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Vicoa indica

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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
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Details Top

Internal ID UUID643fd1c995a61595330307
Scientific name Vicoa indica
Authority DC.
First published in Contr. Bot. India : 10 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vicoa appendiculata DC. Prodr. 5: 474 (1836)
Erigeron sanguineus Parsa Kew Bull. 3(2): 208 (1948)
Inulaster kotschyi Sch.Bip. Flora 24(1, Intelligenzbl.): 42. 1841 ; in Flora, 25(1, Beibl.): 134, 147 (1842)
Inula auriculata Wall. Numer. List : n.° 2965 (1831)
Vicoa leptoclada (Webb) Dandy Fl. Pl. Sudan iii. 62 (1956)
Doronicum calcaratum Roxb. Hort. Bengal. 61; Fl. Ind. iii. 434
Aster lofouensis H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 281 (1910)
Inulaster kotschyi Sch.Bip. ex Hochst.
Inula appendiculata Wall. Numer. List : n.° 2966 (1831)
Inulaster hotschyi Sch.Bip. ex Hochst. Flora 25(1): 42 1841
Jacobaea indica Kuntze Revis. Gen. Pl. 1: 347 (1891)
Vicoa auriculata Cass. Ann. Sci. Nat. (Paris) 17: 418 (1829)
Vicoa aurita DC. Prodr. 5: 474 (1836)
Erigeron linearis Spreng. ex DC. Prodr. 5: 474 (1836)
Inula indica var. hypoleuca Hand.-Mazz. Symbolae Sinicae 7(4): 1107 1936
Varthemia kotschyi Sch.Bip. Beitr. Fl. Aethiop. 161, 307
Inula leptoclada Webb Niger Fl. : 137 (1849)
Varthemia kotschyi Sch.Bip. ex Schweinf. & Asch.
Pentanema indicum var. hypoleucum (Hand.-Mazz.) Ling Acta Phytotax. Sin. 10(2): 179-180 (1965)
Inula indica L. Sp. Pl., ed. 2. 2: 1236. 1763 [Aug 1763]
Inula indica A.Chev. Exploration Botanique de l'Afrique Occidentale Francaise ... 366 1920
Pentanema indicum (L.) Y.Ling Acta Phytotax. Sin. 10: 179 (1965)
Inula scabra Wall. ex DC. Prodr. 5: 474 (1836)
Pentanema indicum var. sivarajanianum R.R.V.Raju & C.P.Raju Rheedea 6(2): 55 (1996)

Common names Top

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Language Common/alternative name
Tamil கூத்தன் குதம்பை

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000118235
KEW urn:lsid:ipni.org:names:259717-1
GBIF 3146542
EPPO VCOIN
USDA GRIN 401877
IPNI 259717-1

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)!
Title Authors Publication Released IDs
Antiviral Constituents from Vicoa indica B. L. Chowdhury, F. A. Hussaini, A. Shoeb Informa UK Limited 25-Nov-2007
doi:10.3109/13880209009082791
Isolation and Characterization of Vicodiol, a New Monoterpenediol from Vicoa indica Saradha Vasanth, A. B. Kundu, K. K. Purushothaman, A. Patra, Vasantha Pattabhi, J. D. Connolly American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50068A013
A germacranolide from Vicoa indica Dilip D. Sawaikar, Supada R. Rojatkar, Bhimsen A. Nagasampagi, Vedavati G. Puranik Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(97)01136-9
Vicogenin, a 28-nor-12-oleanenepentol from Vicoa indica K. Balakrishna, Saradha Vasanth, Amit B. Kundu, R. Bhima Rao, Joseph D. Connolly Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00232-V
Vicoside A, a 28-nortriterpenoid glucoside from Vicoa indica Saradha Vasanth, A.B. Kundu, S.K. Panda, A. Patra Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98251-7
A germacranolide from Inula indica Bhimsen A. Nagasampagi, Uppoor G. Bhatt, Ferdinand Bohlmann, Christa Zdero Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)84062-9
Antifeedant activity of vicolides from Pentanema indicum Saradha Vasanth, Regina Mary, S Govindarajan Elsevier BV 25-Jul-2002
doi:10.1016/S0367-326X(99)00106-9
A cis,cis-germacrenolide from Vicoa indica D.D. Sawaikar, S.R. Rojatkar, B.A. Nagasampagi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(94)85105-0

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,2S,4R,7R)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol 163086581 Click to see CC12CCC(C1(C)CO)CC2O 170.25 unknown https://doi.org/10.1021/NP50068A013
(2S,4R,7R)-7-(hydroxymethyl)-1,7-dimethylbicyclo[2.2.1]heptan-2-ol 163193318 Click to see CC12CCC(C1(C)CO)CC2O 170.25 unknown https://doi.org/10.1021/NP50068A013
Vicodiol 182938 Click to see CC12CCC(C1(C)CO)CC2O 170.25 unknown https://doi.org/10.1021/NP50068A013
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(8,11-Dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl) 2-methylbutanoate 162908011 Click to see CCC(C)C(=O)OC1C=C(CC(C=C(C(C2C1C(=C)C(=O)O2)O)C)O)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)85105-0
[(3aR,4R,5R,6R,9Z,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-2,8-dioxo-4,5,6,7,11,11a-hexahydro-3aH-cyclodeca[b]furan-5-yl] (E)-2-methylbut-2-enoate 6445538 Click to see CC=C(C)C(=O)OC1C(CC(=O)C=C(CC2C(C1O)C(=C)C(=O)O2)C)C 362.40 unknown https://doi.org/10.1016/S0367-326X(99)00106-9
[(3aS,4R,5Z,8S,9Z,11R,11aR)-8,11-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] (2R)-2-methylbutanoate 162908012 Click to see CCC(C)C(=O)OC1C=C(CC(C=C(C(C2C1C(=C)C(=O)O2)O)C)O)C 364.40 unknown https://doi.org/10.1016/0031-9422(94)85105-0
Vicolide B 76326827 Click to see CC=C(C)C(=O)OC1C(CC(=O)C=C(CC2C(C1O)C(=C)C(=O)O2)C)C 362.40 unknown https://doi.org/10.1016/S0367-326X(99)00106-9
Vicolide D 6450513 Click to see CC1CC(=O)C=C(CC2C(C(C1OC(=O)C3(C(O3)C)C)O)C(=C)C(=O)O2)C 378.40 unknown https://doi.org/10.1016/S0367-326X(99)00106-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Vicoa indica VI 2 5477684 Click to see CC=C(C)C(=O)OC1C(C2C(C3C(C1O)C(=C)C(=O)O3)C(=CC2=O)C)C 360.40 unknown https://doi.org/10.1016/S0367-326X(99)00106-9
Vicolide A 9998617 Click to see CC=C(C)C(=O)OC1C(C2C(C3C(C1O)C(=C)C(=O)O3)C(=CC2=O)C)C 360.40 unknown https://doi.org/10.1016/S0367-326X(99)00106-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4R,4aR,6aR,6bS,8S,8aR,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-2,3,8,8a-tetrol 15765108 Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C)O)C 476.70 unknown https://doi.org/10.1016/0031-9422(95)00232-V
(4aR,6aR,6aR,6bR,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 138113838 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.3109/13880209009082791
[(4aR,5S,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-5,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl] formate 101609009 Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)OC=O)C 666.80 unknown https://doi.org/10.1016/S0031-9422(00)98251-7
[5,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl] formate 75110966 Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)OC=O)C 666.80 unknown https://doi.org/10.1016/S0031-9422(00)98251-7
4-(Hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-2,3,8,8a-tetrol 162923270 Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C)O)C 476.70 unknown https://doi.org/10.1016/0031-9422(95)00232-V
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.3109/13880209009082791
Epilupeol 5270628 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/10.3109/13880209009082791
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.3109/13880209009082791
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(2,10-Diacetyloxy-3-methyl-8,12-dimethylidene-6,13-dioxo-4,14-dioxatricyclo[9.3.0.03,5]tetradecan-9-yl) 2-methylbutanoate 162983888 Click to see CCC(C)C(=O)OC1C(C2C(C(C3(C(O3)C(=O)CC1=C)C)OC(=O)C)OC(=O)C2=C)OC(=O)C 478.50 unknown https://doi.org/10.1016/S0031-9422(97)01136-9
[(1R,2S,3R,5R,9R,10R,11R)-2,10-diacetyloxy-3-methyl-8,12-dimethylidene-6,13-dioxo-4,14-dioxatricyclo[9.3.0.03,5]tetradecan-9-yl] (2R)-2-methylbutanoate 162983889 Click to see CCC(C)C(=O)OC1C(C2C(C(C3(C(O3)C(=O)CC1=C)C)OC(=O)C)OC(=O)C2=C)OC(=O)C 478.50 unknown https://doi.org/10.1016/S0031-9422(97)01136-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(9-Acetyloxy-2,6-dihydroxy-3,8-dimethyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl) 2-methylbutanoate 434232 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(O3)C(CC(C1OC(=O)C)C)O)C)O)OC(=O)C2=C 440.50 unknown https://doi.org/10.1016/0031-9422(81)84062-9
[(1R,2S,3R,5R,6S,8S,9R,10S,11R)-9-acetyloxy-2,6-dihydroxy-3,8-dimethyl-12-methylidene-13-oxo-4,14-dioxatricyclo[9.3.0.03,5]tetradecan-10-yl] (2R)-2-methylbutanoate 163011214 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(O3)C(CC(C1OC(=O)C)C)O)C)O)OC(=O)C2=C 440.50 unknown https://doi.org/10.1016/0031-9422(81)84062-9
Vicolide C 76312409 Click to see CCC(C)C(=O)OC1C2C(C(C3(C(O3)C(CC(C1OC(=O)C)C)O)C)O)OC(=O)C2=C 440.50 unknown https://doi.org/10.1016/S0367-326X(99)00106-9

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