4,8-Dimethyltridecane

Details

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Internal ID d033edf7-4756-4549-a6f6-4a2c5a98c6a3
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 4,8-dimethyltridecane
SMILES (Canonical) CCCCCC(C)CCCC(C)CCC
SMILES (Isomeric) CCCCCC(C)CCCC(C)CCC
InChI InChI=1S/C15H32/c1-5-7-8-11-15(4)13-9-12-14(3)10-6-2/h14-15H,5-13H2,1-4H3
InChI Key IRMGDQSAWLAMIV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H32
Molecular Weight 212.41 g/mol
Exact Mass 212.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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Tridecane, 4,8-dimethyl-
55030-62-1
4,8-Dimethyltridecan
4,8-Dimethyltridecane #
DTXSID60970391
IRMGDQSAWLAMIV-UHFFFAOYSA-N

2D Structure

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2D Structure of 4,8-Dimethyltridecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9359 93.59%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.5432 54.32%
OATP2B1 inhibitior - 0.8434 84.34%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6723 67.23%
P-glycoprotein inhibitior - 0.9281 92.81%
P-glycoprotein substrate - 0.8525 85.25%
CYP3A4 substrate - 0.7122 71.22%
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 - 0.9851 98.51%
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 + 0.9590 95.90%
Skin irritation + 0.8624 86.24%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6666 66.66%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6849 68.49%
skin sensitisation + 0.9268 92.68%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.9086 90.86%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.5784 57.84%
Acute Oral Toxicity (c) III 0.5369 53.69%
Estrogen receptor binding - 0.7191 71.91%
Androgen receptor binding - 0.8468 84.68%
Thyroid receptor binding - 0.5202 52.02%
Glucocorticoid receptor binding - 0.7835 78.35%
Aromatase binding - 0.7418 74.18%
PPAR gamma - 0.7995 79.95%
Honey bee toxicity - 0.9853 98.53%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5234 52.34%
Fish aquatic toxicity + 0.9752 97.52%

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 94.10% 89.63%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.07% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.49% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.31% 92.86%
CHEMBL1907 P15144 Aminopeptidase N 90.85% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 89.74% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.70% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.30% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.76% 91.81%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.47% 93.56%
CHEMBL2996 Q05655 Protein kinase C delta 85.78% 97.79%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 84.53% 95.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.02% 92.08%
CHEMBL260 Q16539 MAP kinase p38 alpha 83.36% 97.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.13% 99.17%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 82.47% 90.24%
CHEMBL299 P17252 Protein kinase C alpha 81.69% 98.03%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.30% 97.23%

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.
Artemisia capillaris

Cross-Links

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PubChem 41306
NPASS NPC219733