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Thamnosma montana

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffea6db3ae747145170
Scientific name Thamnosma montana
Authority Torr. & Frém.
First published in Rep. Exped. Rocky Mts. : 313 (1845)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English turpentinebroom

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
  • Northern America
    • Mexico
      • Mexico Northwest
    • 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-0000455271
USDA Plants THMO
Tropicos 28100524
KEW urn:lsid:ipni.org:names:775385-1
Open Tree Of Life 504816
NCBI Taxonomy 452797
Nature Serve 2.137815
IPNI 775385-1
iNaturalist 68403
GBIF 3190417
Freebase /m/0dlm18z
FEIS plants/shrub/thamon
EOL 581905
Calflora (Californian flora) 7954
USDA GRIN 451579
Wikipedia Thamnosma_montana

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
The Different Composition of Coumarins and Antibacterial Activity of Phlojodicarpus sibiricus and Phlojodicarpus villosus Root Extracts Khandy MT, Grigorchuk VP, Sofronova AK, Gorpenchenko TY Plants (Basel) 22-Feb-2024
PMCID:PMC10933757
doi:10.3390/plants13050601
PMID:38475448
Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae) Liu Q, Gao Y, Dong W, Zhao L Ecol Evol 09-Feb-2023
PMCID:PMC9911629
doi:10.1002/ece3.9821
PMID:36789335
ISOLATION OF PLANT GROWTH INHIBITORS FROM THAMNOSMA MONTANA Edward L. Bennett, James Bonner Wiley 31-Jan-2018
doi:10.1002/J.1537-2197.1953.TB06445.X
Disturbance and Plant Succession in the Mojave and Sonoran Deserts of the American Southwest Abella SR Int J Environ Res Public Health 25-Mar-2010
PMCID:PMC2872343
doi:10.3390/ijerph7041248
PMID:20617030
Further studies on constituents of Thamnosma montana Torr. and Frem. J.P. Kutney, T. Inaba, D.L. Dreyer Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)92898-4
Alkaloids and coumarins of Citrus grandis Tian-Shung Wu Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80815-X
Constituents of Thamnosma montana Torr. and Frem. D.L. Dreyer Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)99086-6
Novel epoxides from Thamnosma Montana Torr. and Frem. James P. Kutney, Robert N. Young, Ashok K. Verma Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)88028-X
Heterocycle-Fused Acridines Groundwater PW, Munawar MA Adv Heterocycl Chem 01-Jan-1997
PMCID:PMC7112105
doi:10.1016/S0065-2725(08)60930-7
PMID:32287461
Acridone Alkaloids from Cell Suspension Cultures of Thamnosma montana. Baumert A, Maier W, Matern U, Schmidt J, Schumann B, Gröger D Planta Med 01-Apr-1994
doi:10.1055/S-2006-959437
PMID:17236030

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
(-)-1,11-Dihydro-5-hydroxy-11-methyl-2-(1-methylethenyl)furo(2,3-c)acridin-6(2H)-one 11623705 Click to see 307.30 unknown https://doi.org/10.1055/S-2006-959437
(2R)-2-[(2S)-1,2-dihydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 162890122 Click to see 341.40 unknown https://doi.org/10.1055/S-2006-959437
(2R)-2-acetyl-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 162857567 Click to see 309.30 unknown https://doi.org/10.1055/S-2006-959437
(2R)-5-hydroxy-11-methyl-2-(1,2,3-trihydroxypropan-2-yl)-1,2-dihydrofuro[2,3-c]acridin-6-one 163100007 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C4=C(C=C3O)OC(C4)C(CO)(CO)O 357.40 unknown https://doi.org/10.1055/S-2006-959437
(2R)-5-hydroxy-11-methyl-2-[(2S)-2-methyloxiran-2-yl]-1,2-dihydrofuro[2,3-c]acridin-6-one 163002735 Click to see CC1(CO1)C2CC3=C(O2)C=C(C4=C3N(C5=CC=CC=C5C4=O)C)O 323.30 unknown https://doi.org/10.1055/S-2006-959437
(2R)-5-hydroxy-2-(3-hydroxyprop-1-en-2-yl)-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 162911975 Click to see 323.30 unknown https://doi.org/10.1055/S-2006-959437
(2S)-2-[(2R)-1-chloro-2-hydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 16040191 Click to see 359.80 unknown https://doi.org/10.1055/S-2006-959437
1-Hydroxy-3-methoxy-10-methylacridone 5377412 Click to see CN1C2=CC=CC=C2C(=O)C3=C1C=C(C=C3O)OC 255.27 unknown https://doi.org/10.1055/S-2006-959437
2-(1,2-Dihydroxy-1-methylethyl)-1,11-dihydro-5-hydroxy-11-methylfuro(2,3-c)acridin-6(2H)-one 5317836 Click to see 341.40 unknown https://doi.org/10.1055/S-2006-959437
2-Acetyl-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one 11034226 Click to see CC(=O)C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O 309.30 unknown https://doi.org/10.1055/S-2006-959437
Acridone 2015 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3N2 195.22 unknown https://doi.org/10.1016/0031-9422(88)80815-X
Gravacridonetriol 21586648 Click to see 357.40 unknown https://doi.org/10.1055/S-2006-959437
Gravacridonol 14805775 Click to see 323.30 unknown https://doi.org/10.1055/S-2006-959437
Hallacridone 14380428 Click to see CC(=O)C1=CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O 307.30 unknown https://doi.org/10.1055/S-2006-959437
Isogravacridonechlorine 5486900 Click to see CC(CCl)(C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O 359.80 unknown https://doi.org/10.1055/S-2006-959437
N-Methylacridone 69751 Click to see 209.24 unknown https://doi.org/10.1055/S-2006-959437
https://doi.org/10.1016/0031-9422(88)80815-X
Rutacridone 5281849 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O 307.30 unknown https://doi.org/10.1055/S-2006-959437
Rutacridone epoxide 5281850 Click to see CC1(CO1)C2CC3=C(O2)C=C(C4=C3N(C5=CC=CC=C5C4=O)C)O 323.30 unknown https://doi.org/10.1055/S-2006-959437
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine 164950 Click to see 215.20 unknown https://doi.org/10.1016/0031-9422(88)80815-X
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 7-methoxy-6-[2-[2-(7-methoxy-2-oxo-2H-1-benzopyran-6-yl)-1,4-dimethyl-3-cyclohexen-1-yl]ethenyl]- 618027 Click to see CC1=CC(C(CC1)(C)C=CC2=C(C=C3C(=C2)C=CC(=O)O3)OC)C4=C(C=C5C(=C4)C=CC(=O)O5)OC 484.50 unknown https://doi.org/10.1016/S0040-4020(01)92898-4
7-methoxy-6-[(E)-2-[(1S,2R)-2-(7-methoxy-2-oxochromen-6-yl)-1,4-dimethylcyclohex-3-en-1-yl]ethenyl]chromen-2-one 92469808 Click to see 484.50 unknown https://doi.org/10.1016/S0040-4020(01)92898-4
Thamnosin 5377043 Click to see CC1=CC(C(CC1)(C)C=CC2=C(C=C3C(=C2)C=CC(=O)O3)OC)C4=C(C=C5C(=C4)C=CC(=O)O5)OC 484.50 unknown https://doi.org/10.1016/S0040-4039(01)88028-X
Thamnosmonin 312089 Click to see 276.28 unknown https://doi.org/10.1016/0031-9422(88)80815-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
(+)-Byakangelicin 10211 Click to see 334.30 unknown https://doi.org/10.1002/J.1537-2197.1953.TB06445.X
(Rac)-Byakangelicin 616063 Click to see CC(C)(C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O)O 334.30 unknown https://doi.org/10.1002/J.1537-2197.1953.TB06445.X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
4-[(2S)-2,3-dihydroxy-3-methylbutyl]-9-methoxyfuro[3,2-g]chromen-7-one 162848123 Click to see 318.32 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
7H-Furo(3,2-g)(1)benzopyran-7-one, 4-(2,3-dihydroxy-3-methylbutyl)-9-methoxy- 4981 Click to see 318.32 unknown https://doi.org/10.1016/S0040-4020(01)99086-6
9-Methoxy-4-(1,2,3-trihydroxy-3-methylbutyl)-7h-furo[3,2-g][1]benzopyran-7-one 71438820 Click to see 334.30 unknown https://doi.org/10.1016/0031-9422(88)80815-X
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1002/J.1537-2197.1953.TB06445.X

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