Cyclopentane, hexyl-

Details

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Internal ID f8dcea67-7b6b-4c24-a18c-0094928374d4
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name hexylcyclopentane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H22/c1-2-3-4-5-8-11-9-6-7-10-11/h11H,2-10H2,1H3
InChI Key LKHGKBBAJAFMSQ-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22
Molecular Weight 154.29 g/mol
Exact Mass 154.172150702 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 5

Synonyms

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Cyclopentane, hexyl-
4457-00-5
Hexylcyclopentane #
(1-Methylpentyl)cyclopentane
DTXSID90196224
LKHGKBBAJAFMSQ-UHFFFAOYSA-N
J-500246

2D Structure

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2D Structure of Cyclopentane, hexyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.8666 86.66%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.6558 65.58%
OATP2B1 inhibitior - 0.8467 84.67%
OATP1B1 inhibitior + 0.9525 95.25%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8470 84.70%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.8296 82.96%
CYP3A4 substrate - 0.6412 64.12%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9834 98.34%
CYP2C9 inhibition - 0.9031 90.31%
CYP2C19 inhibition - 0.9105 91.05%
CYP2D6 inhibition - 0.9351 93.51%
CYP1A2 inhibition - 0.6037 60.37%
CYP2C8 inhibition - 0.8280 82.80%
CYP inhibitory promiscuity - 0.7462 74.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5345 53.45%
Eye corrosion + 0.9885 98.85%
Eye irritation + 0.9842 98.42%
Skin irritation + 0.8313 83.13%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.9491 94.91%
Human Ether-a-go-go-Related Gene inhibition - 0.5873 58.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5333 53.33%
skin sensitisation + 0.9137 91.37%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7112 71.12%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.6292 62.92%
Acute Oral Toxicity (c) III 0.6460 64.60%
Estrogen receptor binding - 0.9024 90.24%
Androgen receptor binding - 0.8637 86.37%
Thyroid receptor binding - 0.7541 75.41%
Glucocorticoid receptor binding - 0.8532 85.32%
Aromatase binding - 0.8857 88.57%
PPAR gamma - 0.8822 88.22%
Honey bee toxicity - 0.9909 99.09%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.7990 79.90%
Fish aquatic toxicity + 0.9828 98.28%

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
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 98.38% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.09% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 96.09% 89.63%
CHEMBL240 Q12809 HERG 94.70% 89.76%
CHEMBL2581 P07339 Cathepsin D 94.02% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.89% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 91.68% 91.81%
CHEMBL1968 P07099 Epoxide hydrolase 1 91.63% 98.57%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.89% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 90.70% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.07% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.26% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.94% 93.56%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.78% 92.86%
CHEMBL1914 P06276 Butyrylcholinesterase 87.17% 95.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.10% 95.17%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.93% 99.18%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.21% 92.08%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 84.92% 95.27%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.08% 97.29%
CHEMBL5255 O00206 Toll-like receptor 4 83.71% 92.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.61% 92.62%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.60% 85.94%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.72% 98.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.63% 93.04%
CHEMBL237 P41145 Kappa opioid receptor 82.45% 98.10%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.43% 96.00%

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.
Caryocar coriaceum

Cross-Links

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PubChem 138257
LOTUS LTS0146635
wikiData Q83069296