3-butyl-5,6,7,7a-tetrahydro-3H-2-benzofuran-1-one

Details

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Internal ID 5db5e712-6666-4f98-8fed-3ea784829ac1
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name 3-butyl-5,6,7,7a-tetrahydro-3H-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O2/c1-2-3-8-11-9-6-4-5-7-10(9)12(13)14-11/h6,10-11H,2-5,7-8H2,1H3
InChI Key MJPMPMZXJIZPRE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O2
Molecular Weight 194.27 g/mol
Exact Mass 194.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-butyl-5,6,7,7a-tetrahydro-3H-2-benzofuran-1-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 + 0.7481 74.81%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.6904 69.04%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8510 85.10%
P-glycoprotein inhibitior - 0.9438 94.38%
P-glycoprotein substrate - 0.7938 79.38%
CYP3A4 substrate - 0.5499 54.99%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8426 84.26%
CYP3A4 inhibition - 0.7461 74.61%
CYP2C9 inhibition - 0.8855 88.55%
CYP2C19 inhibition - 0.5220 52.20%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition + 0.5570 55.70%
CYP2C8 inhibition - 0.8932 89.32%
CYP inhibitory promiscuity - 0.6275 62.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5262 52.62%
Eye corrosion - 0.8133 81.33%
Eye irritation + 0.7937 79.37%
Skin irritation - 0.5192 51.92%
Skin corrosion - 0.9367 93.67%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7651 76.51%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.7266 72.66%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6101 61.01%
Acute Oral Toxicity (c) III 0.7513 75.13%
Estrogen receptor binding - 0.7297 72.97%
Androgen receptor binding - 0.5982 59.82%
Thyroid receptor binding - 0.6564 65.64%
Glucocorticoid receptor binding - 0.5805 58.05%
Aromatase binding - 0.8400 84.00%
PPAR gamma - 0.6943 69.43%
Honey bee toxicity - 0.9838 98.38%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9421 94.21%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.87% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 95.78% 89.63%
CHEMBL2581 P07339 Cathepsin D 95.24% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.06% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.04% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.66% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.20% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 84.65% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.50% 100.00%
CHEMBL1978 P11511 Cytochrome P450 19A1 82.18% 91.76%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.80% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 80.57% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.16% 92.62%

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.
Angelica taiwaniana
Conioselinum anthriscoides

Cross-Links

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PubChem 5315981
NPASS NPC167488