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Internal ID UUID643ffae7021d7097814853
Scientific name Vincetoxicum glaucescens
Authority (Decne.) C.Y.Wu & D.Z.Li
First published in Acta Bot. Yunnan. 11: 48 (1989)

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Synonyms Top

Scientific name Authority First published in
Pentasacme glaucescens Decne. Prodr. 8: 627 (1844)
Cynanchum glaucescens (Decne.) Hand.-Mazz. Symb. Sin. 7: 994 (1936)
Cynanchum lightii Dunn Kew Bull., Addit. Ser. 10: 171 (1913)

Common names Top

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Language Common/alternative name
Chinese 白前

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000421691
Tropicos 2610849
KEW urn:lsid:ipni.org:names:946566-1
Open Tree Of Life 482843
NCBI Taxonomy 1165889
IPNI 946566-1
GBIF 5525657
USDA GRIN 464432
CMAUP NPO4460

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
Effects of Juhongtanke oral solution on alleviating the symptoms of community-acquired pneumonia: A multicenter, prospective, randomized controlled trial Liang M, Hu L, Luo N, Lv H, Chen Z, Mo J, Yang M, Lin Y, Chen C Front Pharmacol 20-Oct-2022
PMCID:PMC9630601
doi:10.3389/fphar.2022.1027901
PMID:36339599
Dataset, including a photo-guide, of alien plants sold in traditional medicine markets and healthcare outlets in three South African cities, specifically by traders of Indian, West African, East African, and Chinese origin Williams VL, Burness A, Wojtasik EM, Byrne MJ Data Brief 21-Sep-2021
PMCID:PMC8479245
doi:10.1016/j.dib.2021.107395
PMID:34621926
Isolation and Identification of Chemical Constituents from Zhideke Granules by Ultra-Performance Liquid Chromatography Coupled with Mass Spectrometry Huang G, Liang J, Chen X, Lin J, Wei J, Huang D, Zhou Y, Sun Z, Zhao L J Anal Methods Chem 27-Dec-2020
PMCID:PMC7785344
doi:10.1155/2020/8889607
PMID:33457039
Zhisou powder in treatment of postinfectious cough: A protocol for systematic review and meta-analysis Cai H, Li W, Kang S, He J, Yu P, Li H Medicine (Baltimore) 20-Nov-2020
PMCID:PMC7676576
doi:10.1097/MD.0000000000023117
PMID:33217813
Research Progress on Main Symptoms of Novel Coronavirus Pneumonia Improved by Traditional Chinese Medicine Luo CH, Ma LL, Liu HM, Liao W, Xu RC, Ci ZM, Lin JZ, Han L, Zhang DK Front Pharmacol 11-Sep-2020
PMCID:PMC7516165
doi:10.3389/fphar.2020.556885
PMID:33013395
Clinical Practice Guidelines for Diagnosis and Management of Cough—Chinese Thoracic Society (CTS) Asthma Consortium Lai K, Shen H, Zhou X, Qiu Z, Cai S, Huang K, Wang Q, Wang C, Lin J, Hao C, Kong L, Zhang S, Chen Y, Luo W, Jiang M, Xie J, Zhong N J Thorac Dis 01-Nov-2018
PMCID:PMC6297434
doi:10.21037/jtd.2018.09.153
PMID:30622806
Ethnobotany, Phytochemistry and Pharmacological Effects of Plants in Genus Cynanchum Linn. (Asclepiadaceae) Han L, Zhou X, Yang M, Zhou L, Deng X, Wei S, Wang W, Wang Z, Qiao X, Bai C Molecules 16-May-2018
PMCID:PMC6099929
doi:10.3390/molecules23051194
PMID:29772722
Inspecting the True Identity of Herbal Materials from Cynanchum Using ITS2 Barcode Guo M, Ren L, Pang X Front Plant Sci 13-Nov-2017
PMCID:PMC5694171
doi:10.3389/fpls.2017.01945
PMID:29181014
Identification of the protective effects of traditional medicinal plants against SDS-induced Drosophila gut damage Zhou Y, Liu Z, Chen Y, Jin LH Exp Ther Med 31-Aug-2016
PMCID:PMC5038347
doi:10.3892/etm.2016.3641
PMID:27698771
An Emerging Translational Model to Screen Potential Medicinal Plants for Nephrolithiasis, an Independent Risk Factor for Chronic Kidney Disease Wu SY, Shen JL, Man KM, Lee YJ, Chen HY, Chen YH, Tsai KS, Tsai FJ, Lin WY, Chen WC Evid Based Complement Alternat Med 06-Jul-2014
PMCID:PMC4109113
doi:10.1155/2014/972958
PMID:25097661
Studies on the constituents of asclepiadaceae plants. LV. The structures of three new glycosides, glaucoside-H, -I, and -J from the chinese drug "pai-ch'ien," Cynanchum glaucescens Hand-Mazz. TAKASHI NAKAGAWA, KOJI HAYASHI, HIROSHI MITSUHASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.2244
Studies on the constituents of asclepiadaceae plants. LIII. The structures of glaucogenin-A, -B, and -C mono-D-thevetoside from the chinese drug "pai-ch'ien," Cynanchum glaucescens Hand-Mazz. TAKASHI NAKAGAWA, KOJI HAYASHI, HIROSHI MITSUHASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.870
Studies on the constituents of asclepiadaceae plants. LIV. The structures of glaucoside-F and -G from the chinese drug "pai-ch'ien," Cynanchum glaucescens Hand-Mazz. TAKASHI NAKAGAWA, KOJI HAYASHI, HIROSHI MITSUHASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.879
Seco-pregnane steroids target the subgenomic RNA of alphavirus-like RNA viruses Li Y, Wang L, Li S, Chen X, Shen Y, Zhang Z, He H, Xu W, Shu Y, Liang G, Fang R, Hao X Proc Natl Acad Sci U S A 30-Apr-2007
PMCID:PMC1876575
doi:10.1073/pnas.0702398104
PMID:17470783
Chemical composition of the volatile oil from Cynanchum stauntonii and its activities of anti-influenza virus. Zai-Chang Y, Bo-Chu W, Xiao-Sheng Y, Qiang W Colloids Surf B Biointerfaces 10-Jul-2005
doi:10.1016/J.COLSURFB.2005.05.003
PMID:15975773

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
Fenipentol 3338 Click to see CCCCC(C1=CC=CC=C1)O 164.24 unknown https://doi.org/10.1016/J.COLSURFB.2005.05.003
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
Butylated Hydroxytoluene 31404 Click to see CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C 220.35 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
beta-Asarone 5281758 Click to see CC=CC1=CC(=C(C=C1OC)OC)OC 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
2-Butyl-6-methylphenol 15570435 Click to see CCCCC1=CC=CC(=C1O)C 164.24 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown via CMAUP database
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown via CMAUP database
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown via CMAUP database
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown via CMAUP database
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown via CMAUP database
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown via CMAUP database
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown via CMAUP database
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown via CMAUP database
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown via CMAUP database
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown via CMAUP database
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown via CMAUP database
Tridecane 12388 Click to see CCCCCCCCCCCCC 184.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see CCCCCCCCCCCCCCCC(=O)OCC 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(9Z,12Z)-Ethyl octadeca-9,12-dienoate 11001 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(+)-tau-Muurolol 51394521 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown via CMAUP database
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Isocaryophyllene oxide 1742211 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(S)-3-Ethyl-4-methylpentanol 59911029 Click to see CCC(CCO)C(C)C 130.23 unknown via CMAUP database
3-Ethyl-4-methylpentan-1-ol 549664 Click to see CCC(CCO)C(C)C 130.23 unknown https://doi.org/10.1016/J.COLSURFB.2005.05.003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S,5R,13R,16S,19R,22R)-8-[(2R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 138114005 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)O)OC)O 520.60 unknown https://doi.org/10.1248/CPB.31.870
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Glaucoside H 3086256 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CC4=CCC5C(C4(CC3O)C)CCC6=COC7(C6C(CO7)OC5=O)C)C)O)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC 957.10 unknown https://doi.org/10.1248/CPB.31.2244
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(E,Z)-2,4-Decadienal 6427087 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
(E)-2-butyl-2-octenal 5352696 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
2-Butyl-2-octenal 5362697 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Butyloctenal 25610 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
Nona-2,4-dienal 23203 Click to see CCCCC=CC=CC=O 138.21 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1016/J.COLSURFB.2005.05.003
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown https://doi.org/10.1016/J.COLSURFB.2005.05.003
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5-pentyl-3H-furan-2-one 10725569 Click to see CCCCCC1=CCC(=O)O1 154.21 unknown https://doi.org/10.1016/J.COLSURFB.2005.05.003
> Organoheterocyclic compounds / Epoxides
Humulene epoxide 5352470 Click to see CC1=CCCC2(C(O2)CC(C=CC1)(C)C)C 220.35 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
(4S,5R,7R,8R,12S,13S,16S,19R,22R)-7,8,12-trihydroxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 101953051 Click to see CC12CC(C(CC1=CC(C3C2CCC4=COC5(C4C(CO5)OC3=O)C)O)O)O 392.40 unknown https://doi.org/10.1248/CPB.31.870
(4S,5R,7R,8R,13R,16S,19R,22R)-7,8-dihydroxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 21574519 Click to see CC12CC(C(CC1=CCC3C2CCC4=COC5(C4C(CO5)OC3=O)C)O)O 376.40 unknown https://doi.org/10.1248/CPB.31.879
https://doi.org/10.1248/CPB.31.870
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(R)-(+)-gamma-Nonalactone 11094875 Click to see CCCCCC1CCC(=O)O1 156.22 unknown via CMAUP database
Gamma-nonalactone 7710 Click to see CCCCCC1CCC(=O)O1 156.22 unknown via CMAUP database

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