1-(2,6-Dihydroxy-4-methoxyphenyl)-1-hexanone

Details

Top
Internal ID b8a5ed64-3a1b-420e-8bd6-5cf756b1972f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,6-dihydroxy-4-methoxyphenyl)hexan-1-one
SMILES (Canonical) CCCCCC(=O)C1=C(C=C(C=C1O)OC)O
SMILES (Isomeric) CCCCCC(=O)C1=C(C=C(C=C1O)OC)O
InChI InChI=1S/C13H18O4/c1-3-4-5-6-10(14)13-11(15)7-9(17-2)8-12(13)16/h7-8,15-16H,3-6H2,1-2H3
InChI Key XQQUKAGHLDAJGO-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H18O4
Molecular Weight 238.28 g/mol
Exact Mass 238.12050905 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

Top
SCHEMBL13002149
XQQUKAGHLDAJGO-UHFFFAOYSA-N
1-(2,6-dihydroxy-4-methoxyphenyl)-1-hexanone

2D Structure

Top
2D Structure of 1-(2,6-Dihydroxy-4-methoxyphenyl)-1-hexanone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9705 97.05%
Caco-2 + 0.9328 93.28%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8849 88.49%
OATP2B1 inhibitior - 0.8511 85.11%
OATP1B1 inhibitior + 0.8417 84.17%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8181 81.81%
P-glycoprotein inhibitior - 0.8939 89.39%
P-glycoprotein substrate - 0.8716 87.16%
CYP3A4 substrate - 0.6448 64.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7801 78.01%
CYP3A4 inhibition + 0.6521 65.21%
CYP2C9 inhibition - 0.5973 59.73%
CYP2C19 inhibition + 0.7052 70.52%
CYP2D6 inhibition - 0.6471 64.71%
CYP1A2 inhibition + 0.7144 71.44%
CYP2C8 inhibition - 0.6205 62.05%
CYP inhibitory promiscuity + 0.5442 54.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7634 76.34%
Carcinogenicity (trinary) Non-required 0.7590 75.90%
Eye corrosion - 0.9570 95.70%
Eye irritation + 0.9411 94.11%
Skin irritation - 0.6354 63.54%
Skin corrosion - 0.8838 88.38%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4593 45.93%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5885 58.85%
skin sensitisation - 0.5297 52.97%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5612 56.12%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding + 0.8304 83.04%
Androgen receptor binding + 0.6129 61.29%
Thyroid receptor binding - 0.5057 50.57%
Glucocorticoid receptor binding + 0.7095 70.95%
Aromatase binding + 0.5814 58.14%
PPAR gamma + 0.8276 82.76%
Honey bee toxicity - 0.9861 98.61%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6244 62.44%
Fish aquatic toxicity + 0.9732 97.32%

Targets

Top

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 96.94% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.91% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.66% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.47% 92.08%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.76% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.42% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.75% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.27% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.14% 96.95%

Plants that contains it

Top
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.
Ephedra equisetina
Morus alba
Syzygium levinei

Cross-Links

Top
PubChem 11957913
NPASS NPC165761
LOTUS LTS0259694
wikiData Q105339978