2-Chlorotrideca-3,11-dien-5,7,9-triynyl acetate

Details

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Internal ID f605ffe5-559f-4611-b06a-57c6be16fd3d
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 2-chlorotrideca-3,11-dien-5,7,9-triynyl acetate
SMILES (Canonical) CC=CC#CC#CC#CC=CC(COC(=O)C)Cl
SMILES (Isomeric) CC=CC#CC#CC#CC=CC(COC(=O)C)Cl
InChI InChI=1S/C15H13ClO2/c1-3-4-5-6-7-8-9-10-11-12-15(16)13-18-14(2)17/h3-4,11-12,15H,13H2,1-2H3
InChI Key HMOUISDJRBMADQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13ClO2
Molecular Weight 260.71 g/mol
Exact Mass 260.0604073 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Chlorotrideca-3,11-dien-5,7,9-triynyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7613 76.13%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7433 74.33%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8321 83.21%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6041 60.41%
P-glycoprotein inhibitior - 0.8660 86.60%
P-glycoprotein substrate - 0.8995 89.95%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8787 87.87%
CYP3A4 inhibition - 0.9307 93.07%
CYP2C9 inhibition - 0.8800 88.00%
CYP2C19 inhibition - 0.7178 71.78%
CYP2D6 inhibition - 0.9385 93.85%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8850 88.50%
CYP inhibitory promiscuity - 0.7809 78.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5650 56.50%
Carcinogenicity (trinary) Non-required 0.6469 64.69%
Eye corrosion + 0.9801 98.01%
Eye irritation - 0.9277 92.77%
Skin irritation + 0.8476 84.76%
Skin corrosion + 0.7568 75.68%
Ames mutagenesis + 0.5763 57.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5475 54.75%
Micronuclear - 0.9226 92.26%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation + 0.6213 62.13%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.8340 83.40%
Acute Oral Toxicity (c) II 0.5527 55.27%
Estrogen receptor binding - 0.4949 49.49%
Androgen receptor binding - 0.8421 84.21%
Thyroid receptor binding - 0.5329 53.29%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6076 60.76%
PPAR gamma - 0.5173 51.73%
Honey bee toxicity - 0.6613 66.13%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7155 71.55%
Fish aquatic toxicity + 0.9502 95.02%

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 94.77% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.21% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.02% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.72% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.77% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.29% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.74% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.61% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.31% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.37% 91.11%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.04% 98.75%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.83% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.68% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 80.06% 91.19%

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.
Carthamus lanatus
Coreopsis nodosa

Cross-Links

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PubChem 162957752
LOTUS LTS0164955
wikiData Q105030610