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Salvia cilicica

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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 UUID643feba4d0f8a344921968
Scientific name Salvia cilicica
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 4: 19 (1859)

Description Top

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Synonyms Top

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Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300690
Tropicos 17600579
KEW urn:lsid:ipni.org:names:455957-1
The Plant List kew-182358
Open Tree Of Life 6083095
IPNI 455957-1
GBIF 3906023

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
Abietane diterpenoids and triterpenoic acids from Salvia cilicica and their antileishmanial activities. Tan N, Kaloga M, Radtke OA, Kiderlen AF, Oksüz S, Ulubelen A, Kolodziej H Phytochemistry 01-Dec-2002
doi:10.1016/S0031-9422(02)00361-8
PMID:12453510

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 / Tetralins
CID 9906686 9906686 Click to see CC1(CC2=C(C(=O)C1)C34C(C5=C(C(C3(O4)C=C2)O)C(=CC=C5)OC)O)O 356.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol 101219048 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
(4bS,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione 124511152 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCCC3(C)C)C 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione 2751812 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCCC3(C)C)C 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
4b,8,8-Trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione 4012024 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCCC3(C)C)C 300.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 71438639 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3CC2=O)(C)C)C)O 346.50 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Cryptanol 184179 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3C=C2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Inuroyleanol 15386508 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3CC2=O)(C)C)C)O 346.50 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00361-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3S,4R,5R,6S)-6-[[(3S,4R,4aR)-4-ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101394761 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)OC(=O)C=CC4=CC=C(C=C4)O)O)O 520.50 unknown https://doi.org/10.1016/S0031-9422(02)00361-8

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