Dihydroxy-beta-ionone

Details

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Internal ID 9c04de86-e370-4c22-baa7-08d6ee96459b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-4-[(1R,2R)-1,2-dihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O3/c1-10(14)6-9-13(16)11(2,3)7-5-8-12(13,4)15/h6,9,15-16H,5,7-8H2,1-4H3/b9-6+/t12-,13-/m1/s1
InChI Key AYWGPQFATRWJMF-BHAGLWOSSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O3
Molecular Weight 226.31 g/mol
Exact Mass 226.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dihydroxy-beta-ionone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.8841 88.41%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8571 85.71%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9658 96.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8654 86.54%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.9483 94.83%
CYP3A4 substrate + 0.5276 52.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8714 87.14%
CYP3A4 inhibition - 0.8615 86.15%
CYP2C9 inhibition - 0.8485 84.85%
CYP2C19 inhibition - 0.8828 88.28%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.8348 83.48%
CYP2C8 inhibition - 0.9679 96.79%
CYP inhibitory promiscuity - 0.9703 97.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6516 65.16%
Eye corrosion - 0.9718 97.18%
Eye irritation + 0.8028 80.28%
Skin irritation + 0.6364 63.64%
Skin corrosion - 0.8909 89.09%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8561 85.61%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6627 66.27%
skin sensitisation + 0.6767 67.67%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5755 57.55%
Acute Oral Toxicity (c) III 0.7526 75.26%
Estrogen receptor binding + 0.5450 54.50%
Androgen receptor binding - 0.5675 56.75%
Thyroid receptor binding - 0.6166 61.66%
Glucocorticoid receptor binding - 0.4822 48.22%
Aromatase binding - 0.7087 70.87%
PPAR gamma - 0.8258 82.58%
Honey bee toxicity - 0.9078 90.78%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9247 92.47%

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 91.50% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.71% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.82% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.63% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15693868
LOTUS LTS0070859
wikiData Q104921418