Bicycloheptane

Details

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Internal ID 1a07a9b1-ff29-4f16-bfcd-d4ed466a84af
Taxonomy Hydrocarbons > Saturated hydrocarbons
IUPAC Name cycloheptylcycloheptane
SMILES (Canonical) C1CCCC(CC1)C2CCCCCC2
SMILES (Isomeric) C1CCCC(CC1)C2CCCCCC2
InChI InChI=1S/C14H26/c1-2-6-10-13(9-5-1)14-11-7-3-4-8-12-14/h13-14H,1-12H2
InChI Key ARUKYTASOALXFG-UHFFFAOYSA-N
Popularity 102 references in papers

Physical and Chemical Properties

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Molecular Formula C14H26
Molecular Weight 194.36 g/mol
Exact Mass 194.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 4.93
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Cycloheptylcycloheptane
Bicycloheptyl
1,1'-Bicycloheptyl
12622-04-7
23183-11-1
1,1'-Bi(cycloheptane)
ARUKYTASOALXFG-UHFFFAOYSA-
DTXSID10177757
AKOS006277186
LS-43629
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bicycloheptane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 + 0.6743 67.43%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4720 47.20%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.9833 98.33%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8091 80.91%
P-glycoprotein inhibitior - 0.9609 96.09%
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 - 0.9878 98.78%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.9573 95.73%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition - 0.8256 82.56%
CYP2C8 inhibition - 0.9828 98.28%
CYP inhibitory promiscuity - 0.7975 79.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.4815 48.15%
Eye corrosion + 0.9849 98.49%
Eye irritation + 0.9945 99.45%
Skin irritation + 0.7872 78.72%
Skin corrosion - 0.8372 83.72%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6782 67.82%
skin sensitisation - 0.5489 54.89%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9738 97.38%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5509 55.09%
Acute Oral Toxicity (c) III 0.3787 37.87%
Estrogen receptor binding - 0.8487 84.87%
Androgen receptor binding - 0.7187 71.87%
Thyroid receptor binding - 0.8365 83.65%
Glucocorticoid receptor binding - 0.8445 84.45%
Aromatase binding - 0.8324 83.24%
PPAR gamma - 0.8936 89.36%
Honey bee toxicity - 0.9294 92.94%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.8447 84.47%

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.
Curcuma zedoaria

Cross-Links

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PubChem 141010
NPASS NPC270406