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Prangos tschimganica

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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 UUID643ff76b5bfe2048213252
Scientific name Prangos tschimganica
Authority Fedtsch.
First published in Bull. Herb. Boissier 7: 180 (1899)

Description Top

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Synonyms Top

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Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000391236
Tropicos 1700214
KEW urn:lsid:ipni.org:names:847491-1
Open Tree Of Life 3888519
Observations.org 148558
NCBI Taxonomy 1585712
IPNI 847491-1
iNaturalist 1225568
GBIF 3630157
USDA GRIN 29558

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
Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV Int J Mol Sci 02-Feb-2023
PMCID:PMC9917851
doi:10.3390/ijms24032839
PMID:36769163
Pharmacological perspectives and molecular mechanisms of coumarin derivatives against virus disease Li Z, Kong D, Liu Y, Li M Genes Dis 20-Apr-2021
PMCID:PMC8720699
doi:10.1016/j.gendis.2021.03.007
PMID:35005109
In silico molecular docking: Evaluation of coumarin based derivatives against SARS-CoV-2 Chidambaram SK, Ali D, Alarifi S, Radhakrishnan S, Akbar I J Infect Public Health 21-Sep-2020
PMCID:PMC7505582
doi:10.1016/j.jiph.2020.09.002
PMID:33008777
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products Kaur R, Sharma P, Gupta GK, Ntie-Kang F, Kumar D Molecules 29-Apr-2020
PMCID:PMC7249135
doi:10.3390/molecules25092070
PMID:32365518
Changes of Metabolomic Profile in Helianthus annuus under Exposure to Chromium(VI) Studied by capHPLC-ESI-QTOF-MS and MS/MS Gonzalez Ibarra AA, Wrobel K, Yanez Barrientos E, Corrales Escobosa AR, Gutierrez Corona JF, Enciso Donis I, Wrobel K J Anal Methods Chem 22-Nov-2017
PMCID:PMC5735654
doi:10.1155/2017/3568621
PMID:29359067
Therapeutic potential of coumarins as antiviral agents Hassan MZ, Osman H, Ali MA, Ahsan MJ Eur J Med Chem 25-Jul-2016
PMCID:PMC7115672
doi:10.1016/j.ejmech.2016.07.056
PMID:27484512
Antiviral Activity of Phytochemicals: A Current Perspective Naithani R, Mehta RG, Shukla D, Chandersekera SN, Moriarty RM Dietary Components and Immune Function 07-Jun-2010
PMCID:PMC7121922
doi:10.1007/978-1-60761-061-8_24
Chemical constituents of Prangos tschiniganica; structure elucidation and absolute configuration of coumarin and furanocoumarin derivatives with anti-HIV activity. Shikishima Y, Takaishi Y, Honda G, Ito M, Takfda Y, Kodzhimatov OK, Ashurmetov O, Lee KH Chem Pharm Bull (Tokyo) 01-Jul-2001
doi:10.1248/CPB.49.877
PMID:11456095
Terpenoids and gamma-pyrone derivatives from Prangos tschimganica. Shikishima Y, Takaishi Y, Honda G, Ito M, Takeda Y, Kodzhimatov OK, Ashurmetov O Phytochemistry 01-May-2001
doi:10.1016/S0031-9422(00)00407-6
PMID:11336255

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 / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
[3-hydroxy-1-(7-methoxy-2-oxochromen-8-yl)-3-methylbutan-2-yl] (3R,5R)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylate 10884893 Click to see CC(C)(C(CC1=C(C=CC2=C1OC(=O)C=C2)OC)OC(=O)C3(CC(C(C(C3)O)O)O)O)O 452.50 unknown https://doi.org/10.1248/CPB.49.877
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(3S)-3-methoxy-4,6,6-trimethylcyclohexa-1,4-diene-1-carbaldehyde 162858747 Click to see CC1=CC(C(=CC1OC)C=O)(C)C 180.24 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
(5R)-5-methoxy-4,6,6-trimethylcyclohexa-1,3-diene-1-carbaldehyde 162847541 Click to see CC1=CC=C(C(C1OC)(C)C)C=O 180.24 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Maltol 8369 Click to see CC1=C(C(=O)C=CO1)O 126.11 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
[3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] (3R,5R)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylate 10961807 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)OC(=O)C4(CC(C(C(C4)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.49.877
[3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-9-yl)oxybutan-2-yl] (3R,5R)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylate 11812811 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(=O)C4(CC(C(C(C4)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/CPB.49.877
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1248/CPB.49.877
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1248/CPB.49.877
Isogosferol 148619 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 286.28 unknown https://doi.org/10.1248/CPB.49.877
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1248/CPB.49.877
Marmesin 334704 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O 246.26 unknown https://doi.org/10.1248/CPB.49.877
Pabularinone 14521099 Click to see CC(C)C(=O)COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 286.28 unknown https://doi.org/10.1248/CPB.49.877
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1248/CPB.49.877
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
2H-1-Benzopyran-2-one, 6-(2,3-dihydroxy-3-methylbutyl)-7-hydroxy- 5374451 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)O)O)O 264.27 unknown https://doi.org/10.1248/CPB.49.877
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1248/CPB.49.877

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