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Iris tingitana

Iris tingitana - 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 UUID644027c227ed7063591988
Scientific name Iris tingitana
Authority Boiss. & Reut.
First published in Pugill. Pl. Afr. Bor. Hispan. : 113 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Iris coronaria Salisb. Prodr. Stirp. Chap. Allerton : 45 (1796)
Iris fontanesii Godr. Fl. France 3: 245 (1855)
Iris fontanesii var. mellorii C.Ingram Iris Year Book 1973: 97 (1973)
Iris theresiae Sennen & Mauricio Diagn. Nouv. : 206 (1936)
Iris xiphia St.-Lag. Ann. Soc. Bot. Lyon 7: 128 (1880)
Iris xiphium var. lusitanica (Ker Gawl.) Franco in J. do Amaral Franco & M. da Luz da Rocha Afonso, Nova Fl. Portugal 3(1): 135. 1994
Xiphion tingitanum Baker J. Bot. 9: 13 (1871)
Xiphion fontanesii Baker Gard. Chron. , n.s., 5: 559 (1876)
Xiphion sordidum Salisb. Trans. Hort. Soc. London 1: 303 (1812)
Iris tingitana var. fontanesii (Godr.) Maire Bull. Soc. Hist. Nat. Afrique N. 20: 204. 1929
Iris lusitanica var. sordida (Salisb.) Nyman Consp. Fl. Eur. 699 1882
Iris variabilis subsp. lusitanica (Ker Gawl.) K.Richt. Pl. Eur. 1: 258. 1890 (1890)
Iris variabilis subsp. sordida (Salisb.) K.Richt. Pl. Eur. 1: 258 1890

Common names Top

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Language Common/alternative name
English morocco iris
Arabic سوسن تينجيتانا

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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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000783967
USDA Plants IRTI
Tropicos 100206900
INPN 788886
KEW urn:lsid:ipni.org:names:439190-1
The Plant List kew-322495
Open Tree Of Life 573863
Observations.org 147875
NCBI Taxonomy 292520
NBN Atlas NHMSYS0020704152
IPNI 439190-1
iNaturalist 508389
GBIF 5298377
Freebase /m/011jj6cw
EPPO IRITI
EOL 487184
USDA GRIN 20432
Wikipedia Iris_tingitana

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)!
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Title Authors Publication Released IDs
Stilbene glucosides from the bulbs of Iris tingitana Salwa F. Farag, Yoshiaki Takaya, Masatake Niwa Elsevier BV 29-May-2009
doi:10.1016/J.PHYTOL.2009.05.001
The Chemical Examination of Iris nepalensis. III. Isolation and Structure of Irisolidone Lalit Prakash, Asif Zaman, A. R. Kidwai American Chemical Society (ACS) 29-May-2007
doi:10.1021/JO01021A504
Two isoflavonoids from the fresh bulbs of Iris tingitana Nasr A. El-Emary, Yoshimasa Kobayashi, Yukio Ogihara Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83844-3

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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(3R,4S,5S,6R)-2-[3-hydroxy-5-[(2S,3S)-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-6-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydro-1-benzofuran-3-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163070503 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C6)OC7C(C(C(C(O7)CO)O)O)O)O)O 778.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001
(3R,4S,5S,6R)-2-[3-hydroxy-5-[(2S,3S)-8-hydroxy-2-(4-hydroxyphenyl)-10-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydronaphtho[2,1-e][1]benzofuran-3-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163070407 Click to see C1=CC(=CC2=C1C=CC3=C4C(C(OC4=CC(=C32)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)OC8C(C(C(C(O8)CO)O)O)O)O)O 776.70 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-O-Methylgenistein 5748551 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001
Betavulgarin 442668 Click to see COC1=C2C(=CC3=C1OCO3)OC=C(C2=O)C4=CC=CC=C4O 312.27 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-O-Methylgenistein 7-O-glucoside 44257327 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Irigenin 5464170 Click to see COC1=CC(=CC(=C1OC)O)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
Iriskumaonin 44257359 Click to see COC1=C(C=C(C=C1)C2=COC3=CC4=C(C(=C3C2=O)OC)OCO4)O 342.30 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Iriskumaonin methyl ether 14507159 Click to see COC1=C(C=C(C=C1)C2=COC3=CC4=C(C(=C3C2=O)OC)OCO4)OC 356.30 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
Irisolidone 5281781 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
https://doi.org/10.1021/JO01021A504
Irisolone methyl ether 14539329 Click to see COC1=CC=C(C=C1)C2=COC3=CC4=C(C(=C3C2=O)OC)OCO4 326.30 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Resveratrol 3-Glucoside 25579167 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1016/J.PHYTOL.2009.05.001

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