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Marsdenia roylei

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404b8e2a063015162674
Scientific name Marsdenia roylei
Authority Wight
First published in Contr. Bot. India : 40 (1834)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pergularia roylei (Wight) D.Dietr. Syn. Pl. 1: 894 (1839)

Common names Top

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Language Common/alternative name
Chinese 吉隆牛奶菜
Chinese 吉隆牛嬭菜

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001102198
Tropicos 2601792
KEW urn:lsid:ipni.org:names:99281-1
The Plant List tro-2601792
Open Tree Of Life 6067183
Observations.org 751416
IPNI 99281-1
GBIF 3575513
Elurikkus 376301

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
Pregnanes and pregnane glycosides from Marsdenia roylei. Gupta VS, Kumar A, Deepak D, Khare A, Khare NK Phytochemistry 01-Dec-2003
doi:10.1016/S0031-9422(03)00468-0
PMID:14629995
Trisaccharides from Marsdenia roylei. Kumar A, Khare A, Khare NK Phytochemistry 01-Oct-1999
doi:10.1016/S0031-9422(99)00253-8
PMID:10570829
Two oligosaccharides from Marsdenia roylei. Kumar A, Khare A, Khare NK Phytochemistry 01-Apr-1999
doi:10.1016/S0031-9422(98)00691-8
PMID:10326255

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 / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(3S,8R,9S,10R,11S,12S,13S,14S,17S)-17-(1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,11,12,14,17-pentol 101268474 Click to see CC(C1(CCC2(C1(C(C(C3C2CC=C4C3(CCC(C4)O)C)O)O)C)O)O)O 382.50 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
(3S,8R,9S,10R,11S,12S,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,11,12,14,17-pentol 163012543 Click to see 382.50 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3S,5S,8R,9S,10S,11S,12S,13S,14S,17S)-11,12-diacetyloxy-17-[(1S)-1-acetyloxyethyl]-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] acetate 163106968 Click to see 536.70 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5R,6R)-2-[(2S,3S,4S,5S,6R)-4,5-dihydroxy-2-methyl-6-[[(3S,5S,8R,9S,10S,11S,12S,13S,14S,17S)-11,12,14-trihydroxy-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162897408 Click to see 676.80 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5S,6R)-4,5-dihydroxy-2-methyl-6-[[(3S,8R,9S,10S,11S,12S,13S,14S,17S)-11,12,14-trihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101268475 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3C(C(C5(C4(CCC5C(C)O)O)C)O)O)C)O)O)OC6C(C(C(C(O6)CO)O)O)O 676.80 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
1-[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone 11282994 Click to see 478.60 unknown https://doi.org/10.1016/S0031-9422(03)00468-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,6R)-3-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4S)-4-methoxy-2-methyl-3,4-dihydro-2H-pyran-3-yl]oxy]-2-methyloxan-4-ol 163104066 Click to see 418.50 unknown https://doi.org/10.1016/S0031-9422(98)00691-8
(2R,3S,4S,6S)-3-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4S)-4-methoxy-2-methyl-3,4-dihydro-2H-pyran-3-yl]oxy]-2-methyloxan-4-ol 5320270 Click to see 418.50 unknown https://doi.org/10.1016/S0031-9422(98)00691-8
Oli3Me(b1-4)Qui3Me(b)-O-Et 162842519 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(98)00691-8
Rolinose 5317259 Click to see 350.40 unknown https://doi.org/10.1016/S0031-9422(98)00691-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Deniose 10741574 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00253-8
Royleose 10765968 Click to see 450.50 unknown https://doi.org/10.1016/S0031-9422(99)00253-8
> Organoheterocyclic compounds / Oxazinanes / Morpholines / Phenylmorpholines
Phenmetrazine 4762 Click to see 177.24 unknown https://doi.org/10.1016/S0031-9422(03)00468-0

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