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Psorothamnus arborescens

Psorothamnus arborescens - 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 UUID643fd84b2ef59387505515
Scientific name Psorothamnus arborescens
Authority (Torr. ex A.Gray) Barneby
First published in Mem. New York Bot. Gard.27: 33 (1977)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psorodendron arborescens (A.Gray) Rydb. N.L.Britton & al. (eds.), N. Amer. Fl.24: 42 (1919)
Parosela arborescens (A.Gray) A.Heller Cat. N. Amer. Pl., ed. 2: 5 (1900)
Dalea arborescens Torr. ex A.Gray Mem. Amer. Acad. Arts, n.s., 5: 316 (1855)

Common names Top

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Language Common/alternative name
English mojave indigobush

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Psorothamnus arborescens var. arborescens (A.Gray) Barneby Unknown
Psorothamnus arborescens var. californicus (S.Watson) D.Sutherl., Gandhi & Vincent J. Bot. Res. Inst. Texas14: 188 (2020)
Psorothamnus arborescens var. minutifolius (Parish) Barneby Mem. New York Bot. Gard.27: 35 (1977)
Psorothamnus arborescens var. pubescens (Parish) Barneby Mem. New York Bot. Gard.27: 38 (1977)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000178794
USDA Plants PSAR4
Tropicos 13056266
KEW urn:lsid:ipni.org:names:212358-2
The Plant List ild-24858
Open Tree Of Life 189648
NCBI Taxonomy 248527
Nature Serve 2.152655
IPNI 212358-2
iNaturalist 78772
GBIF 2940467
Freebase /m/0br_j4q
EOL 642687
Calflora (Californian flora) 6918
USDA GRIN 408796
Wikipedia Psorothamnus_arborescens
CMAUP NPO11841

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
An overview on medicinal plants used for combating coronavirus: Current potentials and challenges Abou Baker DH, Hassan EM, El Gengaihi S J Agric Food Res 20-May-2023
PMCID:PMC10198795
doi:10.1016/j.jafr.2023.100632
PMID:37251276
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
Tocilizumab-coated solid lipid nanoparticles loaded with cannabidiol as a novel drug delivery strategy for treating COVID-19: A review Zielińska A, Eder P, Karczewski J, Szalata M, Hryhorowicz S, Wielgus K, Szalata M, Dobrowolska A, Atanasov AG, Słomski R, Souto EB Front Immunol 22-Mar-2023
PMCID:PMC10073701
doi:10.3389/fimmu.2023.1147991
PMID:37033914
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Natural compounds may contribute in preventing SARS-CoV-2 infection: a narrative review Bizzoca ME, Leuci S, Mignogna MD, Muzio EL, Caponio VC, Muzio LL 02-Jun-2022
PMCID:PMC9160299
doi:10.1016/j.fshw.2022.04.005
Pharmacogenetics and Precision Medicine Approaches for the Improvement of COVID-19 Therapies Biswas M, Sawajan N, Rungrotmongkol T, Sanachai K, Ershadian M, Sukasem C Front Pharmacol 18-Feb-2022
PMCID:PMC8894812
doi:10.3389/fphar.2022.835136
PMID:35250581
The Effect of Phytocompounds of Medicinal Plants on Coronavirus (2019-NCOV) Infection Zrig A Pharm Chem J 31-Jan-2022
PMCID:PMC8801268
doi:10.1007/s11094-021-02540-8
PMID:35125554
Identification of antiviral phytochemicals as a potential SARS-CoV-2 main protease (Mpro) inhibitor using docking and molecular dynamics simulations Patel CN, Jani SP, Jaiswal DG, Kumar SP, Mangukia N, Parmar RM, Rawal RM, Pandya HA Sci Rep 13-Oct-2021
PMCID:PMC8514552
doi:10.1038/s41598-021-99165-4
PMID:34645849
Drug Design Strategies for the Treatment of Viral Disease. Plant Phenolic Compounds and Their Derivatives Kowalczyk M, Golonko A, Świsłocka R, Kalinowska M, Parcheta M, Swiergiel A, Lewandowski W Front Pharmacol 30-Jul-2021
PMCID:PMC8363300
doi:10.3389/fphar.2021.709104
PMID:34393787
Bioactive molecules from plants: a prospective approach to combat SARS-CoV-2 Panigrahi GK, Sahoo SK, Sahoo A, Behera S, Sahu S, Dash A, Satapathy KB 20-Jul-2021
PMCID:PMC8290388
doi:10.1007/s13596-021-00599-y
Anti–SARS-CoV-2 Natural Products as Potentially Therapeutic Agents Kim CH Front Pharmacol 27-May-2021
PMCID:PMC8194829
doi:10.3389/fphar.2021.590509
PMID:34122058
Therapeutic Potentials of Antiviral Plants Used in Traditional African Medicine With COVID-19 in Focus: A Nigerian Perspective Attah AF, Fagbemi AA, Olubiyi O, Dada-Adegbola H, Oluwadotun A, Elujoba A, Babalola CP Front Pharmacol 26-Apr-2021
PMCID:PMC8108136
doi:10.3389/fphar.2021.596855
PMID:33981214
Medicinal Plants, Phytochemicals, and Herbs to Combat Viral Pathogens Including SARS-CoV-2 Anand AV, Balamuralikrishnan B, Kaviya M, Bharathi K, Parithathvi A, Arun M, Senthilkumar N, Velayuthaprabhu S, Saradhadevi M, Al-Dhabi NA, Arasu MV, Yatoo MI, Tiwari R, Dhama K Molecules 22-Mar-2021
PMCID:PMC8004635
doi:10.3390/molecules26061775
PMID:33809963
Structural insights on the interaction potential of natural leads against major protein targets of SARS-CoV-2: Molecular modelling, docking and dynamic simulation studies Skariyachan S, Gopal D, Muddebihalkar AG, Uttarkar A, Niranjan V Comput Biol Med 13-Mar-2021
PMCID:PMC7954774
doi:10.1016/j.compbiomed.2021.104325
PMID:33751995
Structural Basis of Potential Inhibitors Targeting SARS-CoV-2 Main Protease Mengist HM, Dilnessa T, Jin T Front Chem 12-Mar-2021
PMCID:PMC8056153
doi:10.3389/fchem.2021.622898
PMID:33889562

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
Ambelline 25092366 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown via CMAUP database
Buphanidrine 338023 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1 315.40 unknown via CMAUP database
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP0502600
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP0502600
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP0502600
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(5-Hydroxy-1,3-benzodioxole-6-yl)-6-methoxybenzofuran-3-carbaldehyde 11587670 Click to see COC1=CC2=C(C=C1)C(=C(O2)C3=CC4=C(C=C3O)OCO4)C=O 312.27 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,12R)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene-16,17-diol 11472095 Click to see C1C2C(C3=C(O1)C(=C(C=C3)O)O)OC4=CC5=C(C=C24)OCO5 300.26 unknown https://doi.org/10.1021/NP0502600
(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene-16,17-diol 9994947 Click to see C1C2C(C3=C(O1)C(=C(C=C3)O)O)OC4=CC5=C(C=C24)OCO5 300.26 unknown https://doi.org/10.1021/NP0502600
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/NP0502600
3,4-Dihydroxy-8,9-methylenedioxypterocarpan 24013844 Click to see C1C2C(C3=C(O1)C(=C(C=C3)O)O)OC4=CC5=C(C=C24)OCO5 300.26 unknown https://doi.org/10.1021/NP0502600
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3-[4,5-Dihydroxy-2-(2-methylbut-3-en-2-yl)phenyl]-5,7-dihydroxychromen-4-one 11646071 Click to see CC(C)(C=C)C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 354.40 unknown https://doi.org/10.3184/030823407X215591
https://doi.org/10.1021/NP0502600
Fremontin 5487268 Click to see CC(C)(C=C)C1=C(C=C(C(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 354.40 unknown https://doi.org/10.1021/NP0502600
Fremontin tetraacetate 44566227 Click to see CC(=O)OC1=CC2=C(C(=C1)OC(=O)C)C(=O)C(=CO2)C3=CC(=C(C=C3C(C)(C)C=C)OC(=O)C)OC(=O)C 522.50 unknown https://doi.org/10.1021/NP0502600
Glycyrrhisoflavone 5317764 Click to see CC(=CCC1=C(C(=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones / 2-prenylated isoflavones
5,7,3',4'-Tetrahydroxy-2'-(3,3-dimethylallyl)isoflavone 11610052 Click to see CC(=CCC1=C(C=CC(=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O)C 354.40 unknown https://doi.org/10.1021/NP0502600
Acid-Catalyzed Cyclization of 5,7,3',4'-tetrahydroxy-2'-(3,3-dimethylallyl)isoflavone 11494111 Click to see CC1(CCC2=C(C=CC(=C2O1)O)C3=COC4=CC(=CC(=C4C3=O)O)O)C 354.40 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
5,7-Dihydroxy-3-[5-hydroxy-4-methoxy-2-(2-methylbut-3-en-2-yl)phenyl]chromen-4-one 24180054 Click to see CC(C)(C=C)C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)OC 368.40 unknown https://doi.org/10.3184/030823407X215591
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-[3,4-Dimethoxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dimethoxychromen-4-one 11495231 Click to see CC(=CCC1=C(C(=CC(=C1)C2=COC3=C(C2=O)C(=CC(=C3)OC)OC)OC)OC)C 410.50 unknown https://doi.org/10.1021/NP0502600
3-[4,5-Dimethoxy-2-(2-methylbut-3-en-2-yl)phenyl]-5,7-dimethoxychromen-4-one 11661504 Click to see CC(C)(C=C)C1=CC(=C(C=C1C2=COC3=C(C2=O)C(=CC(=C3)OC)OC)OC)OC 410.50 unknown https://doi.org/10.1021/NP0502600
Trimethyl fremontin 11589323 Click to see CC(C)(C=C)C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)OC)OC)OC 396.40 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
2',3'-Dihydro-5,7,8'-trihydroxy-2',2'-dimethyl[3,6'-bi-4H-1-benzopyran]-4-one 10736822 Click to see CC1(CCC2=C(O1)C(=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP0502600
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP0502600
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP0502600

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