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Marah fabacea

Marah fabacea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

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

Description Top

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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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Language Common/alternative name
Vietnamese marah fabaceus

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

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

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
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 CC(=O)OC1CC2(C3CC=C4C(C3(C(=O)CC2(C1C(C)(C(=O)C=CC(C)(C)OC(=O)C)O)C)C)CC(C(=O)C4(C)C)O)C 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 CC(=O)OC1CC2(C3CC=C4C(C3(C(=O)CC2(C1C(C)(C(=O)C=CC(C)(C)OC(=O)C)O)C)C)CC(C(=O)C4(C)C)O)C 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,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)-5alpha-Hydroxy-6beta-methyl-6-(4-bromo-1H-pyrrole-2-ylcarbonyloxymethyl)-1,4,5,6-tetrahydropyrimidine-4alpha-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
(6S)-6beta-(4-Bromo-1H-pyrrole-2-ylcarbonyloxymethyl)-6-methyl-1,4,5,6-tetrahydropyrimidine-4alpha-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 CC1(CC(N=CN1)C(=O)O)COC(=O)C2=CC(=CN2)Br 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 C1=C(NC(=C1Br)Br)C(=O)NCC=CC2=CN=C(N2)N 389.05 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrroloazepines
(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 C1CNC(=O)C2=C(C1=C3C(=O)N=C(N3)N)C=CN2 245.24 unknown via CMAUP database
(R)-2,3-Dibromo-4-(2-amino-1H-imidazol-4-yl)-4,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8(1H)-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
2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione 11064594 Click to see C1CNC(=O)C2=C(C1=O)C=C(N2)Br 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 C1CNC(=O)C2=C(C1=C3C(=O)N=C(N3)N)C=CN2 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 C1CNC(=O)C2=C(C1=C3C(=O)N=C(N3)N)C=C(N2)Br 324.13 unknown via CMAUP database
6,7-dihydropyrrolo[2,3-c]azepine-4,8(1H,5H)-dione 3085877 Click to see C1CNC(=O)C2=C(C1=O)C=CN2 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP50022A016
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/NP50022A016

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