beta-Irone

Details

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Internal ID 94efa37a-dc03-4dd9-a6b4-a10eaf4409c2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-4-(2,5,6,6-tetramethylcyclohexen-1-yl)but-3-en-2-one
SMILES (Canonical) CC1CCC(=C(C1(C)C)C=CC(=O)C)C
SMILES (Isomeric) CC1CCC(=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/h8-9,11H,6-7H2,1-5H3/b9-8+
InChI Key BGKCUGPVLVNPSG-CMDGGOBGSA-N
Popularity 0 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) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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79-70-9
6-Methyl-.beta.-ionone
.beta.-Irone
W8NW93JQ9H
beta-Irone [MI]
3-Buten-2-one, 4-(2,5,6,6-tetramethyl-1-cyclohexen-1-yl)-
6-Methyl-beta-ionone
(+/-)-beta-irone
beta-Ionone, 6-methyl-
BETA-N-METHYLIONONE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Irone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9399 93.99%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3995 39.95%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior - 0.2205 22.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7602 76.02%
P-glycoprotein inhibitior - 0.9636 96.36%
P-glycoprotein substrate - 0.9198 91.98%
CYP3A4 substrate + 0.5289 52.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8682 86.82%
CYP3A4 inhibition - 0.9247 92.47%
CYP2C9 inhibition - 0.8719 87.19%
CYP2C19 inhibition - 0.8075 80.75%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.7017 70.17%
CYP2C8 inhibition - 0.9008 90.08%
CYP inhibitory promiscuity - 0.6218 62.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5250 52.50%
Eye corrosion - 0.8866 88.66%
Eye irritation - 0.6014 60.14%
Skin irritation + 0.8968 89.68%
Skin corrosion - 0.9613 96.13%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4655 46.55%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5769 57.69%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4737 47.37%
Acute Oral Toxicity (c) III 0.8297 82.97%
Estrogen receptor binding - 0.8879 88.79%
Androgen receptor binding - 0.8453 84.53%
Thyroid receptor binding - 0.6439 64.39%
Glucocorticoid receptor binding - 0.8748 87.48%
Aromatase binding - 0.7586 75.86%
PPAR gamma - 0.7907 79.07%
Honey bee toxicity - 0.9380 93.80%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9543 95.43%

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 91.06% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.26% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.91% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.91% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.27% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 81.22% 91.19%

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 florentina
Iris sibirica

Cross-Links

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PubChem 5375215
LOTUS LTS0024809
wikiData Q27292468