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Ligularia hodgsonii

Ligularia hodgsonii - Unknown
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Author: Public Domain - WikiMedia
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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 UUID643fd29c7b4b1098017019
Scientific name Ligularia hodgsonii
Authority Hook.
First published in t. 5417 1863

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Senecio yesoensis Franch. Bull. Soc. Bot. France 39: 306 (1893)
Senecillis hodgsonii (Hook.f.) Kitam. Acta Phytotax. Geobot. 8: 82 (1939)
Ligularia yesoensis var. pulchella Pamp. Nuovo Giornale Botanico Italiano, new series 18(1): 142 1911
Ligularia yesoensis (Franch.) Diels Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 29(5): 622 1900
Senecio yesoensis var. creniferus Franch. Bulletin de la Societe Botanique de France 39: 307 1892
Ligularia yesoensis var. sutchuenensis (Franch.) Diels Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 29(5): 622 1901
Ligularia hodgsonii var. sutchuenensis (Franch.) A.Henry Gardener's chronicle, ser. 3 32: 218 1902
Ligularia hodgsonii var. pulchella (Pamp.) Hand.-Mazz. Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 69(1): 115 1938
Ligularia yesoensis var. crenifera (Franch.) Diels Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 29(5): 622 1901
Ligularia hodgsonii var. crenifera (Franch.) Hand.-Mazz. Botanische Jahrbucher fur Systematik, Pflanzengeschichte und Pflanzengeographie 69(1): 115-116 1938

Common names Top

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Language Common/alternative name
Japanese トウゲブキ
Chinese 紫菀
Chinese 山紫菀
Chinese 鹿蹄橐吾
Chinese 鹿蹄橐吾（滇紫菀）

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

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
    • Eastern Asia
      • Japan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000125196
Tropicos 2730419
KEW urn:lsid:ipni.org:names:230755-1
The Plant List gcc-86281
Open Tree Of Life 619949
Observations.org 128329
NCBI Taxonomy 186955
IPNI 230755-1
iNaturalist 911884
GBIF 5395405

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
Chloroplast genome analysis and evolutionary insights in the versatile medicinal plant Calendula officinalis L. Zhang N, Huang K, Xie P, Deng A, Tang X, Jiang M, Mo P, Yin H, Huang R, Liang J, He F, Liu Y, Hu H, Wang Y Sci Rep 26-Apr-2024
PMCID:PMC11053094
doi:10.1038/s41598-024-60455-2
PMID:38671173
The microbial biosynthesis of noncanonical terpenoids Ma M, Li M, Wu Z, Liang X, Zheng Q, Li D, Wang G, An T Appl Microbiol Biotechnol 21-Feb-2024
PMCID:PMC10881772
doi:10.1007/s00253-024-13048-y
PMID:38381229
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Allopatric Lineage Divergence of the East Asian Endemic Herb Conandron ramondioides Inferred from Low-Copy Nuclear and Plastid Markers Hsin KT, Kuo HC, Kokubugata G, Möller M, Wang CN, Cheng YS Int J Mol Sci 29-Nov-2022
PMCID:PMC9740071
doi:10.3390/ijms232314932
PMID:36499259
Mitochondrial toxicity evaluation of traditional Chinese medicine injections with a dual in vitro approach Shen Y, Guo K, Ma A, Huang Z, Du J, Chen J, Lin Q, Wei C, Wang Z, Zhang F, Zhang J, Lin W, Feng N, Ma W Front Pharmacol 02-Nov-2022
PMCID:PMC9667049
doi:10.3389/fphar.2022.1039235
PMID:36408232
Complete chloroplast genome of Ligularia biceps Kitam, 1941 (Asteraceae) Song YY, Shi CN, Bian C, Xu L, Yang YY, Xie M, Kang TG Mitochondrial DNA B Resour 12-Oct-2022
PMCID:PMC9559319
doi:10.1080/23802359.2022.2130716
PMID:36245813
Complete chloroplast genome sequences of Sinosenecio baojingensis Ying Liu & Q.E. Yang (Asteraceae) Xie JN, Wang D, Peng JY, Wang Y, Zhou Q Mitochondrial DNA B Resour 12-Jul-2022
PMCID:PMC9278445
doi:10.1080/23802359.2022.2097026
PMID:35844976
Stepped Geomorphology Shaped the Phylogeographic Structure of a Widespread Tree Species (Toxicodendron vernicifluum, Anacardiaceae) in East Asia Wang L, Li Y, Noshiro S, Suzuki M, Arai T, Kobayashi K, Xie L, Zhang M, He N, Fang Y, Zhang F Front Plant Sci 02-Jun-2022
PMCID:PMC9201781
doi:10.3389/fpls.2022.920054
PMID:35720535
The complete chloroplast genome sequence of Tussilago farfara (Asteraceae) Yizhong D, Lu K, Zhongyu D, Shen Y Mitochondrial DNA B Resour 25-Mar-2022
PMCID:PMC8959504
doi:10.1080/23802359.2021.2005494
PMID:35356793
Identification of Pyrrolizidine Alkaloids in Senecio Plants by Liquid Chromatography-Mass Spectrometry Lu AJ, Lu YL, Tan DP, Qin L, Ling H, Wang CH, He YQ J Anal Methods Chem 16-Nov-2021
PMCID:PMC8610691
doi:10.1155/2021/1957863
PMID:34824876
Ethnobotany and diversity of medicinal plants used by the Buyi in eastern Yunnan, China Xiong Y, Sui X, Ahmed S, Wang Z, Long C Plant Divers 07-Oct-2020
PMCID:PMC7936110
doi:10.1016/j.pld.2020.09.004
PMID:33733008
Comparison of chloroplast genomes of Gynura species: sequence variation, genome rearrangement and divergence studies Han T, Li M, Li J, Lv H, Ren B, Chen J, Li W BMC Genomics 29-Oct-2019
PMCID:PMC6821010
doi:10.1186/s12864-019-6196-x
PMID:31664913
Characterization of the complete chloroplast genome of Sinosenecio oldhamianus (Compositae) Xu J, Gong Y, Hao G Mitochondrial DNA B Resour 11-Oct-2019
PMCID:PMC7707185
doi:10.1080/23802359.2019.1675483
PMID:33366056
New insight into the phylogeographic pattern of Liriodendron chinense (Magnoliaceae) revealed by chloroplast DNA: east–west lineage split and genetic mixture within western subtropical China Yang A, Zhong Y, Liu S, Liu L, Liu T, Li Y, Yu F PeerJ 01-Feb-2019
PMCID:PMC6361005
doi:10.7717/peerj.6355
PMID:30723627
Nuclear and chloroplast DNA phylogeography suggests an Early Miocene southward expansion of Lithocarpus (Fagaceae) on the Asian continent and islands Yang CK, Chiang YC, Huang BH, Ju LP, Liao PC Bot Stud 08-Nov-2018
PMCID:PMC6223401
doi:10.1186/s40529-018-0244-8
PMID:30406863

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 / Tetralins
Liguhodgsonal 14681764 Click to see CC(=C)C1CCC2=C(C1)C(=CC(=C2)O)C=O 216.27 unknown https://doi.org/10.1002/CBER.19771100721
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3-acetyl-6-acetyloxy-8a-hydroxy-4a,5-dimethyl-2-oxo-5,6,7,8-tetrahydro-1H-naphthalen-1-yl) 2-methylbut-2-enoate 162926465 Click to see CC=C(C)C(=O)OC1C(=O)C(=CC2(C1(CCC(C2C)OC(=O)C)O)C)C(=O)C 392.40 unknown https://doi.org/10.1002/JCCS.200200022
(4-Acetyloxy-8a-hydroxy-3,4a,5-trimethyl-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl) acetate 163039028 Click to see CC1C(CCC2(C1(C(C3=C(C2)OC=C3C)OC(=O)C)C)O)OC(=O)C 350.40 unknown https://doi.org/10.1002/CBDV.200800346
(4S,4aS,5S,8aR)-3,4a-dimethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 101473339 Click to see CC=C(C)C(=O)OC1C2=C(CC3C1(C(CCC3)C(=O)O)C)OC=C2C 346.40 unknown https://doi.org/10.1002/CBDV.200800346
(6-Acetyloxy-8a-hydroxy-3,4a,5-trimethyl-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-4-yl) 2-methylbutanoate 163017800 Click to see CCC(C)C(=O)OC1C2=C(CC3(C1(C(C(CC3)OC(=O)C)C)C)O)OC=C2C 392.50 unknown https://doi.org/10.1002/CBDV.200800346
[(1S,4aR,5R,6S,8aR)-3-acetyl-6-acetyloxy-8a-hydroxy-4a,5-dimethyl-2-oxo-5,6,7,8-tetrahydro-1H-naphthalen-1-yl] (Z)-2-methylbut-2-enoate 162926466 Click to see CC=C(C)C(=O)OC1C(=O)C(=CC2(C1(CCC(C2C)OC(=O)C)O)C)C(=O)C 392.40 unknown https://doi.org/10.1002/JCCS.200200022
[(4S,4aS,5R,6S,8aS)-4-acetyloxy-8a-hydroxy-3,4a,5-trimethyl-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-6-yl] acetate 101473340 Click to see CC1C(CCC2(C1(C(C3=C(C2)OC=C3C)OC(=O)C)C)O)OC(=O)C 350.40 unknown https://doi.org/10.1002/CBDV.200800346
[(4S,4aS,5R,6S,8aS)-6-acetyloxy-8a-hydroxy-3,4a,5-trimethyl-4,5,6,7,8,9-hexahydrobenzo[f][1]benzofuran-4-yl] (2R)-2-methylbutanoate 163017801 Click to see CCC(C)C(=O)OC1C2=C(CC3(C1(C(C(CC3)OC(=O)C)C)C)O)OC=C2C 392.50 unknown https://doi.org/10.1002/CBDV.200800346
3,4a-dimethyl-4-(2-methylbut-2-enoyloxy)-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 163007436 Click to see CC=C(C)C(=O)OC1C2=C(CC3C1(C(CCC3)C(=O)O)C)OC=C2C 346.40 unknown https://doi.org/10.1002/CBDV.200800346
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,6R,8aS)-8a-methyl-4-methylidene-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,4a-diol 636618 Click to see CC(C)C1CCC2(C(CCC(=C)C2(C1)O)O)C 238.37 unknown https://doi.org/10.1002/JCCS.200200022
8a-methyl-4-methylidene-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,4a-diol 20979096 Click to see CC(C)C1CCC2(C(CCC(=C)C2(C1)O)O)C 238.37 unknown https://doi.org/10.1002/JCCS.200200022
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4R,4aS,5S,8aR,9aR)-9a-ethoxy-3,4a-dimethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-2-oxo-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 25223261 Click to see CCOC12CC3CCCC(C3(C(C1=C(C(=O)O2)C)OC(=O)C(=CC)C)C)C(=O)O 406.50 unknown https://doi.org/10.1002/HLCA.200800250
(4S,4aS,5S,8aR,9aR)-9a-ethoxy-3,4a-dimethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-2-oxo-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 25223360 Click to see CCOC12CC3CCCC(C3(C(C1=C(C(=O)O2)C)OC(=O)C(=CC)C)C)C(=O)O 406.50 unknown https://doi.org/10.1002/HLCA.200800250
9a-ethoxy-3,4a-dimethyl-4-(2-methylbut-2-enoyloxy)-2-oxo-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylic acid 74433668 Click to see CCOC12CC3CCCC(C3(C(C1=C(C(=O)O2)C)OC(=O)C(=CC)C)C)C(=O)O 406.50 unknown https://doi.org/10.1002/HLCA.200800250
methyl (4R,4aS,5S,8aR,9aR)-9a-hydroxy-3,4a-dimethyl-4-[(Z)-2-methylbut-2-enoyl]oxy-2-oxo-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylate 25223260 Click to see CC=C(C)C(=O)OC1C2=C(C(=O)OC2(CC3C1(C(CCC3)C(=O)OC)C)O)C 392.40 unknown https://doi.org/10.1002/HLCA.200800250
methyl 9a-hydroxy-3,4a-dimethyl-4-(2-methylbut-2-enoyloxy)-2-oxo-5,6,7,8,8a,9-hexahydro-4H-benzo[f][1]benzofuran-5-carboxylate 74433667 Click to see CC=C(C)C(=O)OC1C2=C(C(=O)OC2(CC3C1(C(CCC3)C(=O)OC)C)O)C 392.40 unknown https://doi.org/10.1002/HLCA.200800250
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200200022
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200200022
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/10.1002/JCCS.200200022
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/10.1002/JCCS.200200022
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(7-Acetyloxy-4-ethylidene-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-5-yl) acetate 73800155 Click to see CC=C1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)OC(=O)C)C)OC(=O)C 465.50 unknown https://doi.org/10.1021/NP9906119
[(1R,4Z,5S,6S,7S,11Z)-7-acetyloxy-4-ethylidene-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-5-yl] acetate 21606532 Click to see CC=C1C(C(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)OC(=O)C)C)OC(=O)C 465.50 unknown https://doi.org/10.1021/NP9906119
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(4-Ethenyl-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadeca-4,11-dien-7-yl) acetate 5090286 Click to see CC1C=C(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)C=C 405.40 unknown https://doi.org/10.1021/NP9906119
[(1R,4Z,6R,7S)-4-ethenyl-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadeca-4,11-dien-7-yl] acetate 162960365 Click to see CC1C=C(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)C=C 405.40 unknown https://doi.org/10.1021/NP9906119
Clivoline 5284370 Click to see CC1C=C(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)C=C 405.40 unknown https://doi.org/10.1021/NP9906119
Clivorine 5363807 Click to see CC1C=C(C(=O)OC2CC[N+]3(C2(C(=CC3)COC(=O)C1(C)OC(=O)C)O)C)C=C 406.40 unknown https://doi.org/10.1021/NP9906119
Clivorine (neutral) 10069841 Click to see CC1C=C(C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)OC(=O)C)C)C=C 405.40 unknown https://doi.org/10.1021/NP9906119
Liguhodgcins A 60154789 Click to see CC1CC(OC(=O)C1(C)OC(=O)C)(C(C)Cl)C(=O)OC 306.74 unknown https://doi.org/10.1021/NP200693Z
> Organoheterocyclic compounds / Isobenzofurans
(3R,3aS,4R,7aS)-3-[(2R)-2-hydroxy-3-methyl-5-oxo-2H-furan-4-yl]-3a-methyl-1-oxo-3,4,5,6,7,7a-hexahydro-2-benzofuran-4-carbaldehyde 162942923 Click to see CC1=C(C(=O)OC1O)C2C3(C(CCCC3C(=O)O2)C=O)C 294.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.01.008
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Liguhodgcins B 60154790 Click to see CC1CC2(C(O2)C)C(=O)OC1(C)C(=O)OC 228.24 unknown https://doi.org/10.1021/NP200693Z
> Organoheterocyclic compounds / Naphthofurans
(1R,8R,12R,15S)-3,15-dimethyl-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadeca-2(6),3-dien-13-one 14307935 Click to see CC1=COC2=C1C3C4(C(C2)CCCC4C(=O)O3)C 246.30 unknown https://doi.org/10.1246/BCSJ.52.1182
(3,15-Dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-9-yl) acetate 74433713 Click to see CC1=C2C(CC3C(CCC4C3(C2OC4=O)C)OC(=O)C)OC1=O 320.30 unknown https://doi.org/10.1002/HLCA.200800250
(6-Hydroxy-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-7-yl) 2-methylbut-2-enoate 74433666 Click to see CC=C(C)C(=O)OC1C2CCCC3C2(C(C4=C(C(=O)OC14O)C)OC3=O)C 376.40 unknown https://doi.org/10.1002/HLCA.200800250
(6-Hydroxy-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-9-yl) acetate 74433665 Click to see CC1=C2C3C4(C(CCC(C4CC2(OC1=O)O)OC(=O)C)C(=O)O3)C 336.30 unknown https://doi.org/10.1002/HLCA.200800250
[(1R,6R,7S,8S,12S,15S)-6-hydroxy-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-7-yl] (Z)-2-methylbut-2-enoate 25223259 Click to see CC=C(C)C(=O)OC1C2CCCC3C2(C(C4=C(C(=O)OC14O)C)OC3=O)C 376.40 unknown https://doi.org/10.1002/HLCA.200800250
[(1R,6S,8R,9R,12S,15S)-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-9-yl] acetate 25223358 Click to see CC1=C2C(CC3C(CCC4C3(C2OC4=O)C)OC(=O)C)OC1=O 320.30 unknown https://doi.org/10.1002/HLCA.200800250
[(1R,6S,8R,9R,12S,15S)-6-hydroxy-3,15-dimethyl-4,13-dioxo-5,14-dioxatetracyclo[6.6.1.02,6.012,15]pentadec-2-en-9-yl] acetate 25223258 Click to see CC1=C2C3C4(C(CCC(C4CC2(OC1=O)O)OC(=O)C)C(=O)O3)C 336.30 unknown https://doi.org/10.1002/HLCA.200800250
9,9cbeta-Dimethyl-2aalpha,3,4,5,5abeta,6,9bbeta,9c-octahydro-2H-naphtho[1,8-bc:3,2-b']difuran-2-one 14307934 Click to see CC1=COC2=C1C3C4(C(C2)CCCC4C(=O)O3)C 246.30 unknown https://doi.org/10.1002/CBDV.200800346
https://doi.org/10.1039/C29690000551
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Decursidate 102004630 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(C2=CC=C(C=C2)O)O)O 330.30 unknown https://doi.org/10.1002/CBDV.200800346

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