2,6-Dimethylcyclohexanol

Details

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Internal ID 7bc3be39-6f4c-49f2-ba30-21d7f9cf12fd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclohexanols
IUPAC Name 2,6-dimethylcyclohexan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16O/c1-6-4-3-5-7(2)8(6)9/h6-9H,3-5H2,1-2H3
InChI Key MOISVRZIQDQVPF-UHFFFAOYSA-N
Popularity 20 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 2.10
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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5337-72-4
2,6-Dimethylcyclohexan-1-ol
DTXSID70871123
RefChem:83313
DTXCID70818795
226-264-9
Cyclohexanol, 2,6-dimethyl-
MFCD00001502
alpha,alpha,alpha-2,6-Dimethylcyclohexanol
2,6-Dimethylcyclohexanol,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 2,6-Dimethylcyclohexanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.6988 69.88%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5798 57.98%
OATP2B1 inhibitior - 0.8390 83.90%
OATP1B1 inhibitior + 0.9715 97.15%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9621 96.21%
P-glycoprotein inhibitior - 0.9781 97.81%
P-glycoprotein substrate - 0.9851 98.51%
CYP3A4 substrate - 0.6907 69.07%
CYP2C9 substrate - 0.7877 78.77%
CYP2D6 substrate - 0.6998 69.98%
CYP3A4 inhibition - 0.9565 95.65%
CYP2C9 inhibition - 0.9004 90.04%
CYP2C19 inhibition - 0.9379 93.79%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.7541 75.41%
CYP2C8 inhibition - 0.9922 99.22%
CYP inhibitory promiscuity - 0.9367 93.67%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6760 67.60%
Eye corrosion + 0.8943 89.43%
Eye irritation + 0.9753 97.53%
Skin irritation + 0.7732 77.32%
Skin corrosion + 0.8468 84.68%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6765 67.65%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5282 52.82%
skin sensitisation + 0.8622 86.22%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.5949 59.49%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6449 64.49%
Acute Oral Toxicity (c) III 0.8456 84.56%
Estrogen receptor binding - 0.9341 93.41%
Androgen receptor binding - 0.7250 72.50%
Thyroid receptor binding - 0.8628 86.28%
Glucocorticoid receptor binding - 0.8647 86.47%
Aromatase binding - 0.8911 89.11%
PPAR gamma - 0.8877 88.77%
Honey bee toxicity - 0.9599 95.99%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8955 89.55%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.15% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.62% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.71% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.52% 97.25%
CHEMBL2581 P07339 Cathepsin D 82.95% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.26% 86.00%

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.
Capsella bursa-pastoris

Cross-Links

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PubChem 21428
NPASS NPC143880