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Calycanthus chinensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64400ef8a81d7254422885
Scientific name Calycanthus chinensis
Authority (W.C.Cheng & S.Y.Chang) P.T.Li
First published in J. S. China Agric. Univ. 21(4): 60 (2000)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Sinocalycanthus chinensis W.C.Cheng & S.Y.Chang Acta Phytotax. Sin. 9: 137 (1964)

Common names Top

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Language Common/alternative name
Czech sazaník čínský
Japanese ナツロウバイ
Polish chinokalikantus
Polish kielichowiec chiński
Chinese 牡丹木
Chinese 蜡木
Chinese 黄梅花
Chinese 夏蜡梅
Chinese 夏腊梅
Chinese 夏梅
Chinese 大叶柴
Chinese 夏臘梅

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000581794
KEW urn:lsid:ipni.org:names:77067552-1
The Plant List kew-2693988
Missouri Botanical Garden 278795
Open Tree Of Life 913239
NCBI Taxonomy 3431
IPNI 77214976-1
iNaturalist 430771
GBIF 3915848
EPPO CALCH
EOL 5392767
USDA GRIN 402389
Wikipedia Calycanthus_chinensis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_049901955.1 ASM4990195v1 Scaffold Huazhong Agricultural University 2025-04-24 224 707.16 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
Long-term organogenic callus cultivation of Ranunculus illyricus L.: a blueprint for sustainable ex situ conservation of the species in urban greenery Kocot D, Nowak B, Sitek E BMC Plant Biol 25-Mar-2024
PMCID:PMC10962190
doi:10.1186/s12870-024-04901-3
PMID:38528451
New insights into the plastome evolution of Lauraceae using herbariomics Yang Z, Ferguson DK, Yang Y BMC Plant Biol 10-Aug-2023
PMCID:PMC10413609
doi:10.1186/s12870-023-04396-4
PMID:37563571
Living on the edge: morphological, karyological and genetic diversity studies of the Hungarian Plantago maxima populations and established ex situ collection Kovács Z, Mlinarec J, Höhn M Bot Stud 24-Jan-2023
PMCID:PMC9873897
doi:10.1186/s40529-022-00365-6
PMID:36692644
The chloroplast genome of black pepper (Piper nigrum L.) and its comparative analysis with related Piper species Gaikwad AB, Kaila T, Maurya A, Kumari R, Rangan P, Wankhede DP, Bhat KV Front Plant Sci 12-Jan-2023
PMCID:PMC9878596
doi:10.3389/fpls.2022.1095781
PMID:36714762
The complete plastid genome sequence of Chloranthus fortunei (A. Gray) Solms-Laub. in Chloranthaceae Kang JS, Kim BY, Yoo KO Mitochondrial DNA B Resour 25-Oct-2022
PMCID:PMC9621198
doi:10.1080/23802359.2022.2132840
PMID:36325282
Comparative Chloroplast Genome Analyses of the Winter-Blooming Eastern Asian Endemic Genus Chimonanthus (Calycanthaceae) With Implications For Its Phylogeny and Diversification Jamal A, Wen J, Ma ZY, Ahmed I, Abdullah, Chen LQ, Nie ZL, Liu XQ Front Genet 30-Nov-2021
PMCID:PMC8670589
doi:10.3389/fgene.2021.709996
PMID:34917123
Advances in Research on the Mechanism of Heterosis in Plants Wu X, Liu Y, Zhang Y, Gu R Front Plant Sci 27-Sep-2021
PMCID:PMC8502865
doi:10.3389/fpls.2021.745726
PMID:34646291
Phytochemical studies on traditional herbal medicines based on the ethnopharmacological information obtained by field studies Tanaka N, Kashiwada Y J Nat Med 13-Jul-2021
PMCID:PMC8397699
doi:10.1007/s11418-021-01545-7
PMID:34255289
The complete chloroplast genome sequence of Machilus robusta W. W. Smith (Lauraceae) from Jiangxi Province, China Wu Y, Zheng Y, Liu X, Dai X, Li S, Xu H Mitochondrial DNA B Resour 07-Jun-2021
PMCID:PMC8189048
doi:10.1080/23802359.2021.1934160
PMID:34151010
The complete chloroplast genome sequence of Acorus tatarinowii (Araceae) from Fujian, China Ma L, Jiang SZ, Lian H, Xiong YF, Liu ZJ, Chen SP Mitochondrial DNA B Resour 12-Aug-2020
PMCID:PMC7782871
doi:10.1080/23802359.2020.1806133
PMID:33458094
The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter Shang J, Tian J, Cheng H, Yan Q, Li L, Jamal A, Xu Z, Xiang L, Saski CA, Jin S, Zhao K, Liu X, Chen L Genome Biol 10-Aug-2020
PMCID:PMC7419205
doi:10.1186/s13059-020-02088-y
PMID:32778152
Evolutionary directions of single nucleotide substitutions and structural mutations in the chloroplast genomes of the family Calycanthaceae Dong W, Xu C, Wen J, Zhou S BMC Evol Biol 31-Jul-2020
PMCID:PMC7393888
doi:10.1186/s12862-020-01661-0
PMID:32736519
Pollen limitation in the endangered Chinese endemic species Sinocalycanthus chinensis Li J, Gu J, Wang X, Zhang W, Jin Z Ecol Evol 16-Jul-2020
PMCID:PMC7417249
doi:10.1002/ece3.6550
PMID:32788992
An invasive plant experiences greater benefits of root morphology from enhancing nutrient competition associated with arbuscular mycorrhizae in karst soil than a native plant Xia T, Wang Y, He Y, Wu C, Shen K, Tan Q, Kang L, Guo Y, Wu B, Han X PLoS One 09-Jun-2020
PMCID:PMC7282705
doi:10.1371/journal.pone.0234410
PMID:32516341
Effect of sire population on the genetic diversity and fitness of F1 progeny in the endangered Chinese endemic Sinocalycanthus chinensis Li J, Qi C, Gu J, Jin Z Ecol Evol 03-Apr-2020
PMCID:PMC7244809
doi:10.1002/ece3.6179
PMID:32489633

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Isopropyl 4-hydroxy-3-methoxybenzoate 347415 Click to see CC(C)OC(=O)C1=CC(=C(C=C1)O)OC 210.23 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexan-1-ol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown https://doi.org/10.1016/J.BMC.2011.03.055
[(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138886 Click to see 280.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055
[5-Ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138885 Click to see 280.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2S,3S,4aR,8S,8aS)-3-methoxy-4a,8-dimethyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]propan-2-ol 162869408 Click to see 254.41 unknown https://doi.org/10.1016/J.BMC.2011.03.055
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 4655876 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O 240.38 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Cryptomeridiol 165258 Click to see 240.38 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Sinocalycanchinensin E 54581329 Click to see 468.70 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(11S)-11-[(4-hydroxy-8,8-dimethyl-5-oxo-2-propan-2-yl-6,7-dihydrophenanthren-3-yl)oxy]-8,8-dimethyl-4-propan-2-yl-10,11-dihydro-9H-benzo[i][2]benzoxepine-1,3-dione 163035220 Click to see 594.70 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-[(2R,4aR,8aS)-4a-methyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]propan-2-ol 162981184 Click to see CC12CCCCC1CC(CC2)C(C)(C)O 210.36 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/J.BMC.2011.03.055
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/J.BMC.2011.03.055
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/J.BMC.2011.03.055
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/J.BMC.2011.03.055

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