3-Ethyl-2,3-dimethylpentane

Details

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Internal ID c600ff96-4b98-49d6-94bb-e942d93bc6e8
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 3-ethyl-2,3-dimethylpentane
SMILES (Canonical) CCC(C)(CC)C(C)C
SMILES (Isomeric) CCC(C)(CC)C(C)C
InChI InChI=1S/C9H20/c1-6-9(5,7-2)8(3)4/h8H,6-7H2,1-5H3
InChI Key MMASVVOQIKCFJZ-UHFFFAOYSA-N
Popularity 10 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 4.40
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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16747-33-4
Pentane, 3-ethyl-2,3-dimethyl-
3-ETHYL-2,3-DIMETHYL-PENTANE
2,3-dimethyl-3-ethyl-pentane
DTXSID60168291
MMASVVOQIKCFJZ-UHFFFAOYSA-N
2,3-DIMETHYL-3-ETHYLPENTANE
Q5651936

2D Structure

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2D Structure of 3-Ethyl-2,3-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 + 0.8707 87.07%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.5935 59.35%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9140 91.40%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.7807 78.07%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7490 74.90%
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 - 0.9924 99.24%
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 + 0.9915 99.15%
Skin irritation + 0.8851 88.51%
Skin corrosion - 0.9353 93.53%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8009 80.09%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7475 74.75%
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 - 0.5739 57.39%
Acute Oral Toxicity (c) III 0.6680 66.80%
Estrogen receptor binding - 0.8806 88.06%
Androgen receptor binding - 0.8720 87.20%
Thyroid receptor binding - 0.8693 86.93%
Glucocorticoid receptor binding - 0.9273 92.73%
Aromatase binding - 0.8210 82.10%
PPAR gamma - 0.8515 85.15%
Honey bee toxicity - 0.8698 86.98%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7300 73.00%
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 96.23% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.86% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.72% 97.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.59% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.32% 97.29%
CHEMBL2996 Q05655 Protein kinase C delta 85.93% 97.79%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.34% 93.56%
CHEMBL1907 P15144 Aminopeptidase N 81.01% 93.31%
CHEMBL299 P17252 Protein kinase C alpha 80.73% 98.03%

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.
Crataegus pinnatifida
Picrasma quassioides

Cross-Links

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PubChem 28027
NPASS NPC72157