2,3-Dimethylhexane

Details

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Internal ID 23fba82c-534d-4398-9468-973be413c8e0
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,3-dimethylhexane
SMILES (Canonical) CCCC(C)C(C)C
SMILES (Isomeric) CCCC(C)C(C)C
InChI InChI=1S/C8H18/c1-5-6-8(4)7(2)3/h7-8H,5-6H2,1-4H3
InChI Key JXPOLSKBTUYKJB-UHFFFAOYSA-N
Popularity 124 references in papers

Physical and Chemical Properties

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Molecular Formula C8H18
Molecular Weight 114.23 g/mol
Exact Mass 114.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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584-94-1
xi-2,3-Dimethylhexane
Hexane, 2,3-dimethyl-
EINECS 209-547-1
NSC 74170
2,3-DIMETHYL HEXANE
NSC74170
2,3-dimethyl-hexane
DTXSID40862240
CHEBI:173398
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3-Dimethylhexane

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 + 0.7963 79.63%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Nucleus 0.4002 40.02%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9412 94.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9547 95.47%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9410 94.10%
CYP3A4 substrate - 0.7884 78.84%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9913 99.13%
CYP2C9 inhibition - 0.9436 94.36%
CYP2C19 inhibition - 0.9554 95.54%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.7687 76.87%
CYP2C8 inhibition - 0.9968 99.68%
CYP inhibitory promiscuity - 0.8579 85.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5766 57.66%
Eye corrosion + 0.9881 98.81%
Eye irritation + 0.9856 98.56%
Skin irritation + 0.8808 88.08%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6465 64.65%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation + 0.9268 92.68%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.8294 82.94%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.6609 66.09%
Acute Oral Toxicity (c) III 0.5044 50.44%
Estrogen receptor binding - 0.9232 92.32%
Androgen receptor binding - 0.9019 90.19%
Thyroid receptor binding - 0.8445 84.45%
Glucocorticoid receptor binding - 0.9435 94.35%
Aromatase binding - 0.8687 86.87%
PPAR gamma - 0.9189 91.89%
Honey bee toxicity - 0.9662 96.62%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8791 87.91%

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
CHEMBL2581 P07339 Cathepsin D 92.18% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.86% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.02% 97.25%
CHEMBL1907 P15144 Aminopeptidase N 83.74% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.59% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 81.94% 90.17%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.22% 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.
Cnidium monnieri
Elsholtzia ciliata
Mosla chinensis

Cross-Links

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PubChem 11447
NPASS NPC34857