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Acanthophyllum squarrosum

Acanthophyllum squarrosum - 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 UUID6440069eed32a847083598
Scientific name Acanthophyllum squarrosum
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 1: 81 (1854)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acanthophyllum pungens var. squarrosum Golenkin Trudy Imp. S.-Peterburgsk. Bot. Sada 12: 83 1893

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
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000513722
Tropicos 6302068
KEW urn:lsid:ipni.org:names:150278-1
The Plant List kew-2615124
Open Tree Of Life 5728530
NCBI Taxonomy 1524381
IPNI 150278-1
iNaturalist 850942
GBIF 5585890

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
A critical look at challenges and future scopes of bioactive compounds and their incorporations in the food, energy, and pharmaceutical sector Pai S, Hebbar A, Selvaraj S Environ Sci Pollut Res Int 02-Mar-2022
PMCID:PMC9079019
doi:10.1007/s11356-022-19423-4
PMID:35233673
Ethnoveterinary botanical survey of medicinal plants used in Pashto, Punjabi and Saraiki communities of Southwest Pakistan Abidin SZ, Munem A, Khan R, Batiha GE, Amhad M, Zafar M, Khalil AA, Hetta HF, Mahmoud MH, Sami A, Bhatti MZ Vet Med Sci 22-Jul-2021
PMCID:PMC8464251
doi:10.1002/vms3.582
PMID:34291882
Analysis and review of trichomes in plants Wang X, Shen C, Meng P, Tan G, Lv L BMC Plant Biol 01-Feb-2021
PMCID:PMC7852143
doi:10.1186/s12870-021-02840-x
PMID:33526015
Formulation and Evaluation of Licorice Shampoo in Comparison with Commercial Shampoo Azadbakht M, Monadi T, Esmaeili Z, Chabra A, Tavakoli N J Pharm Bioallied Sci 01-Oct-2018
PMCID:PMC6266641
doi:10.4103/JPBS.JPBS_243_17
PMID:30568378
Brush border membrane vesicle and Caco-2 cell line: Two experimental models for evaluation of absorption enhancing effects of saponins, bile salts, and some synthetic surfactants Moghimipour E, Tabassi SA, Ramezani M, Handali S, Löbenberg R J Adv Pharm Technol Res 01-Jul-2016
PMCID:PMC4932809
doi:10.4103/2231-4040.184588
PMID:27429925
Medicinal plants of the family Caryophyllaceae: a review of ethno-medicinal uses and pharmacological properties Chandra S, Rawat DS Integr Med Res 04-Jul-2015
PMCID:PMC5481791
doi:10.1016/j.imr.2015.06.004
PMID:28664118
An ethnobotanical survey on hormozgan province, Iran Safa O, Soltanipoor MA, Rastegar S, Kazemi M, Nourbakhsh Dehkordi K, Ghannadi A Avicenna J Phytomed 01-Jan-2013
PMCID:PMC4075690
PMID:25050260
Large scale screening of commonly used Iranian traditional medicinal plants against urease activity Nabati F, Mojab F, Habibi-Rezaei M, Bagherzadeh K, Amanlou M, Yousefi B Daru 31-Oct-2012
PMCID:PMC3556030
doi:10.1186/2008-2231-20-72
PMID:23351780
Three new acylated triterpene saponins from Acanthophyllum squarrosum. Gaidi G, Miyamoto T, Rustaiyan A, Lacaille-Dubois MA J Nat Prod 01-Jul-2001
doi:10.1021/NP010002C
PMID:11473424
Two new biologically active triterpene saponins from Acanthophyllum squarrosum. Gaidi G, Miyamoto T, Rustaiyan A, Laurens V, Lacaille-Dubois MA J Nat Prod 01-Nov-2000
doi:10.1021/NP000212+
PMID:11087591

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxycarbonyl-4-formyl-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 44558934 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC4C(C(C(CO4)O)OC5C(C(C(CO5)O)O)O)O)O)O)C)OC(=O)C67CCC(CC6C8=CCC9C1(CCC(C(C1CCC9(C8(CC7)C)C)(C)C=O)OC1C(C(C(C(O1)C(=O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)(C)C)O)O)O)O 1643.70 unknown https://doi.org/10.1021/NP000212+
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-5-hydroxy-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21592243 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5O)C)C)(C)C=O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)O 1251.40 unknown https://doi.org/10.1021/NP010002C
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10748900 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C=O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)O 1235.40 unknown https://doi.org/10.1021/NP000212+
[3-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 9-formyl-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 85255217 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C=O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)O 1235.40 unknown https://doi.org/10.1021/NP000212+
[3-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 9-formyl-5-hydroxy-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73809253 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5O)C)C)(C)C=O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)O 1251.40 unknown https://doi.org/10.1021/NP010002C

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