Scientific name	Authority	First published in
Meratia fragrans	Loisel.	Herb. Gén. Amat. 3: t. 173 (1819)
Meratia praecox	Rehder & E.H.Wilson	Pl. Wilson. 1: 419 (1913)
Meratia yunnanensis	Hu	J. Arnold Arbor. 6: 140 (1925)
Chimonanthus praecox f. intermedius	(Makino) Okuyama	J. Jap. Bot. 30: 42 1955
Chimonanthus praecox var. luteus	G.Don	Gen. Hist. 2: 652. 1832
Chimonanthus praecox f. luteus	(G.Don) Okuyama	J. Jap. Bot. 30: 42 1955
Chimonanthus praecox var. reflexus	B.Zhao	Bull. Bot. Res., Harbin 27: 131 (2007)
Chimonanthus praecox f. versicolor	B.Zhao	Bull. Bot. Res., Harbin 27: 132 (2007)
Beureria praecox	Kuntze	Revis. Gen. Pl. 1: 361 (1891)
Calycanthus praecox	L.	Sp. Pl. ed. 2 : 718 (1762)
Calycanthus suaveolens	Salisb.	Prodr. Stirp. Chap. Allerton : 379 (1796)
Chimonanthus caespitosus	T.B.Chao, Zhi X.Chen & Zhen Q.Li	Bull. Bot. Res., Harbin 9(4): 47 (1989)
Chimonanthus fragrans	Lindl.	Bot. Reg. 6: t. 451 (1820)
Chimonanthus fragrans var. grandiflorus	Lindl.	Bot. Reg. 6: t. 451. 1820
Chimonanthus grandiflorus	Steud.	Nomencl. Bot. , ed. 2, 1: 350 (1840)
Chimonanthus luteus	Hort ex Bielawski	Ann. Soc. Linn. Dép. Maine-et-Loire 9: 96 (1867)
Chimonanthus parviflorus	Raf.	Alsogr. Amer. : 6 (1838)
Chimonanthus praecox var. concolor	Makino	Bot. Mag. (Tokyo) 23: 23. 1909
Chimonanthus praecox var. grandiflorus	(Lindl.) Makino	Bot. Mag. (Tokyo) 24: 301 1910
Chimonanthus praecox var. intermedius	Makino	Bot. Mag. (Tokyo) 24: 300. 1910
Chimonanthus verus	hort. ex Bielawski	Ann. Soc. Linn. Dép. Maine-et-Loire 9: 96 (1867)
Chimonanthus yunnanensis	W.W.Sm.	Notes Roy. Bot. Gard. Edinburgh 8: 182 (1914)
Meratia praecox var. grandiflora	(Lindl.) Rehder & E.H.Wilson	Pl. Wilson. 1: 420 1913
Chimonanthus baokanensis	D.M.Chen & Z.L.Dai
Chimonanthus baokanensis var. yupiensis	D.M.Chen & Z.L.Dai
Butneria praecox	(L.) C.K.Schneid.	Dendr. Winterstud. 204, 241, f. 221i–o 1903

Common names Top

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Filter by language:

Language	Common/alternative name
English	fragrant wintersweet
English	wintersweet
Spanish	masacar
Azerbaijani	İlkin ximonant
Czech	zimnokvět časný
German	chinesische winterblüte
Persian	گل یخ ژاپنی
Finnish	tuoksutalvenlahja
Japanese	臘梅
Japanese	ロウバイ
Japanese	蠟梅
Japanese	蝋梅
Japanese	唐梅
Korean	납매
Polish	zimokwiat wczesny
Russian	Химонант скороспелый
Slovenian	zgodnji zimski cvet
Serbian	Зимоцвет
Turkish	kış tatlısı
Turkish	kış tatlısı çiçeği
Chinese	蜡梅
Chinese	腊梅
Chinese	臘梅
Chinese	蜡梅（素心蜡梅、磬口蜡梅、红心腊梅）
Chinese	蜡梅花
Chinese	蜡木
Chinese	黄梅花
Chinese	磬口蜡梅
Chinese	素心蜡梅
Chinese	铁筷子
Chinese	红心腊梅
Chinese	蠟梅

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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 click to expand
- China
  - China North-central
  - China South-central
  - China Southeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000602230
UNII	5Y143KS0YL
Tropicos	5300007
INPN	991589
Flora of Italy	11384
KEW	urn:lsid:ipni.org:names:139248-1
The Plant List	kew-2718305
Missouri Botanical Garden	278793
Open Tree Of Life	324777
NCBI Taxonomy	13419
IUCN Red List	147377321
IPNI	139248-1
iNaturalist	49080
GBIF	7275851
Freebase	/m/047gpmx
EPPO	CHSPR
EOL	5392977
USDA GRIN	10204
Wikipedia	Chimonanthus_praecox
CMAUP	NPO22216

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_022113865.1	ASM2211386v1	Chromosome	Henan Academy of Forestry	2022-02-10	202.0x	702.88 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

Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus

Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W

BMC Genomics

19-Mar-2024

PMCID:	PMC10949689
doi:	10.1186/s12864-024-10202-8
PMID:	38504151

The Relationship between Endophytic Fungi of Chimonanthus praecox and Volatile Metabolites under Different Circadian Rhythms and Blooming Stages

Li Y, Hei J, He X, Rui R, Wang S

J Fungi (Basel)

11-Feb-2024

PMCID:	PMC10890430
doi:	10.3390/jof10020145
PMID:	38392817

Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids

Yu X, Feng Y, Zhang J

Life (Basel)

25-Jan-2024

PMCID:	PMC10890521
doi:	10.3390/life14020182
PMID:	38398691

Special Issue “Phytohormones: Important Participators in Plant Growth and Development”

Kudoyarova G

Int J Mol Sci

23-Jan-2024

PMCID:	PMC10855094
doi:	10.3390/ijms25031380
PMID:	38338660

Optimizing DUS testing for Chimonanthus praecox using feature selection based on a genetic algorithm

Zhu T, Feng Y, Dong X, Yang X, Liu B, Yuan P, Song X, Chen S, Sui S

Front Plant Sci

18-Jan-2024

PMCID:	PMC10835806
doi:	10.3389/fpls.2023.1328603
PMID:	38312354

DNA methylome analysis reveals novel insights into active hypomethylated regulatory mechanisms of temperature-dependent flower opening in Osmanthus fragrans

Zhong S, Zhu H, Li W, Wu D, Miao Y, Dong B, Wang Y, Xiao Z, Fang Q, Deng J, Zhao H

Hortic Res

10-Jan-2024

PMCID:	PMC10923647
doi:	10.1093/hr/uhae010
PMID:	38464472

Overview of molecular mechanisms of plant leaf development: a systematic review

Lv Z, Zhao W, Kong S, Li L, Lin S

Front Plant Sci

07-Dec-2023

PMCID:	PMC10749370
doi:	10.3389/fpls.2023.1293424
PMID:	38146273

Transcriptome and metabolome analyses of anthocyanin biosynthesis in post-harvest fruits of a full red-type kiwifruit (Actinidia arguta) ‘Jinhongguan’

Ye L, Bai F, Zhang L, Luo M, Gao L, Wang Z, Peng J, Chen Q, Luo X

Front Plant Sci

09-Oct-2023

PMCID:	PMC10591155
doi:	10.3389/fpls.2023.1280970
PMID:	37877082

Family characteristics, phylogenetic reconstruction, and potential applications of the plant BAHD acyltransferase family

Xu D, Wang Z, Zhuang W, Wang T, Xie Y

Front Plant Sci

05-Oct-2023

PMCID:	PMC10585174
doi:	10.3389/fpls.2023.1218914
PMID:	37868312

Comprehensive evaluation of carbon sequestration potential of landscape tree species and its influencing factors analysis: implications for urban green space management

Jin S, Zhang E, Guo H, Hu C, Zhang Y, Yan D

Carbon Balance Manag

05-Sep-2023

PMCID:	PMC10481583
doi:	10.1186/s13021-023-00238-w
PMID:	37668811

Genome-Wide Identification and Expression Analysis of the bHLH Transcription Factor Family in Wintersweet (Chimonanthus praecox)

Kamran HM, Fu X, Wang H, Yang N, Chen L

Int J Mol Sci

30-Aug-2023

PMCID:	PMC10487621
doi:	10.3390/ijms241713462
PMID:	37686265

Characterization of Volatile Organic Compounds in Five Celery (Apium graveolens L.) Cultivars with Different Petiole Colors by HS-SPME-GC-MS

Sun Y, Li M, Li X, Du J, Li W, Lin Y, Zhang Y, Wang Y, He W, Chen Q, Zhang Y, Wang X, Luo Y, Xiong A, Tang H

Int J Mol Sci

28-Aug-2023

PMCID:	PMC10488006
doi:	10.3390/ijms241713343
PMID:	37686147

CpCAF1 from Chimonanthus praecox Promotes Flowering and Low-Temperature Tolerance When Expressed in Arabidopsis thaliana

Lv Y, Xie M, Zhou S, Wen B, Sui S, Li M, Ma J

Int J Mol Sci

18-Aug-2023

PMCID:	PMC10455127
doi:	10.3390/ijms241612945
PMID:	37629126

Mesosphaerum suaveolens Essential Oil Attenuates Inflammatory Response and Oxidative Stress in LPS-Stimulated RAW 264.7 Macrophages by Regulating NF-κB Signaling Pathway

Mohanta O, Ray A, Jena S, Sahoo A, Panda SS, Das PK, Nayak S, Panda PC

Molecules

02-Aug-2023

PMCID:	PMC10420984
doi:	10.3390/molecules28155817
PMID:	37570786

Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches

Yang J, Wang Z, Pan Y, Zheng Y

Ecol Evol

31-Jul-2023

PMCID:	PMC10388403
doi:	10.1002/ece3.10366
PMID:	37529580

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Merulinic acid A	21591019	Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C(=O)O	390.60	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1002/FFJ.2730050205
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate	8785	Click to see CC(=O)OCC1=CC=CC=C1	150.17	unknown	via CMAUP database
> Benzenoids / Phenol ethers
N,N,N-trimethyl-2-phenoxyethanaminium	9725	Click to see C[N+](C)(C)CCOC1=CC=CC=C1	180.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
6-Methyloctan-1-ol	520908	Click to see CCC(C)CCCCCO	144.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1002/FFJ.2730050205
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730050205
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730050205
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1002/FFJ.2730050205
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730050205
(1S,2R,5S,6S,7S,8S)-2,8-dimethyl-5-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undecane-1,8-diol	154496736	Click to see CC(C)C1CCC2(C1C3C(CCC2(O3)O)(C)O)C	254.36	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
(3R,3aR,4R,7R,7aR)-3-(2-hydroxy-2-methylpropyl)-4,7a-dimethyl-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol	162866802	Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O	256.38	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
(Z)-3,7,11-trimethyldodec-6-en-1-ol	42626572	Click to see CC(C)CCCC(=CCCC(C)CCO)C	226.40	unknown	via CMAUP database
3-(2-Hydroxy-2-methylpropyl)-4,7a-dimethyl-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol	78069537	Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O	256.38	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol	85401441	Click to see CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
7,10-Dihydroxy-1,7-dimethyl-4-isopropylbicyclo[4.4.0]dec-3-ene	12313755	Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Bullatantriol	71430886	Click to see CC12CCC(C1C(CCC2O)(C)O)CC(C)(C)O	256.38	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730050205
Farnesyl acetate	638500	Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C	264.40	unknown	via CMAUP database
Homalomenol A	91884956	Click to see CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Oplodiol	12313756	Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)O)C	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
trans,trans-Farnesol	445070	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730050205
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730050205
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
3-Eudesmene-1beta,11-diol	101928774	Click to see CC1=CCC(C2(C1CC(CC2)C(C)(C)O)C)O	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-2,4a,5,6,7,8-hexahydro-1H-naphthalen-1-ol	155899197	Click to see CC1=CCC(C2(C1CC(CC2)C(C)(C)O)C)O	238.37	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3R,3aR,4R,5S,8aR)-3-methyl-8-methylidene-5-propan-2-yl-2,3,3a,4,5,6,7,8a-octahydro-1H-azulen-4-ol	163037008	Click to see CC1CCC2C1C(C(CCC2=C)C(C)C)O	222.37	unknown	https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1016/J.TETLET.2006.03.047
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(5-hydroxy-3-methyl-4-oxochromen-7-yl)oxyoxan-2-yl]methyl 4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	5315626	Click to see CC1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C4=CCC(CC4)C(C)(C)O)O)O)O	520.50	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Nucleoside and nucleotide analogues / 1-pyranosylindoles
[1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]indol-3-yl]methyl acetate	162866801	Click to see CC(=O)OCC1=CN(C2=CC=CC=C21)C3C(C(C(C(O3)CO)O)O)O	351.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Taxiphyllin	107721	Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O	311.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[[(1S,3S,6R)-6-[(3R)-3-hydroxybut-1-enyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162969512	Click to see CC(C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C)O	388.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
(2R,3R,4S,5S,6R)-2-[[(1S,3S,6R)-6-[(E,3R)-3-hydroxybut-1-enyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163194579	Click to see CC(C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C)O	388.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Benzyl alcohol xylopyranosyl-(1-6)-glucopyranoside	14730864	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Benzyl beta-primeveroside	131248	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O	402.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
methyl (E)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate	101842686	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)OC2C(C(C(C(O2)CO)O)O)O	370.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
Methyl 3-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate	162856907	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)OC2C(C(C(C(O2)CO)O)O)O	370.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1002/FFJ.2730050205
> Organoheterocyclic compounds / Indoles and derivatives
hydron;1H-indole	22035206	Click to see [H+].C1=CC=C2C(=C1)C=CN2	118.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(-)-Calycanthidine	16722158	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4N(C6=CC=CC=C56)C)C	360.50	unknown	https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1016/J.PHYTOL.2011.04.012
(-)-Chimonanthine	599086	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C	346.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047 https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.1016/J.TET.2003.11.034
(-)-Folicanthine	16722157	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)C45CCN(C4N(C6=CC=CC=C56)C)C	374.50	unknown	https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1016/J.PHYTOL.2011.04.012
(+)-Calycanthidine	442031	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4N(C6=CC=CC=C56)C)C	360.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
(+)-Folicanthine	16720248	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)C45CCN(C4N(C6=CC=CC=C56)C)C	374.50	unknown	https://doi.org/10.1002/CBDV.200800089 https://doi.org/10.1016/J.TETLET.2006.03.047
(3aR,8bR)-8b-methoxy-3,4-dimethyl-2,3a-dihydro-1H-pyrrolo[2,3-b]indole	24861868	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)OC	218.29	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
(3aR,8bS)-8b-[(3aR,8bS)-4-methyl-1,2,3,3a-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3,4-dimethyl-2,3a-dihydro-1H-pyrrolo[2,3-b]indole	11371848	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)C45CCNC4N(C6=CC=CC=C56)C	360.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047 https://doi.org/10.1016/J.TET.2003.11.034
(3aR,8bS)-8b-[(3aS,8bR)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole	162897041	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C	346.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
8b-methoxy-3,4-dimethyl-2,3a-dihydro-1H-pyrrolo[2,3-b]indole	74336515	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)OC	218.29	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
Calycanthidine	599113	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4N(C6=CC=CC=C56)C)C	360.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1016/J.TETLET.2006.03.047
Chimonanthine	3083909	Click to see CN1CCC2(C1NC3=CC=CC=C32)C45CCN(C4NC6=CC=CC=C56)C	346.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047 https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.1016/J.TET.2003.11.034
Folicanthine	604246	Click to see CN1CCC2(C1N(C3=CC=CC=C32)C)C45CCN(C4N(C6=CC=CC=C56)C)C	374.50	unknown	https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1002/CBDV.200800089 https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.1016/J.TETLET.2006.03.047
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Indole, 3-(2-(methylamino)ethyl)-1-methyl-	37796	Click to see CNCCC1=CN(C2=CC=CC=C21)C	188.27	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
Tryptamine	1150	Click to see C1=CC=C2C(=C1)C(=CN2)CCN	160.22	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
> Organoheterocyclic compounds / Isobenzofurans
(3S,3aR)-3-(furan-3-yl)-3a,7-dimethyl-3,4,5,6-tetrahydro-2-benzofuran-1-one	776141	Click to see CC1=C2C(=O)OC(C2(CCC1)C)C3=COC=C3	232.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Aminoquinolines and derivatives
(+)-Calycanthine	264115	Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C	346.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.1016/J.TETLET.2006.03.047 https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1021/JA01381A034 https://doi.org/10.1002/CBDV.200800089
(1S,2S,10R,11R)-21,24-dimethyl-3,12,21,24-tetrazahexacyclo[9.7.3.32,10.01,10.04,9.013,18]tetracosa-4,6,8,13,15,17-hexaene	11035395	Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C	346.50	unknown	via CMAUP database
(1S,9R,13S,21R)-10,22-dimethyl-8,10,20,22-tetrazahexacyclo[11.11.0.01,21.02,7.09,13.014,19]tetracosa-2,4,6,14,16,18-hexaene	102179239	Click to see CN1CCC23C1NC4=CC=CC=C4C25CCN(C5NC6=CC=CC=C36)C	346.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047
Calycanthine	5392245	Click to see CN1CCC23C4NC5=CC=CC=C5C2(C1NC6=CC=CC=C36)CCN4C	346.50	unknown	https://doi.org/10.1021/JA01381A034 https://doi.org/10.1002/CBDV.200800089 https://doi.org/10.1016/J.TET.2003.11.034 https://doi.org/10.1016/J.TETLET.2006.03.047 https://doi.org/10.1016/J.PHYTOL.2011.04.012 https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Triazinanes / 1,3,5-triazinanes
1,3,5-Tributyl-1,3,5-triazinane	83069	Click to see CCCCN1CN(CN(C1)CCCC)CCCC	255.44	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-hydroxy-6-methoxy-8-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	7275751	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5,5'-dihydroxy-2,2'-bis(4-hydroxyphenyl)-7,7'-dimethoxy-4H,4'H-[6,8'-bichromene]-4,4'-dione	9985405	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC	566.50	unknown	via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-hydroxyphenyl)chromen-4-one	13888657	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	552.50	unknown	via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-methoxyphenyl)chromen-4-one	102115496	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC	566.50	unknown	via CMAUP database
8,8''-Bisgenkwanin	5316884	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OC	566.50	unknown	via CMAUP database
Cupressuflavone	5281609	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O	538.50	unknown	via CMAUP database
Cupressuflavone-7-methyl ether	102115497	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	552.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercetin 3-diglucoside	10211337	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	626.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(R)-Hispaglabridin A	4484221	Click to see CC(=CCC1=C(C=CC(=C1O)C2CC3=C(C4=C(C=C3)OC(C=C4)(C)C)OC2)O)C	392.50	unknown	https://doi.org/10.1016/J.TETLET.2006.03.047

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Chimonanthus praecox

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