Methylcyclohexane

Details

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Internal ID 3d2ed78e-821f-47b5-b933-ccb0b12ed8ed
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name methylcyclohexane
SMILES (Canonical) CC1CCCCC1
SMILES (Isomeric) CC1CCCCC1
InChI InChI=1S/C7H14/c1-7-5-3-2-4-6-7/h7H,2-6H2,1H3
InChI Key UAEPNZWRGJTJPN-UHFFFAOYSA-N
Popularity 3,292 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14
Molecular Weight 98.19 g/mol
Exact Mass 98.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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108-87-2
Cyclohexane, methyl-
Hexahydrotoluene
Cyclohexylmethane
Toluene hexahydride
Hexahydroxytoluene
Sextone B
Toluene, hexahydro-
methyl cyclohexane
Metylocykloheksan
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methylcyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8303 83.03%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.6682 66.82%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.9760 97.60%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9781 97.81%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9833 98.33%
CYP3A4 substrate - 0.7448 74.48%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7481 74.81%
CYP3A4 inhibition - 0.9841 98.41%
CYP2C9 inhibition - 0.9592 95.92%
CYP2C19 inhibition - 0.9661 96.61%
CYP2D6 inhibition - 0.9640 96.40%
CYP1A2 inhibition - 0.8122 81.22%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.9018 90.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5191 51.91%
Eye corrosion + 0.9963 99.63%
Eye irritation + 0.9969 99.69%
Skin irritation + 0.8954 89.54%
Skin corrosion - 0.8964 89.64%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6711 67.11%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6782 67.82%
skin sensitisation + 0.8749 87.49%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4881 48.81%
Acute Oral Toxicity (c) III 0.8627 86.27%
Estrogen receptor binding - 0.9385 93.85%
Androgen receptor binding - 0.9173 91.73%
Thyroid receptor binding - 0.8804 88.04%
Glucocorticoid receptor binding - 0.9062 90.62%
Aromatase binding - 0.8521 85.21%
PPAR gamma - 0.9389 93.89%
Honey bee toxicity - 0.9609 96.09%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9819 98.19%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.85% 97.25%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 88.49% 95.27%
CHEMBL3012 Q13946 Phosphodiesterase 7A 87.66% 99.29%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.19% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.80% 96.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.66% 99.18%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.69% 86.00%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.63% 90.71%
CHEMBL1968 P07099 Epoxide hydrolase 1 81.50% 98.57%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.90% 95.50%

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.
Carica papaya
Caryocar coriaceum
Glycyrrhiza
Opuntia ficus-indica

Cross-Links

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PubChem 7962
NPASS NPC96657
LOTUS LTS0171505
wikiData Q419330