2,4,6-Trimethylheptane

Details

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Internal ID d229f8f2-b43a-4025-9b08-9b147e36a2ba
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,4,6-trimethylheptane
SMILES (Canonical) CC(C)CC(C)CC(C)C
SMILES (Isomeric) CC(C)CC(C)CC(C)C
InChI InChI=1S/C10H22/c1-8(2)6-10(5)7-9(3)4/h8-10H,6-7H2,1-5H3
InChI Key YNLBBDHDNIXQNL-UHFFFAOYSA-N
Popularity 25 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 4.80
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2613-61-8
2,4,6-TRIMETHYL HEPTANE
Heptane, 2,4,6-trimethyl-
DTXSID30180763
YNLBBDHDNIXQNL-UHFFFAOYSA-N
2-Bromo-2,4-Difluoroacetophenone
FT-0634395
EN300-7055778
Q5651210
Z1255415595

2D Structure

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2D Structure of 2,4,6-Trimethylheptane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.7117 71.17%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.4438 44.38%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9665 96.65%
OATP1B3 inhibitior + 0.9486 94.86%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9035 90.35%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9426 94.26%
CYP3A4 substrate - 0.7925 79.25%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9742 97.42%
CYP2C9 inhibition - 0.9517 95.17%
CYP2C19 inhibition - 0.9643 96.43%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.8755 87.55%
CYP2C8 inhibition - 0.9967 99.67%
CYP inhibitory promiscuity - 0.8861 88.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6483 64.83%
Carcinogenicity (trinary) Warning 0.4815 48.15%
Eye corrosion + 0.9929 99.29%
Eye irritation + 0.9920 99.20%
Skin irritation + 0.8206 82.06%
Skin corrosion - 0.9872 98.72%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7649 76.49%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8943 89.43%
skin sensitisation + 0.8527 85.27%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.5638 56.38%
Acute Oral Toxicity (c) III 0.5721 57.21%
Estrogen receptor binding - 0.9196 91.96%
Androgen receptor binding - 0.8968 89.68%
Thyroid receptor binding - 0.7959 79.59%
Glucocorticoid receptor binding - 0.8905 89.05%
Aromatase binding - 0.7198 71.98%
PPAR gamma - 0.8983 89.83%
Honey bee toxicity - 0.9259 92.59%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.7733 77.33%

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 90.68% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 87.59% 93.31%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.27% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.53% 96.09%
CHEMBL3837 P07711 Cathepsin L 86.23% 96.61%
CHEMBL2885 P07451 Carbonic anhydrase III 83.14% 87.45%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 137658
NPASS NPC80642