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Knautia tatarica

Knautia tatarica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643ff3d1da25a600322468
Scientific name Knautia tatarica
Authority (L.) Szabó
First published in Bot. Közlem. 13: 65 (1914)

Description Top

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Synonyms Top

Scientific name Authority First published in
Knautia montana (Roem. & Schult.) DC. Prodr. 4: 651 (1830)
Knautia heterotricha K.Koch Linnaea 24: 444 (1851)
Trichera tatarica (L.) Soják Cas. Nár. Mus., Odd. Prír. 148: 198 (1979 publ. 1980)
Trichera montana Roem. & Schult. Syst. Veg., ed. 15 bis 3: 57 (1818)
Scabiosa heterotricha Opiz Lotos 2: 229 (1852)
Scabiosa tatarica L. Sp. Pl. : 99 (1753)
Astrocephalus tatarica (L.) Raf. Fl. Tellur. 4: 94. 1838 [1836 publ. mid-1838]

Common names Top

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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-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000357776
Tropicos 11200271
KEW urn:lsid:ipni.org:names:319488-1
The Plant List kew-2336390
Observations.org 147096
IPNI 319488-1
iNaturalist 777603
GBIF 4103943
Elurikkus 654579
CMAUP NPO4209

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
> Alkaloids and derivatives / Corynanthean-type alkaloids
7-Hydroxymitragynine 44301524 Click to see CCC1CN2CCC3(C(=NC4=C3C(=CC=C4)OC)C2CC1C(=COC)C(=O)OC)O 414.50 unknown via CMAUP database
7beta-Hydroxy-7H-mitraciliatine 102232174 Click to see CCC1CN2CCC3(C(=NC4=C3C(=CC=C4)OC)C2CC1C(=COC)C(=O)OC)O 414.50 unknown via CMAUP database
Corynantheidine 3000341 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown via CMAUP database
Isopaynantheine 101804033 Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=C(N3)C=CC=C4OC)C(=O)OC 396.50 unknown via CMAUP database
methyl 2-[(2S,3S,12bS)-3-ethyl-8-methoxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 92204 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC 398.50 unknown via CMAUP database
Mitraciliatine 11741588 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC 398.50 unknown via CMAUP database
Mitragynine 3034396 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC 398.50 unknown via CMAUP database
Paynantheine 3037629 Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=C(N3)C=CC=C4OC)C(=O)OC 396.50 unknown via CMAUP database
Speciociliatine 15560576 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC 398.50 unknown via CMAUP database
Speciogynine 15560577 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=C3C(=CC=C4)OC 398.50 unknown via CMAUP database
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1S,2S,3S)-2-[(E)-1,3-dimethoxy-3-oxoprop-1-en-2-yl]-3-ethyl-8-methoxy-2,3,4,6,7,12-hexahydro-1H-indolo[2,3-a]quinolizin-5-ium-1-sulfonate 10552557 Click to see CCC1C[N+]2=C(C(C1C(=COC)C(=O)OC)S(=O)(=O)[O-])C3=C(CC2)C4=C(N3)C=CC=C4OC 476.50 unknown via CMAUP database
(8S)-8-ethyl-15-methoxy-5-oxo-4-oxa-10,20-diazapentacyclo[11.7.0.02,10.03,7.014,19]icosa-1(13),2,6,14(19),15,17-hexaene-6-carbaldehyde 10690137 Click to see CCC1CN2CCC3=C(C2=C4C1=C(C(=O)O4)C=O)NC5=C3C(=CC=C5)OC 364.40 unknown via CMAUP database
Corynantheidinaline 14804152 Click to see CCC1=C(C(=C2C3=C(CCN2C1=O)C4=CC=CC=C4N3)C=O)C(=O)OC 350.40 unknown via CMAUP database
methyl (8R)-8-ethyl-6-oxo-7-oxa-10,20-diazapentacyclo[11.7.0.02,10.04,8.014,19]icosa-1(13),2,4,14,16,18-hexaene-5-carboxylate 10522789 Click to see CCC12CN3CCC4=C(C3=CC1=C(C(=O)O2)C(=O)OC)NC5=CC=CC=C45 364.40 unknown via CMAUP database
methyl (E)-2-[(2S,3S)-3-ethyl-8-methoxy-2,3,4,12-tetrahydro-1H-indolo[2,3-a]quinolizin-5-ium-2-yl]-3-methoxyprop-2-enoate 10741318 Click to see CCC1C[N+]2=C(CC1C(=COC)C(=O)OC)C3=C(C=C2)C4=C(N3)C=CC=C4OC 395.50 unknown via CMAUP database
Mitragynaline 636690 Click to see CCC1=C(C(=C2C3=C(CCN2C1=O)C4=C(N3)C=CC=C4OC)C=O)C(=O)OC 380.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
Isopteropodine 9885603 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
Isorotundifoline 102232176 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 400.50 unknown via CMAUP database
Isospeciofoleine 102232175 Click to see COC=C(C1CC2C3(CCN2CC1C=C)C4=C(C=CC=C4O)NC3=O)C(=O)OC 398.50 unknown via CMAUP database
Isospeciofoline 101289836 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 400.50 unknown via CMAUP database
Mitrafo;ine 101666873 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=C(C=CC=C4O)NC3=O 400.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
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 via CMAUP database
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 via CMAUP database
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 via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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