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Rothia indica

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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
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Details Top

Internal ID UUID643fd9520258f985054118
Scientific name Rothia indica
Authority (L.) Druce
First published in Rep. Bot. Exch. Club Soc. Brit. Isles3: 423 (1913 publ. 1914)

Description Top

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Synonyms Top

Scientific name Authority First published in
Trigonella indica L. Sp. Pl.: 778 (1753)
Lotus indicus (L.) Desr. J.B.A.M.de Lamarck, Encycl.3: 606 (1792)
Hosackia indica (L.) Graham N.Wallich, Numer. List: n.° 5940 (1831)
Westonia indica (L.) Kuntze Revis. Gen. Pl.1: 213 (1891)

Common names Top

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Language Common/alternative name
Chinese 落地豆

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Rothia indica subsp. australis A.E.Holland Austrobaileya5: 94 (1997)
Rothia indica subsp. indica Unknown

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185014
Tropicos 13060940
KEW urn:lsid:ipni.org:names:517807-1
The Plant List ild-31140
Open Tree Of Life 3928189
NCBI Taxonomy 1977627
IPNI 944798-1
GBIF 5353606
EOL 643840
USDA GRIN 32211

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)!
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Title Authors Publication Released IDs
Soyasaponin I from Rothia trifoliata G. Venkateshwar Rao, P. S. Rao, Tsuyoshi Tomimori, Haruhisa Kizu American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50037A027
Alkaloids of Rothia trifoliata and Rothia hirsuta. Hussain RA, Kinghorn AD, Molyneux RJ J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A033
PMID:21401151

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
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(14-Oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl) 4-hydroxy-3-methoxybenzoate 14109020 Click to see COC1=C(C=CC(=C1)C(=O)OC2CCN3CC4CC(C3C2)CN5C4CCCC5=O)O 414.50 unknown https://doi.org/10.1021/NP50058A033
(1S,2R,9R,10S,12S)-12-[(E)-but-2-en-2-yl]oxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163068328 Click to see CC=C(C)OC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 318.50 unknown https://doi.org/10.1021/NP50058A033
(1S,2S,9S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 1274462 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/NP50058A033
(1S,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 131705291 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/NP50058A033
(2R,4S,10S)-4-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 139031198 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O 264.36 unknown https://doi.org/10.1021/NP50058A033
[(1R,2S,4S,9R,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-3-phenylprop-2-enoate 162896409 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)OC(=O)C=CC5=CC=CC=C5 394.50 unknown https://doi.org/10.1021/NP50058A033
[(1R,2S,4S,9R,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (Z)-2-methylbut-2-enoate 163002242 Click to see CC=C(C)C(=O)OC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 346.50 unknown https://doi.org/10.1021/NP50058A033
[(1R,2S,4S,9R,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] 3-methylbutanoate 162850223 Click to see CC(C)CC(=O)OC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 348.50 unknown https://doi.org/10.1021/NP50058A033
[(1S,2S,4S,9S,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] acetate 163106852 Click to see CC(=O)OC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 306.40 unknown https://doi.org/10.1021/NP50058A033
[(2S,4S,9S,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] acetate 163188591 Click to see CC(=O)OC1CCN2CC3CC(C2C1)CN4C3CCCC4=O 306.40 unknown https://doi.org/10.1021/NP50058A033
4-Hydroxyspartein-2-one 442958 Click to see C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O 264.36 unknown https://doi.org/10.1021/NP50058A033
7,14-Methano-2H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocine, dodecahydro-, [7S-(7alpha,7abeta,14alpha,14abeta)]- 1774551 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/NP50058A033
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1021/NP50058A033
alpha-ISOSPARTEINE 92759 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1021/NP50058A033
Cinevanine 15939895 Click to see COC1=C(C=C(C=C1)C(=O)OC2CCN3CC4CC(C3C2)CN5C4CCCC5=O)O 414.50 unknown https://doi.org/10.1021/NP50058A033
Hydroxylupanine 73404 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1021/NP50058A033
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown https://doi.org/10.1021/NP50037A027
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1021/NP50058A033

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