Heliotropium indicum - Unknown
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Internal ID UUID64402007eaa72857826830
Scientific name Heliotropium indicum
Authority L.
First published in Species Plantarum 2 1753

Description Top

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The plant is toxic to humans and animals.

Indian heliotrope (Heliotropium indicum) is an annual, hirsute plant native to Asia. It is widely used in native medicine in Tamil Nadu, India, and is a common weed in waste places and settled areas. It grows to a height of 15-50 cm and has small white or purple flowers with a green calyx, five stamens, a terminal style, and a four-lobed ovary. Extracts from the plant are used as a traditional medicine, but it is toxic to humans and animals due to its pyrrolizidine alkaloids.

Synonyms Top

Scientific name Authority First published in
Tiaridium velutinum Lehm. Pl. Asperif. Nucif. : 15 (1818)
Tiaridium indicum Lehm. Pl. Asperif. Nucif. : 14 (1818)
Tiaridium anisophyllum G.Don Gen. Hist. 4: 364 (1837)
Eliopia riparia Raf. Sylva Tellur. : 90 (1838)
Eliopia serrata Raf. Sylva Tellur. : 90 (1838)
Heliophytum foetidum DC. Prodr. 9: 553 (1845)
Heliophytum indicum DC. Prodr. 9: 556 (1845)
Heliophytum velutinum DC. Prodr. 9: 557 (1845)
Heliotropium africanum Schumach. & Thonn. Beskr. Guin. Pl. : 87 (1827)
Heliotropium anisophyllum P.Beauv. Fl. Oware 2: 62 (1818)
Heliotropium cordifolium Moench Methodus : 415 (1794)
Heliotropium horminifolium Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Heliotropium foetidum Salisb. Prodr. Stirp. Chap. Allerton : 112 (1796)
Heliotropium parviflorum Blanco Fl. Filip. : 80 (1837)
Tiaridium indicum var. mexicanum M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11: 337 (1844)

Common names Top

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Language Common/alternative name
English indian heliotrope
English indian turnsole
Spanish alacrancillo
Arabic رقيب الشمس الهندي
Bambara nɔɔnsiku
Bengali হাতিশুঁড়
Bengali মহাশুণ্ডী
Bengali শ্রীহস্তিনী
Bengali হস্তীশুণ্ডী
Bengali হাতিশুঁড়ি
Bengali হাতিশুণ্ডি
dag kpansogwa
ht vèvenn pyan
Indonesian sangketan
jv tlalé gajah
Malayalam തേൾക്കട
Malayalam തേക്കട
mnw လပှ်စိင်၊ တၞံ
Oriya ହାତିଶୁଣ୍ଢ
Oriya ନାଗଦନ୍ତୀ
pam uladulad
Portuguese cravo de urubu
Tamil தேள் கொடுக்கி
Telugu నాగదంతి
Thai หญ้างวงช้าง
Vietnamese vòi voi
Chinese 大尾摇
Chinese 狗尾天芥菜
Chinese 狗尾草
Chinese 象鼻草
Chinese 大尾搖

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000718658
Florida Plant Atlas 1753
Flora of Alabama 1177
USDA Plants HEIN
Tropicos 4000972
INPN 445521
KEW urn:lsid:ipni.org:names:116938-1
The Plant List kew-2844124
Open Tree Of Life 1063716
Observations.org 198725
NCBI Taxonomy 248297
Nature Serve 2.135348
IPNI 116884-3
iNaturalist 83492
GBIF 2925788
Freebase /m/05n_zmc
EPPO HEOIN
EOL 580404
Elurikkus 335410
USDA GRIN 18825
Wikipedia Heliotropium_indicum
CMAUP NPO146

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
Climate and soil factors co-derive the functional traits variations in naturalized downy thorn apple (Datura innoxia Mill.) along the altitudinal gradient in the semi-arid environment Khan N, Ullah R, Okla MK, Abdel-Maksoud MA, Saleh IA, Abu-Harirah HA, AlRamadneh TN, AbdElgawad H Heliyon 14-Mar-2024
PMCID:PMC10957434
doi:10.1016/j.heliyon.2024.e27811
PMID:38524627
Late-instar monarch caterpillars sabotage milkweed to acquire toxins, not to disarm plant defence Betz A, Bischoff R, Petschenka G Proc Biol Sci 21-Feb-2024
PMCID:PMC10878802
doi:10.1098/rspb.2023.2721
PMID:38378155
Efficacy of 2,4-Di-tert-butylphenol in Reducing Ralstonia solanacearum Virulence: Insights into the Underlying Mechanisms Yang L, Wang R, Lin W, Li B, Jin T, Weng Q, Zhang M, Liu P ACS Omega 16-Jan-2024
PMCID:PMC10831823
doi:10.1021/acsomega.3c07887
PMID:38313526
Genome-Wide Identification, Characterization, and Expression Analysis of the Copper-Containing Amine Oxidase Gene Family in Mangrove Kandelia obovata Hussain Q, Ye T, Shang C, Li S, Nkoh JN, Li W, Hu Z Int J Mol Sci 09-Dec-2023
PMCID:PMC10743698
doi:10.3390/ijms242417312
PMID:38139139
The Optimization of Medium Conditions and Auxins in the Induction of Adventitious Roots of Pokeweed (Phytolacca americana L.) and Their Phytochemical Constituents Trunjaruen A, Luecha P, Taratima W Scientifica (Cairo) 21-Aug-2023
PMCID:PMC10462441
doi:10.1155/2023/2983812
PMID:37645570
Molecular dynamics and simulation analysis against superoxide dismutase (SOD) target of Micrococcus luteus with secondary metabolites from Bacillus licheniformis recognized by genome mining approach Bagewadi ZK, Yunus Khan TM, Gangadharappa B, Kamalapurkar A, Mohamed Shamsudeen S, Yaraguppi DA Saudi J Biol Sci 01-Aug-2023
PMCID:PMC10424208
doi:10.1016/j.sjbs.2023.103753
PMID:37583871
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Marine Algal Polyphenols as Skin Protective Agents: Current Status and Future Prospectives Jayawardhana HH, Jayawardena TU, Sanjeewa KK, Liyanage NM, Nagahawatta DP, Lee HG, Kim JI, Jeon YJ Mar Drugs 30-Apr-2023
PMCID:PMC10222755
doi:10.3390/md21050285
PMID:37233479
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
Recent advances in the area of plant-based anti-cancer drug discovery using computational approaches Das AP, Agarwal SM Mol Divers 21-Jan-2023
PMCID:PMC9859751
doi:10.1007/s11030-022-10590-7
PMID:36670282
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 09-Jan-2023
PMCID:PMC9827234
doi:10.2903/j.efsa.2023.7726
PMID:36628332
Medicinal plants used by rural Thai people to treat non-communicable diseases and related symptoms Nguanchoo V, Balslev H, Sadgrove NJ, Phumthum M Heliyon 04-Jan-2023
PMCID:PMC9850000
doi:10.1016/j.heliyon.2022.e12758
PMID:36685400
Biomedical Applications of Plant Extract-Synthesized Silver Nanoparticles Simon S, Sibuyi NR, Fadaka AO, Meyer S, Josephs J, Onani MO, Meyer M, Madiehe AM Biomedicines 02-Nov-2022
PMCID:PMC9687463
doi:10.3390/biomedicines10112792
PMID:36359308
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100
Ethnomedicinal Use, Phytochemistry, and Other Potential Application of Aquatic and Semiaquatic Medicinal Plants Arya AK, Durgapal M, Bachheti A, Deepti, Joshi KK, Gonfa YH, Bachheti RK, Husen A Evid Based Complement Alternat Med 10-Aug-2022
PMCID:PMC9385301
doi:10.1155/2022/4931556
PMID:35990854

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
> Alkaloids and derivatives
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 78384682 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1039/J39670000329
[(4S,7R,8R)-7-hydroxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl (2R)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 163024928 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CC[N+]2(C1C(CC2)O)[O-])O 315.36 unknown https://doi.org/10.1039/J39670000329
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1S)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 162973293 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1039/J39670000329
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 44285612 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-methoxyethyl)-3-methylbutanoate 6420067 Click to see CC(C)C(C(C)OC)(C(=O)OCC1=CCN2C1C(CC2)O)O 313.39 unknown via CMAUP database
[(7S)-7-hydroxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 10018581 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CC[N+]2(C1C(CC2)O)[O-])O 315.36 unknown via CMAUP database
[(7S)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 5315902 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown via CMAUP database
[(8R)-7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2,3-dihydroxy-2-(1-methoxyethyl)-3-methylbutanoate 138112573 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)OC)(C(C)(C)O)O 411.50 unknown https://doi.org/10.1039/J39670000329
[(8S)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 6326108 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown via CMAUP database
1H-Pyrrolizine-7-methanol, 2,3,5,7a-tetrahydro-1-hydroxy-, (1S-cis)- 10626 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
5,6,7,8-Tetrahydro-3H-pyrrolizin-1-ylmethanol 186156 Click to see C1CC2C(=CCN2C1)CO 139.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
Echinatine 22384 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1039/J39670000329
Echinatine, N-oxide 38946 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CC[N+]2(C1C(CC2)O)[O-])O 315.36 unknown https://doi.org/10.1039/J39670000329
Heliotrine 906426 Click to see CC(C)C(C(C)OC)(C(=O)OCC1=CCN2C1C(CC2)O)O 313.39 unknown https://doi.org/10.1039/J39670000329
Indicine N-oxide 280564 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CC[N+]2(C1C(CC2)O)[O-])O 315.36 unknown https://doi.org/10.1039/J39670000329
Lycopsamine 107938 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1039/J39670000329
Retronecine 10198 Click to see C1CN2CC=C(C2C1O)CO 155.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
https://doi.org/10.1016/S0031-9422(00)82598-4
Supinidine 164663 Click to see C1CC2C(=CCN2C1)CO 139.19 unknown https://doi.org/10.1016/0031-9422(82)83097-5
Unii-743IO8efvg 12310804 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Helioxanthin 177023 Click to see C1C2=C(C=C3C=CC4=C(C3=C2C5=CC6=C(C=C5)OCO6)OCO4)C(=O)O1 348.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Surangin A 5321563 Click to see CCCC1=CC(=O)OC2=C1C(=C(C(=C2C(=O)C(C)CC)O)CC=C(C)CCC=C(C)C)O 440.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
2,4,4-trimethyl-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17Z)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-2-en-1-one 6436871 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(=O)CCC2(C)C)C)C)C 550.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1039/J39670000329
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/10.1039/J39670000329
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methyl-5-methyleneheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 134688501 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1039/J39670000329
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1039/J39670000329
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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/10.1039/J39670000329
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/10.1039/J39670000329
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/10.1039/J39670000329
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/10.1039/J39670000329
> Nucleosides, nucleotides, and analogues / Ribonucleoside 3-phosphates
3'-Adenylic acid 41211 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)O)O)N 347.22 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Spermidine 1102 Click to see C(CCNCCCN)CN 145.25 unknown https://doi.org/10.1016/S0031-9422(00)82598-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses / Pentose phosphates
2'-Cytidylic acid 101544 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)OP(=O)(O)O 323.20 unknown via CMAUP database
Cytidine 3'-monophosphate 66535 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)OP(=O)(O)O)O 323.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
3-Ethyl-2,5-dihydroxy-1,4-benzoquinone 821411 Click to see CCC1=C(C(=O)C=C(C1=O)O)O 168.15 unknown via CMAUP database
Rapanone 100659 Click to see CCCCCCCCCCCCCC1=C(C(=O)C=C(C1=O)O)O 322.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(2Z)-2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one 5354391 Click to see C1=CC=C2C(=C1)C(=O)C(=C3C(=O)C4=CC=CC=C4N3)N2 262.26 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
1H-Pyrrolizine-1-methanol, hexahydro-, (1S-cis)- 94259 Click to see C1CC2C(CCN2C1)CO 141.21 unknown https://doi.org/10.1016/0031-9422(82)83097-5
Lindelofidine 11126361 Click to see C1CC2C(CCN2C1)CO 141.21 unknown https://doi.org/10.1016/0031-9422(82)83097-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
7-Hydroxyflavanone 1890 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown https://doi.org/10.1039/J39670000329
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
2-[6,7-Dihydroxy-5-(hydroxymethyl)-1-benzofuran-4-yl]-6-[2-[6,7-dihydroxy-5-(hydroxymethyl)-1-benzofuran-4-yl]-5,9-dihydroxy-4-oxobenzo[h]chromen-6-yl]-5,9-dihydroxybenzo[h]chromen-4-one 12992492 Click to see C1=CC2=C(C=C1O)C3=C(C(=O)C=C(O3)C4=C5C=COC5=C(C(=C4CO)O)O)C(=C2C6=C(C7=C(C8=C6C=CC(=C8)O)OC(=CC7=O)C9=C1C=COC1=C(C(=C9CO)O)O)O)O 810.70 unknown https://doi.org/10.1016/0031-9422(82)83097-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Naringenin 5-methyl ether 188424 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1039/J39670000329

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