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Rohdea wattii

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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 UUID6440291f21b96283431011
Scientific name Rohdea wattii
Authority (C.B.Clarke) Yamashita & M.N.Tamura
First published in J. Pl. Res. 117: 369 (2004)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tupistra wattii (C.B.Clarke) Hook.f. Fl. Brit. India 6: 325 (1892)
Campylandra cauliflora Chun Sunyatsenia 1: 213 (1934)
Campylandra wattii C.B.Clarke J. Linn. Soc., Bot. 25: 78 (1889)

Common names Top

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Language Common/alternative name
Chinese 弯蕊开口箭

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
      • East Himalaya
    • Indo-China
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000799606
Tropicos 100252000
KEW urn:lsid:ipni.org:names:77065524-1
The Plant List kew-338069
Open Tree Of Life 797564
NCBI Taxonomy 1045279
IPNI 77065524-1
iNaturalist 863236
GBIF 5303903
CMAUP NPO8818

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
Characterization of the complete chloroplast genome of Rohdea wattii (Asparagaceae) Wang Y, Zhang Y, Li C, Zhao B Mitochondrial DNA B Resour 25-Aug-2021
PMCID:PMC8405109
doi:10.1080/23802359.2021.1967801
PMID:34471695
Ethnobotany and diversity of medicinal plants used by the Buyi in eastern Yunnan, China Xiong Y, Sui X, Ahmed S, Wang Z, Long C Plant Divers 07-Oct-2020
PMCID:PMC7936110
doi:10.1016/j.pld.2020.09.004
PMID:33733008
Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C J Ethnobiol Ethnomed 19-Aug-2019
PMCID:PMC6699132
doi:10.1186/s13002-019-0316-1
PMID:31426826
Steroidal Saponins from Rhizomes of Tupistra wattii Hook. f. Ping Shen, San‐Long Wang, Xi‐Kui Liu, Chong‐Ren Yang, Bing Cai, Xin‐Sheng Yao Wiley 29-Jun-2005
doi:10.1002/CHIN.200334177
Steroidal saponins from rhizomes of Tupistra wattii Hook. f. Shen P, Wang SL, Liu XK, Yang CR, Cai B, Yao XS Chem Pharm Bull (Tokyo) 01-Mar-2003
doi:10.1248/CPB.51.305
PMID:12612416

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 / Triterpenoids
29-Hydroxyfriedelan-3-one 14108943 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Hennadiol 489919 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(=C)CO)C)C)C)C 442.70 unknown via CMAUP database
Octandronic acid 14108946 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C 456.70 unknown via CMAUP database
Octandronol 14108942 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown via CMAUP database
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1S,2S,4S,4'S,5'S,6R,7S,8R,9S,12S,13S,14S,15S,16S,17S,18R,20R)-14,15,16,17,18,20-hexahydroxy-5',7,9,13-tetramethyl-4'-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 101228123 Click to see CC1COC2(CC1OC3C(C(C(C(O3)CO)O)O)O)C(C4C(O2)CC5C4(CCC6C5C(C(=O)C7(C6(C(C(C(C7O)O)O)O)C)O)O)C)C 688.80 unknown https://doi.org/10.1248/CPB.51.305
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13S,14S,15S,16S,17S,18R)-5',7,9,13-tetramethyl-17-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14,15,16,18-tetrol 101228122 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6(C5(C(C(C(C6OC7C(C(C(CO7)O)O)O)O)O)O)C)O)C)C)OC1 612.70 unknown https://doi.org/10.1248/CPB.51.305
(2R,3R,4S,5R,6R)-2-[[(2R,3R,4S,5R,6R)-6-[(1S,2S,4S,4'S,5'S,6R,7S,8R,9S,12S,13S,14R,16R,18R)-14,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-4'-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163060762 Click to see CC1COC2(CC1OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(C5C(O2)CC6C5(CCC7C6CCC8C7(C(CC(C8)O)O)C)C)C 772.90 unknown https://doi.org/10.1248/CPB.51.305
14,15,16,17,18,20-Hexahydroxy-5',7,9,13-tetramethyl-4'-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 85143562 Click to see CC1COC2(CC1OC3C(C(C(C(O3)CO)O)O)O)C(C4C(O2)CC5C4(CCC6C5C(C(=O)C7(C6(C(C(C(C7O)O)O)O)C)O)O)C)C 688.80 unknown https://doi.org/10.1002/CHIN.200334177
2-[[6-(14,16-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-4'-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85143831 Click to see CC1COC2(CC1OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(C5C(O2)CC6C5(CCC7C6CCC8C7(C(CC(C8)O)O)C)C)C 772.90 unknown https://doi.org/10.1002/CHIN.200334177
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(6aS,6bS,8aS,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-8,9,12,12a,13,14-hexahydro-7H-picen-2-one 46881919 Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C 404.60 unknown via CMAUP database
Tingenone 101520 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C 420.60 unknown via CMAUP database

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