Citrus cavaleriei - Unknown
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Internal ID UUID6440118cc4df6718827190
Scientific name Citrus cavaleriei
Authority H.Lév. ex Cavalerie
First published in Bull. Acad. Int. Géogr. Bot. 21: 211 (1911)

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Synonyms Top

Scientific name Authority First published in
Citrus aurantium subsp. ichangensis (Swingle) Guillaumin Cit. Cult. Sauv. 28
Citrus hongheensis Y.Ye, X.Liu, S.Q.Ding & M.Liang Acta Phytotax. Sin. 14(1): 57 (1976)
Citrus ichangensis Swingle J. Agric. Res. 1: 1 (1913)
Citrus macrosperma T.C.Guo & Y.M.Ye Acta Phytotax. Sin. 35: 353 (1997)

Common names Top

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Language Common/alternative name
English ichang lemon or ichang papeda
Japanese イーチャンチー
Japanese 宜昌橙
Japanese イーチャンパペダ
Korean 의창지
Lithuanian rytinis citrinmedis
Thai มะส้าน
Chinese 野柑子
Chinese 橘红
Chinese 红河橙
Chinese 宜昌橙
Chinese 宜昌橙(野柑子)
Chinese 大种橙

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000607966
Tropicos 50119416
KEW urn:lsid:ipni.org:names:771870-1
The Plant List kew-2724045
Open Tree Of Life 929667
NCBI Taxonomy 2709
IPNI 771870-1
iNaturalist 765425
GBIF 3832575
Freebase /m/01hnh8
USDA GRIN 461658
Wikipedia Citrus_cavaleriei

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_030448935.1 ASM3044893v1 Contig Huazhong Agriculture University 2023-07-13 85.0x 347.63 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
Preparation, Characterization and Application of Active Food Packaging Films Based on Sodium Alginate and Twelve Varieties of Mandarin Peel Powder Yun D, Liu J Foods 12-Apr-2024
PMCID:PMC11048805
doi:10.3390/foods13081174
PMID:38672846
The lemon genome and DNA methylome unveil epigenetic regulation of citric acid biosynthesis during fruit development Yu H, Zhang C, Lu C, Wang Y, Ge C, Huang G, Wang H Hortic Res 05-Jan-2024
PMCID:PMC10923643
doi:10.1093/hr/uhae005
PMID:38464476
Transposable elements cause the loss of self‐incompatibility in citrus Hu J, Liu C, Du Z, Guo F, Song D, Wang N, Wei Z, Jiang J, Cao Z, Shi C, Zhang S, Zhu C, Chen P, Larkin RM, Lin Z, Xu Q, Ye J, Deng X, Bosch M, Franklin‐Tong VE, Chai L Plant Biotechnol J 01-Dec-2023
PMCID:PMC11022811
doi:10.1111/pbi.14250
PMID:38038155
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Bayesian phylodynamic analysis reveals the evolutionary history and the dispersal patterns of citrus tristeza virus in China based on the p25 gene Wang C, Chen C, Chen Y, Zhong K, Yi L Virol J 03-Oct-2023
PMCID:PMC10548698
doi:10.1186/s12985-023-02190-0
PMID:37789347
Comprehensive analyses of the citrus WRKY gene family involved in the metabolism of fruit sugars and organic acids Zhang M, Lu W, Yang X, Li Q, Lin X, Liu K, Yin C, Xiong B, Liao L, Sun G, He S, He J, Wang X, Wang Z Front Plant Sci 15-Sep-2023
PMCID:PMC10540311
doi:10.3389/fpls.2023.1264283
PMID:37780491
Evolutionary assessment of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE genes in citrus relatives with a specific focus on flowering Li Y, Wang S, Adhikari PB, Liu B, Liu S, Huang Y, Hu G, Notaguchi M, Xu Q Mol Hortic 20-Jul-2023
PMCID:PMC10515035
doi:10.1186/s43897-023-00061-4
PMID:37789480
Evolution‐guided multiomics provide insights into the strengthening of bioactive flavone biosynthesis in medicinal pummelo Zheng W, Zhang W, Liu D, Yin M, Wang X, Wang S, Shen S, Liu S, Huang Y, Li X, Zhao Q, Yan L, Xu Y, Yu S, Hu B, Yuan T, Mei Z, Guo L, Luo J, Deng X, Xu Q, Huang L, Ma Z Plant Biotechnol J 28-Apr-2023
PMCID:PMC10363765
doi:10.1111/pbi.14058
PMID:37115171
Citrus genomic resources unravel putative genetic determinants of Huanglongbing pathogenicity Gao Y, Xu J, Li Z, Zhang Y, Riera N, Xiong Z, Ouyang Z, Liu X, Lu Z, Seymour D, Zhong B, Wang N iScience 23-Jan-2023
PMCID:PMC9941208
doi:10.1016/j.isci.2023.106024
PMID:36824272
Nanopore long-read RNAseq reveals transcriptional variations in citrus species Hu XL, You C, Zhu K, Li X, Gong J, Ma H, Sun X Front Plant Sci 04-Jan-2023
PMCID:PMC9845879
doi:10.3389/fpls.2022.1077797
PMID:36684788
A chromosome-level phased genome enabling allele-level studies in sweet orange: a case study on citrus Huanglongbing tolerance Wu B, Yu Q, Deng Z, Duan Y, Luo F, Gmitter Jr F Hortic Res 03-Nov-2022
PMCID:PMC9832951
doi:10.1093/hr/uhac247
PMID:36643761
Insights into the mechanism of Huanglongbing tolerance in the Australian finger lime (Citrus australasica) Weber KC, Mahmoud LM, Stanton D, Welker S, Qiu W, Grosser JW, Levy A, Dutt M Front Plant Sci 21-Oct-2022
PMCID:PMC9634478
doi:10.3389/fpls.2022.1019295
PMID:36340410
Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification Wang N, Li C, Kuang L, Wu X, Xie K, Zhu A, Xu Q, Larkin RM, Zhou Y, Deng X, Guo W Proc Natl Acad Sci U S A 19-Oct-2022
PMCID:PMC9618123
doi:10.1073/pnas.2206076119
PMID:36260744
The complex genome and adaptive evolution of polyploid Chinese pepper (Zanthoxylum armatum and Zanthoxylum bungeanum) Hu L, Xu Z, Fan R, Wang G, Wang F, Qin X, Yan L, Ji X, Meng M, Sim S, Chen W, Hao C, Wang Q, Zhu H, Zhu S, Xu P, Zhao H, Lindsey K, Daniell H, Wendel JF, Jin S Plant Biotechnol J 07-Oct-2022
PMCID:PMC9829393
doi:10.1111/pbi.13926
PMID:36117410
Transcriptome analysis of the pulp of citrus fruitlets suggests that domestication enhanced growth processes and reduced chemical defenses increasing palatability Perez-Roman E, Borredá C, Tadeo FR, Talon M Front Plant Sci 02-Sep-2022
PMCID:PMC9478336
doi:10.3389/fpls.2022.982683
PMID:36119632

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 / Terpene lactones
Ichangin 441801 Click to see CC12CCC3C(C14C(O4)C(=O)OC2C5=COC=C5)(C(=O)CC(C36COC(=O)CC6O)C(C)(C)O)C 488.50 unknown https://doi.org/10.1016/S0031-9422(00)90464-3
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids
(6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 134781708 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C3C=C4C(CC(CC4(O3)C)O)(C)C 600.90 unknown https://doi.org/10.1007/BF00579990
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Phytofluene 6436722 Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C 542.90 unknown https://doi.org/10.1007/BF00579990
Tetrahydro-beta-carotene/eta-Carotene 16061254 Click to see CC1=C(C(CCC1)(C)C)CCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)CCC2=C(CCCC2(C)C)C)C)C 540.90 unknown https://doi.org/10.1007/BF00579990
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(6S,7Ar)-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 134737870 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C 584.90 unknown https://doi.org/10.1007/BF00579990
2-[(2Z,4E,6E,8E,10E,12E,14E,16E)-17-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 101526841 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown https://doi.org/10.1007/BF00579990
Citroxanthin 5281246 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CCCC3(O2)C)(C)C)C)C 552.90 unknown https://doi.org/10.1007/BF00579990
Cryptoflavin 5376350 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CCCC3(O2)C)(C)C)C)C 568.90 unknown https://doi.org/10.1007/BF00579990
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,2R,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-13-yl] acetate 137706495 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C 514.60 unknown https://doi.org/10.1016/S0031-9422(00)90464-3
https://doi.org/10.1021/JF00088A003
CID 326240 326240 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C 514.60 unknown https://doi.org/10.1016/S0031-9422(00)90464-3
https://doi.org/10.1021/JF00088A003
Deacetylnomilin 139082180 Click to see CC1(C2CC(=O)C3(C(C2(C(CC(=O)O1)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 472.50 unknown https://doi.org/10.1021/JF00088A003
https://doi.org/10.1016/S0031-9422(00)90464-3
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1021/JF00088A003
https://doi.org/10.1016/S0031-9422(00)90464-3
Obacunone 119041 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown https://doi.org/10.1021/JF00088A003
https://doi.org/10.1016/S0031-9422(00)90464-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1R,2R,4S,7S,8S,11R,12R,13S,16R)-7-(furan-3-yl)-13-hydroxy-1,8,12,13,15,15-hexamethyl-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecane-5,18-dione 101592373 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)(C)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 444.50 unknown https://doi.org/10.1021/JF00088A003
https://doi.org/10.1016/S0031-9422(00)90464-3
https://doi.org/10.1016/0031-9422(88)80238-3
(1R,2R,5R,6R,7R,10S,11S,14S)-6-acetyl-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-3,13-dione 163013248 Click to see CC(=O)C1(C2CCC3(C(OC(=O)C4C3(C2(C(=O)CC1C(C)(C)O)C)O4)C5=COC=C5)C)C 444.50 unknown https://doi.org/10.1016/0031-9422(88)80238-3
3-[(1R,2R,5R,6R,7R,10S,11S,14S)-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-3,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]-3-hydroxypropanoic acid 101601415 Click to see CC12CCC3C(C(CC(=O)C3(C14C(O4)C(=O)OC2C5=COC=C5)C)C(C)(C)O)(C)C(CC(=O)O)O 490.50 unknown https://doi.org/10.1021/JF00088A003
https://doi.org/10.1016/S0031-9422(00)90464-3
6-Acetyl-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-3,13-dione 14037477 Click to see CC(=O)C1(C2CCC3(C(OC(=O)C4C3(C2(C(=O)CC1C(C)(C)O)C)O4)C5=COC=C5)C)C 444.50 unknown https://doi.org/10.1016/0031-9422(88)80238-3
Nomilinic acid 131751863 Click to see CC(=O)OC(CC(=O)O)C1(C2CCC3(C(OC(=O)C4C3(C2(C(=O)CC1C(C)(C)O)C)O4)C5=COC=C5)C)C 532.60 unknown https://doi.org/10.1016/S0031-9422(00)90464-3
https://doi.org/10.1021/JF00088A003
> Organoheterocyclic compounds / Naphthofurans
9b-(2-Carboxy-1-hydroxyethyl)-7-[furan-3-yl(hydroxy)methyl]-3,3,5a,7-tetramethyl-5-oxospiro[1,3a,4,8,9,9a-hexahydrobenzo[e][2]benzofuran-6,3'-oxirane]-2'-carboxylic acid 162818618 Click to see CC1(C2CC(=O)C3(C(C2(CO1)C(CC(=O)O)O)CCC(C34C(O4)C(=O)O)(C)C(C5=COC=C5)O)C)C 506.50 unknown https://doi.org/10.1016/S0031-9422(00)90464-3
https://doi.org/10.1021/JF00088A003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1016/0305-1978(95)00109-3
Didymin 16760075 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 594.60 unknown https://doi.org/10.1016/0305-1978(95)00109-3

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