5,5'-Dibutoxy-2,2'-bifuran

Details

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Internal ID 0ff59464-a603-4195-8446-453fd14cccef
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name 2-butoxy-5-(5-butoxyfuran-2-yl)furan
SMILES (Canonical) CCCCOC1=CC=C(O1)C2=CC=C(O2)OCCCC
SMILES (Isomeric) CCCCOC1=CC=C(O1)C2=CC=C(O2)OCCCC
InChI InChI=1S/C16H22O4/c1-3-5-11-17-15-9-7-13(19-15)14-8-10-16(20-14)18-12-6-4-2/h7-10H,3-6,11-12H2,1-2H3
InChI Key BQFASOONPNRMGH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H22O4
Molecular Weight 278.34 g/mol
Exact Mass 278.15180918 g/mol
Topological Polar Surface Area (TPSA) 44.70 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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CHEBI:65763
RefChem:101012
2-butoxy-5-(5-butoxyfuran-2-yl)furan
1035897-79-0
Q27134249

2D Structure

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2D Structure of 5,5'-Dibutoxy-2,2'-bifuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.8752 87.52%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7277 72.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.8945 89.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6165 61.65%
P-glycoprotein inhibitior - 0.4881 48.81%
P-glycoprotein substrate - 0.8805 88.05%
CYP3A4 substrate - 0.6657 66.57%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate + 0.3871 38.71%
CYP3A4 inhibition - 0.7946 79.46%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition - 0.6010 60.10%
CYP2D6 inhibition - 0.8646 86.46%
CYP1A2 inhibition + 0.6178 61.78%
CYP2C8 inhibition - 0.6283 62.83%
CYP inhibitory promiscuity + 0.5627 56.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.4233 42.33%
Eye corrosion - 0.9688 96.88%
Eye irritation + 0.6649 66.49%
Skin irritation - 0.8039 80.39%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8485 84.85%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8349 83.49%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.4675 46.75%
Acute Oral Toxicity (c) III 0.8098 80.98%
Estrogen receptor binding + 0.5839 58.39%
Androgen receptor binding + 0.7201 72.01%
Thyroid receptor binding + 0.6810 68.10%
Glucocorticoid receptor binding - 0.5060 50.60%
Aromatase binding + 0.7480 74.80%
PPAR gamma + 0.5787 57.87%
Honey bee toxicity - 0.9845 98.45%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8959 89.59%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 91.38% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.50% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.48% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 88.72% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.12% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.92% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.42% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.09% 94.00%

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.
Cyathula officinalis

Cross-Links

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PubChem 70697742
LOTUS LTS0223453
wikiData Q27134249