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Iris crocea

Iris crocea - 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 UUID644027ac1917f045919904
Scientific name Iris crocea
Authority Jacquem. ex R.C.Foster
First published in Contr. Gray Herb. 114: 41 (1936)

Description Top

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Synonyms Top

Scientific name Authority First published in
Iris aurea Lindl. Edwards's Bot. Reg. 33: t. 59. 1847
Iris spuria subsp. aurea Dykes Gen. Iris 65. 1913 (1913)

Common names Top

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Language Common/alternative name
Arabic سوسن مذهب
Persian زنبق زعفرانی
Chinese 鲜黄鸢尾

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

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-0000783242
KEW urn:lsid:ipni.org:names:438518-1
The Plant List kew-321731
Open Tree Of Life 3998472
IPNI 438518-1
iNaturalist 486413
GBIF 5297956
Freebase /m/012smyzw
EOL 2902996
USDA GRIN 428732
Wikipedia Iris_crocea

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)!
Title Authors Publication Released IDs
Isoflavonoids from Iris crocea Abdul S Shawl, Tej Kumar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80300-4

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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-alpinone 46883390 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1016/0031-9422(92)80300-4
(2S,3S)-3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 90646612 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1016/0031-9422(92)80300-4
Alpinone 5317747 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1016/0031-9422(92)80300-4
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
[4-(5,7-Diacetyloxy-6-methoxy-4-oxochromen-3-yl)phenyl] acetate 162915533 Click to see CC(=O)OC1=CC=C(C=C1)C2=COC3=CC(=C(C(=C3C2=O)OC(=O)C)OC)OC(=O)C 426.40 unknown https://doi.org/10.1016/0031-9422(92)80300-4
5,7-Dihydroxy-2',6-dimethoxyisoflavone 5491794 Click to see COC1=CC=CC=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/0031-9422(92)80300-4
Tectorigenin 5281811 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(92)80300-4
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154497558 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(92)80300-4
5-Hydroxy-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162916994 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1016/0031-9422(92)80300-4
5,7-dihydroxy-6-methoxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 44133603 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(92)80300-4
5,7-Dihydroxy-6-methoxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 163021887 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(92)80300-4
Tectorigenin-7-O-beta-glucosyl-4'-O-beta-glucoside 16126681 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 624.50 unknown https://doi.org/10.1016/0031-9422(92)80300-4
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(6aR,12aR)-11,12a-dihydroxy-9,10-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 162938165 Click to see COC1=C(C(=C2C(=C1)OC3COC4=CC=CC=C4C3(C2=O)O)O)OC 344.30 unknown https://doi.org/10.1016/0031-9422(92)80300-4
11,12a-Dihydroxy-9,10-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 73175724 Click to see COC1=C(C(=C2C(=C1)OC3COC4=CC=CC=C4C3(C2=O)O)O)OC 344.30 unknown https://doi.org/10.1016/0031-9422(92)80300-4
Coccineone 15385379 Click to see COC1=C(C(=C2C(=C1)OC3COC4=CC=CC=C4C3(C2=O)O)O)OC 344.30 unknown https://doi.org/10.1016/0031-9422(92)80300-4

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