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Heliotropium sarmentosum

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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 UUID64402012044f3030317894
Scientific name Heliotropium sarmentosum
Authority (Lam.) Craven
First published in Blumea 50: 380 (2005)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tournefortia glabrifolia Domin Biblioth. Bot. 22(89): 544 (1928)
Tournefortia frangulifolia Zipp. ex Span. Linnaea 15: 334 (1841)
Tournefortia orientalis R.Br. Prodr. Fl. Nov. Holland. : 497 (1810)
Tournefortia horsfieldii Miq. Fl. Ned. Ind. 2: 927 (1858)
Tournefortia acclinis F.Muell. Fragm. 4: 95 (1864)
Tournefortia urvilleana Cham. Linnaea 4: 465 (1829)
Bourreria setosa G.Don Gen. Hist. 4: 390 (1837)
Tournefortia sarmentosa Lam. Tabl. Encycl. 1: 416 (1792)
Tournefortia sarmentosa var. magnifolia Domin Biblioth. Bot. 22(89): 1097 (1928)

Common names Top

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Language Common/alternative name
Chinese 冷飯藤

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
    • Indo-China
      • Andaman Islands
      • Laos
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000718904
Tropicos 100385186
KEW urn:lsid:ipni.org:names:77069573-1
The Plant List kew-2844445
IPNI 77069573-1
iNaturalist 370499
GBIF 4062031
Open Tree Of Life 579114

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
Protective effect of Heliotropium foertherianum (Boraginaceae) folk remedy and its active compound, rosmarinic acid, against a Pacific ciguatoxin. Rossi F, Jullian V, Pawlowiez R, Kumar-Roiné S, Haddad M, Darius HT, Gaertner-Mazouni N, Chinain M, Laurent D J Ethnopharmacol 30-Aug-2012
doi:10.1016/J.JEP.2012.05.045
PMID:22706150
The Alkaloids of Heliotropium supinum L., with Observations on Viridifloric Acid HC Crowley, CCJ Culvenor CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9590694
Occurrence of supinine in Tournefortia sarmentosa Lam C Crowley, CCJ Culvenor CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9550464
Anti-lipid-peroxidative principles from Tournefortia sarmentosa. Lin YL, Chang YY, Kuo YH, Shiao MS J Nat Prod 01-May-2002
doi:10.1021/NP010538Y
PMID:12027757
Phenolic compounds from tournefortia sarmentosa. Lin YL, Tsai YL, Kuo YH, Liu YH, Shiao MS J Nat Prod 01-Nov-1999
doi:10.1021/NP9901332
PMID:10579860

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
5,6,7,8-tetrahydro-3H-pyrrolizin-1-ylmethyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 259729 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown https://doi.org/10.1071/CH9550464
https://doi.org/10.1071/CH9590694
Supinine 108053 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown https://doi.org/10.1071/CH9590694
https://doi.org/10.1071/CH9550464
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2-Ethoxy-4,5-dihydroxybenzoic acid 10821779 Click to see CCOC1=CC(=C(C=C1C(=O)O)O)O 198.17 unknown https://doi.org/10.1021/NP9901332
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1021/NP9901332
> Benzenoids / Phenols / 4-alkoxyphenols
2-Ethoxy-4,5-dihydroxybenzaldehyde 10821281 Click to see CCOC1=CC(=C(C=C1C=O)O)O 182.17 unknown https://doi.org/10.1021/NP9901332
> Benzenoids / Phenols / Benzenediols / Hydroquinones
2,5-Bis(4-methyloxolan-2-yl)benzene-1,4-diol 85158798 Click to see CC1CC(OC1)C2=CC(=C(C=C2O)C3CC(CO3)C)O 278.34 unknown https://doi.org/10.1021/NP9901332
5-[(2S,4R)-4-methyloxolan-2-yl]-2-[(2R,4R)-4-methyloxolan-2-yl]benzene-1,4-diol 10492852 Click to see CC1CC(OC1)C2=CC(=C(C=C2O)C3CC(CO3)C)O 278.34 unknown https://doi.org/10.1021/NP9901332
5-[(2S,4S)-4-methyloxolan-2-yl]-2-[(2R,4S)-4-methyloxolan-2-yl]benzene-1,4-diol 163094159 Click to see CC1CC(OC1)C2=CC(=C(C=C2O)C3CC(CO3)C)O 278.34 unknown https://doi.org/10.1021/NP9901332
> Benzenoids / Phenols / Methoxyphenols
Methyl 5-(5-hydroxy-2-methoxyphenyl)furan-3-carboxylate 5324825 Click to see COC1=C(C=C(C=C1)O)C2=CC(=CO2)C(=O)OC 248.23 unknown https://doi.org/10.1021/NP9901332
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1021/NP9901332
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin 439714 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1021/NP9901332
Allantoin, (-)- 439713 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1021/NP9901332
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
(2S)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(2,3,10-trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoyl]oxypropanoic acid 163187826 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=CC4=CC(=C(C=C4OC3=C(C=C2)O)O)O)O)O 492.40 unknown https://doi.org/10.1021/NP010538Y
3-(2,3,10-Trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoic acid 85094112 Click to see C1=CC2=C(C=CC(=C2OC3=CC(=C(C=C31)O)O)O)C=CC(=O)O 312.27 unknown https://doi.org/10.1021/NP010538Y
3-(3,4-Dihydroxyphenyl)-2-[3-(2,3,10-trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoyloxy]propanoic acid 75072247 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=CC4=CC(=C(C=C4OC3=C(C=C2)O)O)O)O)O 492.40 unknown https://doi.org/10.1021/NP010538Y
isosalvianolic acid C 44566967 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=CC4=CC(=C(C=C4OC3=C(C=C2)O)O)O)O)O 492.40 unknown https://doi.org/10.1021/NP010538Y
Tournefolic Acid B 10018390 Click to see C1=CC2=C(C=CC(=C2OC3=CC(=C(C=C31)O)O)O)C=CC(=O)O 312.27 unknown https://doi.org/10.1021/NP010538Y
Tournefolic acid B ethylester 10042848 Click to see CCOC(=O)C=CC1=C2C=CC3=CC(=C(C=C3OC2=C(C=C1)O)O)O 340.30 unknown https://doi.org/10.1021/NP010538Y
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acid esters
Methyl 5-(2,5-dihydroxyphenyl)furan-3-carboxylate 5324826 Click to see COC(=O)C1=COC(=C1)C2=C(C=CC(=C2)O)O 234.20 unknown https://doi.org/10.1021/NP9901332
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Lithospermic acid 4482010 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
(2R,3R)-4-[(1E)-3-[(1R)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propen-1-yl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylic acid 92212909 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
(2R,3R)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 95224953 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
(2S,3S)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 95359683 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
2-(3,4-Dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-carbaldehyde 636753 Click to see C1=CC(=C(C=C1C2=CC3=C(C=CC(=C3O2)O)C=O)O)O 270.24 unknown https://doi.org/10.1021/NP010538Y
2-(3,4-Dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-carboxylic acid 141732624 Click to see C1=CC(=C(C=C1C2=CC3=C(C=CC(=C3O2)O)C(=O)O)O)O 286.24 unknown https://doi.org/10.1021/NP010538Y
3-[2-(3,4-Dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-yl]prop-2-enoic acid 85133477 Click to see C1=CC(=C(C=C1C2=CC3=C(C=CC(=C3O2)O)C=CC(=O)O)O)O 312.27 unknown https://doi.org/10.1021/NP010538Y
CID 5281302 5281302 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
Lithospermic acid 6441498 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown https://doi.org/10.1021/NP010538Y
Tournefolic acid A 10403222 Click to see C1=CC(=C(C=C1C2=CC3=C(C=CC(=C3O2)O)C=CC(=O)O)O)O 312.27 unknown https://doi.org/10.1021/NP010538Y
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1021/NP010538Y
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/J.JEP.2012.05.045
https://doi.org/10.1021/NP010538Y
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1021/NP010538Y
> Phenylpropanoids and polyketides / Stilbenes
(2S)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-[2-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoyl]oxypropanoic acid 29927682 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown https://doi.org/10.1021/NP010538Y
3-[2-[2-(3,4-Dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoic acid 54208832 Click to see C1=CC(=C(C=C1C=CC2=C(C=CC(=C2O)O)C=CC(=O)O)O)O 314.29 unknown https://doi.org/10.1021/NP010538Y
N-Boc-amino-(3-thienyl)aceticacid 502233 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown https://doi.org/10.1021/NP010538Y
Salvianolic acid A 5281793 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O 494.40 unknown https://doi.org/10.1021/NP010538Y
salvianolic acid F 10903113 Click to see C1=CC(=C(C=C1C=CC2=C(C=CC(=C2O)O)C=CC(=O)O)O)O 314.29 unknown https://doi.org/10.1021/NP010538Y

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