1,4-Bis(2-hydroxy-5-methylphenyl)butane-1,4-dione

Details

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Internal ID fec678f4-ed61-4c17-9d65-7e88c164ce34
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1,4-bis(2-hydroxy-5-methylphenyl)butane-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H18O4/c1-11-3-5-15(19)13(9-11)17(21)7-8-18(22)14-10-12(2)4-6-16(14)20/h3-6,9-10,19-20H,7-8H2,1-2H3
InChI Key IXLWDOWATMXBRE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O4
Molecular Weight 298.30 g/mol
Exact Mass 298.12050905 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.56
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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1,4-bis(2-hydroxy-5-methylphenyl)-1,4-butanedione
AKOS024327387

2D Structure

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2D Structure of 1,4-Bis(2-hydroxy-5-methylphenyl)butane-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9441 94.41%
Caco-2 + 0.7366 73.66%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.9574 95.74%
OATP2B1 inhibitior - 0.5740 57.40%
OATP1B1 inhibitior + 0.9353 93.53%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5691 56.91%
P-glycoprotein inhibitior - 0.8546 85.46%
P-glycoprotein substrate - 0.9865 98.65%
CYP3A4 substrate - 0.7422 74.22%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8096 80.96%
CYP3A4 inhibition - 0.5383 53.83%
CYP2C9 inhibition + 0.8257 82.57%
CYP2C19 inhibition + 0.7915 79.15%
CYP2D6 inhibition - 0.6183 61.83%
CYP1A2 inhibition + 0.8345 83.45%
CYP2C8 inhibition - 0.9269 92.69%
CYP inhibitory promiscuity - 0.5875 58.75%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7099 70.99%
Carcinogenicity (trinary) Non-required 0.7281 72.81%
Eye corrosion - 0.9849 98.49%
Eye irritation + 0.7657 76.57%
Skin irritation - 0.7657 76.57%
Skin corrosion - 0.8259 82.59%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6566 65.66%
Micronuclear - 0.5782 57.82%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.8816 88.16%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6145 61.45%
Acute Oral Toxicity (c) III 0.7353 73.53%
Estrogen receptor binding + 0.8135 81.35%
Androgen receptor binding + 0.5352 53.52%
Thyroid receptor binding - 0.5699 56.99%
Glucocorticoid receptor binding + 0.5660 56.60%
Aromatase binding - 0.5417 54.17%
PPAR gamma + 0.6549 65.49%
Honey bee toxicity - 0.9851 98.51%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9666 96.66%

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 91.51% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.99% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.55% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.51% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.80% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.80% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.74% 99.17%

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.
Berberis coriaria

Cross-Links

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PubChem 4139276
LOTUS LTS0076910
wikiData Q105122252