1-(3-Methylbutoxy)non-2-en-4,6-diyne

Details

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Internal ID 30009408-80c4-4e16-8265-c0aedf7fceae
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-(3-methylbutoxy)non-2-en-4,6-diyne
SMILES (Canonical) CCC#CC#CC=CCOCCC(C)C
SMILES (Isomeric) CCC#CC#CC=CCOCCC(C)C
InChI InChI=1S/C14H20O/c1-4-5-6-7-8-9-10-12-15-13-11-14(2)3/h9-10,14H,4,11-13H2,1-3H3
InChI Key LKZQIVWWONRZTQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H20O
Molecular Weight 204.31 g/mol
Exact Mass 204.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3-Methylbutoxy)non-2-en-4,6-diyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 + 0.8616 86.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.3951 39.51%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8678 86.78%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9080 90.80%
P-glycoprotein inhibitior - 0.9613 96.13%
P-glycoprotein substrate - 0.8090 80.90%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5886 58.86%
CYP2D6 substrate - 0.7883 78.83%
CYP3A4 inhibition - 0.9431 94.31%
CYP2C9 inhibition - 0.9011 90.11%
CYP2C19 inhibition - 0.8581 85.81%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition - 0.6470 64.70%
CYP2C8 inhibition - 0.8818 88.18%
CYP inhibitory promiscuity - 0.7921 79.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.4899 48.99%
Eye corrosion + 0.7424 74.24%
Eye irritation - 0.5873 58.73%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9088 90.88%
Ames mutagenesis - 0.6408 64.08%
Human Ether-a-go-go-Related Gene inhibition - 0.4817 48.17%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation + 0.8853 88.53%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8410 84.10%
Estrogen receptor binding - 0.6855 68.55%
Androgen receptor binding - 0.8373 83.73%
Thyroid receptor binding - 0.4915 49.15%
Glucocorticoid receptor binding - 0.6093 60.93%
Aromatase binding + 0.6178 61.78%
PPAR gamma - 0.7576 75.76%
Honey bee toxicity - 0.7852 78.52%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8722 87.22%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.79% 96.09%
CHEMBL3837 P07711 Cathepsin L 87.59% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.35% 94.45%
CHEMBL2581 P07339 Cathepsin D 86.30% 98.95%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.71% 95.58%
CHEMBL1907 P15144 Aminopeptidase N 84.49% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.33% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 84.10% 94.73%
CHEMBL202 P00374 Dihydrofolate reductase 82.33% 89.92%
CHEMBL221 P23219 Cyclooxygenase-1 82.24% 90.17%
CHEMBL2885 P07451 Carbonic anhydrase III 81.70% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.11% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.70% 99.17%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.64% 96.38%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.46% 89.34%

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.
Ursinia eckloniana

Cross-Links

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PubChem 163040109
LOTUS LTS0043243
wikiData Q105153368