Details Top

Internal ID UUID64405c225eaa3908653845
Scientific name Marah fabacea
Authority (Naudin) Greene
First published in Leafl. Bot. Observ. Crit. 2: 36 (1910)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Marah fabacea (synonym of Marah macrocarpa) yields a starchy tuber that, after processing, is ground into flour. The tuber is harvested in early spring, cut into pieces, soaked in water for several days to leach out bitter cucurbitacin compounds, boiled or roasted until soft, dried, and milled to produce a flour used in traditional carbohydrate foods.

Industrial and craft applications:
The woody stems are used as a source of bast fiber. After the stems are cut and the outer bark removed, the inner fibers are split and twisted into rope. Historically, the rope has been employed for tying bundles, constructing fishing nets, and other cordage needs.

Food and beverages (non‑medicinal):
Processed tuber flour is incorporated into porridges, flatbreads, and as a thickener in sauces. The flour swells and forms a viscous gel when cooked, providing texture and binding properties. No commercial production of the flour has been reported; its use remains within traditional food practices.

Wood and fiber:
Although the plant does not produce timber, the stems supply bast fibers for rope. The fibers consist primarily of cellulose within a lignin matrix, giving the rope tensile strength and modest resistance to decay.

Properties relevant to use:
The tuber contains a high proportion of starch that forms a gel upon cooking, making it suitable for flour. Leaching removes water‑soluble cucurbitacin glycosides, eliminating bitterness and reducing mild toxicity. The bast fibers are long and rich in cellulose, with lignin providing structural integrity for cordage applications.

Standards and regulation:
No species‑specific standards exist for Marah fabacea starch or fiber. Where marketed, general food safety regulations (e.g., Codex Alimentarius for flour) and textile standards (e.g., ASTM D1425 for rope tensile testing) apply.

Sustainability and sourcing:
Marah fabacea is wild‑harvested across arid and semi‑arid habitats of western North America. Populations are generally stable, but selective harvesting of tubers can deplete local stands. Sustainable practices—such as allowing regrowth, avoiding over‑harvest, and protecting habitats—are recommended to maintain long‑term availability. Because Marah fabacea is a perennial, its tuber regrows annually, allowing limited harvest while preserving the plant.

Synonyms Top

Scientific name Authority First published in
Echinocystis fabacea Naudin Ann. Sci. Nat., Bot. , sér. 4, 12: 154 (1859)
Echinocystis fabacea var. inermis Jeps. Fl. Calif. 2: 554 (1936)
Echinocystis inermis Congdon Zoe 5: 134 (1901)
Echinocystis scabrida Eastw. Bull. Torrey Bot. Club 30: 500 (1903)
Micrampelis fabacea (Naudin) Greene Pittonia 2: 129 (1890)
Micrampelis fabacea var. agrestis Greene Fl. Francisc. : 236 (1891)
Megarrhiza californica Torr. Pacif. Railr. Rep. Stevens, Bot. 12(2): 61 (1860)
Marah fabacea var. agrestis (Greene) Stocking Madroño 13: 130 (1955)
Marah inermis (Congdon) Dunn Bull. Misc. Inform. Kew 1913: 153 (1913)
Micrampelis fabaceus var. agrestis Greene Fl. Francisc. : 236 (1891)
Echinocystis fabacea var. agrestis Congdon Zoe 5: 133 (1901)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001300992
Tropicos 9200469
KEW urn:lsid:ipni.org:names:152827-2
The Plant List tro-9200469
Open Tree Of Life 696888
NCBI Taxonomy 329128
IPNI 152827-2
iNaturalist 205330
GBIF 3622328
Freebase /m/02x1_5
EOL 584299
Calflora (Californian flora) 11820
USDA GRIN 455995
Wikipedia Marah_fabacea
CMAUP NPO8562

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_043882805.1 ddMarFaba1.0.p Scaffold University of California, Santa Cruz 2024-10-25 22 1.00 Gb

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
Arabidopsis Phototropins Participate in the Regulation of Dark-Induced Leaf Senescence Eckstein A, Grzyb J, Hermanowicz P, Zgłobicki P, Łabuz J, Strzałka W, Dziga D, Banaś AK Int J Mol Sci 12-Feb-2021
PMCID:PMC7918785
doi:10.3390/ijms22041836
PMID:33673252
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Ethylene Stimulates Nutations That Are Dependent on the ETR1 Receptor Binder BM, O'Malley RC, Wang W, Zutz TC, Bleecker AB Plant Physiol 01-Dec-2006
PMCID:PMC1676061
doi:10.1104/pp.106.087858
PMID:17071649
Flavonoids of Marah oreganus K. W. Nicholls, B. A. Bohm American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50022A016
Bitter Principles from Echinocystis Fabacea<sup>1</sup> W. O. EISENHUT, C. R. NOLLER American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO01106A048

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[17-(6-acetyloxy-2-hydroxy-6-methyl-3-oxohept-4-en-2-yl)-2-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-16-yl] acetate 3574185 Click to see 600.70 unknown https://doi.org/10.1021/JO01106A048
[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 2885 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1021/JO01106A048
Cucurbitacin B 5281316 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1021/JO01106A048
Fabacein 5356030 Click to see 600.70 unknown https://doi.org/10.1021/JO01106A048
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(4S,5S,6S)-6-(((4-Bromo-1H-pyrrole-2-carbonyl)oxy)methyl)-5-hydroxy-6-methyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid 5323782 Click to see CC1(C(C(N=CN1)C(=O)O)O)COC(=O)C2=CC(=CN2)Br 360.16 unknown via CMAUP database
(4S,6S)-6-(((4-Bromo-1H-pyrrole-2-carbonyl)oxy)methyl)-1,6-dimethyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid 101136769 Click to see CC1(CC(N=CN1C)C(=O)O)COC(=O)C2=CC(=CN2)Br 358.19 unknown via CMAUP database
(4S,6S)-6-(((4-Bromo-1H-pyrrole-2-carbonyl)oxy)methyl)-6-methyl-1,4,5,6-tetrahydropyrimidine-4-carboxylic acid 11739421 Click to see CC1(CC(N=CN1)C(=O)O)COC(=O)C2=CC(=CN2)Br 344.16 unknown via CMAUP database
Manzacidin A 179267 Click to see 344.16 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid amides / 2-heteroaryl carboxamides
4,5-Dibromo-1h-pyrrole-2-carboxamide 14056555 Click to see C1=C(NC(=C1Br)Br)C(=O)N 267.91 unknown via CMAUP database
Oroidin 6312649 Click to see 389.05 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroloazepines
(4R)-4-(2-amino-1H-imidazol-5-yl)-2,3-dibromo-4,5,6,7-tetrahydro-1H-pyrrolo[2,3-c]azepin-8-one 25774437 Click to see C1CNC(=O)C2=C(C1C3=CN=C(N3)N)C(=C(N2)Br)Br 389.05 unknown via CMAUP database
(4Z)-4-(2-amino-4-oxo-1H-imidazol-5-ylidene)-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one 5288032 Click to see 245.24 unknown via CMAUP database
2-Bromoaldisin 11064594 Click to see 243.06 unknown via CMAUP database
4-(2-amino-4-oxo-1H-imidazol-5-ylidene)-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one 2960 Click to see 245.24 unknown via CMAUP database
4-(2-amino-4-oxo-1H-imidazol-5-ylidene)-2-bromo-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one 122778 Click to see 324.13 unknown via CMAUP database
Aldisine 3085877 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1021/NP50022A016
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50022A016
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1021/NP50022A016
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1021/NP50022A016

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