Iris sanguinea
Table of Contents
Details Top
Internal ID | UUID644027bd592e6315982996 |
Scientific name | Iris sanguinea |
Authority | Hornem. |
First published in | Hort. Bot. Hafn. 1: 58 (1813) |
Description Top
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No description added yet. Help us by writing one.
Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Iris haematophylla | Fisch. | Index Seminum (LE) 1823: 401 1823 |
Iris sibirica var. orientalis | (Schrank) Baker | J. Linn. Soc., Bot. 16: 139. 1877 |
Iris sibirica var. sanguinea | (Donn ex Hornem.) Ker Gawl. | Bot. Mag. 35: t. 1604 1813 |
Iris nertschinskia var. pumila | Makino | Ill. Fl. Japan 713 1940 |
Iris sanguinea f. albiflora | Y.N.Lee | Fl. Korea (Lee) 1163, without type. 1996 |
Limniris sanguinea | (Hornem.) Rodion. | Bot. Zhurn. (Moscow & Leningrad) 92: 551 (2007) |
Common names Top
Add a new one! Suggest a correction!Language | Common/alternative name |
---|---|
English | blood iris |
Arabic | سوسن دموي |
German | ostsibirische schwertlilie |
Persian | زنبق سنگونیا |
Japanese | 文目 |
Japanese | 綾目 |
Japanese | 菖蒲 |
Japanese | アヤメ |
Korean | 붓꽃 |
Norwegian Nynorsk | fioliris |
Swedish | violiris |
Chinese | 溪蓀 |
Chinese | 溪荪鸢尾 |
Chinese | 东方鸢尾 |
Chinese | 西伯利亚鸢尾东方变种 |
Chinese | 东方鸢属 |
Chinese | 溪荪 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!Name | Authority | First published in |
---|---|---|
Iris sanguinea var. sanguinea | Unknown | |
Iris sanguinea var. tobataensis | S.Akiyama & Iwashina | Bull. Natl. Mus. Nat. Sci., Tokyo, B. 35: 207 (2009) |
Iris sanguinea var. violacea | Makino | J. Jap. Bot. 6: 32 (1929) |
Iris sanguinea var. yixingensis | Y.T.Zhao | Acta Phytotax. Sin. 20: 99 (1982) |
Germination/Propagation Top
Suggest a correction or add new data!Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated. |
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper. |
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water. |
nick carefully; sow fresh or soak old seed; prechill 4 weeks, (or L), bring indoors once germinated to avoid temperature shock; transplant at 4 leaves |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China North-central
- China Southeast
- Manchuria
-
Eastern Asia
- Japan
- Korea
-
Mongolia
- Mongolia
-
Russian Far East
- Amur
- Khabarovsk
- Kuril Islands
- Primorye
- Sakhalin
-
Siberia
- Buryatiya
- Chita
- Irkutsk
- Yakutskiya
-
China
-
Asia-tropical click to expand
-
Indian Subcontinent
- Assam
-
Indian Subcontinent
-
Europe click to expand
-
Middle Europe
- Austria
-
Middle Europe
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000783823 |
USDA Plants | IRSA2 |
Tropicos | 16600260 |
KEW | urn:lsid:ipni.org:names:439065-1 |
The Plant List | kew-322345 |
Open Tree Of Life | 43092 |
Observations.org | 142405 |
NCBI Taxonomy | 198824 |
Nature Serve | 2.133461 |
IPNI | 439065-1 |
iNaturalist | 164133 |
GBIF | 5298821 |
Freebase | /m/0_qctgx |
EOL | 487183 |
USDA GRIN | 20393 |
Wikipedia | Iris_sanguinea |
CMAUP | NPO24890 |
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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Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
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Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
---|---|---|---|---|---|
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles | |||||
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde | 189687 | Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O | 241.24 | unknown | via CMAUP database |
2-methoxy-9H-carbazol-3-ol | 15182256 | Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)O | 213.23 | unknown | via CMAUP database |
2-methoxy-9H-carbazole-3-carbaldehyde | 6483032 | Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 | 225.24 | unknown | via CMAUP database |
3-Formyl-2-hydroxy-6-methoxycarbazole | 101508363 | Click to see C1=CC2=C(C=C1O)C3=C(N2)C=C(C(=C3)C=O)O | 227.21 | unknown | via CMAUP database |
3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carbaldehyde | 71623858 | Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C | 277.30 | unknown | via CMAUP database |
7-Hydroxyheptaphylline | 15767846 | Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)O)C=O)O)C | 295.30 | unknown | via CMAUP database |
7-Methoxyheptaphylline | 189688 | Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C | 309.40 | unknown | via CMAUP database |
9H-Carbazole-3-carbaldehyde | 504067 | Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O | 195.22 | unknown | via CMAUP database |
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- | 5317755 | Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC | 255.27 | unknown | via CMAUP database |
Clauraila D | 51039828 | Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)C | 293.30 | unknown | via CMAUP database |
Clausenawalline H | 71623801 | Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=C(C(=C3)C=O)O)O)C | 295.30 | unknown | via CMAUP database |
Clausenawalline K | 71623860 | Click to see CC1(C(C(C2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)O)O)C | 327.30 | unknown | via CMAUP database |
Clausine H | 5315952 | Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)OC | 285.29 | unknown | via CMAUP database |
Clausine K | 504070 | Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)O | 271.27 | unknown | via CMAUP database |
Clauszoline K | 10537169 | Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O | 225.24 | unknown | via CMAUP database |
Girinimbine | 96943 | Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 | 263.30 | unknown | via CMAUP database |
Heptaphylline | 5318015 | Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C | 279.30 | unknown | via CMAUP database |
Lansine | 5278451 | Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O | 241.24 | unknown | via CMAUP database |
methyl 1,6-dihydroxy-5-(3-methylbut-2-enyl)-9H-carbazole-3-carboxylate | 71623800 | Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C(=CC(=C3)C(=O)OC)O)O)C | 325.40 | unknown | via CMAUP database |
Methyl 3-carbazolecarboxylate | 504069 | Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 | 225.24 | unknown | via CMAUP database |
methyl 8-hydroxy-3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carboxylate | 71623859 | Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C(=CC(=C4)C(=O)OC)O)C | 323.30 | unknown | via CMAUP database |
Mukonal | 504068 | Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O | 211.22 | unknown | via CMAUP database |
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines | |||||
Dictamnine | 68085 | Click to see COC1=C2C=COC2=NC3=CC=CC=C31 | 199.20 | unknown | via CMAUP database |
Gamma-Fagarine | 107936 | Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 | 229.23 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides | |||||
Swertiamacroside | 6443992 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O)O | 488.40 | unknown | via CMAUP database |
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides | |||||
6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone | 44258368 | Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O | 462.40 | unknown | via CMAUP database |
Collections Top
In private collections | 0 |
In public collections | 0 |