4,4-Dimethylnonane

Details

Top
Internal ID e67cb474-f1f6-41ab-a882-0fabb28a7dfd
Taxonomy Hydrocarbons > Saturated hydrocarbons
IUPAC Name 4,4-dimethylnonane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H24/c1-5-7-8-10-11(3,4)9-6-2/h5-10H2,1-4H3
InChI Key HARRKRKVTQABSF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H24
Molecular Weight 156.31 g/mol
Exact Mass 156.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
DTXSID60699035
17302-18-0
RefChem:96372
DTXCID30649784
Nonane, 4,4-dimethyl-
SCHEMBL1971884
SCHEMBL3885284
SCHEMBL21925320
SCHEMBL28153732
HARRKRKVTQABSF-UHFFFAOYSA-N

2D Structure

Top
2D Structure of 4,4-Dimethylnonane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.9772 97.72%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.5678 56.78%
OATP2B1 inhibitior - 0.8422 84.22%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8598 85.98%
P-glycoprotein inhibitior - 0.9679 96.79%
P-glycoprotein substrate - 0.8887 88.87%
CYP3A4 substrate - 0.6843 68.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9682 96.82%
CYP2C9 inhibition - 0.9046 90.46%
CYP2C19 inhibition - 0.9441 94.41%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.7620 76.20%
CYP2C8 inhibition - 0.9292 92.92%
CYP inhibitory promiscuity - 0.8359 83.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6078 60.78%
Eye corrosion + 0.9741 97.41%
Eye irritation + 0.9932 99.32%
Skin irritation + 0.7207 72.07%
Skin corrosion - 0.9906 99.06%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6467 64.67%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.9320 93.20%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9188 91.88%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.5500 55.00%
Acute Oral Toxicity (c) IV 0.7268 72.68%
Estrogen receptor binding - 0.9272 92.72%
Androgen receptor binding - 0.7910 79.10%
Thyroid receptor binding - 0.7476 74.76%
Glucocorticoid receptor binding - 0.9092 90.92%
Aromatase binding - 0.9214 92.14%
PPAR gamma - 0.8835 88.35%
Honey bee toxicity - 0.9825 98.25%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5182 51.82%
Fish aquatic toxicity + 0.9805 98.05%

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
CHEMBL230 P35354 Cyclooxygenase-2 94.98% 89.63%
CHEMBL2581 P07339 Cathepsin D 92.31% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 92.08% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.99% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.66% 92.08%
CHEMBL2996 Q05655 Protein kinase C delta 87.95% 97.79%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 84.59% 85.40%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.57% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 84.55% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 84.20% 94.73%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.14% 92.86%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.22% 96.95%
CHEMBL2885 P07451 Carbonic anhydrase III 82.04% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.73% 91.81%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.71% 92.68%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.44% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.03% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.73% 99.17%
CHEMBL4581 P52732 Kinesin-like protein 1 80.71% 93.18%

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.
Agastache foeniculum

Cross-Links

Top
PubChem 53425988
LOTUS LTS0260862
wikiData Q82629707