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Iris nigricans

Iris nigricans - 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 UUID644027b80ff4b945874458
Scientific name Iris nigricans
Authority Dinsm.
First published in Fl. Syria , ed. 2, 2: 600 (1933)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English black iris
Arabic سوسن أسود
Persian زنبق سیاهچرده
Russian Ирис чернеющий
Slovenian črna perunika
Slovenian črni iris

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-0000783669
Tropicos 16600252
KEW urn:lsid:ipni.org:names:438911-1
The Plant List kew-322175
Open Tree Of Life 614404
NCBI Taxonomy 995810
IUCN Red List 13161765
IPNI 438911-1
iNaturalist 508329
GBIF 5298042
Freebase /m/0s8vsxh
EOL 5866838
USDA GRIN 20369
Wikipedia Iris_nigricans

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
The Cryopreservation of Medicinal and Ornamental Geophytes: Application and Challenges El Merzougui S, Benelli C, El Boullani R, Serghini MA Plants (Basel) 29-May-2023
PMCID:PMC10255897
doi:10.3390/plants12112143
PMID:37299120
The diversity of bacterial endophytes from Iris pseudacorus L. and their plant beneficial traits Shurigin V, Alimov J, Davranov K, Gulyamova T, Egamberdieva D Curr Res Microb Sci 12-Apr-2022
PMCID:PMC9325737
doi:10.1016/j.crmicr.2022.100133
PMID:35909614
Xanthone Glucosides: Isolation, Bioactivity and Synthesis Huang Q, Wang Y, Wu H, Yuan M, Zheng C, Xu H Molecules 14-Sep-2021
PMCID:PMC8465223
doi:10.3390/molecules26185575
PMID:34577044
Composition of Volatile Oil of Iris pallida Lam. from Ukraine MYKHAILENKO O Turk J Pharm Sci 02-Apr-2018
PMCID:PMC7227901
doi:10.4274/tjps.07379
PMID:32454644
In vitro propagation of an endangered medicinal herb Chlorophytum borivilianum Sant. et Fernand. through somatic embryogenesis Rizvi MZ, Kukreja AK, Bisht NS Physiol Mol Biol Plants 30-Nov-2010
PMCID:PMC3550677
doi:10.1007/s12298-010-0026-6
PMID:23572975
Capillary electrophoresis as a screening tool for alpha amylase inhibitors in plant extracts Hamdan II, Afifi FU Saudi Pharm J 13-Feb-2010
PMCID:PMC3792626
doi:10.1016/j.jsps.2010.02.004
PMID:24115900
New Isoflavones from Iris nigricans S. Al-Khalil, D. Al-Eisawi, Masaya Kato, Munekazu Iinuma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50104A001
A xanthone C-glycoside from Iris nigricans Suleiman Al-Khalil, Hideki Tosa, Munekazu Iinuma Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00641-6

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 / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP50104A001
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP50104A001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/NP50104A001
> 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/10.1021/NP50104A001
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5,8-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 92029589 Click to see C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(94)00641-6
1,3,5,8-Tetrahydroxyxanthone 5281626 Click to see C1=CC(=C2C(=C1O)C(=O)C3=C(C=C(C=C3O2)O)O)O 260.20 unknown https://doi.org/10.1016/0031-9422(94)00641-6
1,3,8-Trihydroxy-7-methoxyxanthone 14839957 Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1016/0031-9422(94)00641-6
1,4,5,7-tetrahydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 162941046 Click to see C1=CC(=C2C(=C1O)C(=O)C3=CC(=C(C(=C3O2)O)C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(94)00641-6
1,4,5,7-Tetrahydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 162941045 Click to see C1=CC(=C2C(=C1O)C(=O)C3=CC(=C(C(=C3O2)O)C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(94)00641-6
1,6-Dihydroxy-3,7-dimethoxyxanthone 5316766 Click to see COC1=CC(=C2C(=C1)OC3=CC(=C(C=C3C2=O)OC)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(94)00641-6
7-O-Methylmangiferin 101916326 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(94)00641-6
Bellidifolin 5281623 Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1016/0031-9422(94)00641-6
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(94)00641-6
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown https://doi.org/10.1016/0031-9422(94)00641-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1021/NP50104A001
> Phenylpropanoids and polyketides / Coumarins and derivatives
Nigricanin 101733537 Click to see COC1C2=C3C4=C(C=CC(=C4O1)O)C(=O)OC3=C(C=C2)O 286.24 unknown https://doi.org/10.1021/NP50104A001
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Irilone 5281779 Click to see C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=C(C=C4)O)O 298.25 unknown https://doi.org/10.1021/NP50104A001
Irisolone 165103 Click to see COC1=C2C(=CC3=C1OCO3)OC=C(C2=O)C4=CC=C(C=C4)O 312.27 unknown https://doi.org/10.1021/NP50104A001

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