PlantaeDB Logo
Login Sign-up

Artemisia tridentata

Artemisia tridentata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Artemisia tridentata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fd2ab16cbf467740353
Scientific name Artemisia tridentata
Authority Nutt.
First published in Trans. Amer. Philos. Soc. , ser. 2, 7: 398 (1841)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Artemisia tridentata subsp. xericensis Winward J. Range Managem. 44: 334. 1991 15792
Artemisia tridentata subsp. xericensis Winward ex Rosentr. & R.G.Kelsey J. Range Managem. 44: 334 (1991)
Seriphidium tridentatum (Nutt.) W.A.Weber Phytologia 55(1): 8. 1984

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English sagebrush
English big sagebrush
Catalan artemisa tridentada
chy vánó'êstse
Czech pelyněk trojzubý
German artemisia parishii
German artemisia vaseyana
German seriphidium tridentatum
German steppen-beifuß
German wüsten-beifuss
German wüsten-salbei
German wüstenbeifuss
German wüstenbeifuß
German wüstensalbei
German wüsten-beifuß
Persian درمنه بزرگ
French armoise tridentée
Hebrew לענה משוננת
Italian sagebrush
Norwegian Bokmål sagebrush
nv ts'ah
nv tsʼah
Chinese 三齒蒿
Chinese 三齿蒿

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Artemisia tridentata subsp. parishii (A.Gray) H.M.Hall & Clem. Publ. Carnegie Inst. Wash. 326: 137 (1923)
Artemisia tridentata subsp. tridentata Nutt.
Artemisia tridentata subsp. vaseyana (Rydb.) Beetle Rhodora 61: 83 (1959)
Artemisia tridentata subsp. wyomingensis Beetle & A.L.Young Rhodora 67: 405 (1965)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • North-central U.S.A.
      • Nebraska
      • North Dakota
      • South Dakota
    • Northeastern U.S.A.
      • New York
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000125631
UNII 45E08M336T
Canadensys 2914
USDA Plants ARTR2
Tropicos 2701811
KEW urn:lsid:ipni.org:names:20780-2
The Plant List gcc-86701
PFAF Artemisia tridentata
Open Tree Of Life 368822
Observations.org 195419
NCBI Taxonomy 55611
Nature Serve 2.130545
IUCN Red List 156820993
IPNI 20780-2
iNaturalist 75598
GBIF 3121335
Freebase /m/02m7hm
EPPO ARTTR
EOL 850413
Calflora (Californian flora) 725
USDA GRIN 103973
Wikipedia Artemisia_tridentata

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_021014915.2 BSU_IDT2_0.1 Chromosome Boise State University 2024-03-22 109.0x 3.66 Gb

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 Essential Oil Compositions of Ambrosia acanthicarpa Hook., Artemisia ludoviciana Nutt., and Gutierrezia sarothrae (Pursh) Britton & Rusby (Asteraceae) from the Owyhee Mountains of Idaho Swor K, Poudel A, Satyal P, Setzer WN Molecules 20-Mar-2024
PMCID:PMC10976104
doi:10.3390/molecules29061383
PMID:38543021
The Effects of Heavy Metal Pollution on Soil Nitrogen Transformation and Rice Volatile Organic Compounds under Different Water Management Practices Afzal M, Muhammad S, Tan D, Kaleem S, Khattak AA, Wang X, Chen X, Ma L, Mo J, Muhammad N, Jan M, Tan Z Plants (Basel) 18-Mar-2024
PMCID:PMC10976017
doi:10.3390/plants13060871
PMID:38592896
Plant–plant communication in Camellia japonica and C. rusticana via volatiles Sakurai Y, Ishizaki S Sci Rep 15-Mar-2024
PMCID:PMC10943193
doi:10.1038/s41598-024-56268-y
PMID:38491033
Evolution of sensitivity to warning cues from kin in plants with a structured population Yamauchi A, Takabayashi J, Shiojiri K, Karban R Ecol Evol 21-Feb-2024
PMCID:PMC10879904
doi:10.1002/ece3.11057
PMID:38384830
Sesquiterpene Lactones and Flavonoid from the Leaves of Basin Big Sagebrush (Artemisia tridentata subsp. tridentata): Isolation, Characterization and Biological Activities Anibogwu R, Jesus KD, Pradhan S, Leuven SV, Sharma K Molecules 09-Feb-2024
PMCID:PMC10892904
doi:10.3390/molecules29040802
PMID:38398555
Immunocontraceptive Efficacy of Native Porcine Zona Pellucida (pZP) Treatment of Nevada’s Virginia Range Free-Roaming Horse Population Schulman ML, Hayes NK, Wilson TA, Grewar JD Vaccines (Basel) 18-Jan-2024
PMCID:PMC10820100
doi:10.3390/vaccines12010096
PMID:38250909
Psyllids in Natural Habitats as Alternative Resources for Key Natural Enemies of the Pear Psyllids (Hemiptera: Psylloidea) Horton DR Insects 06-Jan-2024
PMCID:PMC10816694
doi:10.3390/insects15010037
PMID:38249044
Food availability leads to more connected contact networks among peridomestic zoonotic reservoir hosts Kuenzi AJ, Luis AD R Soc Open Sci 15-Nov-2023
PMCID:PMC10646467
doi:10.1098/rsos.230809
PMID:38026027
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Arbuscular Mycorrhizae Alter Photosynthetic Responses to Drought in Seedlings of Artemisia tridentata Geisler M, Buerki S, Serpe MD Plants (Basel) 19-Aug-2023
PMCID:PMC10458374
doi:10.3390/plants12162990
PMID:37631200
The Legacy of Plant Invasion: Impacts on Soil Nitrification and Management Implications Afzal MR, Naz M, Ashraf W, Du D Plants (Basel) 18-Aug-2023
PMCID:PMC10458916
doi:10.3390/plants12162980
PMID:37631191
Movement patterns and habitat use for the sympatric species: Gambelia wislizenii and Aspidoscelis tigris McAlpine‐Bellis E, Utsumi KL, Diamond KM, Klein J, Gilbert‐Smith S, Garrison GE, Eifler MA, Eifler DA Ecol Evol 10-Aug-2023
PMCID:PMC10413956
doi:10.1002/ece3.10422
PMID:37575589
The influence of disturbance scale on the natural recovery of biological soil crusts on the Colorado Plateau Jech SD, Havrilla CA, Barger NN Front Microbiol 03-Aug-2023
PMCID:PMC10434622
doi:10.3389/fmicb.2023.1176760
PMID:37601344
A genotype × environment experiment reveals contrasting response strategies to drought between populations of a keystone species (Artemisia tridentata; Asteraceae) Melton AE, Moran K, Martinez P, Ellestad P, Milliken E, Morales W, Child AW, Richardson BA, Serpe M, Novak SJ, Buerki S Plant Environ Interact 24-Jul-2023
PMCID:PMC10423975
doi:10.1002/pei3.10119
PMID:37583876
Potential use of saline resources for biofuel production using halophytes and marine algae: prospects and pitfalls Abideen Z, Ansari R, Hasnain M, Flowers TJ, Koyro HW, El-Keblawy A, Abouleish M, Khan MA Front Plant Sci 02-Jun-2023
PMCID:PMC10272829
doi:10.3389/fpls.2023.1026063
PMID:37332715

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Santolina triene 519872 Click to see CC(=CC(C=C)C(=C)C)C 136.23 unknown https://doi.org/10.1021/JO00189A021
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
methyl (2R,3S)-3-ethenyl-2,5-dimethylhex-4-enoate 13076812 Click to see CC(C(C=C)C=C(C)C)C(=O)OC 182.26 unknown https://doi.org/10.1021/JF60210A021
Methyl santolinate 565394 Click to see CC(C(C=C)C=C(C)C)C(=O)OC 182.26 unknown https://doi.org/10.1021/JF60210A021
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dien-1-ol 162933896 Click to see CC(=C)C(C=C)C=C(C)CO 152.23 unknown https://doi.org/10.1021/JO00014A023
(2R,3E)-5-methyl-2-prop-1-en-2-ylhexa-3,5-dien-1-ol 162915795 Click to see CC(=C)C=CC(CO)C(=C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(01)00438-1
(3S)-3-ethenyl-5-methyl-2-methylidenehex-4-en-1-ol 101293645 Click to see CC(=CC(C=C)C(=C)CO)C 152.23 unknown https://doi.org/10.1021/JO00189A021
3-Ethenyl-5-methyl-2-methylidenehex-4-en-1-ol 101409165 Click to see CC(=CC(C=C)C(=C)CO)C 152.23 unknown https://doi.org/10.1021/JO00189A021
4-Ethenyl-2,5-dimethylhexa-2,5-dien-1-ol 519722 Click to see CC(=C)C(C=C)C=C(C)CO 152.23 unknown https://doi.org/10.1021/JO00014A023
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Methyl isopimarate 3032412 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)OC)C)C1)C=C 316.50 unknown https://doi.org/10.1021/JF60210A021
Methyl levopimarate 13710755 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)OC)C 316.50 unknown https://doi.org/10.1021/JF60210A021
Methyl palustrate 13710758 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)OC)C 316.50 unknown https://doi.org/10.1021/JF60210A021
Methyl trans-communate 11141639 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)C=C 316.50 unknown https://doi.org/10.1021/JF60210A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
Lavandulol 5464156 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(01)00438-1
Lavandulol, (+/-)- 94060 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(01)00438-1
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1021/JF60210A021
> 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/10.1021/JF60210A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/JO00189A021
https://doi.org/10.1021/JA01317A054
(1S,5R,7R)-1,7-Bis(3-methyl-2-butenyl)-2-hydroxy-3-isobutyryl-5,8,8-trimethylbicyclo[3.3.1]nona-2-ene-4,9-dione 101117444 Click to see CC(C)C(=O)C1=C(C2(CC(C(C(C1=O)(C2=O)CC=C(C)C)(C)C)CC=C(C)C)C)O 414.60 unknown https://doi.org/10.1021/JO00189A021
https://doi.org/10.1021/JO00340A047
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/10.1021/JF60210A021
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/JF60210A021
https://doi.org/10.2307/3897909
https://doi.org/10.1016/S0031-9422(01)00438-1
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
https://doi.org/10.1021/JO00189A021
https://doi.org/10.2307/3897909
alpha-Thujone 12304613 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/JF60210A021
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF60210A021
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.2307/3897909
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
https://doi.org/10.1021/JO00189A021
https://doi.org/10.2307/3897909
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/JA01317A054
https://doi.org/10.1021/JF60210A021
https://doi.org/10.1021/JO00189A021
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.2307/3897909
Fenchol 15406 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown https://doi.org/10.1021/JF60210A021
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1021/JF60210A021
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JO00189A021
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.2307/3897909
https://doi.org/10.1016/S0031-9422(01)00438-1
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60210A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/JF60210A021
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60210A021
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/JF60210A021
https://doi.org/10.2307/3897909
Cyclohexaneethanol, beta,4-dimethyl-, cis- 346868 Click to see CC1CCC(CC1)C(C)CO 156.26 unknown https://doi.org/10.1021/JO01204A015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(1R,2S)-1-(2-methylprop-1-enyl)-2-prop-1-en-2-ylcyclopropane 11126315 Click to see CC(=CC1CC1C(=C)C)C 136.23 unknown https://doi.org/10.1021/JO00189A021
(1S,2R)-1-(2-methylprop-1-enyl)-2-prop-1-en-2-ylcyclopropane 13745740 Click to see CC(=CC1CC1C(=C)C)C 136.23 unknown https://doi.org/10.1021/JO00189A021
https://doi.org/10.1021/JO00340A047
(R,R)-chrysanthemol 2724508 Click to see CC(=CC1C(C1(C)C)CO)C 154.25 unknown https://doi.org/10.1021/JO00014A023
[2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methyl acetate 233175 Click to see CC(=CC1C(C1(C)C)COC(=O)C)C 196.29 unknown https://doi.org/10.1021/JO00014A023
Chrysanthemol 110685 Click to see CC(=CC1C(C1(C)C)CO)C 154.25 unknown https://doi.org/10.1021/JO00014A023
Cyclopropanemethanol, 2,2-dimethyl-3-(2-methylpropenyl)-, acetate, trans- 91710959 Click to see CC(=CC1C(C1(C)C)COC(=O)C)C 196.29 unknown https://doi.org/10.1021/JO00014A023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1021/JF60210A021
alpha-IONONE 5282108 Click to see CC1=CCCC(C1C=CC(=O)C)(C)C 192.30 unknown https://doi.org/10.1021/JF60210A021
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF60210A021
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1021/JF60210A021
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2S,3R,5S,8Z,11S)-2-hydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-8-en-13-one 101316855 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(73)80691-0
2-Hydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-8-en-13-one 181707 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(73)80691-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4S,5aS,9aR,9bS)-4,9a-dihydroxy-5a-methyl-3,9-dimethylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 162914552 Click to see CC12CCCC(=C)C1(C3C(C(C2)O)C(=C)C(=O)O3)O 264.32 unknown https://doi.org/10.1016/0031-9422(73)80562-X
Ridentin B 14779603 Click to see CC12CCC3C(C1C(=C)C(CC2O)O)OC(=O)C3=C 264.32 unknown https://doi.org/10.1016/0031-9422(73)80693-4
Rothin B 157009946 Click to see CC12CCCC(=C)C1(C3C(C(C2)O)C(=C)C(=O)O3)O 264.32 unknown https://doi.org/10.1016/0031-9422(73)80562-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,5E,9R,10E,11aR)-4,9-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one 163075603 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/0031-9422(73)80691-0
4,9-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72731791 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/0031-9422(73)80691-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(4-Ethenyl-2,5-dimethylhexa-2,5-dienyl) acetate 78409237 Click to see CC(=C)C(C=C)C=C(C)COC(=O)C 194.27 unknown https://doi.org/10.1021/JO00014A023
[(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dienyl] acetate 162943767 Click to see CC(=C)C(C=C)C=C(C)COC(=O)C 194.27 unknown https://doi.org/10.1021/JO00014A023
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
N-[2,5-dibenzyl-8-butan-2-yl-21-hydroxy-4,11-dimethyl-15-(2-methylpropyl)-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]-2,3-dihydroxypropanamide 75582685 Click to see CCC(C)C1C(=O)OC(C(C(=O)NC(C(=O)NC2CCC(N(C2=O)C(C(=O)N(C(C(=O)N1)CC3=CC=CC=C3)C)CC4=CC=CC=C4)O)CC(C)C)NC(=O)C(CO)O)C 837.00 unknown https://doi.org/10.1021/JO01204A015
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dienal 163020116 Click to see CC(=C)C(C=C)C=C(C)C=O 150.22 unknown https://doi.org/10.1021/JO00014A023
4-Ethenyl-2,5-dimethylhexa-2,5-dienal 71435827 Click to see CC(=C)C(C=C)C=C(C)C=O 150.22 unknown https://doi.org/10.1021/JO00014A023
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4S,5R)-4-ethenyl-3-methyl-5-prop-1-en-2-yloxolan-2-one 163016730 Click to see CC1C(C(OC1=O)C(=C)C)C=C 166.22 unknown https://doi.org/10.1021/JO01332A006
(3R,4S,5S)-4-ethenyl-3-methyl-5-prop-1-en-2-yloxolan-2-one 11789573 Click to see CC1C(C(OC1=O)C(=C)C)C=C 166.22 unknown https://doi.org/10.1021/JO01332A006
(3S,4S,5S)-4-ethenyl-3-methyl-5-prop-1-en-2-yloxolan-2-one 10855848 Click to see CC1C(C(OC1=O)C(=C)C)C=C 166.22 unknown https://doi.org/10.1021/JO01332A006
4-Ethenyl-3-methyl-5-prop-1-en-2-yloxolan-2-one 73102414 Click to see CC1C(C(OC1=O)C(=C)C)C=C 166.22 unknown https://doi.org/10.1021/JO01332A006
> Organoheterocyclic compounds / Oxanes
Artemiseole 521927 Click to see CC1(C2C(C2(CO1)C)C=C)C 152.23 unknown https://doi.org/10.1021/JO00189A021
> Organoheterocyclic compounds / Pyrans
2,3-Dimethyl-6-isopropyl-4h-pyran 12070933 Click to see CC1=C(OC(=CC1)C(C)C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(01)00438-1
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
2,2-dimethyl-6-propan-2-yl-3H-pyran-4-one 13611567 Click to see CC(C)C1=CC(=O)CC(O1)(C)C 168.23 unknown https://doi.org/10.1016/S0031-9422(01)00438-1
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/0305-1978(92)90072-L
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1016/0305-1978(92)90072-L
https://doi.org/10.1016/S0021-9673(01)97678-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)85324-8
https://doi.org/10.1016/0305-1978(92)90072-L
https://doi.org/10.1016/S0021-9673(01)97678-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1016/S0031-9422(00)85324-8
https://doi.org/10.1016/0305-1978(92)90072-L
https://doi.org/10.1016/S0021-9673(01)97678-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/0305-1978(92)90072-L
https://doi.org/10.1016/S0031-9422(00)85324-8
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/0305-1978(92)90072-L
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6-Hydroxyluteolin 5281642 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O 302.23 unknown https://doi.org/10.1515/ZNC-1995-5-604
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0021-9673(01)97678-2
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/10.1016/0305-1978(92)90072-L
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin 5281680 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O)O 318.23 unknown https://doi.org/10.1016/0305-1978(92)90072-L
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/10.1016/0305-1978(92)90072-L
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(92)90072-L
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1016/0305-1978(92)90072-L

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.