(s)-(+)-gamma-Ionone

Details

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Internal ID 723c3cd1-6cd2-4999-9ea9-45b7a347cb23
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-4-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-one
SMILES (Canonical) CC(=O)C=CC1C(=C)CCCC1(C)C
SMILES (Isomeric) CC(=O)/C=C/[C@@H]1C(=C)CCCC1(C)C
InChI InChI=1S/C13H20O/c1-10-6-5-9-13(3,4)12(10)8-7-11(2)14/h7-8,12H,1,5-6,9H2,2-4H3/b8-7+/t12-/m1/s1
InChI Key SFEOKXHPFMOVRM-ABZNLYFFSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O
Molecular Weight 192.30 g/mol
Exact Mass 192.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.51
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (s)-(+)-gamma-Ionone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.9082 90.82%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4400 44.00%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9056 90.56%
OATP1B3 inhibitior - 0.4166 41.66%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8941 89.41%
P-glycoprotein inhibitior - 0.9684 96.84%
P-glycoprotein substrate - 0.9520 95.20%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8845 88.45%
CYP3A4 inhibition - 0.9207 92.07%
CYP2C9 inhibition - 0.8306 83.06%
CYP2C19 inhibition - 0.7772 77.72%
CYP2D6 inhibition - 0.9499 94.99%
CYP1A2 inhibition - 0.7407 74.07%
CYP2C8 inhibition - 0.8625 86.25%
CYP inhibitory promiscuity - 0.7217 72.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5473 54.73%
Eye corrosion - 0.8853 88.53%
Eye irritation + 0.6606 66.06%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9809 98.09%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6346 63.46%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6667 66.67%
skin sensitisation + 0.9207 92.07%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5578 55.78%
Acute Oral Toxicity (c) III 0.8392 83.92%
Estrogen receptor binding - 0.9268 92.68%
Androgen receptor binding - 0.8527 85.27%
Thyroid receptor binding - 0.7299 72.99%
Glucocorticoid receptor binding - 0.7129 71.29%
Aromatase binding - 0.8499 84.99%
PPAR gamma - 0.9199 91.99%
Honey bee toxicity - 0.8816 88.16%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9899 98.99%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.21% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.94% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 87.46% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.16% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 83.99% 91.19%
CHEMBL1937 Q92769 Histone deacetylase 2 83.43% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.70% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.96% 95.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.05% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Sideritis hirsuta

Cross-Links

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PubChem 11194862
LOTUS LTS0102379
wikiData Q105251708