Bicyclohexyl

Details

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Internal ID e9074b50-1505-4138-9172-af3a9f41fdd1
Taxonomy Hydrocarbons > Saturated hydrocarbons
IUPAC Name cyclohexylcyclohexane
SMILES (Canonical) C1CCC(CC1)C2CCCCC2
SMILES (Isomeric) C1CCC(CC1)C2CCCCC2
InChI InChI=1S/C12H22/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h11-12H,1-10H2
InChI Key WVIIMZNLDWSIRH-UHFFFAOYSA-N
Popularity 652 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22
Molecular Weight 166.30 g/mol
Exact Mass 166.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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92-51-3
1,1'-Bicyclohexyl
DICYCLOHEXYL
Cyclohexylcyclohexane
Bicyclohexane
Dicyclohexane
Dodecahydrobiphenyl
Cyclohexane, cyclohexyl-
1,1'-Biphenyl, dodecahydro-
NSC 59855
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bicyclohexyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.6938 69.38%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5396 53.96%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.9833 98.33%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8559 85.59%
P-glycoprotein inhibitior - 0.9657 96.57%
P-glycoprotein substrate - 0.9936 99.36%
CYP3A4 substrate - 0.7917 79.17%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.6797 67.97%
CYP3A4 inhibition - 0.9723 97.23%
CYP2C9 inhibition - 0.8530 85.30%
CYP2C19 inhibition - 0.9223 92.23%
CYP2D6 inhibition - 0.9638 96.38%
CYP1A2 inhibition - 0.7314 73.14%
CYP2C8 inhibition - 0.9828 98.28%
CYP inhibitory promiscuity + 0.5691 56.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.4485 44.85%
Eye corrosion + 0.9761 97.61%
Eye irritation + 0.9947 99.47%
Skin irritation + 0.6010 60.10%
Skin corrosion - 0.5449 54.49%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5177 51.77%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6782 67.82%
skin sensitisation - 0.5838 58.38%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5509 55.09%
Acute Oral Toxicity (c) III 0.6993 69.93%
Estrogen receptor binding - 0.8683 86.83%
Androgen receptor binding - 0.7187 71.87%
Thyroid receptor binding - 0.8530 85.30%
Glucocorticoid receptor binding - 0.8525 85.25%
Aromatase binding - 0.8251 82.51%
PPAR gamma - 0.9119 91.19%
Honey bee toxicity - 0.9294 92.94%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9519 95.19%

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
CHEMBL3012 Q13946 Phosphodiesterase 7A 88.44% 99.29%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.61% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.60% 97.25%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.65% 99.18%
CHEMBL1968 P07099 Epoxide hydrolase 1 84.29% 98.57%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.06% 94.78%

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.
Acacia aulacocarpa
Anemonastrum flaccidum
Ardisia neriifolia
Aspidosperma subincanum
Cryptocarya aschersoniana
Eupatorium argentinum
Garcinia madruno
Guatteria ucayalina
Juniperus brevifolia
Lonicera japonica
Peritassa compta
Psiadia dentata
Pulicaria arabica

Cross-Links

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PubChem 7094
NPASS NPC7777
LOTUS LTS0120733
wikiData Q21099094