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Pfaffia iresinoides

Pfaffia iresinoides - 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 UUID643ff7cb9583c203027154
Scientific name Pfaffia iresinoides
Authority Spreng.
First published in Syst. Veg. 4(2): 103 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alternanthera iresinoides Kunth Nov. Gen. Sp. 2: 209 (1818)
Gomphrena iresinoides Moq. Prodr. 13(2): 383 (1849)
Gomphrena iresinoides var. martiana Seub. Fl. Bras. 5(1): 190 (1875)
Gomphrena iresinoides var. riedeliana Seub. Fl. Bras. 5(1): 191 (1875)
Iresine luzuliflora Griseb. Fl. Brit. W. I. : 65 (1859)
Sertuernera iresinoides Mart. Nov. Gen. Sp. Pl. Bras. 2: 48 (1826)

Common names Top

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Language Common/alternative name
English illecebrum iresinoides

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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No forms added yet.

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
  • Southern America
    • Caribbean
      • Haiti
      • Leeward Islands
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000394289
UNII KY5OZ3A24T
Tropicos 1101158
INPN 630372
KEW urn:lsid:ipni.org:names:61055-1
The Plant List kew-2407785
Open Tree Of Life 780108
NCBI Taxonomy 451963
IPNI 61055-1
iNaturalist 279373
GBIF 7323495
EPPO PFFIR
USDA GRIN 27475

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
Evaluation of Ajuga bracteosa for antioxidant, anti-inflammatory, analgesic, antidepressant and anticoagulant activities Kayani WK, Dilshad E, Ahmed T, Ismail H, Mirza B BMC Complement Altern Med 27-Sep-2016
PMCID:PMC5039935
doi:10.1186/s12906-016-1363-y
PMID:27677846
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467
Practical uses for ecdysteroids in mammals including humans: an update Lafont R, Dinan L J Insect Sci 14-Mar-2003
PMCID:PMC524647
doi:10.1093/jis/3.1.7
PMID:15844229
Iresinoside, a yellow pigment from Pfaffia iresinoides Y Shiobara Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80192-H
Three ecdysteroid glycosides from Pfaffia iresinoides Nobushige Nishimoto, Yoshinori Shiobara, Shun-suke Inoue, Masumi Fujino, Tsunematsu Takemoto, Cheow Lin Yeoh, Fernando de Oliveira, Gokithi Akisue, Maria Kubota Akisue, Goro Hashimoto Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80422-9
Ecdysteroids from Pfaffia iresinoides and reassignment of some 13CNMR chemical shifts☆ Nobushige Nishimoto, Yoshinori Shiobara, Masumi Fujino, Shun-Suke Inoue, Tsunematsu Takemoto, Fernando De Oliveira, Gokithi Akisue, Maria Kubota Akisue, Goro Hashimoto, Osamu Tanaka Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83865-0
Ecdysteroid 7,9(11)-dien-6-ones as potential photoaffinity labels for ecdysteroid binding proteins Bourne PC, Whiting P, Dhadialla TS, Hormann RE, Girault JP, Harmatha J, Lafont R, Dinan L J Insect Sci 28-Jun-2002
PMCID:PMC355911
doi:10.1093/jis/2.1.11
PMID:15455045

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 / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(88)80422-9
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(88)80422-9
https://doi.org/10.1016/S0031-9422(00)83865-0
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0031-9422(00)83865-0
https://doi.org/10.1016/0031-9422(88)80422-9
Pterosterone 441836 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(88)80422-9
https://doi.org/10.1016/S0031-9422(00)83865-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(2R,3R,5S)-2,3-dihydroxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162893359 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 642.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11039514 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 642.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
17-[2,3-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 14132163 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 642.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
17-[2,3-dihydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 14132157 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 642.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,5R,10S,13R,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,11,12,16,17-decahydrocyclopenta[a]phenanthren-6-one 14132162 Click to see CC12CCC3=C(C1=CCC2C(C)(C(CCC(C)(C)OC4C(C(C(C(O4)CO)O)O)O)O)O)CC(=O)C5C3(CC(C(C5)O)O)C 624.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
17-[2,3-Dihydroxy-6-methyl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,11,12,16,17-decahydrocyclopenta[a]phenanthren-6-one 14132161 Click to see CC12CCC3=C(C1=CCC2C(C)(C(CCC(C)(C)OC4C(C(C(C(O4)CO)O)O)O)O)O)CC(=O)C5C3(CC(C(C5)O)O)C 624.80 unknown https://doi.org/10.1016/0031-9422(88)80422-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[7-methoxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 78124326 Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)C3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)OC 554.50 unknown https://doi.org/10.1016/0031-9422(92)80192-H

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