Gentiana depressa - Unknown
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Internal ID UUID64401d9db6ad1452076730
Scientific name Gentiana depressa
Authority D.Don
First published in Prodr. Fl. Nepal. : 125 (1825)

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Synonyms Top

Scientific name Authority First published in
Pneumonanthe depressa G.Don London Edinburgh Philos. Mag. & J. Sci. 1836: 76 (1836)
Ericala depressa D.Don ex G.Don Gen. Hist. iv. 189.
Gentiana depressa var. stenophylla T.N.Ho Bull. Nat. Hist. Mus. (London), Bot. 23: 57 (1993)
Gentianodes depressa (D.Don) Á.Löve & D.Löve Bot. Not. 125: 257 (1972)

Common names Top

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Language Common/alternative name
Chinese 平龙胆

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
avoid pricking out individually, transplant seedlings in clumps

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-0000697370
Tropicos 13802135
KEW urn:lsid:ipni.org:names:368076-1
The Plant List kew-2820368
Open Tree Of Life 836877
NCBI Taxonomy 50762
IPNI 368076-1
iNaturalist 602697
GBIF 7269866
EOL 2892487
USDA GRIN 17369

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
Olive Fruit and Leaf Wastes as Bioactive Ingredients for Cosmetics—A Preliminary Study Cádiz-Gurrea MD, Pinto D, Delerue-Matos C, Rodrigues F Antioxidants (Basel) 05-Feb-2021
PMCID:PMC7914505
doi:10.3390/antiox10020245
PMID:33562523
First Report on the Ethnopharmacological Uses of Medicinal Plants by Monpa Tribe from the Zemithang Region of Arunachal Pradesh, Eastern Himalayas, India Chakraborty T, Saha S, Bisht NS Plants (Basel) 02-Mar-2017
PMCID:PMC5371772
doi:10.3390/plants6010013
PMID:28257092
Ecological correlates of ex situ seed longevity: a comparative study on 195 species Probert RJ, Daws MI, Hay FR Ann Bot 09-Apr-2009
PMCID:PMC2706723
doi:10.1093/aob/mcp082
PMID:19359301
Depressoside, Nouvel Iridoïde Isole de Gentiana depressa Albert J. Chulia, Mourad Kaouadji American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50037A009
Iridoids and flavones from Gentiana depressa Albert J. Chulia, Joseph Vercauteren, Anne Marie Mariotte Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00900-0
Depresteroside, a mixed iridoid-secoiridoid structure from Gentiana depressa Albert J. Chulia, Joseph Vercauteren, Mourad Kaouadji Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97079-1

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 / Prenol lipids / Terpene glycosides
Depressine 101696497 Click to see COC(=O)C1=COC(C(C1CCOC(=O)C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O 688.60 unknown https://doi.org/10.1016/0031-9422(95)00900-0
methyl 3-ethenyl-4-[2-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxyethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 146160886 Click to see COC(=O)C1=COC(C(C1CCOC(=O)C2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O 688.60 unknown https://doi.org/10.1016/0031-9422(95)00900-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
2-[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]ethyl (1S,4aS,6S,7R,7aS)-6-(2,3-dihydroxybenzoyl)oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101663344 Click to see CC1C(CC2C1C(OC=C2C(=O)OCCC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C6=C(C(=CC=C6)O)O 884.80 unknown https://doi.org/10.1016/S0031-9422(00)97079-1
2-[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]ethyl (1S,4aS,6S,7R,7aS)-6-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162926434 Click to see CC1C(CC2C1C(OC=C2C(=O)OCCC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)O 1047.00 unknown https://doi.org/10.1016/0031-9422(95)00900-0
2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]ethyl 6-(2,3-dihydroxybenzoyl)oxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163076464 Click to see CC1C(CC2C1C(OC=C2C(=O)OCCC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C6=C(C(=CC=C6)O)O 884.80 unknown https://doi.org/10.1016/S0031-9422(00)97079-1
2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]ethyl 6-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoyl]oxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162926433 Click to see CC1C(CC2C1C(OC=C2C(=O)OCCC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)O 1047.00 unknown https://doi.org/10.1016/0031-9422(95)00900-0
Depressoside 180722 Click to see CC1C(CC2C1C(OC=C2C(=O)OC3=CC=CC(=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC(=O)C6=C(C(=CC=C6)O)O)O)O)O 782.70 unknown https://doi.org/10.1021/NP50037A009
Loganin 87691 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(95)00900-0
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(95)00900-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50037A009
Isoscoparin 442611 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(95)00900-0
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP50037A009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50037A009

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