Isobutyrophenone

Details

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Internal ID da8ac96b-1aaf-44a8-be4c-d84264b16a78
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 2-methyl-1-phenylpropan-1-one
SMILES (Canonical) CC(C)C(=O)C1=CC=CC=C1
SMILES (Isomeric) CC(C)C(=O)C1=CC=CC=C1
InChI InChI=1S/C10H12O/c1-8(2)10(11)9-6-4-3-5-7-9/h3-8H,1-2H3
InChI Key BSMGLVDZZMBWQB-UHFFFAOYSA-N
Popularity 211 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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611-70-1
2-methyl-1-phenylpropan-1-one
Isopropyl phenyl ketone
1-Propanone, 2-methyl-1-phenyl-
Phenyl isopropyl ketone
2-Methylpropiophenone
Isopropyl phenyl keton
alpha-Methylpropiophenone
2-Methyl-1-phenyl-1-propanone
.alpha.-Methylpropiophenone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isobutyrophenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.9301 93.01%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.7185 71.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9681 96.81%
OATP1B3 inhibitior + 0.9718 97.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9202 92.02%
P-glycoprotein inhibitior - 0.9892 98.92%
P-glycoprotein substrate - 0.9842 98.42%
CYP3A4 substrate - 0.8193 81.93%
CYP2C9 substrate - 0.8216 82.16%
CYP2D6 substrate - 0.7909 79.09%
CYP3A4 inhibition - 0.9669 96.69%
CYP2C9 inhibition - 0.9360 93.60%
CYP2C19 inhibition - 0.9317 93.17%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.5224 52.24%
CYP2C8 inhibition - 0.9854 98.54%
CYP inhibitory promiscuity - 0.8282 82.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5336 53.36%
Carcinogenicity (trinary) Non-required 0.7203 72.03%
Eye corrosion + 0.9823 98.23%
Eye irritation + 0.9614 96.14%
Skin irritation + 0.8566 85.66%
Skin corrosion - 0.9639 96.39%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8154 81.54%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation + 0.9110 91.10%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.4627 46.27%
Acute Oral Toxicity (c) III 0.8398 83.98%
Estrogen receptor binding - 0.9496 94.96%
Androgen receptor binding - 0.8180 81.80%
Thyroid receptor binding - 0.8963 89.63%
Glucocorticoid receptor binding - 0.9255 92.55%
Aromatase binding - 0.8892 88.92%
PPAR gamma - 0.8985 89.85%
Honey bee toxicity - 0.9875 98.75%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7349 73.49%

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 91.86% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.58% 95.56%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 90.49% 98.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 90.49% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.14% 90.17%
CHEMBL2535 P11166 Glucose transporter 83.65% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.95% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.38% 94.73%

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.
Conioselinum anthriscoides
Ligusticum officinale
Ligusticum striatum

Cross-Links

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PubChem 69144
NPASS NPC190567