3,7-Dimethylnonane

Details

Top
Internal ID 1567aed4-014e-4d49-bc80-2be086a2311a
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 3,7-dimethylnonane
SMILES (Canonical) CCC(C)CCCC(C)CC
SMILES (Isomeric) CCC(C)CCCC(C)CC
InChI InChI=1S/C11H24/c1-5-10(3)8-7-9-11(4)6-2/h10-11H,5-9H2,1-4H3
InChI Key YGPVLXJHRFZYJJ-UHFFFAOYSA-N
Popularity 10 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 5.60
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
Nonane, 3,7-dimethyl-
17302-32-8
Nonane,3,7-dimethyl-
DTXSID80873315
YGPVLXJHRFZYJJ-UHFFFAOYSA-N
LMFA11000616

2D Structure

Top
2D Structure of 3,7-Dimethylnonane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9436 94.36%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.5432 54.32%
OATP2B1 inhibitior - 0.8403 84.03%
OATP1B1 inhibitior + 0.9546 95.46%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8583 85.83%
P-glycoprotein inhibitior - 0.9634 96.34%
P-glycoprotein substrate - 0.9083 90.83%
CYP3A4 substrate - 0.7584 75.84%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9842 98.42%
CYP2C9 inhibition - 0.9267 92.67%
CYP2C19 inhibition - 0.9483 94.83%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.6549 65.49%
CYP2C8 inhibition - 0.9932 99.32%
CYP inhibitory promiscuity - 0.7959 79.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6062 60.62%
Eye corrosion + 0.9906 99.06%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.8624 86.24%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5920 59.20%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7552 75.52%
skin sensitisation + 0.9268 92.68%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity - 0.9086 90.86%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.4821 48.21%
Acute Oral Toxicity (c) III 0.5369 53.69%
Estrogen receptor binding - 0.8976 89.76%
Androgen receptor binding - 0.8754 87.54%
Thyroid receptor binding - 0.6564 65.64%
Glucocorticoid receptor binding - 0.9021 90.21%
Aromatase binding - 0.8500 85.00%
PPAR gamma - 0.9010 90.10%
Honey bee toxicity - 0.9797 97.97%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9752 97.52%

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
CHEMBL2581 P07339 Cathepsin D 90.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.82% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.05% 87.45%
CHEMBL1907 P15144 Aminopeptidase N 82.56% 93.31%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.27% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.06% 93.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.84% 97.25%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.45% 92.86%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

Top
PubChem 28458
NPASS NPC151273