2-Methyldecane

Details

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Internal ID 684e2b45-4e96-48a4-a751-d9b663873ac4
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2-methyldecane
SMILES (Canonical) CCCCCCCCC(C)C
SMILES (Isomeric) CCCCCCCCC(C)C
InChI InChI=1S/C11H24/c1-4-5-6-7-8-9-10-11(2)3/h11H,4-10H2,1-3H3
InChI Key CNPVJWYWYZMPDS-UHFFFAOYSA-N
Popularity 93 references in papers

Physical and Chemical Properties

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Molecular Formula C11H24
Molecular Weight 156.31 g/mol
Exact Mass 156.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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6975-98-0
Decane, 2-methyl-
90622-57-4
ISOUNDECANE
Isopar G
Isopar H
Dimethylnonane
Shellsol K
2-Methyl-Decane
Nonane, dimethyl-
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-Methyldecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9106 91.06%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4437 44.37%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.9701 97.01%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9029 90.29%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.8560 85.60%
CYP3A4 substrate - 0.7190 71.90%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9872 98.72%
CYP2C9 inhibition - 0.9221 92.21%
CYP2C19 inhibition - 0.9470 94.70%
CYP2D6 inhibition - 0.9457 94.57%
CYP1A2 inhibition - 0.6898 68.98%
CYP2C8 inhibition - 0.9855 98.55%
CYP inhibitory promiscuity - 0.8241 82.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6183 61.83%
Eye corrosion + 0.9891 98.91%
Eye irritation + 0.9927 99.27%
Skin irritation + 0.8188 81.88%
Skin corrosion - 0.9798 97.98%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6506 65.06%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7810 78.10%
skin sensitisation + 0.9360 93.60%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.9674 96.74%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.5208 52.08%
Acute Oral Toxicity (c) IV 0.4917 49.17%
Estrogen receptor binding - 0.9315 93.15%
Androgen receptor binding - 0.8184 81.84%
Thyroid receptor binding - 0.7121 71.21%
Glucocorticoid receptor binding - 0.9208 92.08%
Aromatase binding - 0.8870 88.70%
PPAR gamma - 0.9020 90.20%
Honey bee toxicity - 0.9898 98.98%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.7782 77.82%
Fish aquatic toxicity + 0.9819 98.19%

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 96.46% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.90% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 95.49% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 94.68% 93.31%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.80% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.29% 92.08%
CHEMBL2885 P07451 Carbonic anhydrase III 92.43% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.86% 93.56%
CHEMBL2996 Q05655 Protein kinase C delta 89.60% 97.79%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 88.73% 90.24%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.15% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.14% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.26% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.21% 99.17%
CHEMBL299 P17252 Protein kinase C alpha 83.82% 98.03%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.13% 96.47%
CHEMBL283 P08254 Matrix metalloproteinase 3 81.06% 97.29%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.00% 100.00%
CHEMBL240 Q12809 HERG 80.54% 89.76%
CHEMBL221 P23219 Cyclooxygenase-1 80.52% 90.17%

Cross-Links

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PubChem 23415
NPASS NPC107015
LOTUS LTS0016558
wikiData Q82921599