alpha-Irone

Details

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Internal ID 881598b0-9660-4913-b43a-12be8c5103aa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-4-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)but-3-en-2-one
SMILES (Canonical) CC1CC=C(C(C1(C)C)C=CC(=O)C)C
SMILES (Isomeric) CC1CC=C(C(C1(C)C)/C=C/C(=O)C)C
InChI InChI=1S/C14H22O/c1-10-6-7-11(2)14(4,5)13(10)9-8-12(3)15/h6,8-9,11,13H,7H2,1-5H3/b9-8+
InChI Key JZQOJFLIJNRDHK-CMDGGOBGSA-N
Popularity 1,249 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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79-69-6
Methyl alpha-ionone
6-Methyl-alpha-ionone
Irone
alpha-Iron
4-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)but-3-en-2-one
alpha-Ionone, methyl-
6-Methyl ionone
Irone, alpha-
4-(2,5,6,6-Tetramethylcyclohex-2-enyl)but-3-en-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of alpha-Irone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8124 81.24%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5093 50.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9466 94.66%
OATP1B3 inhibitior + 0.8943 89.43%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7684 76.84%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.8906 89.06%
CYP3A4 substrate - 0.5073 50.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8845 88.45%
CYP3A4 inhibition - 0.8407 84.07%
CYP2C9 inhibition - 0.8469 84.69%
CYP2C19 inhibition - 0.7140 71.40%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition - 0.7487 74.87%
CYP2C8 inhibition - 0.9277 92.77%
CYP inhibitory promiscuity - 0.5239 52.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5717 57.17%
Carcinogenicity (trinary) Non-required 0.5569 55.69%
Eye corrosion - 0.6591 65.91%
Eye irritation - 0.6523 65.23%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9141 91.41%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5701 57.01%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6144 61.44%
skin sensitisation + 0.9578 95.78%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.5539 55.39%
Acute Oral Toxicity (c) III 0.7656 76.56%
Estrogen receptor binding - 0.7392 73.92%
Androgen receptor binding - 0.7342 73.42%
Thyroid receptor binding - 0.7780 77.80%
Glucocorticoid receptor binding - 0.8403 84.03%
Aromatase binding - 0.8539 85.39%
PPAR gamma - 0.7996 79.96%
Honey bee toxicity - 0.8730 87.30%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9717 97.17%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.58% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.53% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.48% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.65% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.17% 96.95%

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.
Iris sibirica
Trifolium pratense

Cross-Links

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PubChem 5371002
NPASS NPC5626
LOTUS LTS0067996
wikiData Q27108610