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Limnophila geoffrayi

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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 UUID643ffda475edc955501776
Scientific name Limnophila geoffrayi
Authority Bonati
First published in Bull. Soc. Bot. France 55: 510 (1908)

Description Top

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Synonyms Top

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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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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-0000445583
KEW urn:lsid:ipni.org:names:804316-1
The Plant List kew-2497805
Open Tree Of Life 3883276
IUCN Red List 199707
IPNI 804316-1
iNaturalist 439662
GBIF 6711389
EPPO LIOGE
Elurikkus 579023
USDA GRIN 465240

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)!
Title Authors Publication Released IDs
Limnophilaspiroketone, a highly oxygenated phenolic derivative from Limnophila geoffrayi. Jang DS, Su BN, Pawlus AD, Jones WP, Kleps RA, Bunyapraphatsara N, Fong HH, Pezzuto JM, Kinghorn AD J Nat Prod 01-Jul-2005
doi:10.1021/NP050132B
PMID:16038568
Antimycobacterial and antioxidant flavones from Limnophila geoffrayi. Suksamrarn A, Poomsing P, Aroonrerk N, Punjanon T, Suksamrarn S, Kongkun S Arch Pharm Res 01-Oct-2003
doi:10.1007/BF02980026
PMID:14609129

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-15-ol 625708 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1021/NP050132B
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Limnophilaspiroketone 11428821 Click to see COC1=C(C(C2(C1=O)C(=O)C=C(O2)C3=CC=C(C=C3)O)(C(=O)OC)O)OC 376.30 unknown https://doi.org/10.1021/NP050132B
Methyl 9-hydroxy-2-(4-hydroxyphenyl)-7,8-dimethoxy-4,6-dioxo-1-oxaspiro[4.4]nona-2,7-diene-9-carboxylate 72957880 Click to see COC1=C(C(C2(C1=O)C(=O)C=C(O2)C3=CC=C(C=C3)O)(C(=O)OC)O)OC 376.30 unknown https://doi.org/10.1021/NP050132B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3-Farnesyl-4-hydroxybenzoesaure 54248366 Click to see CC(=CCCC(=CCCC(=CCC1=C(C=CC(=C1)C(=O)O)O)C)C)C 342.50 unknown https://doi.org/10.1021/NP050132B
4-Hydroxy-3-(3,7,11-trimethyldodeca-2,6,10-trienoxy)benzoic acid 162983666 Click to see CC(=CCCC(=CCCC(=CCOC1=C(C=CC(=C1)C(=O)O)O)C)C)C 358.50 unknown https://doi.org/10.1021/NP050132B
4-hydroxy-3-[(2Z,6Z)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzoic acid 44559229 Click to see CC(=CCCC(=CCCC(=CCC1=C(C=CC(=C1)C(=O)O)O)C)C)C 342.50 unknown https://doi.org/10.1021/NP050132B
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4aS,6aS,6aS,6bR,8aS,12aR,14bR)-1,8,10-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 129316997 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP050132B
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid 14355557 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP050132B
1,10-Dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 12315074 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP050132B
4-Epihederagenin 12302577 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050132B
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP050132B
alpha-Hederagenin 258538 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050132B
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP050132B
Rotungenic acid 12315077 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP050132B
Sumaresinol 12443148 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050132B
Sumaresinolic acid 4660579 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP050132B
Uncaric acid 10838721 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1021/NP050132B
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Isothymusin 630253 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)O)OC 330.29 unknown https://doi.org/10.1021/NP050132B
https://doi.org/10.1007/BF02980026
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1021/NP050132B
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1021/NP050132B
https://doi.org/10.1007/BF02980026

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