4-Isopropylbenzoic acid

Details

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Internal ID 27c577d8-d201-43b5-a62c-4257fa62adec
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-propan-2-ylbenzoic acid
SMILES (Canonical) CC(C)C1=CC=C(C=C1)C(=O)O
SMILES (Isomeric) CC(C)C1=CC=C(C=C1)C(=O)O
InChI InChI=1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)
InChI Key CKMXAIVXVKGGFM-UHFFFAOYSA-N
Popularity 116 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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536-66-3
CUMIC ACID
Cuminic acid
p-Isopropylbenzoic acid
4-(1-Methylethyl)benzoic acid
p-cumic acid
4-(propan-2-yl)benzoic acid
Benzoic acid, 4-(1-methylethyl)-
Benzoic acid, p-isopropyl-
4-Isopropyl benzoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Isopropylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9223 92.23%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.7713 77.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9603 96.03%
P-glycoprotein inhibitior - 0.9751 97.51%
P-glycoprotein substrate - 0.9728 97.28%
CYP3A4 substrate - 0.8335 83.35%
CYP2C9 substrate + 0.6830 68.30%
CYP2D6 substrate - 0.9055 90.55%
CYP3A4 inhibition - 0.9753 97.53%
CYP2C9 inhibition - 0.9397 93.97%
CYP2C19 inhibition - 0.9922 99.22%
CYP2D6 inhibition - 0.9535 95.35%
CYP1A2 inhibition - 0.9018 90.18%
CYP2C8 inhibition - 0.9778 97.78%
CYP inhibitory promiscuity - 0.9830 98.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5198 51.98%
Carcinogenicity (trinary) Non-required 0.8052 80.52%
Eye corrosion + 0.8354 83.54%
Eye irritation + 0.9878 98.78%
Skin irritation + 0.8962 89.62%
Skin corrosion + 0.7184 71.84%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8837 88.37%
Micronuclear - 0.8641 86.41%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.5068 50.68%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5430 54.30%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4717 47.17%
Acute Oral Toxicity (c) II 0.5057 50.57%
Estrogen receptor binding - 0.9257 92.57%
Androgen receptor binding - 0.6844 68.44%
Thyroid receptor binding - 0.8327 83.27%
Glucocorticoid receptor binding - 0.9281 92.81%
Aromatase binding - 0.5735 57.35%
PPAR gamma - 0.8294 82.94%
Honey bee toxicity - 0.9784 97.84%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8727 87.27%
Fish aquatic toxicity + 0.8968 89.68%

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
CHEMBL4208 P20618 Proteasome component C5 90.38% 90.00%
CHEMBL2581 P07339 Cathepsin D 87.53% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.28% 87.67%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.40% 100.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.90% 81.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.16% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.02% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.28% 86.33%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 82.98% 98.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.81% 90.24%
CHEMBL221 P23219 Cyclooxygenase-1 80.14% 90.17%

Cross-Links

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PubChem 10820
NPASS NPC304873
LOTUS LTS0264031
wikiData Q1143809