3,3-Dimethylpentane

Details

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Internal ID a7a6e202-7cc6-4072-b9ae-e73835073fdf
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 3,3-dimethylpentane
SMILES (Canonical) CCC(C)(C)CC
SMILES (Isomeric) CCC(C)(C)CC
InChI InChI=1S/C7H16/c1-5-7(3,4)6-2/h5-6H2,1-4H3
InChI Key AEXMKKGTQYQZCS-UHFFFAOYSA-N
Popularity 203 references in papers

Physical and Chemical Properties

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Molecular Formula C7H16
Molecular Weight 100.20 g/mol
Exact Mass 100.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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562-49-2
Pentane, 3,3-dimethyl-
Pentane,3,3-dimethyl-
3,3,-dimethylpentane
3.3-Dimethyl pentane
UNII-R1RH0VBD2L
R1RH0VBD2L
DTXSID0049319
EINECS 209-230-8
NSC 74150
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,3-Dimethylpentane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.9272 92.72%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.5935 59.35%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.9689 96.89%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9026 90.26%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9567 95.67%
CYP3A4 substrate - 0.8180 81.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9348 93.48%
CYP2C9 inhibition - 0.9214 92.14%
CYP2C19 inhibition - 0.9574 95.74%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.8842 88.42%
CYP2C8 inhibition - 0.9843 98.43%
CYP inhibitory promiscuity - 0.8520 85.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5129 51.29%
Eye corrosion + 0.9865 98.65%
Eye irritation + 0.9925 99.25%
Skin irritation + 0.8851 88.51%
Skin corrosion - 0.9353 93.53%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7757 77.57%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7074 70.74%
skin sensitisation + 0.9141 91.41%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity - 0.6716 67.16%
Acute Oral Toxicity (c) III 0.6680 66.80%
Estrogen receptor binding - 0.8917 89.17%
Androgen receptor binding - 0.9208 92.08%
Thyroid receptor binding - 0.8514 85.14%
Glucocorticoid receptor binding - 0.9475 94.75%
Aromatase binding - 0.9077 90.77%
PPAR gamma - 0.8867 88.67%
Honey bee toxicity - 0.8769 87.69%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9035 90.35%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.00% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.11% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.59% 97.29%
CHEMBL2581 P07339 Cathepsin D 81.87% 98.95%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 80.16% 94.01%

Cross-Links

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PubChem 11229
NPASS NPC152459
LOTUS LTS0047677
wikiData Q2815978