1-(3,5-Dihydroxyphenyl)heptan-1-one

Details

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Internal ID 5cd3c958-f3b3-41f2-a175-63614e8b8e45
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(3,5-dihydroxyphenyl)heptan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O3/c1-2-3-4-5-6-13(16)10-7-11(14)9-12(15)8-10/h7-9,14-15H,2-6H2,1H3
InChI Key YAMFGBCNXUCDEQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O3
Molecular Weight 222.28 g/mol
Exact Mass 222.125594432 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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1-(3,5-dihydroxyphenyl)heptan-1-one
1-(3,5-Dihydroxyphenyl)heptan-1'-one

2D Structure

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2D Structure of 1-(3,5-Dihydroxyphenyl)heptan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.7960 79.60%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7035 70.35%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8385 83.85%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9168 91.68%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.8592 85.92%
CYP3A4 substrate - 0.6414 64.14%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7329 73.29%
CYP3A4 inhibition + 0.7543 75.43%
CYP2C9 inhibition - 0.6602 66.02%
CYP2C19 inhibition - 0.5339 53.39%
CYP2D6 inhibition - 0.8222 82.22%
CYP1A2 inhibition + 0.5867 58.67%
CYP2C8 inhibition - 0.7313 73.13%
CYP inhibitory promiscuity - 0.6733 67.33%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7934 79.34%
Carcinogenicity (trinary) Non-required 0.7245 72.45%
Eye corrosion - 0.8322 83.22%
Eye irritation + 0.9308 93.08%
Skin irritation + 0.5800 58.00%
Skin corrosion - 0.6470 64.70%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6067 60.67%
skin sensitisation + 0.5165 51.65%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5796 57.96%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4764 47.64%
Acute Oral Toxicity (c) III 0.7471 74.71%
Estrogen receptor binding - 0.5594 55.94%
Androgen receptor binding - 0.6204 62.04%
Thyroid receptor binding - 0.6720 67.20%
Glucocorticoid receptor binding - 0.4795 47.95%
Aromatase binding - 0.6240 62.40%
PPAR gamma + 0.9162 91.62%
Honey bee toxicity - 0.9948 99.48%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8038 80.38%
Fish aquatic toxicity + 0.9695 96.95%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.36% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.72% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.41% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 93.90% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.83% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.67% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.77% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.54% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.70% 96.95%

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 49778006
LOTUS LTS0242936
wikiData Q105345450