1-(2,4-Dihydroxy-5-methylphenyl)hex-4-en-1-one

Details

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Internal ID 97681eed-fbef-4ee0-8a3f-5b4ddeeef107
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(2,4-dihydroxy-5-methylphenyl)hex-4-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O3/c1-3-4-5-6-11(14)10-7-9(2)12(15)8-13(10)16/h3-4,7-8,15-16H,5-6H2,1-2H3
InChI Key PZLKKLWFFFEJHP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O3
Molecular Weight 220.26 g/mol
Exact Mass 220.109944368 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,4-Dihydroxy-5-methylphenyl)hex-4-en-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 + 0.9859 98.59%
Caco-2 + 0.8773 87.73%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8640 86.40%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior + 0.8236 82.36%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8088 80.88%
BSEP inhibitior - 0.7644 76.44%
P-glycoprotein inhibitior - 0.9772 97.72%
P-glycoprotein substrate - 0.9485 94.85%
CYP3A4 substrate - 0.6490 64.90%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8310 83.10%
CYP3A4 inhibition + 0.7481 74.81%
CYP2C9 inhibition + 0.5532 55.32%
CYP2C19 inhibition + 0.6760 67.60%
CYP2D6 inhibition - 0.7644 76.44%
CYP1A2 inhibition + 0.7421 74.21%
CYP2C8 inhibition - 0.9012 90.12%
CYP inhibitory promiscuity + 0.6632 66.32%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7973 79.73%
Carcinogenicity (trinary) Non-required 0.7408 74.08%
Eye corrosion - 0.8924 89.24%
Eye irritation + 0.8298 82.98%
Skin irritation + 0.6113 61.13%
Skin corrosion - 0.6540 65.40%
Ames mutagenesis - 0.6578 65.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6113 61.13%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.7660 76.60%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6961 69.61%
Acute Oral Toxicity (c) III 0.7471 74.71%
Estrogen receptor binding + 0.5945 59.45%
Androgen receptor binding - 0.8428 84.28%
Thyroid receptor binding - 0.5282 52.82%
Glucocorticoid receptor binding + 0.7366 73.66%
Aromatase binding - 0.4908 49.08%
PPAR gamma + 0.5959 59.59%
Honey bee toxicity - 0.9540 95.40%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9353 93.53%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.48% 91.11%
CHEMBL4208 P20618 Proteasome component C5 90.33% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 89.61% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.98% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.91% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.25% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.66% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.01% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.80% 86.33%

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 72828684
LOTUS LTS0257540
wikiData Q104195595