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Knoxia roxburghii

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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 UUID643fe017d46ea194640953
Scientific name Knoxia roxburghii
Authority (Spreng.) M.A.Rau
First published in Bull. Bot. Surv. India 10(Suppl. 2): 40 (1969)

Description Top

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Synonyms Top

Scientific name Authority First published in
Knoxia brachycarpa R.Br. ex Hook.f. Fl. Brit. India 3: 130 (1880)
Knoxia microcarpa Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 46: 138 (1877)
Knoxia roxburghii subsp. brunonis (Wall. ex G.Don) R.Bhattacharjee & Deb J. Econ. Taxon. Bot. 6: 85 (1985)
Knoxia roxburghii var. glauca (W.W.Sm.) R.Bhattacharjee & Deb J. Econ. Taxon. Bot. 6: 85 (1985)
Knoxia valerianoides Thorel ex Pit. Fl. Indo-Chine 3: 288 (1923)
Knoxia wallichii L.Bruce ex Panigrahi Bull. Bot. Soc. Bengal 21: 29 (1967)
Spermacoce brunonis Wall. ex G.Don Gen. Hist. 3: 621 (1834)
Spermacoce roxburghii Spreng. Syst. Veg. 1: 404 (1824)
Knoxia brachycarpa var. congesta Pit. Fl. Indo-Chine 3: 289. 1924
Knoxia roxburghii var. brunonis (Wall. ex G.Don) R.Bhattacharjee & Deb J. Econ. Taxon. Bot. 6(1): 85 (1985)
Dentillaria brachycarpa (R.Br. ex Hook.f.) Kuntze Revis. Gen. Pl. 1: 280 (1891)
Hedyotis glauca W.W.Sm. Bull. Misc. Inform. Kew 1911: 344 (1911)

Common names Top

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Language Common/alternative name
Chinese 红大戟
Chinese 广大戟
Chinese 紫大戟
Chinese 红芽戟

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Knoxia roxburghii subsp. roxburghii 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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000221137
Tropicos 100211538
KEW urn:lsid:ipni.org:names:754683-1
The Plant List kew-106109
Open Tree Of Life 3870825
NCBI Taxonomy 1905575
IPNI 754683-1
GBIF 2901184
EOL 1104659
CMAUP NPO16765

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_030378225.1 ASM3037822v1 Chromosome Yunnan University of Chinese Medicine 2023-06-30 85.0x 425.63 Mb

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
A chromosome-level genome assembly of the Knoxia roxburghii (Rubiaceae) Zhang Y, Zhang F, Jin L, Zhang T, Pu X, Qiu B, Li G Sci Data 15-Nov-2023
PMCID:PMC10651836
doi:10.1038/s41597-023-02725-8
PMID:37968303
Treating Chronic Wounds Using Photoactive Metabolites: Data Mining the Chinese Pharmacopoeia for Potential Lead Species Scotti F, Mou L, Huang C, Booker A, Weckerle C, Maake C, Heinrich M Planta Med 15-Sep-2021
PMCID:PMC8585569
doi:10.1055/a-1578-8778
PMID:34528222
The Occurrence and Biological Activity of Tormentic Acid—A Review Olech M, Ziemichód W, Nowacka-Jechalke N Molecules 22-Jun-2021
PMCID:PMC8270333
doi:10.3390/molecules26133797
PMID:34206442

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 / Anthracenes / Anthraquinones
Digiferruginol 32209 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)CO)O 254.24 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown via CMAUP database
1,3,5-Trihydroxy-2-methyl-6-methoxyanthraquinone 127173 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C(=C(C=C3)OC)O)O 300.26 unknown via CMAUP database
2-Ethoxymethylknoxiavaledin 91156689 Click to see CCOCC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C(=C(C=C3)OC)O)O 344.30 unknown via CMAUP database
2-Formylknoxiavaledin 101665858 Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(C(=C(C=C3C2=O)O)C=O)O)O 314.25 unknown via CMAUP database
Damnacanthol 160474 Click to see COC1=C2C(=CC(=C1CO)O)C(=O)C3=CC=CC=C3C2=O 284.26 unknown via CMAUP database
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Lucidin ethyl ether 28578 Click to see CCOCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 298.29 unknown via CMAUP database
Nordamnacanthal 160712 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 268.22 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown via CMAUP database
Soranjidiol 124063 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)O 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> 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 via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Eudesmin 73117 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown via CMAUP database
(3R,3aS,6R,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 325601 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown via CMAUP database
Eudesmin 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 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
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 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
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aR,10R,11R,12aS,14bS)-10,11-dihydroxy-9,12a-bis(hydroxymethyl)-2,2,6a,6b,9-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 92043473 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)CO)C)C2C1)C)C(=O)O)C 504.70 unknown via CMAUP database
2-Oxopomolic acid 44593379 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown via CMAUP database
Arjugenin 12444386 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C 504.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Rotungenic acid 12315077 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 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 / Stigmastanes and derivatives
4,22-Stigmastadiene-3-one 12611207 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 410.70 unknown via CMAUP database
7-Oxostigmasterol 12044013 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Koaburaside 5318820 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)CO)O)O)O 332.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C 300.30 unknown via CMAUP database

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