1-Ethyl-1-methylcyclohexane

Details

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Internal ID 95d4a0e7-7e7e-4271-ac35-ef780915f73d
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name 1-ethyl-1-methylcyclohexane
SMILES (Canonical) CCC1(CCCCC1)C
SMILES (Isomeric) CCC1(CCCCC1)C
InChI InChI=1S/C9H18/c1-3-9(2)7-5-4-6-8-9/h3-8H2,1-2H3
InChI Key YPJRYQGOKHKNKZ-UHFFFAOYSA-N
Popularity 16 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 4.40
Atomic LogP (AlogP) 3.37
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4926-90-3
1-Methyl-1-ethylcyclohexane
Cyclohexane, 1-ethyl-1-methyl-
Cyclohexane, ethylmethyl-
methylethylcyclohexane
1-ethyl-1-methyl-cyclohexane
NSC 73962
NSC-73962
30677-34-0
NSC73962
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-Ethyl-1-methylcyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.9637 96.37%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.6638 66.38%
OATP2B1 inhibitior - 0.8417 84.17%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9448 94.48%
P-glycoprotein inhibitior - 0.9879 98.79%
P-glycoprotein substrate - 0.9657 96.57%
CYP3A4 substrate - 0.6940 69.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9304 93.04%
CYP2C9 inhibition - 0.9010 90.10%
CYP2C19 inhibition - 0.9451 94.51%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition - 0.7823 78.23%
CYP2C8 inhibition - 0.9722 97.22%
CYP inhibitory promiscuity - 0.7953 79.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5679 56.79%
Eye corrosion + 0.9398 93.98%
Eye irritation + 0.9888 98.88%
Skin irritation - 0.5727 57.27%
Skin corrosion - 0.9945 99.45%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6587 65.87%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5452 54.52%
skin sensitisation + 0.9445 94.45%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7523 75.23%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6107 61.07%
Acute Oral Toxicity (c) III 0.5767 57.67%
Estrogen receptor binding - 0.9353 93.53%
Androgen receptor binding - 0.8183 81.83%
Thyroid receptor binding - 0.8651 86.51%
Glucocorticoid receptor binding - 0.9172 91.72%
Aromatase binding - 0.8782 87.82%
PPAR gamma - 0.9139 91.39%
Honey bee toxicity - 0.9670 96.70%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9900 99.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.83% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.65% 97.25%
CHEMBL233 P35372 Mu opioid receptor 88.45% 97.93%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.41% 96.38%
CHEMBL230 P35354 Cyclooxygenase-2 87.18% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 87.03% 90.17%
CHEMBL2581 P07339 Cathepsin D 86.79% 98.95%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.01% 99.29%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.78% 95.17%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.61% 96.61%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 35411
NPASS NPC267056