Ruscodibenzofuran

Details

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Internal ID bc3a5f04-3735-455b-bb90-bdd3b1ced8fc
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name 1-(3-hydroxy-6,9-dimethyldibenzofuran-2-yl)ethanone
SMILES (Canonical) CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C
SMILES (Isomeric) CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C
InChI InChI=1S/C16H14O3/c1-8-4-5-9(2)16-15(8)12-6-11(10(3)17)13(18)7-14(12)19-16/h4-7,18H,1-3H3
InChI Key WSSVACUQZZCDCW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O3
Molecular Weight 254.28 g/mol
Exact Mass 254.094294304 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.11
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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65432-28-2
NSC285245
DTXSID20314550
NSC-285245
Ethanone,9-dimethyl-2-dibenzofuranyl)-
RUSCODIBENZOFURAN FROM RUSCUS ACULETUS (LILIACEAE)
Ethanone, 1-(3-hydroxy-6,9-dimethyl-2-dibenzofuranyl)-

2D Structure

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2D Structure of Ruscodibenzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7911 79.11%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7588 75.88%
OATP2B1 inhibitior - 0.7202 72.02%
OATP1B1 inhibitior + 0.9551 95.51%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6881 68.81%
P-glycoprotein inhibitior - 0.7579 75.79%
P-glycoprotein substrate - 0.8495 84.95%
CYP3A4 substrate - 0.5722 57.22%
CYP2C9 substrate - 0.6016 60.16%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition - 0.8665 86.65%
CYP2C9 inhibition - 0.6438 64.38%
CYP2C19 inhibition + 0.5752 57.52%
CYP2D6 inhibition - 0.9550 95.50%
CYP1A2 inhibition + 0.9898 98.98%
CYP2C8 inhibition - 0.6246 62.46%
CYP inhibitory promiscuity + 0.6523 65.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4079 40.79%
Eye corrosion - 0.9845 98.45%
Eye irritation + 0.5649 56.49%
Skin irritation - 0.5638 56.38%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5310 53.10%
Micronuclear + 0.7559 75.59%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7536 75.36%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8106 81.06%
Acute Oral Toxicity (c) III 0.5522 55.22%
Estrogen receptor binding + 0.8249 82.49%
Androgen receptor binding + 0.6568 65.68%
Thyroid receptor binding - 0.5287 52.87%
Glucocorticoid receptor binding + 0.7499 74.99%
Aromatase binding + 0.7301 73.01%
PPAR gamma + 0.8066 80.66%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9709 97.09%

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 98.79% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 92.60% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.57% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.42% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.54% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.42% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.82% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.27% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.77% 94.42%
CHEMBL2535 P11166 Glucose transporter 81.94% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.06% 94.45%

Cross-Links

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PubChem 323624
NPASS NPC36565