Abies delavayi - Unknown
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Internal ID UUID6440063c7b55f016817667
Scientific name Abies delavayi
Authority Franch.
First published in J. Bot. (Morot) 13: 255 (1899)

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Synonyms Top

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Common names Top

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Language Common/alternative name
English delavay's fir
Arabic شوح دولافي
Czech jedle delavayova
German delavays tanne
German abies fansipanensis
German abies nukiangensis
German yunnan-tanne
Persian نراد دلاوی
Finnish delavaynpihta
Italian abete di delavay
koi Делавей ньыв
udm Делавей ньылпу
Chinese 蒼山冷杉
Chinese 高山枞
Chinese 冷杉果
Chinese 苍山冷杉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Abies delavayi subsp. delavayi Unknown
Abies delavayi subsp. fansipanensis (Q.P.Xiang, L.K.Fu & Nan Li) Rushforth Int. Dendrol. Soc. Year Book 1998: 62 (1999)

Varieties (abbr. var.) Top

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Name Authority First published in
Abies delavayi var. motuoensis W.C.Cheng & L.K.Fu Acta Phytotax. Sin. 13(4): 83 (1975)
Abies delavayi var. nukiangensis (W.C.Cheng & L.K.Fu) Farjon & Silba Phytologia 68: 13 (1990)

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
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000511092
Tropicos 24901013
INPN 717026
KEW urn:lsid:ipni.org:names:261505-1
The Plant List kew-2609799
PFAF Abies delavayi
Open Tree Of Life 723562
NCBI Taxonomy 425837
NBN Atlas NHMSYS0000455516
IUCN Red List 42277
IPNI 261505-1
iNaturalist 136300
GBIF 2685456
Freebase /m/027y6k1
EPPO ABIDE
EOL 1061730
USDA GRIN 653
Wikipedia Abies_delavayi

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
Vertical distribution characteristics of soil organic carbon and vegetation types under different elevation gradients in Cangshan, Dali Yang X, Xu J, Wang H, Quan H, Yu H, Luan J, Wang D, Li Y, Lv D PeerJ 04-Jan-2024
PMCID:PMC10771771
doi:10.7717/peerj.16686
PMID:38188153
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Liverwort and Hornwort Flora of Hoàng Liên National Park and the Adjacent Areas (North Vietnam, Indochina) Bakalin VA, Klimova KG, Nguyen VS, Nguyen HM, Bakalin DA, Choi SS Plants (Basel) 29-Apr-2023
PMCID:PMC10181137
doi:10.3390/plants12091841
PMID:37176900
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA Pharmaceuticals (Basel) 11-Nov-2022
PMCID:PMC9699253
doi:10.3390/ph15111392
PMID:36422521
Forest characteristics, population structure and growth trends of threatened relict Pseudotsuga forrestii in China Tang CQ, Yao SQ, Han PB, Wen JR, Li S, Peng MC, Wang CY, Matsui T, Li YP, Lu S, He Y Plant Divers 07-Nov-2022
PMCID:PMC10435900
doi:10.1016/j.pld.2022.10.005
PMID:37601542
Extraction Techniques and Analytical Methods for Isolation and Characterization of Lignans Patyra A, Kołtun-Jasion M, Jakubiak O, Kiss AK Plants (Basel) 05-Sep-2022
PMCID:PMC9460740
doi:10.3390/plants11172323
PMID:36079704
Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K Plants (Basel) 28-Apr-2022
PMCID:PMC9105001
doi:10.3390/plants11091194
PMID:35567195
Calypogeia (Calypogeiaceae, Marchantiophyta) in Pacific Asia: Updates from Molecular Revision with Particular Attention to the Genus in North Indochina Bakalin VA, Maltseva YD, Müller F, Klimova KG, Nguyen VS, Choi SS, Troitsky AV Plants (Basel) 04-Apr-2022
PMCID:PMC9002642
doi:10.3390/plants11070983
PMID:35406962
Ethnobotanical study on plants used for traditional beekeeping by Dulong people in Yunnan, China Cheng Z, Luo B, Fang Q, Long C J Ethnobiol Ethnomed 14-Oct-2020
PMCID:PMC7559768
doi:10.1186/s13002-020-00414-z
PMID:33054863
Total Synthesis, Biological Evaluation, and Target Identification of Rare Abies Sesquiterpenoids Davis DC, Hoch DG, Wu L, Abegg D, Martin BS, Zhang ZY, Adibekian A, Dai M J Am Chem Soc 06-Dec-2018
PMCID:PMC6470006
doi:10.1021/jacs.8b07652
PMID:30461272
Geophysical upheavals and evolutionary diversification of plant species in the Himalaya Manish K, Pandit MK PeerJ 07-Nov-2018
PMCID:PMC6228543
doi:10.7717/peerj.5919
PMID:30425898
Elevation Shift in Abies Mill. (Pinaceae) of Subtropical and Temperate China and Vietnam—Corroborative Evidence from Cytoplasmic DNA and Ecological Niche Modeling Shao YZ, Zhang XC, Phan LK, Xiang QP Front Plant Sci 18-Apr-2017
PMCID:PMC5394127
doi:10.3389/fpls.2017.00578
PMID:28458681
Triterpenes as Potentially Cytotoxic Compounds Chudzik M, Korzonek-Szlacheta I, Król W Molecules 19-Jan-2015
PMCID:PMC6272502
doi:10.3390/molecules20011610
PMID:25608043
Abiespiroside A, an Unprecedented Sesquiterpenoid Spirolactone with a 6/6/5 Ring System from <i>Abies delavayi</i> Xian‐Wen Yang, Su‐Mei Li, Yong‐Li Li, Jia‐Han Xia, Liang Wu, Yun‐Heng Shen, Jun‐Mian Tian, Ning Wang, Yonghong Liu, Wei‐Dong Zhang Wiley 19-Oct-2010
doi:10.1002/EJOC.201001203
Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a Tool Li XC, Ferreira D, Ding Y Curr Org Chem 01-Oct-2010
PMCID:PMC3983998
doi:10.2174/138527210792927717
PMID:24729741

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 / Prenol lipids / Sesquiterpenoids
(4R,5R)-4-hydroxy-5-[(1S)-1-(3-hydroxy-4-methylphenyl)ethyl]-3-methylcyclopent-2-en-1-one 44179910 Click to see CC1=C(C=C(C=C1)C(C)C2C(C(=CC2=O)C)O)O 246.30 unknown https://doi.org/10.1039/B905710B
4-Hydroxy-5-[1-(3-hydroxy-4-methylphenyl)ethyl]-3-methylcyclopent-2-en-1-one 74942013 Click to see CC1=C(C=C(C=C1)C(C)C2C(C(=CC2=O)C)O)O 246.30 unknown https://doi.org/10.1039/B905710B
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,4S,4aR,8R,8aR)-3',4,7-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,4a,5,8,8a-hexahydrochromene-2,5'-furan]-2'-one 50925084 Click to see CC1CC2(C=C(C(=O)O2)C)OC3C1CC=C(C3OC4C(C(C(C(O4)CO)O)O)O)C 426.50 unknown https://doi.org/10.1002/EJOC.201001203
3',4,7-Trimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,4,4a,5,8,8a-hexahydrochromene-2,5'-furan]-2'-one 75583139 Click to see CC1CC2(C=C(C(=O)O2)C)OC3C1CC=C(C3OC4C(C(C(C(O4)CO)O)O)O)C 426.50 unknown https://doi.org/10.1002/EJOC.201001203

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