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Heliotropium sarmentosum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

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

Ethnobotanical Use Top

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General Uses Top

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Common products:
Industrial and craft applications:
Food and beverages (non-medicinal):
Colorants and tanning:
Wood and fiber:
Fragrance and cosmetics:
Properties relevant to use:
Standards and regulation:
Sustainability and sourcing:

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

Suggest others/fix!
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!
You can also contribute to this by clicking here.
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 283.36 unknown https://doi.org/10.1071/CH9590694
https://doi.org/10.1071/CH9550464
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 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 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-[(2R,4S)-4-methyloxolan-2-yl]-2-[(2S,4S)-4-methyloxolan-2-yl]benzene-1,4-diol 163094159 Click to see 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
> 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 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 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 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 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 234.20 unknown https://doi.org/10.1021/NP9901332
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(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 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 538.50 unknown https://doi.org/10.1021/NP010538Y
2-(3,4-Dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-carboxylic acid 141732624 Click to see 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 312.27 unknown https://doi.org/10.1021/NP010538Y
4-[(E)-3-[(1R)-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 5281302 Click to see 538.50 unknown https://doi.org/10.1021/NP010538Y
4-[3-[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 4482010 Click to see 538.50 unknown https://doi.org/10.1021/NP010538Y
Lithospermic Acid 6441498 Click to see 538.50 unknown https://doi.org/10.1021/NP010538Y
Tournefolal 636753 Click to see 270.24 unknown https://doi.org/10.1021/NP010538Y
Tournefolic Acid A 10403222 Click to see 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 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 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 494.40 unknown https://doi.org/10.1021/NP010538Y
2-Propenoic acid,3-[2-[(1E)-2-(3,4-dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]-, (2E)- 54208832 Click to see 314.29 unknown https://doi.org/10.1021/NP010538Y
3-(3,4-Dihydroxyphenyl)-2-[3-[2-[2-(3,4-dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoyloxy]propanoic acid 502233 Click to see 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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