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Heliotropium bovei

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 UUID64402000410f7078533484
Scientific name Heliotropium bovei
Authority Boiss.
First published in Diagn. Pl. Orient. 11: 87 (1849)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Heliotropium kotschyanum Bunge Bull. Soc. Imp. Naturalistes Moscou 42(I): 312 (1869)
Heliotropium prusianum Bunge Bull. Soc. Imp. Naturalistes Moscou 42(I): 310 (1869)
Heliotropium smyrnaeum Bunge Bull. Soc. Imp. Naturalistes Moscou 42(I): 311 (1869)

Common names Top

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Language Common/alternative name
Persian آفتابپرست تهرانی

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000718428
KEW urn:lsid:ipni.org:names:116704-1
Open Tree Of Life 6063691
IPNI 116704-1
iNaturalist 717186
GBIF 4067324
EPPO HEOBO
CMAUP NPO3007

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
A Minor Pyrrolizidine Alkaloid from<i>Heliotropium bovei</i> Matías Reina, Ali H. Meriçli, A. González-Coloma Informa UK Limited 07-Jul-2007
doi:10.1080/10575639808044962
Pyrrolizidine alkaloids from Heliotropium bovei Matías Reina, Ali H. Mericli, Raimundo Cabrera, Azucena González-Coloma Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(94)00580-M

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
(1S,7aR)-7-[({(2S)-2,3-dihydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoyl}oxy)methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate 6321388 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/10.1016/0031-9422(94)00580-M
(7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2,3-dihydroxy-2-(1-methoxyethyl)-3-methylbutanoate 14488205 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)(C(C)(C)O)O)OC 371.40 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-4-oxido-5,6,7,8-tetrahydro-3H-pyrrolizin-4-ium-1-yl]methyl (2R)-3-acetyloxy-2-hydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 101915799 Click to see 469.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-3-acetyloxy-2-hydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 101915797 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)OC)(C(C)(C)OC(=O)C)O 453.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S,8R)-7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-3-acetyloxy-2-hydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 162901632 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)OC)(C(C)(C)OC(=O)C)O 453.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S,8R)-7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2,3-dihydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 163023688 Click to see 371.40 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2,3-dihydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 134715015 Click to see 329.39 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(7S)-7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2,3-dihydroxy-2-[(1S)-1-methoxyethyl]-3-methylbutanoate 101915798 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)(C(C)(C)O)O)OC 371.40 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[(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 411.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 3-acetyloxy-2-hydroxy-2-(1-methoxyethyl)-3-methylbutanoate 162901630 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)OC)(C(C)(C)OC(=O)C)O 453.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
7-({[2,3-Dihydroxy-2-(1-methoxyethyl)-3-methylbutanoyl]oxy}methyl)-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl 2-methylbut-2-enoate 613201 Click to see 411.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
CID 98222 98222 Click to see 329.39 unknown https://doi.org/10.1016/0031-9422(94)00580-M
Lasiocarpine N-oxide 5458800 Click to see 427.50 unknown https://doi.org/10.1016/0031-9422(94)00580-M
> Benzenoids / Benzene and substituted derivatives / Biphenols
4,4',5,5'-Tetrahydroxy-1,1'-binaphthyl 10087226 Click to see 318.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Taraxasterol 115250 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(9R,10R,13R,17R)-17-[(2R,5R)-5,6-Dimethylhept-3-en-2-yl]-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 167799 Click to see 392.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(+)-Mellein 10921069 Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1 178.18 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizines
(7-Oxo-5,6-dihydropyrrolizin-1-yl)methyl 2,3-dihydroxy-2-(1-methoxyethyl)-3-methylbutanoate 163106234 Click to see 325.36 unknown https://doi.org/10.1080/10575639808044962
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown via CMAUP database

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