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Salvia jaminiana

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 UUID643febc08e2c6321105060
Scientific name Salvia jaminiana
Authority de Noé
First published in Bull. Soc. Bot. France 2: 581 (1855)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

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-0000301295
Tropicos 100253807
KEW urn:lsid:ipni.org:names:456463-1
The Plant List kew-182916
Open Tree Of Life 6083285
NCBI Taxonomy 2886708
IPNI 456463-1
iNaturalist 1127681
GBIF 3898985

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H Molecules 27-Nov-2023
PMCID:PMC10708212
doi:10.3390/molecules28237801
PMID:38067531
Cytotoxicity and Apoptosis Induction of 6,7-Dehydroroyleanone from Taiwania cryptomerioides Bark Essential Oil in Hepatocellular Carcinoma Cells Chen GR, Chang ML, Chang ST, Ho YT, Chang HT Pharmaceutics 02-Feb-2022
PMCID:PMC8880271
doi:10.3390/pharmaceutics14020351
PMID:35214084
Components and antibacterial activity of the roots of Salvia jaminiana. Kabouche A, Boutaghane N, Kabouche Z, Seguin E, Tillequin F, Benlabed K Fitoterapia 01-Jul-2005
doi:10.1016/J.FITOTE.2005.03.011
PMID:15893885

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 / Naphthalenes
1-Hydroxy-8,13,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one 50907654 Click to see 298.40 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
Microstegiol 403772 Click to see 298.40 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> 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/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
6a-Hydroxysalvinolone 403771 Click to see CC(C)C1=C(C(=C2C(=C1)CC(=C3C2(CCCC3(C)C)C)O)O)O 316.40 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
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/J.FITOTE.2005.03.011
Cryptanol 184179 Click to see 316.40 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
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/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
6,9-dihydroxy-4,4,8-trimethyl-2,3-dihydro-1H-cyclohepta[a]naphthalen-10-one 163048944 Click to see CC1=C(C(=O)C=C2C3=C(C=C(C2=C1)O)C(CCC3)(C)C)O 284.30 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2R,6R,7R)-2-[2-(furan-3-yl)ethyl]-7-methyl-3-methylidene-9-oxatricyclo[5.3.3.01,6]tridecan-10-one 163001473 Click to see 314.40 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
methyl (E,6R)-6-[(1R,3R,6S,8S,11R,12S,13S,15R,16R,18R)-6,13-diacetyloxy-18-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoate 162863514 Click to see CC(CCC=C(C)C(=O)OC)C1CC(C2(C1(CC(C34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)O)C)C)OC(=O)C 586.80 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campestanol 119394 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C 402.70 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
Ergostan-3-ol, (3beta,5alpha)- 612090 Click to see 402.70 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(E)-2-[[1-[3-chloro-5-(diaminomethylideneamino)-4-hydroxy-2-[[4-methoxy-3-(3-prop-1-en-2-ylquinolin-4-yl)benzoyl]amino]pentanoyl]-3-hydroxy-3-methylpyrrolidine-2-carbonyl]amino]-3-methylpent-2-enoic acid 11125570 Click to see 764.30 unknown https://doi.org/10.1016/J.FITOTE.2005.03.011

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