1,3-Diisopropylbenzene

Details

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Internal ID 5559c773-7685-49f3-abf9-352a21905d76
Taxonomy Benzenoids > Benzene and substituted derivatives > Cumenes
IUPAC Name 1,3-di(propan-2-yl)benzene
SMILES (Canonical) CC(C)C1=CC(=CC=C1)C(C)C
SMILES (Isomeric) CC(C)C1=CC(=CC=C1)C(C)C
InChI InChI=1S/C12H18/c1-9(2)11-6-5-7-12(8-11)10(3)4/h5-10H,1-4H3
InChI Key UNEATYXSUBPPKP-UHFFFAOYSA-N
Popularity 229 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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99-62-7
m-Diisopropylbenzene
Benzene, 1,3-bis(1-methylethyl)-
Benzene, m-diisopropyl-
1,3-Bis(1-methylethyl)benzene
m-Diisopropylbenzol
HSDB 5325
EINECS 202-773-1
BRN 1905828
DTXSID8026640
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3-Diisopropylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.8793 87.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.5463 54.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9290 92.90%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.9541 95.41%
CYP3A4 substrate - 0.8044 80.44%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.7071 70.71%
CYP3A4 inhibition - 0.9512 95.12%
CYP2C9 inhibition - 0.9394 93.94%
CYP2C19 inhibition - 0.9687 96.87%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.7996 79.96%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.8217 82.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5036 50.36%
Carcinogenicity (trinary) Warning 0.5584 55.84%
Eye corrosion + 0.9906 99.06%
Eye irritation + 0.9607 96.07%
Skin irritation + 0.8874 88.74%
Skin corrosion - 0.9468 94.68%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4277 42.77%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.9163 91.63%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7255 72.55%
Nephrotoxicity - 0.6594 65.94%
Acute Oral Toxicity (c) III 0.8434 84.34%
Estrogen receptor binding - 0.8909 89.09%
Androgen receptor binding - 0.8684 86.84%
Thyroid receptor binding - 0.6871 68.71%
Glucocorticoid receptor binding - 0.8840 88.40%
Aromatase binding - 0.8227 82.27%
PPAR gamma - 0.8170 81.70%
Honey bee toxicity - 0.9320 93.20%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9269 92.69%

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 94.35% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 89.45% 97.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.77% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.37% 94.73%
CHEMBL2535 P11166 Glucose transporter 85.23% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.66% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.38% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 82.22% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.04% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.51% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.46% 100.00%

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 7450
NPASS NPC32312