12,14,14-Trimethyl-3,6,9-trioxapentadecan-1-ol

Details

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Internal ID 2b7ff503-5898-4c19-a3d7-ba6f13c75fe0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers > Polyethylene glycols
IUPAC Name 2-[2-[2-(3,5,5-trimethylhexoxy)ethoxy]ethoxy]ethanol
SMILES (Canonical) CC(CCOCCOCCOCCO)CC(C)(C)C
SMILES (Isomeric) CC(CCOCCOCCOCCO)CC(C)(C)C
InChI InChI=1S/C15H32O4/c1-14(13-15(2,3)4)5-7-17-9-11-19-12-10-18-8-6-16/h14,16H,5-13H2,1-4H3
InChI Key CQOVUZIFCWPUOD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H32O4
Molecular Weight 276.41 g/mol
Exact Mass 276.23005950 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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CQOVUZIFCWPUOD-UHFFFAOYSA-N
2-(2-(2-[(3,5,5-Trimethylhexyl)oxy]ethoxy)ethoxy)ethanol #

2D Structure

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2D Structure of 12,14,14-Trimethyl-3,6,9-trioxapentadecan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9150 91.50%
Caco-2 + 0.9144 91.44%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.5063 50.63%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.8962 89.62%
OATP1B3 inhibitior + 0.9162 91.62%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6841 68.41%
P-glycoprotein inhibitior - 0.8955 89.55%
P-glycoprotein substrate - 0.8522 85.22%
CYP3A4 substrate - 0.5719 57.19%
CYP2C9 substrate - 0.8160 81.60%
CYP2D6 substrate - 0.7644 76.44%
CYP3A4 inhibition - 0.8291 82.91%
CYP2C9 inhibition - 0.8990 89.90%
CYP2C19 inhibition - 0.8924 89.24%
CYP2D6 inhibition - 0.9483 94.83%
CYP1A2 inhibition - 0.9349 93.49%
CYP2C8 inhibition - 0.9868 98.68%
CYP inhibitory promiscuity - 0.9762 97.62%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.7628 76.28%
Eye corrosion - 0.7477 74.77%
Eye irritation + 0.7888 78.88%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9901 99.01%
Ames mutagenesis - 0.7973 79.73%
Human Ether-a-go-go-Related Gene inhibition - 0.4780 47.80%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6428 64.28%
skin sensitisation + 0.7838 78.38%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5936 59.36%
Acute Oral Toxicity (c) III 0.6940 69.40%
Estrogen receptor binding - 0.5851 58.51%
Androgen receptor binding - 0.8902 89.02%
Thyroid receptor binding - 0.6344 63.44%
Glucocorticoid receptor binding - 0.5659 56.59%
Aromatase binding - 0.6084 60.84%
PPAR gamma - 0.7404 74.04%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.5226 52.26%

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
CHEMBL2885 P07451 Carbonic anhydrase III 93.48% 87.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.67% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.71% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.62% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.55% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 88.92% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 84.17% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.61% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.65% 99.17%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 545734
NPASS NPC307144