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Ventilago leiocarpa

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffa54593ea502673179
Scientific name Ventilago leiocarpa
Authority Benth.
First published in J. Proc. Linn. Soc., Bot. 5: 77 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Smythea nitida Merr. J. Arnold Arbor. 6: 136 (1925)
Ventilago leiocarpa var. pubescens Y.L.Chen & P.K.Chou Bull. Bot. Lab. N. E. Forest. Inst., Harbin 5: 89 (1979)

Common names Top

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Language Common/alternative name
Chinese 光果翼核木
Chinese 翼核果
Chinese 血风藤
Chinese 铁牛入石
Chinese 扁果藤
Chinese 穿破石
Chinese 血风根
Chinese 青筋藤

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000418340
Tropicos 27501410
KEW urn:lsid:ipni.org:names:719136-1
Open Tree Of Life 706703
Observations.org 353882
NCBI Taxonomy 108868
IPNI 719136-1
iNaturalist 708650
GBIF 7274033
Elurikkus 581423
USDA GRIN 465290
CMAUP NPO23982

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
Neuroprotective, Anti-Inflammatory and Antifibrillogenic Offerings by Emodin against Alzheimer’s Dementia: A Systematic Review Saha P, Ahmad F ACS Omega 07-Feb-2024
PMCID:PMC10882671
doi:10.1021/acsomega.3c07178
PMID:38405501
The complete plastid genome of Rhamnus leptacantha Schneid. (Rhamnaceae) Huang G, Li L, Wang X, Yang L, Wang Y, Wu D, Wu J Mitochondrial DNA B Resour 03-Jan-2024
PMCID:PMC10769139
doi:10.1080/23802359.2023.2300468
PMID:38187011
The complete chloroplast genome of Ziziphus mairei Dode 1908 (Rhamnaceae), an endangered perennial plant in Yunnan, China Wang S, Liu Y, Li R, Wang S, Huang Y Mitochondrial DNA B Resour 24-Dec-2023
PMCID:PMC10763858
doi:10.1080/23802359.2023.2290844
PMID:38173918
Sequencing the chloroplast genome of a jujube genotype (Ziziphus jujuba Mill. 'Fengmiguan') uncovered a 101 bp insertion in the large-single copy region Zhang S, Li B, Han L, Yang M, Liu M Mitochondrial DNA B Resour 06-Jul-2023
PMCID:PMC10327523
doi:10.1080/23802359.2023.2231246
PMID:37426571
Revisiting chloroplast genomic landscape and annotation towards comparative chloroplast genomes of Rhamnaceae Wanichthanarak K, Nookaew I, Pasookhush P, Wongsurawat T, Jenjaroenpun P, Leeratsuwan N, Wattanachaisaereekul S, Visessanguan W, Sirivatanauksorn Y, Nuntasaen N, Kuhakarn C, Reutrakul V, Ajawatanawong P, Khoomrung S BMC Plant Biol 28-Jan-2023
PMCID:PMC9883906
doi:10.1186/s12870-023-04074-5
PMID:36707785
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Ancient Rhamnaceae flowers impute an origin for flowering plants exceeding 250-million-years ago He T, Lamont BB iScience 18-Jun-2022
PMCID:PMC9254029
doi:10.1016/j.isci.2022.104642
PMID:35800761
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Ventilagolin Suppresses Migration, Invasion and Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma Cells by Downregulating Pim-1 Liu Y, Cheng DH, Lai KD, Su H, Lu GS, Wang L, Lv JH Drug Des Devel Ther 01-Dec-2021
PMCID:PMC8647656
doi:10.2147/DDDT.S327270
PMID:34880599
The complete chloroplast genome sequence of Ventilago leiocarpa Benth Lu X, Luo Q, Qin Y, Yan Q, Guo S Mitochondrial DNA B Resour 11-Mar-2021
PMCID:PMC7954415
doi:10.1080/23802359.2020.1861559
PMID:33763564
Phenotyping the genus Hypericum by secondary metabolite profiling: emodin vs. skyrin, two possible key intermediates in hypericin biosynthesis Kimáková K, Kimáková A, Idkowiak J, Stobiecki M, Rodziewicz P, Marczak Ł, Čellárová E Anal Bioanal Chem 05-Oct-2018
PMCID:PMC6244766
doi:10.1007/s00216-018-1384-0
PMID:30291388
Ethnobotanical study on medicinal plants used by Maonan people in China Hong L, Guo Z, Huang K, Wei S, Liu B, Meng S, Long C J Ethnobiol Ethnomed 30-Apr-2015
PMCID:PMC4449599
doi:10.1186/s13002-015-0019-1
PMID:25925830
Samarangenin B from Limonium sinense Suppresses Herpes Simplex Virus Type 1 Replication in Vero Cells by Regulation of Viral Macromolecular Synthesis Kuo YC, Lin LC, Tsai WJ, Chou CJ, Kung SH, Ho YH Antimicrob Agents Chemother 01-Sep-2002
PMCID:PMC127446
doi:10.1128/AAC.46.9.2854-2864.2002
PMID:12183238
Two anthraquinones from Ventilago calyculata B.Kesava Rao, T. Hanumaiah, J.U.M. Rao, K.V.J. Rao, Ronald H. Thomson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84996-1

Phytochemical Profile Top

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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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Leiocarpaquinone 195147 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3C(=O)OC)O)O 312.27 unknown https://doi.org/10.1016/S0031-9422(00)84996-1
> Benzenoids / Anthracenes / Anthraquinones
1-Methoxy-2-methyl-4,5-dihydroxy-9,10-anthraquinone 11119613 Click to see CC1=CC(=C2C(=C1OC)C(=O)C3=C(C2=O)C(=CC=C3)O)O 284.26 unknown https://doi.org/10.1021/NP000569D
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione 24867638 Click to see CC1=CC2C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 256.25 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Erythroglaucin 10152 Click to see CC1=CC(=C2C(=C1O)C(=O)C3=C(C2=O)C(=CC(=C3)OC)O)O 300.26 unknown https://doi.org/10.1021/NP000569D
Islandicin 10151 Click to see CC1=CC(=C2C(=C1O)C(=O)C3=C(C2=O)C(=CC=C3)O)O 270.24 unknown https://doi.org/10.1021/NP000569D
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,2,6-Trihydroxy-3-methyl-7,8-dimethoxyanthraquinone 11131324 Click to see CC1=CC2=C(C(=C1O)O)C(=O)C3=C(C(=C(C=C3C2=O)O)OC)OC 330.29 unknown https://doi.org/10.1021/NP000569D
2,6,8-Trihydroxy-1-methoxy-3-methylanthracene-9,10-dione 10086148 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=C(C2=O)C=C(C=C3O)O 300.26 unknown https://doi.org/10.1021/NP000569D
Catenarin 10150 Click to see CC1=CC(=C2C(=C1O)C(=O)C3=C(C2=O)C(=CC(=C3)O)O)O 286.24 unknown https://doi.org/10.1021/NP000569D
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1016/S0031-9422(00)84996-1
https://doi.org/10.1021/NP000569D
https://doi.org/10.1142/S0192415X96000189
https://doi.org/10.1016/0378-8741(96)01397-9
Emodin(1-) 25201450 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3[O-])O 269.23 unknown via CMAUP database
Skyrin 73071 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(C(=C3C2=O)C4=C5C(=C(C=C4O)O)C(=O)C6=C(C5=O)C=C(C=C6O)C)O)O 538.50 unknown https://doi.org/10.1021/NP000569D
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aR,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 162931937 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP000569D
(3S,4aS,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 11876269 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP000569D
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP000569D
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(8-Acetyloxy-4-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-6,12-dioxatricyclo[9.3.0.05,7]tetradec-9-en-2-yl) 2-methylbut-2-enoate 433433 Click to see CC=C(C)C(=O)OC1CC(C2C(O2)C(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)(C)O 420.50 unknown https://doi.org/10.1021/NP000569D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP000569D
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)84996-1
https://doi.org/10.1021/NP000569D
Monogynol B (6CI) 44586882 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP000569D
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP000569D
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP000569D
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 6-hydroxy-2-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 9986257 Click to see COC1=C(C=CC(=C1C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 614.50 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
6,10-dihydroxy-5,7-dimethoxy-1,3-dimethyl-1H-benzo[g]isochromene-8,9-dione 5315180 Click to see CC1C2=C(C=C(O1)C)C(=C3C(=C2O)C(=O)C(=O)C(=C3O)OC)OC 332.30 unknown via CMAUP database
6,10-dihydroxy-7-methoxy-1,3-dimethyl-3,4-dihydro-1H-benzo[g]isochromene-8,9-dione 14523293 Click to see CC1CC2=CC3=C(C(=C2C(O1)C)O)C(=O)C(=O)C(=C3O)OC 304.29 unknown via CMAUP database
Ventiloquinone K 44584756 Click to see CC1CC2=C(C(O1)C)C(=C3C(=C2OC)C(=C(C(=O)C3=O)OC)O)O 334.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
2-(4,7,8-Trimethoxy-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-9-ium-2-yl)propan-2-ol 4486242 Click to see CC(C)(C1CC2=C(C3=C(C(=C(C=C3)OC)OC)[N+](=C2O1)C)OC)O 334.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-2-phenyl-6,8-diprenyl-4H-1-benzopyran-4-one 25775471 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)CC=C(C)C)O)C 392.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+)-Epiaromadendrin 11449086 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP000569D
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP000569D
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP000569D
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(6S,7S,8R)-5-methoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromene-6,7-diol 11100309 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3O)O)C4=CC=CC=C4)OC)C 354.40 unknown via CMAUP database
(6S,7S,8R)-5,6-dimethoxy-2,2-dimethyl-8-phenyl-7,8-dihydro-6H-pyrano[3,2-g]chromen-7-ol 11014062 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)O)C4=CC=CC=C4)OC)C 368.40 unknown via CMAUP database
2alpha-Phenyl-8,8-dimethyl-4beta-ethoxy-5-methoxy-3,4-dihydro-2H,8H-benzo[1,2-b:5,4-b']dipyran 12016631 Click to see CCOC1CC(OC2=C1C(=C3C=CC(OC3=C2)(C)C)OC)C4=CC=CC=C4 366.40 unknown via CMAUP database
3beta-Methoxyxuulanin 10475006 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)OC)C4=CC=CC=C4)OC)C 382.40 unknown via CMAUP database
3beta,4beta,5-Trimethoxy-4'-hydroxy-(6:7)-2,2-dimethylpyranoflavan 636704 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(C(C3OC)OC)C4=CC=C(C=C4)O)OC)C 398.40 unknown via CMAUP database
5-Hydroxy-8-(4-hydroxy-3-methoxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b']dipyran-6-one 10915521 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC(=C(C=C4)O)OC)C 366.40 unknown via CMAUP database
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
Carpachromene dimethyl ether 14607844 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)C4=CC=C(C=C4)OC)C 364.40 unknown via CMAUP database
Xuuranin 10247444 Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3OC)C4=CC=CC=C4)OC)C 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isochromanequinones
(1R,3S)-5,8,10-trihydroxy-7-methoxy-1,3-dimethyl-3,4-dihydro-1H-benzo[g]isochromene-6,9-dione 163012871 Click to see CC1CC2=C(C(O1)C)C(=C3C(=C2O)C(=O)C(=C(C3=O)O)OC)O 320.29 unknown https://doi.org/10.1021/NP000569D
(1R,3S)-8,10-dihydroxy-7-methoxy-1,3-dimethyl-3,4-dihydro-1H-benzo[g]isochromene-6,9-dione 163184325 Click to see CC1CC2=CC3=C(C(=C2C(O1)C)O)C(=O)C(=C(C3=O)OC)O 304.29 unknown https://doi.org/10.1021/NP000569D
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1021/NP000569D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Glychalcone A 15230651 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=CC3=CC=C(C=C3)OC)O)C 366.40 unknown via CMAUP database
Isobavachromene 5889042 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 322.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Isocordoin 6251270 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O)C 308.40 unknown via CMAUP database

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