2-Hexene, 1-butoxy-, (E)-

Details

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Internal ID d6025076-94c1-40f6-b7c1-07d09593dc84
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name (E)-1-butoxyhex-2-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O/c1-3-5-7-8-10-11-9-6-4-2/h7-8H,3-6,9-10H2,1-2H3/b8-7+
InChI Key LXDQSUZPIXBWIQ-BQYQJAHWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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(E)-1-Butoxy-2-hexene
2-Hexene, 1-butoxy-, (E)-
(2E)-1-Butoxy-2-hexene #
LXDQSUZPIXBWIQ-BQYQJAHWSA-N
DB-310151

2D Structure

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2D Structure of 2-Hexene, 1-butoxy-, (E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.9804 98.04%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4186 41.86%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.8645 86.45%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8691 86.91%
P-glycoprotein inhibitior - 0.9815 98.15%
P-glycoprotein substrate - 0.9332 93.32%
CYP3A4 substrate - 0.5718 57.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7339 73.39%
CYP3A4 inhibition - 0.9729 97.29%
CYP2C9 inhibition - 0.9274 92.74%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.6287 62.87%
CYP2C8 inhibition - 0.8438 84.38%
CYP inhibitory promiscuity - 0.8383 83.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5979 59.79%
Eye corrosion + 0.9263 92.63%
Eye irritation + 0.9829 98.29%
Skin irritation - 0.6641 66.41%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4738 47.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8945 89.45%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.7255 72.55%
Acute Oral Toxicity (c) III 0.7671 76.71%
Estrogen receptor binding - 0.9076 90.76%
Androgen receptor binding - 0.8835 88.35%
Thyroid receptor binding - 0.7478 74.78%
Glucocorticoid receptor binding - 0.7609 76.09%
Aromatase binding - 0.8618 86.18%
PPAR gamma - 0.6907 69.07%
Honey bee toxicity - 0.9774 97.74%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5352 53.52%
Fish aquatic toxicity + 0.8917 89.17%

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
CHEMBL240 Q12809 HERG 96.90% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 89.69% 93.31%
CHEMBL2581 P07339 Cathepsin D 84.57% 98.95%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 84.44% 90.75%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.44% 92.08%
CHEMBL2664 P23526 Adenosylhomocysteinase 81.93% 86.67%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.00% 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.
Glycyrrhiza

Cross-Links

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PubChem 5364961
NPASS NPC150246