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Thalictrum fendleri

Thalictrum fendleri - Unknown
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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 UUID64404d2764801571162586
Scientific name Thalictrum fendleri
Authority Engelm. ex A.Gray
First published in Mem. Amer. Acad. Arts , n.s., 4: 5 (1849)

Description Top

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Synonyms Top

Scientific name Authority First published in
Thalictrum wrightii A.Gray Smithsonian Contr. Knowl. 5(6): 7 (1853)
Thalictrum fendleri var. wrightii Trel. Proc. Boston Soc. Nat. Hist. 23: 304 (1886)
Thalictrum fendleri var. platycarpum Trel. Proc. Boston Soc. Nat. Hist. 23: 304 (1886)
Thalictrum amissum Greene
Thalictrum fendleri var. quadrinervatum B.Boivin Rhodora 46: 463 (1944)
Thalictrum fendleri var. sinuosum B.Boivin Rhodora 46: 462 (1944)

Common names Top

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Language Common/alternative name
English fendler's meadow-rue
nv tązhiiłchiin

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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No forms added yet.

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • North-central U.S.A.
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001129465
USDA Plants THFE
Tropicos 27100844
KEW urn:lsid:ipni.org:names:714419-1
The Plant List tro-27100844
Open Tree Of Life 500543
NCBI Taxonomy 1084669
Nature Serve 2.157543
IPNI 714419-1
iNaturalist 53299
GBIF 3033120
Freebase /m/0dlkrfs
EOL 594646
Calflora (Californian flora) 7949
USDA GRIN 36433
Wikipedia Thalictrum_fendleri

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
Fungal diversity notes 1387–1511: taxonomic and phylogenetic contributions on genera and species of fungal taxa Boonmee S, Wanasinghe DN, Calabon MS, Huanraluek N, Chandrasiri SK, Jones GE, Rossi W, Leonardi M, Singh SK, Rana S, Singh PN, Maurya DK, Lagashetti AC, Choudhary D, Dai YC, Zhao CL, Mu YH, Yuan HS, He SH, Phookamsak R, Jiang HB, Martín MP, Dueñas M, Telleria MT, Kałucka IL, Jagodziński AM, Liimatainen K, Pereira DS, Phillips AJ, Suwannarach N, Kumla J, Khuna S, Lumyong S, Potter TB, Shivas RG, Sparks AH, Vaghefi N, Abdel-Wahab MA, Abdel-Aziz FA, Li GJ, Lin WF, Singh U, Bhatt RP, Lee HB, Nguyen TT, Kirk PM, Dutta AK, Acharya K, Sarma VV, Niranjan M, Rajeshkumar KC, Ashtekar N, Lad S, Wijayawardene NN, Bhat DJ, Xu RJ, Wijesinghe SN, Shen HW, Luo ZL, Zhang JY, Sysouphanthong P, Thongklang N, Bao DF, Aluthmuhandiram JV, Abdollahzadeh J, Javadi A, Dovana F, Usman M, Khalid AN, Dissanayake AJ, Telagathoti A, Probst M, Peintner U, Garrido-Benavent I, Bóna L, Merényi Z, Boros L, Zoltán B, Stielow JB, Jiang N, Tian CM, Shams E, Dehghanizadeh F, Pordel A, Javan-Nikkhah M, Denchev TT, Denchev CM, Kemler M, Begerow D, Deng CY, Harrower E, Bozorov T, Kholmuradova T, Gafforov Y, Abdurazakov A, Xu JC, Mortimer PE, Ren GC, Jeewon R, Maharachchikumbura SS, Phukhamsakda C, Mapook A, Hyde KD Fungal Divers 07-Dec-2021
PMCID:PMC8648402
doi:10.1007/s13225-021-00489-3
PMID:34899100
The ethoxycarbonyl group as both activating and protective group in N-acyl-Pictet–Spengler reactions using methoxystyrenes. A short approach to racemic 1-benzyltetrahydroisoquinoline alkaloids Keller M, Sauvageot-Witzku K, Geisslinger F, Urban N, Schaefer M, Bartel K, Bracher F Beilstein J Org Chem 05-Nov-2021
PMCID:PMC8576818
doi:10.3762/bjoc.17.183
PMID:34804241
Chloroplast primers for clade‐wide phylogenetic studies of Thalictrum Morales‐Briones DF, Arias T, Di Stilio VS, Tank DC Appl Plant Sci 16-Oct-2019
PMCID:PMC6814179
doi:10.1002/aps3.11294
PMID:31667022
Hemiparasitic plants increase alpine plant richness and evenness but reduce arbuscular mycorrhizal fungal colonization in dominant plant species McKibben M, Henning JA PeerJ 07-Nov-2018
PMCID:PMC6228546
doi:10.7717/peerj.5682
PMID:30425882
Plant dominance in a subalpine montane meadow: biotic vs. abiotic controls of subordinate diversity within and across sites LaPlante E, Souza L PeerJ 21-Sep-2018
PMCID:PMC6152469
doi:10.7717/peerj.5619
PMID:30258717
Data-mining of potential antitubercular activities from molecular ingredients of traditional Chinese medicines Jamal S, Scaria V PeerJ 17-Jul-2014
PMCID:PMC4106188
doi:10.7717/peerj.476
PMID:25081126
Dramatic response to climate change in the Southwest: Robert Whittaker's 1963 Arizona Mountain plant transect revisited Brusca RC, Wiens JF, Meyer WM, Eble J, Franklin K, Overpeck JT, Moore W Ecol Evol 13-Aug-2013
PMCID:PMC3797479
doi:10.1002/ece3.720
PMID:24223270
Plant Cuttings Chaffey N Ann Bot 01-Jan-2013
PMCID:PMC3523662
doi:10.1093/aob/mcs291
Introduction to the Arizona Sky Island Arthropod Project (ASAP): Systematics, Biogeography, Ecology, and Population Genetics of Arthropods of the Madrean Sky Islands Moore W, Meyer WM III, Eble JA, Franklin K, Wiens JF, Brusca RC Proc RMRS 01-Jan-2013
PMCID:PMC4260471
PMID:25505938
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899
The Isoquinolone Alkaloids Barry D. Krane, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50022A001
Thalictrum alkaloids—VII M. Shamma, M.A. Podczasy Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)92468-8
Thalictrum alkaloids I. Thalifendlerine and thalifendine Maurice Shamma, Michael A. Greenberg, Bernard S. Dudock Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)99545-0
Thalictrum alkaloids. V. Isolation. Shamma M, Dudock BS J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600570204
PMID:5641669

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Aporphines
(12R)-7,16,17-trimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene 1600002 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC 369.40 unknown https://doi.org/10.1002/JPS.2600570204
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 100020 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC 341.40 unknown https://doi.org/10.2307/4117899
Ocotein 3083793 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC 369.40 unknown https://doi.org/10.1002/JPS.2600570204
Preocoteine 176968 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC 371.40 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
https://doi.org/10.2307/4117899
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(11R)-16-methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene-11,17-diol 154497569 Click to see COC1=C(C=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21)O 338.30 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
(1S)-16-methoxy-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-17-ol 3246443 Click to see COC1=C(C=CC2=C1CN3CCC4=CC5=C(C=C4C3C2)OCO5)O 325.40 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate 10426199 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-] 321.30 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1016/S0040-4020(01)92468-8
Hydroberberubin 276137 Click to see COC1=C(C=CC2=C1CN3CCC4=CC5=C(C=C4C3C2)OCO5)O 325.40 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
Thalifendine 3084288 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O 322.30 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
https://doi.org/10.2307/4117899
> Lignans, neolignans and related compounds
(1S,14S)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol 10627884 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)OC)OC 638.70 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
(9S,27R)-4,15,16,21-tetramethoxy-10,26-dimethyl-2,18-dioxa-10,26-diazaheptacyclo[27.2.2.13,7.19,13.119,23.017,35.027,34]hexatriaconta-1(31),3,5,7(36),13(35),14,16,19,21,23(34),29,32-dodecaen-14-ol 162909659 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7OC3=CC(=C2)OC)OC)OC)O)OC 638.70 unknown https://doi.org/10.1002/JPS.2600570204
4,15,16,21-Tetramethoxy-10,26-dimethyl-2,18-dioxa-10,26-diazaheptacyclo[27.2.2.13,7.19,13.119,23.017,35.027,34]hexatriaconta-1(31),3,5,7(36),13(35),14,16,19,21,23(34),29,32-dodecaen-14-ol 162909658 Click to see CN1CCC2=C3C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7OC3=CC(=C2)OC)OC)OC)O)OC 638.70 unknown https://doi.org/10.1002/JPS.2600570204
Thalidezine 320711 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)OC)OC 638.70 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Dihydroisoquinolines
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene-11,17-diol 12443385 Click to see COC1=C(C=CC2=CC3=[N+](CC(C4=CC5=C(C=C43)OCO5)O)C=C21)O 338.30 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(2S,3R,4R,5R,6S)-2-methyl-6-[4-[[(1R)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]oxane-3,4,5-triol 162894554 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC3C4=CC(=C(C(=C4CCN3C)OC)OC)OC)O)O)O 489.60 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
2-methyl-6-[4-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]oxane-3,4,5-triol 421848 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC3C4=CC(=C(C(=C4CCN3C)OC)OC)OC)O)O)O 489.60 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
4-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenol 12443387 Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC)OC 343.40 unknown https://doi.org/10.1016/S0040-4039(01)99545-0
4-[[(1R)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenol 163070936 Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC)OC 343.40 unknown https://doi.org/10.1016/S0040-4039(01)99545-0
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.2307/4117899
5,6,7-Trimethoxy-2-methyl-3,4-dihydroisoquinolin-1-one 162931699 Click to see CN1CCC2=C(C(=C(C=C2C1=O)OC)OC)OC 251.28 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
N-Methylcorydaldine 303906 Click to see CN1CCC2=CC(=C(C=C2C1=O)OC)OC 221.25 unknown https://doi.org/10.1016/S0040-4020(01)92468-8
https://doi.org/10.1021/NP50022A001
> Phenylpropanoids and polyketides / Tannins
(1R,14S)-9,19,20,21,25-pentamethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-dodecaene 7098682 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)OC)OC 652.80 unknown https://doi.org/10.1002/JPS.2600570204
Hernandezine 72343 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)OC)OC 652.80 unknown https://doi.org/10.2307/4117899
Isohernandezine 308359 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)OC)OC 652.80 unknown https://doi.org/10.1002/JPS.2600570204

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