4-Ethylcyclohexanol

Details

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Internal ID b43815a5-84e0-4dd4-9740-c83e094aae18
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name 4-ethylcyclohexan-1-ol
SMILES (Canonical) CCC1CCC(CC1)O
SMILES (Isomeric) CCC1CCC(CC1)O
InChI InChI=1S/C8H16O/c1-2-7-3-5-8(9)6-4-7/h7-9H,2-6H2,1H3
InChI Key RVTKUJWGFBADIN-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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trans-4-Ethylcyclohexanol
4534-74-1
19781-62-5
CIS-4-ETHYLCYCLOHEXANOL
19781-61-4
4-ethylcyclohexan-1-ol
Cyclohexanol, 4-ethyl-
Cyclohexanol, 4-ethyl-, cis-
Cyclohexanol, 4-ethyl-, trans-
4-Ethylcyclohexanol,c&t
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Ethylcyclohexanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7144 71.44%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5713 57.13%
OATP2B1 inhibitior - 0.8418 84.18%
OATP1B1 inhibitior + 0.9575 95.75%
OATP1B3 inhibitior + 0.9387 93.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9645 96.45%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9263 92.63%
CYP3A4 substrate - 0.6823 68.23%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9552 95.52%
CYP2C9 inhibition - 0.8983 89.83%
CYP2C19 inhibition - 0.9108 91.08%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition - 0.7322 73.22%
CYP2C8 inhibition - 0.9633 96.33%
CYP inhibitory promiscuity - 0.9051 90.51%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.7234 72.34%
Eye corrosion + 0.8517 85.17%
Eye irritation + 0.9786 97.86%
Skin irritation + 0.8375 83.75%
Skin corrosion + 0.5432 54.32%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6240 62.40%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5218 52.18%
skin sensitisation + 0.8676 86.76%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6582 65.82%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.8105 81.05%
Acute Oral Toxicity (c) III 0.8540 85.40%
Estrogen receptor binding - 0.8440 84.40%
Androgen receptor binding - 0.8982 89.82%
Thyroid receptor binding - 0.8454 84.54%
Glucocorticoid receptor binding - 0.8370 83.70%
Aromatase binding - 0.8942 89.42%
PPAR gamma - 0.9235 92.35%
Honey bee toxicity - 0.9396 93.96%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.6433 64.33%

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 95.32% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 95.31% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.95% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.65% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.43% 96.61%
CHEMBL2581 P07339 Cathepsin D 84.06% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 83.76% 90.17%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium
Foeniculum vulgare

Cross-Links

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PubChem 78293
NPASS NPC106958