3-Ethyl-3-methylheptane

Details

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Internal ID 44f78bd7-d39f-4b24-a3c1-b355f06ebcd7
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 3-ethyl-3-methylheptane
SMILES (Canonical) CCCCC(C)(CC)CC
SMILES (Isomeric) CCCCC(C)(CC)CC
InChI InChI=1S/C10H22/c1-5-8-9-10(4,6-2)7-3/h5-9H2,1-4H3
InChI Key HSOMNBKXPGCNBH-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C10H22
Molecular Weight 142.28 g/mol
Exact Mass 142.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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17302-01-1
Heptane, 3-ethyl-3-methyl-
3-ethyl-3-methyl heptane
DTXSID10169495
HSOMNBKXPGCNBH-UHFFFAOYSA-N
MFCD00048812
E0304
FT-0692151
T71920
Q5651948
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-methylheptane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.9695 96.95%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6435 64.35%
OATP2B1 inhibitior - 0.8423 84.23%
OATP1B1 inhibitior + 0.9184 91.84%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9273 92.73%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9040 90.40%
CYP3A4 substrate - 0.7171 71.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.9026 90.26%
CYP2C19 inhibition - 0.9440 94.40%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.7348 73.48%
CYP2C8 inhibition - 0.9527 95.27%
CYP inhibitory promiscuity - 0.8184 81.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6038 60.38%
Eye corrosion + 0.9716 97.16%
Eye irritation + 0.9913 99.13%
Skin irritation + 0.7564 75.64%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5904 59.04%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.9208 92.08%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.8679 86.79%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.6697 66.97%
Acute Oral Toxicity (c) IV 0.6590 65.90%
Estrogen receptor binding - 0.9218 92.18%
Androgen receptor binding - 0.7834 78.34%
Thyroid receptor binding - 0.8263 82.63%
Glucocorticoid receptor binding - 0.9182 91.82%
Aromatase binding - 0.8831 88.31%
PPAR gamma - 0.9017 90.17%
Honey bee toxicity - 0.9815 98.15%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5752 57.52%
Fish aquatic toxicity + 0.9730 97.30%

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 95.10% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.73% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.40% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.83% 85.94%
CHEMBL2996 Q05655 Protein kinase C delta 86.74% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 84.50% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.15% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.97% 92.08%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 80.14% 94.01%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.06% 91.81%

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.
Panax ginseng

Cross-Links

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PubChem 140213
NPASS NPC215322