1-Cyclohexene-1-ethanol, 2,6,6-trimethyl-

Details

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Internal ID 82b143e1-abe6-4cd1-bd5e-93c918b61cd8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 2-(2,6,6-trimethylcyclohexen-1-yl)ethanol
SMILES (Canonical) CC1=C(C(CCC1)(C)C)CCO
SMILES (Isomeric) CC1=C(C(CCC1)(C)C)CCO
InChI InChI=1S/C11H20O/c1-9-5-4-7-11(2,3)10(9)6-8-12/h12H,4-8H2,1-3H3
InChI Key JGJFZOVBBGQGOM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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472-65-1
SCHEMBL4304302
DTXSID00343848
JGJFZOVBBGQGOM-UHFFFAOYSA-N
2,6,6-trimethyl,1-cyclohexene-1-ethanol
2-(2,6,6-Trimethyl-1-cyclohexen-1-yl)ethanol #

2D Structure

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2D Structure of 1-Cyclohexene-1-ethanol, 2,6,6-trimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9399 93.99%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.7726 77.26%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.8197 81.97%
OATP1B3 inhibitior - 0.2159 21.59%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8739 87.39%
P-glycoprotein inhibitior - 0.9724 97.24%
P-glycoprotein substrate - 0.9534 95.34%
CYP3A4 substrate - 0.5759 57.59%
CYP2C9 substrate - 0.8218 82.18%
CYP2D6 substrate - 0.7703 77.03%
CYP3A4 inhibition - 0.7605 76.05%
CYP2C9 inhibition - 0.9177 91.77%
CYP2C19 inhibition - 0.9313 93.13%
CYP2D6 inhibition - 0.9304 93.04%
CYP1A2 inhibition - 0.8951 89.51%
CYP2C8 inhibition - 0.9150 91.50%
CYP inhibitory promiscuity - 0.8262 82.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.6368 63.68%
Eye corrosion - 0.9168 91.68%
Eye irritation + 0.9879 98.79%
Skin irritation + 0.5608 56.08%
Skin corrosion - 0.9767 97.67%
Ames mutagenesis - 0.7916 79.16%
Human Ether-a-go-go-Related Gene inhibition - 0.6438 64.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6180 61.80%
skin sensitisation + 0.8496 84.96%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5666 56.66%
Acute Oral Toxicity (c) III 0.8996 89.96%
Estrogen receptor binding - 0.9773 97.73%
Androgen receptor binding - 0.7082 70.82%
Thyroid receptor binding - 0.8478 84.78%
Glucocorticoid receptor binding - 0.8887 88.87%
Aromatase binding - 0.8864 88.64%
PPAR gamma - 0.8815 88.15%
Honey bee toxicity - 0.9688 96.88%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9524 95.24%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.34% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.08% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.73% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.11% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 81.39% 94.75%
CHEMBL2581 P07339 Cathepsin D 81.36% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.19% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.11% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.86% 95.56%

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.
Carthamus arborescens

Cross-Links

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PubChem 592706
NPASS NPC229197