PlantaeDB Logo
Login Sign-up

Iris tenuifolia

Iris tenuifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID644027c174f7b381654805
Scientific name Iris tenuifolia
Authority Pall.
First published in Reise Russ. Reich. 3: 714 (1776)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Cryptobasis tenuifolia (Pall.) Nevski Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 4: 244 (1937)
Iris acaulis Pall. Reise Russ. Reich. 3: 213 (1776)
Iris regelii Maxim ex Regel Trudy Imp. S.-Peterburgsk. Bot. Sada vi. (1879) 495.
Joniris tenuifolia Klatt Bot. Zeitung (Berlin) 30: 502 (1872)
Neubeckia tenuifolia Alef. Bot. Zeitung (Berlin) 21: 297 (1863)
Xiphion tenuifolium Schrank Flora 7(2 Beibl.): 19 (1824)
Cryptobasis mariae Mavrodiev Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 107(5): 78 (2002)
Cryptobasis regelii (Maxim. ex Regel) M.B.Crespo, Mart.-Azorín & Mavrodiev Phytotaxa 232: 61 (2015)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Azerbaijani nazikyarpaq süsən
Bulgarian тънколистен ирис
mn Нарийн цахилдаг
Russian Ирис тонколистный
Chinese 丝叶马蔺
Chinese 细叶马蔺
Chinese 细叶鸢尾
Chinese 老牛拽
Chinese 老牛揣
Chinese 细叶莺尾
Chinese 老牛揣子

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Siberia
      • Chita
    • Western Asia
      • Afghanistan
      • Iran
  • Europe
    • Eastern Europe
      • East European Russia
      • South European Russia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000783952
Tropicos 16602071
KEW urn:lsid:ipni.org:names:439173-1
The Plant List kew-322479
Plantarium 20835
Open Tree Of Life 43090
Observations.org 147375
NCBI Taxonomy 198827
IPNI 439173-1
iNaturalist 508380
GBIF 5298016
Freebase /m/012r4swq
Elurikkus 507689
USDA GRIN 20429
Wikipedia Iris_tenuifolia

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
Effect of grazing and climatic factors on biodiversity-ecosystem functioning relationships in grassland ecosystems - a case study of typical steppe in Inner Mongolia, China Zhang Y, Wuriliga, Liu P, Fan R, Guo J, Liu L, Ding Y Front Plant Sci 22-Dec-2023
PMCID:PMC10770857
doi:10.3389/fpls.2023.1297061
PMID:38186605
Effects of Spring Drought and Nitrogen Addition on Productivity and Community Composition of Degraded Grasslands Li S, Lu S, Li X, Hou X, Zhao X, Xu X, Zhao N Plants (Basel) 31-Jul-2023
PMCID:PMC10421370
doi:10.3390/plants12152836
PMID:37570989
Study on wild medicinal plant resources and their applied ethnology in multiethnic areas of the Gansu–Ningxia–Inner Mongolia intersection zone Xie J, Luo C, Yang X, Ren Y, Zhang X, Chen H, Zhao Y, Liu S, Wu F J Ethnobiol Ethnomed 20-May-2023
PMCID:PMC10199607
doi:10.1186/s13002-023-00585-5
PMID:37210577
Species richness and asynchrony maintain the stability of primary productivity against seasonal climatic variability Zhang Z, Hautier Y, Bao T, Yang J, Qing H, Liu Z, Wang M, Li T, Yan M, Zhang G Front Plant Sci 28-Oct-2022
PMCID:PMC9650401
doi:10.3389/fpls.2022.1014049
PMID:36388500
Intra‐annual growing season climate variability drives the community intra‐annual stability of a temperate grassland by altering intra‐annual species asynchrony and richness in Inner Mongolia, China Zhang Z, Bao T, Hautier Y, Yang J, Liu Z, Qing H Ecol Evol 04-Oct-2022
PMCID:PMC9532246
doi:10.1002/ece3.9385
PMID:36225823
Ethnobotany of wild edible plants in multiethnic areas of the Gansu–Ningxia–Inner Mongolia junction zone Jia X, Zhao Y, Zhu Y, Zeng X, Liang X, Xie J, Wu F J Ethnobiol Ethnomed 09-Aug-2022
PMCID:PMC9364587
doi:10.1186/s13002-022-00549-1
PMID:35945554
Chromane Derivatives from Underground Parts of Iris tenuifolia and Their In Vitro Antimicrobial, Cytotoxicity and Antiproliferative Evaluation Otgon O, Nadmid S, Paetz C, Dahse HM, Voigt K, Bartram S, Boland W, Dagvadorj E Molecules 05-Nov-2021
PMCID:PMC8588511
doi:10.3390/molecules26216705
PMID:34771113
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Climate variability decreases species richness and community stability in a temperate grassland Zhang Y, Loreau M, He N, Wang J, Pan Q, Bai Y, Han X Oecologia 26-Jun-2018
PMCID:PMC6112414
doi:10.1007/s00442-018-4208-1
PMID:29943096
Productivity depends more on the rate than the frequency of N addition in a temperate grassland Zhang Y, Feng J, Isbell F, Lü X, Han X Sci Rep 28-Jul-2015
PMCID:PMC4517389
doi:10.1038/srep12558
PMID:26218675
The Role of Brain-Derived Neurotrophic Factor in Comorbid Depression: Possible Linkage with Steroid Hormones, Cytokines, and Nutrition Numakawa T, Richards M, Nakajima S, Adachi N, Furuta M, Odaka H, Kunugi H Front Psychiatry 26-Sep-2014
PMCID:PMC4175905
doi:10.3389/fpsyt.2014.00136
PMID:25309465
Synthesis of 4-Methoxybenzoylhydrazones and Evaluation of Their Antiglycation Activity Taha M, Naz H, Rasheed S, Ismail NH, Rahman AA, Yousuf S, Choudhary MI Molecules 21-Jan-2014
PMCID:PMC6271482
doi:10.3390/molecules19011286
PMID:24451249
Interactive Effects of Warming and Increased Precipitation on Community Structure and Composition in an Annual Forb Dominated Desert Steppe Hou Y, Zhou G, Xu Z, Liu T, Zhang X PLoS One 19-Jul-2013
PMCID:PMC3716769
doi:10.1371/journal.pone.0070114
PMID:23894600
Wild plant folk nomenclature of the Mongol herdsmen in the Arhorchin national nature reserve, Inner Mongolia, PR China Soyolt, Galsannorbu, Yongping, Wunenbayar, Liu G, Khasbagan J Ethnobiol Ethnomed 24-Apr-2013
PMCID:PMC3649933
doi:10.1186/1746-4269-9-30
PMID:23628479
Flavans from Iris tenuifolia and their effects on β-amyloid aggregation and neural stem cells proliferation in vitro. Cui YM, Wang H, Liu QR, Han M, Lu Y, Zhao CQ Bioorg Med Chem Lett 01-Aug-2011
doi:10.1016/J.BMCL.2011.06.039
PMID:21737268

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate 163021367 Click to see CCCCCCCCCCCCC(CCCCC(CC(=O)OC(CO)CO)OC(=O)C)OC(=O)C 502.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aR,5bR,7aR,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 12305184 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(3S,3aS,5bS,11aS,13aR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one 5319770 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
3a,5a,8,8,11a,13a-Hexamethyl-3-(propan-2-yl)-1,2,3,3a,4,5,5a,5b,6,7,7a,8,10,11,11a,13,13a,13b-octadecahydro-9h-cyclopenta[a]chrysen-9-one 185590 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Aborenone 12305183 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> 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/10.1016/J.PHYTOCHEM.2008.03.011
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Ethyl glucoside 428040 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(1S,12S)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-ol 162868806 Click to see COC1=C2C3CC(C4=C(O3)C(=CC=C4)O)OC2=CC5=C1OCO5 314.29 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
(1S,9S)-11,13-dimethoxy-8,16-dioxatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10(15),11,13-hexaen-6-ol 46847424 Click to see COC1=CC2=C(C3CC(O2)C4=C(O3)C(=CC=C4)O)C(=C1)OC 300.30 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(6R)-6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one 163079697 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=C(C(=CC=C4)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
(6R)-9-hydroxy-6-(2-hydroxyphenyl)-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one 163022965 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(6S)-6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one 102066375 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=C(C(=CC=C4)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
https://doi.org/10.1016/S0031-9422(96)00596-1
2',5-Dihydroxy-6,7-methylenedioxyflavanone 74819425 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O 300.26 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
https://doi.org/10.1016/J.BMCL.2011.06.039
5,2'-Dihydroxy-6,7-methylenedioxyflavanone 42608090 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O 300.26 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
https://doi.org/10.1016/S0031-9422(96)00596-1
5,2',3'-Trihydroxy-6,7-methylenedioxyflavanone 42608091 Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=C(C(=CC=C4)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
https://doi.org/10.1016/J.BMCL.2011.06.039
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one 162919149 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)O)O 318.28 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
(2R,3R)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 163195576 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)OC)O 332.30 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
(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/J.PHYTOCHEM.2008.03.011
(2R)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 162977634 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
(2S,3R)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 162951471 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)OC)O 332.30 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
(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/J.PHYTOCHEM.2008.03.011
(2S)-2-(2,3-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydrochromen-4-one 163064968 Click to see COC1=C(C(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O)OC 332.30 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
(2S)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one 102066376 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
https://doi.org/10.1016/J.BMCL.2011.06.039
(2S)-5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 102066377 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)OC)O 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
2-(2,3-Dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one 162919148 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)O)O 318.28 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
3,5-Dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 162951470 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)OC)O 332.30 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
5,2',3'-Trihydroxy-7-methoxyflavanone 42607850 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O 302.28 unknown https://doi.org/10.1016/J.BMCL.2011.06.039
https://doi.org/10.1016/S0031-9422(96)00596-1
5,3'-Dihydroxy-7,2'-dimethoxyflavanone 42607852 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)OC)O 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00596-1
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/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Irisoid A 11045683 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)OCC4=C3C(=CC=C4)O)O 328.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
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/J.PHYTOCHEM.2008.03.011
5,7,2'-Trihydroxy-6-methoxyisoflavone 5491551 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=CC=C3O)O 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
7-(2,3-Dihydroxyphenyl)-9-hydroxy-[1,3]dioxolo[4,5-g]chromen-8-one 24970458 Click to see C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=C(C(=CC=C4)O)O)O 314.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
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.PHYTOCHEM.2008.03.011
Irisone A 5491929 Click to see COC1=CC=CC=C1C2=COC3=CC4=C(C(=C3C2=O)O)OCO4 312.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Irisone B 5387194 Click to see C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=CC=C4O)O 298.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Stilbenes
1-(6-Hydroxy-4-methoxy-1,3-benzodioxol-5-yl)-2-(2-hydroxyphenyl)ethane-1,2-dione 24970457 Click to see COC1=C(C(=CC2=C1OCO2)O)C(=O)C(=O)C3=CC=CC=C3O 316.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.