2,3,5,8-Tetramethyldecane

Details

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Internal ID 30838400-9931-409c-95a0-5fd778bb3b76
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,3,5,8-tetramethyldecane
SMILES (Canonical) CCC(C)CCC(C)CC(C)C(C)C
SMILES (Isomeric) CCC(C)CCC(C)CC(C)C(C)C
InChI InChI=1S/C14H30/c1-7-12(4)8-9-13(5)10-14(6)11(2)3/h11-14H,7-10H2,1-6H3
InChI Key XTIADNINQBIUNR-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C14H30
Molecular Weight 198.39 g/mol
Exact Mass 198.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.13
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Decane, 2,3,5,8-tetramethyl-
192823-15-7
2,3,5,8-Tetramethyldecane #
CHEBI:84227
DTXSID70337936
XTIADNINQBIUNR-UHFFFAOYSA-N
Q27157597

2D Structure

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2D Structure of 2,3,5,8-Tetramethyldecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.8599 85.99%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.3794 37.94%
OATP2B1 inhibitior - 0.8463 84.63%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9194 91.94%
P-glycoprotein inhibitior - 0.9280 92.80%
P-glycoprotein substrate - 0.8698 86.98%
CYP3A4 substrate - 0.7012 70.12%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9850 98.50%
CYP2C9 inhibition - 0.9257 92.57%
CYP2C19 inhibition - 0.9460 94.60%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.6934 69.34%
CYP2C8 inhibition - 0.9759 97.59%
CYP inhibitory promiscuity - 0.8121 81.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5801 58.01%
Eye corrosion + 0.9823 98.23%
Eye irritation + 0.6531 65.31%
Skin irritation + 0.8650 86.50%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6521 65.21%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7388 73.88%
skin sensitisation + 0.9351 93.51%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity - 0.9148 91.48%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity + 0.6352 63.52%
Acute Oral Toxicity (c) III 0.4925 49.25%
Estrogen receptor binding - 0.7750 77.50%
Androgen receptor binding - 0.7937 79.37%
Thyroid receptor binding - 0.6045 60.45%
Glucocorticoid receptor binding - 0.8396 83.96%
Aromatase binding - 0.7474 74.74%
PPAR gamma - 0.8629 86.29%
Honey bee toxicity - 0.9468 94.68%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9573 95.73%

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 91.92% 98.95%
CHEMBL206 P03372 Estrogen receptor alpha 87.99% 97.64%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.58% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.25% 96.09%
CHEMBL236 P41143 Delta opioid receptor 84.88% 99.35%
CHEMBL226 P30542 Adenosine A1 receptor 84.22% 95.93%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.53% 97.23%
CHEMBL1907 P15144 Aminopeptidase N 83.35% 93.31%
CHEMBL268 P43235 Cathepsin K 83.34% 96.85%
CHEMBL242 Q92731 Estrogen receptor beta 83.27% 98.35%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.24% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.04% 96.47%

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.
Lycium barbarum
Lycium chinense
Vitis vinifera

Cross-Links

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PubChem 545611
NPASS NPC167545
LOTUS LTS0068825
wikiData Q27157597