2-(2-Hydroxypropan-2-yl)benzofuran-5-carbaldehyde

Details

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Internal ID 072c29b2-5107-47bb-938b-b151422a4455
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 2-(2-hydroxypropan-2-yl)-1-benzofuran-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O3/c1-12(2,14)11-6-9-5-8(7-13)3-4-10(9)15-11/h3-7,14H,1-2H3
InChI Key AUICRIQYGBSWOB-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O3
Molecular Weight 204.22 g/mol
Exact Mass 204.078644241 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-(1-hydroxy-1-methyl-ethyl)-benzofuran-5-carbaldehyde
2-(1-hydroxy-1-methylethyl)-1-benzofuran-5-carbaldehyde

2D Structure

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2D Structure of 2-(2-Hydroxypropan-2-yl)benzofuran-5-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.6832 68.32%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6612 66.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8902 89.02%
P-glycoprotein inhibitior - 0.9267 92.67%
P-glycoprotein substrate - 0.9484 94.84%
CYP3A4 substrate - 0.5930 59.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7933 79.33%
CYP3A4 inhibition - 0.8825 88.25%
CYP2C9 inhibition - 0.8141 81.41%
CYP2C19 inhibition - 0.8670 86.70%
CYP2D6 inhibition - 0.9103 91.03%
CYP1A2 inhibition - 0.5423 54.23%
CYP2C8 inhibition - 0.8480 84.80%
CYP inhibitory promiscuity - 0.7876 78.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7836 78.36%
Carcinogenicity (trinary) Non-required 0.4983 49.83%
Eye corrosion - 0.9310 93.10%
Eye irritation + 0.8419 84.19%
Skin irritation - 0.5553 55.53%
Skin corrosion - 0.9432 94.32%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6875 68.75%
Micronuclear - 0.5299 52.99%
Hepatotoxicity + 0.6327 63.27%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6822 68.22%
Acute Oral Toxicity (c) III 0.8300 83.00%
Estrogen receptor binding + 0.7178 71.78%
Androgen receptor binding + 0.6024 60.24%
Thyroid receptor binding - 0.5308 53.08%
Glucocorticoid receptor binding - 0.6442 64.42%
Aromatase binding + 0.6600 66.00%
PPAR gamma - 0.5655 56.55%
Honey bee toxicity - 0.9541 95.41%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8152 81.52%

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
CHEMBL3401 O75469 Pregnane X receptor 94.79% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.77% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.88% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.32% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.30% 93.65%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.99% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.82% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.28% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.29% 99.17%

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 10998110
LOTUS LTS0093924
wikiData Q104918926