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Internal ID UUID64403bb3c6f6c983297750
Scientific name Euphorbia teheranica
Authority Boiss.
First published in Cent. Euphorb. : 36 (1860)

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Synonyms Top

Scientific name Authority First published in
Tithymalus teheranicus (Boiss.) Soják Cas. Nár. Mus., Odd. Prír. 140: 177 (1972)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000965042
Tropicos 50111292
KEW urn:lsid:ipni.org:names:348456-1
The Plant List kew-82471
Open Tree Of Life 392595
NCBI Taxonomy 1031534
IPNI 348456-1
GBIF 3065278
EOL 1143787

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)!
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Title Authors Publication Released IDs
Jatrophane Diterpenoids from Euphorbia glomerulans. Hasan A, Liu GY, Hu R, Aisa HA J Nat Prod 26-Apr-2019
doi:10.1021/ACS.JNATPROD.8B00507
PMID:30860373
New diterpenoids from euphorbia teheranica. Ahmad VU, Jassbi AR J Nat Prod 01-Jul-1999
doi:10.1021/NP980368Y
PMID:10425130

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1021/ACS.JNATPROD.8B00507
https://doi.org/10.1021/NP980368Y
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
(2,4,7,14,15-Pentaacetyloxy-5,9-dimethyl-11-prop-1-en-2-yl-16-oxatetracyclo[7.5.2.01,10.03,7]hexadec-12-en-8-yl) pyridine-3-carboxylate 73157938 Click to see CC1CC2(C(C1OC(=O)C)C(C34C(C=CC(C3C(C2OC(=O)C5=CN=CC=C5)(OC4OC(=O)C)C)C(=C)C)OC(=O)C)OC(=O)C)OC(=O)C 697.70 unknown https://doi.org/10.1021/NP980368Y
(2,4,7,8,12-Pentaacetyloxy-5,9,12-trimethyl-16-oxo-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-15-yl) 2-methylbutanoate 73804952 Click to see CCC(C)C(=O)OC1C2CC(C2C3C4(C(C5(CC(C(C5C(C3(C1=O)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C)C)(C)OC(=O)C 692.70 unknown https://doi.org/10.1021/NP980368Y
[(1R,2R,3R,4S,5S,7R,8S,9R,10R,11S,14R,15R)-2,4,7,14,15-pentaacetyloxy-5,9-dimethyl-11-prop-1-en-2-yl-16-oxatetracyclo[7.5.2.01,10.03,7]hexadec-12-en-8-yl] pyridine-3-carboxylate 163185189 Click to see CC1CC2(C(C1OC(=O)C)C(C34C(C=CC(C3C(C2OC(=O)C5=CN=CC=C5)(OC4OC(=O)C)C)C(=C)C)OC(=O)C)OC(=O)C)OC(=O)C 697.70 unknown https://doi.org/10.1021/NP980368Y
[(1S,2R,3R,4S,5S,7R,8S,9R,10R,11S,12S,14R,15R)-2,4,7,8,12-pentaacetyloxy-5,9,12-trimethyl-16-oxo-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-15-yl] (2R)-2-methylbutanoate 162906318 Click to see CCC(C)C(=O)OC1C2CC(C2C3C4(C(C5(CC(C(C5C(C3(C1=O)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C)C)(C)OC(=O)C 692.70 unknown https://doi.org/10.1021/NP980368Y
[(1S,2R,3R,4S,5S,7R,8S,9R,10R,11S,12S,14R,15R)-2,7,8,12-tetraacetyloxy-5,9,12-trimethyl-15-[(2R)-2-methylbutanoyl]oxy-16-oxo-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-4-yl] pyridine-3-carboxylate 163096691 Click to see CCC(C)C(=O)OC1C2CC(C2C3C4(C(C5(CC(C(C5C(C3(C1=O)CO4)OC(=O)C)OC(=O)C6=CN=CC=C6)C)OC(=O)C)OC(=O)C)C)(C)OC(=O)C 755.80 unknown https://doi.org/10.1021/NP980368Y
[2,7,8,12-Tetraacetyloxy-5,9,12-trimethyl-15-(2-methylbutanoyloxy)-16-oxo-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-4-yl] pyridine-3-carboxylate 73109100 Click to see CCC(C)C(=O)OC1C2CC(C2C3C4(C(C5(CC(C(C5C(C3(C1=O)CO4)OC(=O)C)OC(=O)C6=CN=CC=C6)C)OC(=O)C)OC(=O)C)C)(C)OC(=O)C 755.80 unknown https://doi.org/10.1021/NP980368Y

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