Isopropylcyclohexane

Details

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Internal ID 4747c2fb-0433-4566-995d-3fdbd678a5db
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name propan-2-ylcyclohexane
SMILES (Canonical) CC(C)C1CCCCC1
SMILES (Isomeric) CC(C)C1CCCCC1
InChI InChI=1S/C9H18/c1-8(2)9-6-4-3-5-7-9/h8-9H,3-7H2,1-2H3
InChI Key GWESVXSMPKAFAS-UHFFFAOYSA-N
Popularity 99 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18
Molecular Weight 126.24 g/mol
Exact Mass 126.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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696-29-7
Hexahydrocumene
propan-2-ylcyclohexane
Normanthane
Cyclohexane, (1-methylethyl)-
Cyclohexane, isopropyl-
(1-Methylethyl)cyclohexane
Isopropyl-cyclohexane
2-Cyclohexylpropane
Iso-propylcyclohexane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopropylcyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8032 80.32%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.6801 68.01%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.9740 97.40%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9604 96.04%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9657 96.57%
CYP3A4 substrate - 0.7414 74.14%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9877 98.77%
CYP2C9 inhibition - 0.9419 94.19%
CYP2C19 inhibition - 0.9607 96.07%
CYP2D6 inhibition - 0.9600 96.00%
CYP1A2 inhibition - 0.8513 85.13%
CYP2C8 inhibition - 0.9824 98.24%
CYP inhibitory promiscuity - 0.9143 91.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5711 57.11%
Eye corrosion + 0.9934 99.34%
Eye irritation + 0.9954 99.54%
Skin irritation + 0.7710 77.10%
Skin corrosion - 0.9719 97.19%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5716 57.16%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5832 58.32%
skin sensitisation + 0.8678 86.78%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8849 88.49%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6367 63.67%
Acute Oral Toxicity (c) IV 0.6539 65.39%
Estrogen receptor binding - 0.9169 91.69%
Androgen receptor binding - 0.8541 85.41%
Thyroid receptor binding - 0.8973 89.73%
Glucocorticoid receptor binding - 0.8764 87.64%
Aromatase binding - 0.8602 86.02%
PPAR gamma - 0.9176 91.76%
Honey bee toxicity - 0.9325 93.25%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9729 97.29%

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
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 91.84% 97.23%
CHEMBL5203 P33316 dUTP pyrophosphatase 90.99% 99.18%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 90.96% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.78% 97.25%
CHEMBL3012 Q13946 Phosphodiesterase 7A 87.71% 99.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.96% 96.09%
CHEMBL1968 P07099 Epoxide hydrolase 1 85.43% 98.57%
CHEMBL2581 P07339 Cathepsin D 84.69% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.90% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.40% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.69% 97.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.07% 95.58%
CHEMBL237 P41145 Kappa opioid receptor 80.14% 98.10%

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.
Artemisia monosperma

Cross-Links

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PubChem 12763
LOTUS LTS0031667
wikiData Q63408583