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Ajania fastigiata

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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 UUID643fc92b12cda482455737
Scientific name Ajania fastigiata
Authority (C.Winkl.) Poljakov
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 17: 428 (1955)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tanacetum fastigiatum (C.Winkl.) Krasch. Spisok Rast. Gerb. Fl. S.S.S.R. Bot. Inst. Vsesojuzn. Akad. Nauk 11: 40 (1949)
Artemisia fastigiata C.Winkl. Trudy Imp. S.-Peterburgsk. Bot. Sada xi. (1891) 373.
Chrysanthemum fastigiatum (C.Winkl.) H.Ohashi & Yonek. J. Jap. Bot. 79(3): 189 (2004)

Common names Top

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Language Common/alternative name
Chinese 新疆亚菊
Chinese 新疆亞菊

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000028276
Tropicos 2728644
KEW urn:lsid:ipni.org:names:175792-1
The Plant List gcc-127327
Open Tree Of Life 729288
Observations.org 124954
NCBI Taxonomy 205360
IPNI 175792-1
iNaturalist 1029625
GBIF 3112246
EPPO AJNFA
EOL 6262495
CMAUP NPO6138

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
Botanicals Against Tetranychus urticae Koch Under Laboratory Conditions: A Survey of Alternatives for Controlling Pest Mites Rincón RA, Rodríguez D, Coy-Barrera E Plants (Basel) 07-Aug-2019
PMCID:PMC6724176
doi:10.3390/plants8080272
PMID:31394806
Dataset of pollen morphological traits of 56 dominant species among desert vegetation in the eastern arid central Asia Lu KQ, Xie G, Li M, Li JF, Trivedi A, Ferguson DK, Yao YF, Wang YF Data Brief 31-Mar-2018
PMCID:PMC5996618
doi:10.1016/j.dib.2018.03.122
PMID:29900271
Differential Growth Inhibitory Effects of Highly Oxygenated Guaianolides Isolated from the Middle Eastern Indigenous Plant Achillea falcata in HCT-116 Colorectal Cancer Cells Tohme R, Aaraj LA, Ghaddar T, Gali-Muhtasib H, Saliba NA, Darwiche N Molecules 15-Jul-2013
PMCID:PMC6269692
doi:10.3390/molecules18078275
PMID:23860275
C-glycosides of Ajania fastigiata T. K. Chumbalov, R. A. Zhubaeva Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00565204
Flavonoids of Ajania fastigiata T. K. Chumbalov, V. I. Glyzin, R. A. Zhubaeva Springer Science and Business Media LLC 07-Jul-2008
doi:10.1007/BF00564014
Flavonoids of Ajania fastigiata T. K. Chumbalov, R. A. Zhubaeva, G. M. Nurgalieva Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580913
Rupicolin B-oxide and isochrysartemin — New guaianolides fromAjania fastigiata M. I. Yusupov, Sh. Z. Kasymov, N. D. Adbullaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00577218
Ajafin ? A new guaianolide from Ajania fastigiata M. I. Yusupov, Sh. Z. Kasymov, G. P. Sidyakin, N. D. Abdullaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00579790
Study of the essential oil of Ajania fastigiata F. S. Sharipova, T. K. Chumbalov, L. A. El'chibekova, R. A. Zhubaeva Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568252
Sesquiterpene lactones ofAjania fastigiata M. I. Yusupov, Sh. Z. Kasymov, G. P. Sidyakin, U. Rakhmankulov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565064

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Heptanoic Acid 8094 Click to see CCCCCCC(=O)O 130.18 unknown https://doi.org/10.1007/BF00568252
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1007/BF00568252
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Butyric Acid 264 Click to see CCCC(=O)O 88.11 unknown https://doi.org/10.1007/BF00568252
Valeric acid 7991 Click to see CCCCC(=O)O 102.13 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00568252
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/BF00568252
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1007/BF00568252
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1007/BF00568252
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF00568252
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1007/BF00568252
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/BF00568252
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1007/BF00568252
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF00568252
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2S,6R,7S,12R,14S)-7-hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradec-9-en-4-one 102060406 Click to see CC1=C2CC3C(C2C4C(C(C1)O)C(=C)C(=O)O4)(O3)C 262.30 unknown https://doi.org/10.1007/BF00565064
(3aR,4R,7R,9R,9aR,9bR)-4,7-dihydroxy-9-methoxy-6,9-dimethyl-3-methylidene-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-2,8-dione 162892919 Click to see CC1=C2C(C3C(C(C1)O)C(=C)C(=O)O3)C(C(=O)C2O)(C)OC 308.33 unknown https://doi.org/10.1007/BF00579790
(3aR,4S,7R,9R,9aS,9bS)-4,7-dihydroxy-9-methoxy-6,9-dimethyl-3-methylidene-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-2,8-dione 162892920 Click to see CC1=C2C(C3C(C(C1)O)C(=C)C(=O)O3)C(C(=O)C2O)(C)OC 308.33 unknown https://doi.org/10.1007/BF00579790
4,7-Dihydroxy-9-methoxy-6,9-dimethyl-3-methylidene-3a,4,5,7,9a,9b-hexahydroazuleno[4,5-b]furan-2,8-dione 162892917 Click to see CC1=C2C(C3C(C(C1)O)C(=C)C(=O)O3)C(C(=O)C2O)(C)OC 308.33 unknown https://doi.org/10.1007/BF00579790
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,2S,6S,7S,10S,12S,14R)-7,10-dihydroxy-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 162884064 Click to see CC12C(O1)CC3(C2C4C(C(CC3=C)O)C(=C)C(=O)O4)O 278.30 unknown https://doi.org/10.1007/BF00577218
(1S,2R,4S,5R,9S,10S,11R,13S,14R)-2,4-dihydroxy-2,11-dimethyl-6-methylidene-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-7-one 101316845 Click to see CC1(CC(C2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O)O 294.30 unknown https://doi.org/10.1007/BF00565064
(1S,2S,5S,9S,10S,11R,13S,14R)-2-hydroxy-2,11-dimethyl-6-methylidene-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-7-one 162947959 Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O 278.30 unknown https://doi.org/10.1007/BF00577218
7,10-Dihydroxy-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 162884063 Click to see CC12C(O1)CC3(C2C4C(C(CC3=C)O)C(=C)C(=O)O4)O 278.30 unknown https://doi.org/10.1007/BF00577218
Artecanin 442147 Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O 278.30 unknown https://doi.org/10.1007/BF00565064
Rupicolin B 3082542 Click to see CC1=CCC2(C1C3C(C(CC2=C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1007/BF00565204
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1007/BF00564014
https://doi.org/10.1007/BF00580913
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1007/BF00580913

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