3-Ethyl-3-methylhexane

Details

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Internal ID ee89e805-b1c8-48a8-8352-03f2c50f2419
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 3-ethyl-3-methylhexane
SMILES (Canonical) CCCC(C)(CC)CC
SMILES (Isomeric) CCCC(C)(CC)CC
InChI InChI=1S/C9H20/c1-5-8-9(4,6-2)7-3/h5-8H2,1-4H3
InChI Key CYWROHZCELEGSE-UHFFFAOYSA-N
Popularity 22 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 4.70
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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3074-76-8
DTXSID30184766
RefChem:1086578
DTXCID70107257
3-ETHYL-3-METHYLHEXANE
3-Methyl-3-ethylhexane
3-ethyl-3-methyl-hexane
SCHEMBL131622
SCHEMBL232421
SCHEMBL598304
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-Ethyl-3-methylhexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.9553 95.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.6176 61.76%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9259 92.59%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9189 91.89%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.9429 94.29%
CYP3A4 substrate - 0.7646 76.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9498 94.98%
CYP2C9 inhibition - 0.9092 90.92%
CYP2C19 inhibition - 0.9431 94.31%
CYP2D6 inhibition - 0.9287 92.87%
CYP1A2 inhibition - 0.7405 74.05%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.7868 78.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5682 56.82%
Eye corrosion + 0.9590 95.90%
Eye irritation + 0.9776 97.76%
Skin irritation + 0.8247 82.47%
Skin corrosion - 0.9832 98.32%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6814 68.14%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.9288 92.88%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.8790 87.90%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity + 0.5542 55.42%
Acute Oral Toxicity (c) IV 0.4913 49.13%
Estrogen receptor binding - 0.9347 93.47%
Androgen receptor binding - 0.8662 86.62%
Thyroid receptor binding - 0.8765 87.65%
Glucocorticoid receptor binding - 0.9420 94.20%
Aromatase binding - 0.8716 87.16%
PPAR gamma - 0.9010 90.10%
Honey bee toxicity - 0.9381 93.81%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9378 93.78%

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 95.19% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.87% 96.09%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.63% 90.93%

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.
Cistanche deserticola

Cross-Links

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PubChem 18313
NPASS NPC16588