3-Ethyl-2,5-dimethylhexane-2,5-diol

Details

Top
Internal ID 9cdd9b1d-ab56-4878-9b40-d0bcd9bf7fe9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 3-ethyl-2,5-dimethylhexane-2,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H22O2/c1-6-8(10(4,5)12)7-9(2,3)11/h8,11-12H,6-7H2,1-5H3
InChI Key UZBOVVCKYSVTPL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H22O2
Molecular Weight 174.28 g/mol
Exact Mass 174.161979940 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-Ethyl-2,5-dimethylhexane-2,5-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.7404 74.04%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4916 49.16%
OATP2B1 inhibitior - 0.8448 84.48%
OATP1B1 inhibitior + 0.9369 93.69%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9437 94.37%
P-glycoprotein inhibitior - 0.9661 96.61%
P-glycoprotein substrate - 0.9193 91.93%
CYP3A4 substrate - 0.7199 71.99%
CYP2C9 substrate - 0.6084 60.84%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.8763 87.63%
CYP2C9 inhibition - 0.8559 85.59%
CYP2C19 inhibition - 0.7837 78.37%
CYP2D6 inhibition - 0.9235 92.35%
CYP1A2 inhibition - 0.7844 78.44%
CYP2C8 inhibition - 0.9795 97.95%
CYP inhibitory promiscuity - 0.7956 79.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.9616 96.16%
Skin irritation + 0.5734 57.34%
Skin corrosion - 0.6640 66.40%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6116 61.16%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5663 56.63%
skin sensitisation + 0.8890 88.90%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5845 58.45%
Acute Oral Toxicity (c) III 0.8966 89.66%
Estrogen receptor binding - 0.8697 86.97%
Androgen receptor binding - 0.8941 89.41%
Thyroid receptor binding - 0.7936 79.36%
Glucocorticoid receptor binding - 0.8694 86.94%
Aromatase binding - 0.7450 74.50%
PPAR gamma - 0.8637 86.37%
Honey bee toxicity - 0.9306 93.06%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.5605 56.05%

Targets

Top

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 96.52% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.94% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.33% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.49% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.76% 96.95%

Plants that contains it

Top
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.
Achillea fragrantissima

Cross-Links

Top
PubChem 148344119
LOTUS LTS0182594
wikiData Q105282086