2,3,5-Trimethylhexane

Details

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Internal ID 54bce7df-456e-41e7-b96a-85e8ae80b95a
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,3,5-trimethylhexane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H20/c1-7(2)6-9(5)8(3)4/h7-9H,6H2,1-5H3
InChI Key ODGLTLJZCVNPBU-UHFFFAOYSA-N
Popularity 48 references in papers

Physical and Chemical Properties

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Molecular Formula C9H20
Molecular Weight 128.25 g/mol
Exact Mass 128.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1069-53-0
Hexane, 2,3,5-trimethyl-
EINECS 213-957-6
CHEBI:141559
DTXSID70870833
RefChem:81410
Hexane, 2,3,5trimethyl
DTXCID30818519
213-957-6
ODGLTLJZCVNPBU-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,5-Trimethylhexane

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 + 0.5800 58.00%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4773 47.73%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9604 96.04%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9701 97.01%
P-glycoprotein inhibitior - 0.9724 97.24%
P-glycoprotein substrate - 0.9145 91.45%
CYP3A4 substrate - 0.7778 77.78%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9812 98.12%
CYP2C9 inhibition - 0.9570 95.70%
CYP2C19 inhibition - 0.9669 96.69%
CYP2D6 inhibition - 0.9318 93.18%
CYP1A2 inhibition - 0.8959 89.59%
CYP2C8 inhibition - 0.9953 99.53%
CYP inhibitory promiscuity - 0.9174 91.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6183 61.83%
Carcinogenicity (trinary) Non-required 0.5421 54.21%
Eye corrosion + 0.9935 99.35%
Eye irritation + 0.9913 99.13%
Skin irritation + 0.8962 89.62%
Skin corrosion - 0.9447 94.47%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6631 66.31%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8213 82.13%
skin sensitisation + 0.8518 85.18%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.5554 55.54%
Acute Oral Toxicity (c) III 0.6589 65.89%
Estrogen receptor binding - 0.9101 91.01%
Androgen receptor binding - 0.8913 89.13%
Thyroid receptor binding - 0.8624 86.24%
Glucocorticoid receptor binding - 0.9321 93.21%
Aromatase binding - 0.7577 75.77%
PPAR gamma - 0.9052 90.52%
Honey bee toxicity - 0.9019 90.19%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8664 86.64%

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 91.52% 98.95%
CHEMBL3837 P07711 Cathepsin L 87.49% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.58% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 85.76% 93.31%
CHEMBL268 P43235 Cathepsin K 85.16% 96.85%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.54% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 80.07% 87.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14045
LOTUS LTS0141177
wikiData Q5651194