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Prangos uloptera

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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 UUID6440471555ad6440464184
Scientific name Prangos uloptera
Authority DC.
First published in Prodr. 4: 239 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Koelzella uloptera (DC.) M.Hiroe Umbell. World : 1286 (1979)
Prangos aucheri Boiss. Ann. Sci. Nat., Bot. , sér. 3, 2: 83 (1844)
Cachrys uloptera (DC.) Takht. Fl. Erevana : 188 (1972)
Cachrys uloptera (DC.) Herrnst. & Heyn Notes Roy. Bot. Gard. Edinburgh 33(3): 443. 1975
Prangos isphairamica B.Fedtsch. Fl. URSS 16: 594 (1950)
Prangos quasiperforata Kuzjmina Bot. Zhurn. (Moscow & Leningrad) 47: 252 (1962)

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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001068746
Tropicos 1703112
KEW urn:lsid:ipni.org:names:847495-1
The Plant List tro-1703112
Open Tree Of Life 413490
Observations.org 149008
NCBI Taxonomy 325744
IPNI 847495-1
iNaturalist 992386
GBIF 7883600
Elurikkus 627836
USDA GRIN 29559

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
Chemical Composition, Antioxidant and Anti-Inflammatory Activities of Clary Sage and Coriander Essential Oils Produced on Polluted and Amended Soils-Phytomanagement Approach Raveau R, Fontaine J, Verdin A, Mistrulli L, Laruelle F, Fourmentin S, Lounès-Hadj Sahraoui A Molecules 01-Sep-2021
PMCID:PMC8434190
doi:10.3390/molecules26175321
PMID:34500751
Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities Mottaghipisheh J Plants (Basel) 30-Jul-2021
PMCID:PMC8401860
doi:10.3390/plants10081577
PMID:34451622
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
Deverra tortuosa (Desf.) DC from Saudi Arabia as a new source of marmin and furanocoumarins derivatives with α-glucosidase, antibacterial and cytotoxic activities Oueslati MH, Guetat A, Bouajila J, Alzahrani AK, Basha J Heliyon 05-Apr-2021
PMCID:PMC8056227
doi:10.1016/j.heliyon.2021.e06656
PMID:33898812
Recent Updates on Anti-Inflammatory and Antimicrobial Effects of Furan Natural Derivatives Alizadeh M, Jalal M, Hamed K, Saber A, Kheirouri S, Pourteymour Fard Tabrizi F, Kamari N J Inflamm Res 19-Aug-2020
PMCID:PMC7443407
doi:10.2147/JIR.S262132
PMID:32884326
A bioclimatic characterization of high elevation habitats in the Alborz mountains of Iran Noroozi J, Körner C Alp Bot 06-Feb-2018
PMCID:PMC5856880
doi:10.1007/s00035-018-0202-9
PMID:29576762
Ethnobotanical knowledge of Apiaceae family in Iran: A review Amiri MS, Joharchi MR Avicenna J Phytomed 01-Nov-2016
PMCID:PMC5206921
PMID:28078243
Coumarins from the roots of Prangos lipskyi T. Yu. Danchul, L. V. Kuz'mina, G. A. Kuznetsova Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570686
Coumarins from the aerial parts of Prangos uloptera (Apiaceae) Seyed Mehdi Razavi, Hossein Nazemiyeh, Rogayeh Hajiboland, Yashodharan Kumarasamy, Abbas Delazar, Lutfun Nahar, Satyajit D. Sarker Springer Science and Business Media LLC 17-Apr-2008
doi:10.1590/S0102-695X2008000100002
The coumarin composition of the roots of Prangos uloptera A. Z. Abyshev, P. P. Denisenko Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580907
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!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> 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/10.1007/BF00580907
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1007/BF00580907
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF00580907
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00580907
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00580907
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1007/BF00580907
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1007/BF00580907
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 124305339 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1007/BF00580907
https://doi.org/10.1016/S0031-9422(00)00407-6
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1007/BF00580907
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1007/BF00580907
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1007/BF00580907
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1007/BF00580907
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
CID 12310408 12310408 Click to see CC=C(C)C(=O)OC1CC2(C(O2)CC(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1248/CPB.49.877
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(5R)-2,4,4-trimethyl-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 162846348 Click to see CC1=CC(C(CC1=O)COC2C(C(C(C(O2)CO)O)O)O)(C)C 330.37 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
Dianthoside 5316639 Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Phenylhydantoins
Methetoin 21908 Click to see CCC1(C(=O)NC(=O)N1C)C2=CC=CC=C2 218.25 unknown https://doi.org/10.1590/S0102-695X2008000100002
> Organoheterocyclic compounds / Isobenzofurans
(1R,3aS,7aS)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one 636977 Click to see CC1=CC(C2C(C1=O)COC2O)(C)C 196.24 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
(1S,3aS,7aS)-1-hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one 163093877 Click to see CC1=CC(C2C(C1=O)COC2O)(C)C 196.24 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
1-Hydroxy-5,7,7-trimethyl-1,3,3a,7a-tetrahydro-2-benzofuran-4-one 22297498 Click to see CC1=CC(C2C(C1=O)COC2O)(C)C 196.24 unknown https://doi.org/10.1016/S0031-9422(00)00407-6
> Phenylpropanoids and polyketides / Coumarins and derivatives
Isomeranzin 473252 Click to see CC(C)C(=O)CC1=C(C=CC2=C1OC(=O)C=C2)OC 260.28 unknown https://doi.org/10.1248/CPB.49.877
Ulopterol 176475 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 278.30 unknown https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin 442104 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1590/S0102-695X2008000100002
2-(7-Oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propyl 3-methylbut-2-enoate 25785 Click to see CC(COC(=O)C=C(C)C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3 328.40 unknown https://doi.org/10.1007/BF00570686
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/10.1590/S0102-695X2008000100002
https://doi.org/10.1007/BF00570686
Ammijin 216283 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O 408.40 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/10.1590/S0102-695X2008000100002
Oxyimperatorin 182251 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1007/BF00570686
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1007/BF00570686
Sprengelianine, (+/-)- 6183350 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3 328.40 unknown https://doi.org/10.1590/S0102-695X2008000100002
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O 202.16 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/10.1007/BF00570686
https://doi.org/10.1590/S0102-695X2008000100002
https://doi.org/10.1248/CPB.49.877
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin 5316525 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C 230.26 unknown https://doi.org/10.1248/CPB.49.877
Osthenol 5320318 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C 230.26 unknown https://doi.org/10.1248/CPB.49.877
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1248/CPB.49.877
https://doi.org/10.1590/S0102-695X2008000100002

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