3-Hydroxy-7,8-dihydro-beta-ionone

Details

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Internal ID 91c0a756-4efd-488f-8c6c-1c628acd5c01
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-(3-hydroxybutyl)-2,2,4-trimethylcyclohex-3-en-1-ol
SMILES (Canonical) CC1=C(C(C(CC1)O)(C)C)CCC(C)O
SMILES (Isomeric) CC1=C(C(C(CC1)O)(C)C)CCC(C)O
InChI InChI=1S/C13H24O2/c1-9-5-8-12(15)13(3,4)11(9)7-6-10(2)14/h10,12,14-15H,5-8H2,1-4H3
InChI Key PCHNRWMSYBNCRR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H24O2
Molecular Weight 212.33 g/mol
Exact Mass 212.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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3-hydroxy-7,8-dihydro-.beta.-ionone

2D Structure

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2D Structure of 3-Hydroxy-7,8-dihydro-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 + 0.9945 99.45%
Caco-2 + 0.8025 80.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6677 66.77%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9373 93.73%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7736 77.36%
P-glycoprotein inhibitior - 0.9303 93.03%
P-glycoprotein substrate - 0.7544 75.44%
CYP3A4 substrate + 0.5138 51.38%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7214 72.14%
CYP3A4 inhibition - 0.7572 75.72%
CYP2C9 inhibition - 0.8783 87.83%
CYP2C19 inhibition - 0.7990 79.90%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition - 0.8712 87.12%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity - 0.7216 72.16%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8828 88.28%
Carcinogenicity (trinary) Non-required 0.6575 65.75%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.6060 60.60%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9741 97.41%
Ames mutagenesis - 0.7837 78.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8103 81.03%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8305 83.05%
Acute Oral Toxicity (c) III 0.8279 82.79%
Estrogen receptor binding - 0.8110 81.10%
Androgen receptor binding - 0.6982 69.82%
Thyroid receptor binding - 0.4887 48.87%
Glucocorticoid receptor binding - 0.6979 69.79%
Aromatase binding - 0.8362 83.62%
PPAR gamma - 0.8047 80.47%
Honey bee toxicity - 0.9674 96.74%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9650 96.50%

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 95.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.03% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.32% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.72% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.85% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.06% 95.89%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.85% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.24% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.94% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.90% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.82% 95.89%
CHEMBL4040 P28482 MAP kinase ERK2 81.68% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 80.12% 90.17%

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.
Tectona grandis

Cross-Links

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PubChem 91747289
LOTUS LTS0179277
wikiData Q105205738