5-(1-Hydroxyethyl)-2-propan-2-ylidene-1-benzofuran-3-one

Details

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Internal ID 09423314-0622-44d1-ad42-124ee7c7ad16
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 5-(1-hydroxyethyl)-2-propan-2-ylidene-1-benzofuran-3-one
SMILES (Canonical) CC(C1=CC2=C(C=C1)OC(=C(C)C)C2=O)O
SMILES (Isomeric) CC(C1=CC2=C(C=C1)OC(=C(C)C)C2=O)O
InChI InChI=1S/C13H14O3/c1-7(2)13-12(15)10-6-9(8(3)14)4-5-11(10)16-13/h4-6,8,14H,1-3H3
InChI Key ROWWZMMEUAEBOW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O3
Molecular Weight 218.25 g/mol
Exact Mass 218.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1-Hydroxyethyl)-2-propan-2-ylidene-1-benzofuran-3-one

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 + 0.5966 59.66%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7678 76.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9563 95.63%
OATP1B3 inhibitior + 0.9716 97.16%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8089 80.89%
P-glycoprotein inhibitior - 0.9348 93.48%
P-glycoprotein substrate - 0.9086 90.86%
CYP3A4 substrate - 0.6288 62.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8247 82.47%
CYP3A4 inhibition - 0.8134 81.34%
CYP2C9 inhibition - 0.6180 61.80%
CYP2C19 inhibition + 0.6187 61.87%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition + 0.9518 95.18%
CYP2C8 inhibition - 0.9654 96.54%
CYP inhibitory promiscuity + 0.8416 84.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4466 44.66%
Eye corrosion - 0.9357 93.57%
Eye irritation + 0.7830 78.30%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9280 92.80%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7178 71.78%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5114 51.14%
skin sensitisation + 0.5852 58.52%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.4633 46.33%
Acute Oral Toxicity (c) III 0.6485 64.85%
Estrogen receptor binding + 0.6446 64.46%
Androgen receptor binding + 0.5532 55.32%
Thyroid receptor binding - 0.5387 53.87%
Glucocorticoid receptor binding - 0.6976 69.76%
Aromatase binding - 0.5308 53.08%
PPAR gamma - 0.6964 69.64%
Honey bee toxicity - 0.7720 77.20%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9687 96.87%

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 97.78% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.35% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.99% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.85% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.30% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.14% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.07% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.57% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.70% 90.71%
CHEMBL4208 P20618 Proteasome component C5 80.69% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.52% 86.33%

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.
Verbesina luetzelburgii

Cross-Links

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PubChem 101417056
LOTUS LTS0002076
wikiData Q105242526