Cyclobutanol, 1-ethyl-

Details

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Internal ID 0ec12f2d-43ed-436e-a143-e03e6ebdd1f5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1-ethylcyclobutan-1-ol
SMILES (Canonical) CCC1(CCC1)O
SMILES (Isomeric) CCC1(CCC1)O
InChI InChI=1S/C6H12O/c1-2-6(7)4-3-5-6/h7H,2-5H2,1H3
InChI Key ZQXBPTKCIMXYMS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 100.16 g/mol
Exact Mass 100.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.31
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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20434-30-4
RefChem:432621
873-439-6
Cyclobutanol, 1-ethyl-
84256-19-9
1-ethylcyclobutanol
2-ethyl-2-hydroxycyclobutane
SCHEMBL126850
SCHEMBL129902
SCHEMBL129903
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclobutanol, 1-ethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.9107 91.07%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5083 50.83%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9591 95.91%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9514 95.14%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9672 96.72%
CYP3A4 substrate - 0.7192 71.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7321 73.21%
CYP3A4 inhibition - 0.9183 91.83%
CYP2C9 inhibition - 0.7695 76.95%
CYP2C19 inhibition - 0.8227 82.27%
CYP2D6 inhibition - 0.9316 93.16%
CYP1A2 inhibition - 0.6890 68.90%
CYP2C8 inhibition - 0.9906 99.06%
CYP inhibitory promiscuity - 0.9322 93.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6171 61.71%
Eye corrosion - 0.5798 57.98%
Eye irritation + 0.9835 98.35%
Skin irritation + 0.7449 74.49%
Skin corrosion - 0.7126 71.26%
Ames mutagenesis - 0.8470 84.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7419 74.19%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5612 56.12%
skin sensitisation + 0.7895 78.95%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6926 69.26%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6296 62.96%
Acute Oral Toxicity (c) III 0.7914 79.14%
Estrogen receptor binding - 0.9225 92.25%
Androgen receptor binding - 0.8546 85.46%
Thyroid receptor binding - 0.8589 85.89%
Glucocorticoid receptor binding - 0.8976 89.76%
Aromatase binding - 0.9289 92.89%
PPAR gamma - 0.8702 87.02%
Honey bee toxicity - 0.9828 98.28%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.4755 47.55%

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 92.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.46% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.92% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 80.76% 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.
Glycyrrhiza

Cross-Links

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PubChem 145025
NPASS NPC45176