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Oxytropis ochrocephala

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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 UUID643fd988a95bd230254742
Scientific name Oxytropis ochrocephala
Authority Bunge
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 22(1): 57 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Spiesia ochrocephala (Bunge) Kuntze Revis. Gen. Pl.1: 207 (1891)

Common names Top

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Language Common/alternative name
Chinese 甘肃棘豆
Chinese 马绊肠
Chinese 鸡翔草
Chinese 黄花棘豆
Chinese 团巴草
Chinese 希日-其其格图-奥日图哲
Chinese 黃花棘豆

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Oxytropis ochrocephala var. latibracteata Y.H.Wu Fl. Kunlunica2: 727 (2015)
Oxytropis ochrocephala var. ochrocephala Bunge Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
      • China South-central
      • Inner Mongolia
      • Qinghai
      • Tibet
      • Xinjiang

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186009
Tropicos 13031179
KEW urn:lsid:ipni.org:names:511732-1
The Plant List ild-32347
Open Tree Of Life 5147767
NCBI Taxonomy 483875
IPNI 511732-1
GBIF 5361417
EPPO OXROC
EOL 644239
CMAUP NPO19803

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_020916435.1 ASM2091643v1 Chromosome Northwestern University 2021-11-22 314.0x 914.49 Mb

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
Vegetation communities and soil properties along the restoration process of the Jinqianghe mine site in the Qilian Mountains, China Yang X, Feng Q, Zhu M, Zhang J, Yang L, Zhang C, Wang Z, Feng Y Front Plant Sci 22-Apr-2024
PMCID:PMC11070538
doi:10.3389/fpls.2024.1358309
PMID:38711611
The loss of plant functional groups increased arthropod diversity in an alpine meadow on the Tibetan Plateau Lu N, Yang H, Zhou X, Tan Y, Cai W, Jiang Q, Lu Y, Chen Y, He H, Wang S Front Plant Sci 16-Feb-2024
PMCID:PMC10904612
doi:10.3389/fpls.2024.1305768
PMID:38434435
Transcriptomic Screening of Alternaria oxytropis Isolated from Locoweed Plants for Genes Involved in Mycotoxin Swaisonine Production Yuan S, Zhao Q, Yu K, Gao Y, Ma Z, Li H, Yu Y J Fungi (Basel) 22-Jan-2024
PMCID:PMC10820250
doi:10.3390/jof10010088
PMID:38276034
Community ecological succession of endophytic fungi associates with medicinal compound accumulation in Sophora alopecuroides Ju M, Zhang Q, Wang R, Yan S, Zhang Q, Li P, Hao F, Gu P Microbiol Spectr 18-Jan-2024
PMCID:PMC10845968
doi:10.1128/spectrum.03076-23
PMID:38236025
Diazotrophic abundance and community structure associated with three meadow plants on the Qinghai-Tibet Plateau Nshimiyimana JB, Zhao K, Wang W, Kong W Front Microbiol 08-Jan-2024
PMCID:PMC10801153
doi:10.3389/fmicb.2023.1292860
PMID:38260880
Plant Secondary Compounds Promote White Adipose Tissue Browning via Modulation of the Gut Microbiota in Small Mammals Ren S, Zhang L, Tang X, Fan C, Zhao Y, Cheng Q, Zhang Y Int J Mol Sci 13-Dec-2023
PMCID:PMC10743627
doi:10.3390/ijms242417420
PMID:38139249
Transcriptome profiling of Bergenia purpurascens under cold stress Zhang X, Yu F, Lyu X, Chen J, Zeng H, Xu N, Wu Y, Zhu Q BMC Genomics 07-Dec-2023
PMCID:PMC10702111
doi:10.1186/s12864-023-09850-z
PMID:38062379
Interactive effects between the invasive weed Stellera chamaejasme and grass: can arbuscular mycorrhizal fungi and fungal pathogens coregulate interspecific relationships? Zhang R, Qu S, Zhang B, Gao Y, Xing F Front Microbiol 30-Aug-2023
PMCID:PMC10498474
doi:10.3389/fmicb.2023.1236891
PMID:37711687
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649
Salt stress responses and alleviation strategies in legumes: a review of the current knowledge Bouzroud S, Henkrar F, Fahr M, Smouni A 3 Biotech 28-Jul-2023
PMCID:PMC10382465
doi:10.1007/s13205-023-03643-7
PMID:37520340
Patterns and drivers of the belowground bud bank in alpine grasslands on the Qinghai-Tibet Plateau Li W, Huang A, Zhou T, Liu M, Ma S, Zhao N, Wang X, Sun J Front Plant Sci 18-Jan-2023
PMCID:PMC9893863
doi:10.3389/fpls.2022.1095864
PMID:36743557
In-depth characterization of phytase-producing plant growth promotion bacteria isolated in alpine grassland of Qinghai-Tibetan Plateau Li Q, Yang X, Li J, Li M, Li C, Yao T Front Microbiol 04-Jan-2023
PMCID:PMC9846362
doi:10.3389/fmicb.2022.1019383
PMID:36687657
Response of soil microbial compositional and functional heterogeneity to grazing exclusion in alpine shrub and meadows in the Qinghai–Tibet Plateau Wang S, Abalori TA, Wang W, Deng X, Liu W, Wang J, Cao W Front Microbiol 30-Nov-2022
PMCID:PMC9748428
doi:10.3389/fmicb.2022.1038805
PMID:36532507
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Soil Fungal Composition Drives Ecosystem Multifunctionality after Long-Term Field Nitrogen and Phosphorus Addition in Alpine Meadows on the Tibetan Plateau Cheng B, Liu H, Bai J, Li J Plants (Basel) 28-Oct-2022
PMCID:PMC9656404
doi:10.3390/plants11212893
PMID:36365345

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one, 7,7a,8,9,10,11,13,14-octahydro-, [7R-(7alpha,7aalpha,14alpha)]- 91746595 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0305-1978(94)90091-4
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0305-1978(94)90091-4
Thermopsine perchlorate 228640 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0305-1978(94)90091-4
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(94)90091-4
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(94)90091-4
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(94)90091-4
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(94)90091-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Octadecene 8217 Click to see CCCCCCCCCCCCCCCCC=C 252.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
Yuanhuacine 5358691 Click to see CCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C7=CC=CC=C7)C)C=C(C6=O)C)O)O)CO 648.70 unknown via CMAUP database
Yuanhuaoate E 73348817 Click to see CCCCCC=CC=CC(=O)OC1C2C3C(O3)(C(C4(C(C2(C(C(C1(C(=C)C)O)OC(=O)C5=CC=CC=C5)C)O)C=C(C4=O)C)O)O)CO 666.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,2'R,3'S,8'S)-3',4,5',6-tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 100885566 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(O3)C5=CC=C(C=C5)O)C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O 542.50 unknown via CMAUP database
Daphnodorin A 72426 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown via CMAUP database
Daphnodorin B 72427 Click to see C1C(C(OC2=C1C(=CC3=C2C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5O)O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown via CMAUP database
Daphnodorin C 72428 Click to see C1CC2=C(C3=C(C=C2O)OC(C34C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5S,6R,13S)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984107 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown via CMAUP database
(1S,5S,13R)-1,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 76317993 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown via CMAUP database
(1S,5S,6R,13R)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984106 Click to see C1C(C(OC2=C1C(=CC3=C2C4(C(=O)C5=C(C=C(C=C5OC4(O3)C6=CC=C(C=C6)O)O)O)O)O)C7=CC=C(C=C7)O)O 558.50 unknown via CMAUP database
daphnodorin D2 13941113 Click to see C1CC2=C(C(=C(C=C2O)O)C3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown via CMAUP database
Daphnodorin F 70688394 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(91)85128-M
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1080/14786419.2012.678350
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(beta-D-glucopyranosyloxy)-5-hydroxy-7-methoxy- 122361335 Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(91)85128-M

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