5,5'-Diisobutoxy-2,2'-bifuran

Details

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Internal ID cfa46658-fbc0-42dd-957f-242e7bdd10af
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name 2-(2-methylpropoxy)-5-[5-(2-methylpropoxy)furan-2-yl]furan
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H22O4/c1-11(2)9-17-15-7-5-13(19-15)14-6-8-16(20-14)18-10-12(3)4/h5-8,11-12H,9-10H2,1-4H3
InChI Key ZNKHZNREKSGKIK-UHFFFAOYSA-N
Popularity 4 references 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 5.00
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,5'-Diisobutoxy-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 + 0.9714 97.14%
Caco-2 + 0.7912 79.12%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7640 76.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9680 96.80%
OATP1B3 inhibitior + 0.8981 89.81%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5696 56.96%
P-glycoprotein inhibitior - 0.5288 52.88%
P-glycoprotein substrate - 0.9091 90.91%
CYP3A4 substrate - 0.7164 71.64%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.6902 69.02%
CYP3A4 inhibition - 0.7805 78.05%
CYP2C9 inhibition - 0.5928 59.28%
CYP2C19 inhibition - 0.5807 58.07%
CYP2D6 inhibition - 0.7879 78.79%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9523 95.23%
CYP inhibitory promiscuity + 0.6075 60.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8131 81.31%
Carcinogenicity (trinary) Warning 0.3506 35.06%
Eye corrosion - 0.9657 96.57%
Eye irritation - 0.8061 80.61%
Skin irritation - 0.8593 85.93%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6464 64.64%
Micronuclear - 0.6545 65.45%
Hepatotoxicity + 0.6704 67.04%
skin sensitisation - 0.6472 64.72%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6523 65.23%
Acute Oral Toxicity (c) III 0.7559 75.59%
Estrogen receptor binding + 0.6997 69.97%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5650 56.50%
Glucocorticoid receptor binding - 0.6347 63.47%
Aromatase binding + 0.8310 83.10%
PPAR gamma - 0.5322 53.22%
Honey bee toxicity - 0.9250 92.50%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9326 93.26%

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
CHEMBL2581 P07339 Cathepsin D 90.28% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.82% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.59% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.00% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.36% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.44% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.36% 94.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.23% 83.57%

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 129881877
LOTUS LTS0151953
wikiData Q105380105