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Cheniella glauca

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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 UUID64406852bfa12073008413
Scientific name Cheniella glauca
Authority (Benth.) R.Clark & Mackinder
First published in Eur. J. Taxon.360: 24 (2017)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bauhinia glauca (Benth.) Wall. ex Benth. Fl. Hongk.: 99 (1861)
Phanera glauca Benth. F.A.W.Miquel, Pl. Jungh.: 265 (1852)
Bauhinia viridiflora Miq.
Bauhinia paraglauca T.Tang & Wang
Bauhinia glauca subsp. glauca (Benth.) Benth.
Bauhinia micrantha Ridl. J. Straits Branch Roy. Asiat. Soc.59: 98 (1911)
Phanera ochroleuca Miq. Fl. Ned. Ind.1(1): 69 (1855)
Bauhinia micrantha var. empetrifolia Benth. Fl. Austral.3: 170 (1867)
Bauhinia micrantha var. puberula Benth. Fl. Austral.3: 170 (1867)

Common names Top

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Language Common/alternative name
Chinese 粉叶首冠藤
Chinese 粉葉首冠藤

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Bauhinia glauca subsp. caterviflora (L.Chen) T.Chen
Bauhinia glauca subsp. pernervosa (L.Chen) T.Chen
Bauhinia glauca subsp. tenuiflora (C.B.Clarke) K.Larsen & S.S.Lar

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001421742
KEW urn:lsid:ipni.org:names:77165916-1
NCBI Taxonomy 228520
IPNI 77165916-1
GBIF 10856210

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
The complete chloroplast genome and phylogenetic analysis of Bauhinia glauca subsp. hupehana (Craib) T. C. Chen 1988 Ke QL, Li RY, Cai SS, Tang MQ, Cui LC, Lai CD, Li YH Mitochondrial DNA B Resour 11-Mar-2024
PMCID:PMC10930098
doi:10.1080/23802359.2024.2324928
PMID:38476838
From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 09-Feb-2024
PMCID:PMC10892999
doi:10.3390/molecules29040815
PMID:38398566
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Impacts of growth form and phylogenetic relatedness on seed germination: A large‐scale analysis of a subtropical regional flora Wang J, Xu G, Chen W, Ma Y, Qi W, Zhang C, Cui X Ecol Evol 07-Jan-2021
PMCID:PMC7863672
doi:10.1002/ece3.7132
PMID:33598130
Isolation of Bioactive Compounds from Calicotome villosa Stems Alhage J, Elbitar H, Taha S, Guegan JP, Dassouki Z, Vives T, Benvegnu T Molecules 08-Apr-2018
PMCID:PMC6017485
doi:10.3390/molecules23040851
PMID:29642501
Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men). Tang Y, Ling J, Zhang P, Zhang X, Zhang N, Wang W, Li J, Li N Bioorg Med Chem Lett 15-Aug-2015
doi:10.1016/J.BMCL.2015.05.089
PMID:26096681
Phytochemical Composition and Antinociceptive Activity of Bauhinia glauca subsp. hupehana in Rats Xu J, Zhao Q, Wei L, Yang Y, Xu R, Yu N, Zhao Y PLoS One 06-Feb-2015
PMCID:PMC4320050
doi:10.1371/journal.pone.0117801
PMID:25658740
Chemical Constituents of Kino Extract from Corymbia torelliana Nobakht M, Grkovic T, Trueman SJ, Wallace HM, Katouli M, Quinn RJ, Brooks PR Molecules 04-Nov-2014
PMCID:PMC6270844
doi:10.3390/molecules191117862
PMID:25375331
Medicinal plants from swidden fallows and sacred forest of the Karen and the Lawa in Thailand Junsongduang A, Balslev H, Inta A, Jampeetong A, Wangpakapattanawong P J Ethnobiol Ethnomed 24-Jun-2013
PMCID:PMC3702467
doi:10.1186/1746-4269-9-44
PMID:23800255
Kaempferia parviflora, a plant used in traditional medicine to enhance sexual performance contains large amounts of low affinity PDE5 inhibitors Temkitthawon P, Hinds TR, Beavo JA, Viyoch J, Suwanborirux K, Pongamornkul W, Sawasdee P, Ingkaninan K J Ethnopharmacol 30-Aug-2011
PMCID:PMC4056445
doi:10.1016/j.jep.2011.08.025
PMID:21884777
Flavonoids from Bauhinia glauca subsp. pernervosa. Wu ZB, Zhao YY, Yang XW, Liang H Chem Pharm Bull (Tokyo) 01-Jun-2009
doi:10.1248/CPB.57.628
PMID:19483349
Seasonal differences in leaf-level physiology give lianas a competitive advantage over trees in a tropical seasonal forest Cai ZQ, Schnitzer SA, Bongers F Oecologia 06-May-2009
PMCID:PMC2700874
doi:10.1007/s00442-009-1355-4
PMID:19418072

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Benzenoids / Phenols / Methoxyphenols
3,5-Dihydroxy-4-Methoxybenzaldehyde 12928004 Click to see COC1=C(C=C(C=C1O)C=O)O 168.15 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442448 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 454.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone 5281343 Click to see C1=COC2=CC(=CC(=C2C1=O)O)O 178.14 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-4-benzopyrone 442396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1248/CPB.57.628
https://doi.org/10.1016/J.BMCL.2015.05.089
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethylchroman-4-one 91144 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1248/CPB.57.628
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
6-C-Methylkaempferol 44259048 Click to see CC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-[2-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-methoxyphenyl)propan-1-one 163041388 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.628
1-[2,4-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]-3-(4-methoxyphenyl)propan-1-one 102508288 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 596.60 unknown https://doi.org/10.1248/CPB.57.628
1-[4-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-methoxyphenyl)propan-1-one 21722185 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.628
1-[4-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-methoxyphenyl)propan-1-one 73830079 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.628
Bauhiniaside B 146116201 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.628
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 40491193 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 122185642 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one 12310452 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.57.628
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methyl-2,3-dihydrochromen-4-one 163040096 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O 316.30 unknown https://doi.org/10.1248/CPB.57.628
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methyl-2,3-dihydrochromen-4-one 74929197 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O 316.30 unknown https://doi.org/10.1248/CPB.57.628
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Fisetin 3-methyl ether 9839293 Click to see COC1=C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2015.05.089
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.57.628
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1248/CPB.57.628
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxy-3-(p-methoxyphenyl)-propiophenone 578444 Click to see COC1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O 272.29 unknown https://doi.org/10.1248/CPB.57.628
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-[3-(4-Hydroxy-3-methoxyphenyl)propyl]benzene-1,3-diol 44130318 Click to see COC1=C(C=CC(=C1)CCCC2=C(C=C(C=C2)O)O)O 274.31 unknown https://doi.org/10.1248/CPB.57.628

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