1-(2,6-Dihydroxyphenyl)-1-octanone

Details

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Internal ID 96590882-ebe3-40a5-aec3-d2ebb34f2313
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,6-dihydroxyphenyl)octan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H20O3/c1-2-3-4-5-6-8-11(15)14-12(16)9-7-10-13(14)17/h7,9-10,16-17H,2-6,8H2,1H3
InChI Key SXJJVNCFPXBQMK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H20O3
Molecular Weight 236.31 g/mol
Exact Mass 236.14124450 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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1-(2,6-dihydroxyphenyl)-1-octanone

2D Structure

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2D Structure of 1-(2,6-Dihydroxyphenyl)-1-octanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.8572 85.72%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8627 86.27%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9138 91.38%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8497 84.97%
P-glycoprotein inhibitior - 0.9588 95.88%
P-glycoprotein substrate - 0.8109 81.09%
CYP3A4 substrate - 0.6657 66.57%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8096 80.96%
CYP3A4 inhibition + 0.6994 69.94%
CYP2C9 inhibition - 0.5741 57.41%
CYP2C19 inhibition + 0.5491 54.91%
CYP2D6 inhibition - 0.7650 76.50%
CYP1A2 inhibition + 0.6691 66.91%
CYP2C8 inhibition - 0.8162 81.62%
CYP inhibitory promiscuity - 0.5166 51.66%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8034 80.34%
Carcinogenicity (trinary) Non-required 0.7301 73.01%
Eye corrosion - 0.9190 91.90%
Eye irritation + 0.9589 95.89%
Skin irritation + 0.6889 68.89%
Skin corrosion - 0.6403 64.03%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5362 53.62%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6192 61.92%
skin sensitisation + 0.6807 68.07%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.5840 58.40%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4580 45.80%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding - 0.5065 50.65%
Androgen receptor binding - 0.7265 72.65%
Thyroid receptor binding - 0.5197 51.97%
Glucocorticoid receptor binding - 0.5831 58.31%
Aromatase binding - 0.7811 78.11%
PPAR gamma + 0.9080 90.80%
Honey bee toxicity - 0.9969 99.69%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7359 73.59%
Fish aquatic toxicity + 0.9889 98.89%

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
CHEMBL2581 P07339 Cathepsin D 97.52% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.67% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.47% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 90.47% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.42% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.49% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.10% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 86.35% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.01% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.21% 99.23%

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.
Metanarthecium luteoviride
Pandanus tectorius
Sarcococca saligna

Cross-Links

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PubChem 58709380
NPASS NPC154719