C)C	474.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054 https://doi.org/10.1021/NP900457U
Balsaminol B	44607277	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)CO)O)OC)C)C)C	488.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054 https://doi.org/10.1021/NP900457U
Balsaminol C	52947022	Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)CO)O)C)C)C	470.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
Balsaminol E	46912852	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)C)O)C)C)C	456.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
Balsaminoside A	44555454	Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C	634.90	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
Cucurbalsaminol A	44607278	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(C(CC3(C2C(C=C4C3CCC(C4(C)C)O)O)C)O)C)C	474.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054 https://doi.org/10.1021/NP900457U
Cucurbalsaminol B	44607451	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(C(CC3(C2C(C=C4C3CCC(C4(C)C)O)OC)C)O)C)C	488.70	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
Karavilagenin C	46182790	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)O)OC)C)C)C	472.70	unknown	https://doi.org/10.1055/S-0029-1234299
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
3-Hydroxy-4-(hydroxymethyl)-4,9,13,14-tetramethyl-17-(4-oxopentan-2-yl)-1,2,3,8,10,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one	75970000	Click to see CC(CC(=O)C)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)CO)O)C)C)C	430.60	unknown	https://doi.org/10.1016/J.BMC.2010.05.054
Balsaminol D	52947048	Click to see CC(CC(=O)C)C1CCC2(C1(CCC3(C2C(=O)C=C4C3CCC(C4(C)CO)O)C)C)C	430.60	unknown	https://doi.org/10.1016/J.BMC.2010.05.054

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Momordica balsamina

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