7-Chloropentadeca-3,9,12-trien-1-yn-6-yl acetate

Details

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Internal ID fc78f2ab-a5c7-4ec3-85c0-8d5b96af0382
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 7-chloropentadeca-3,9,12-trien-1-yn-6-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H23ClO2/c1-4-6-8-9-10-12-13-16(18)17(20-15(3)19)14-11-7-5-2/h2,6-8,10-12,16-17H,4,9,13-14H2,1,3H3
InChI Key OIYRZXJDSDRVQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H23ClO2
Molecular Weight 294.80 g/mol
Exact Mass 294.1386577 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Chloropentadeca-3,9,12-trien-1-yn-6-yl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 - 0.5764 57.64%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6805 68.05%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.8244 82.44%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7936 79.36%
P-glycoprotein inhibitior - 0.6662 66.62%
P-glycoprotein substrate - 0.8951 89.51%
CYP3A4 substrate + 0.5090 50.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.8219 82.19%
CYP2C9 inhibition - 0.7858 78.58%
CYP2C19 inhibition - 0.6238 62.38%
CYP2D6 inhibition - 0.9180 91.80%
CYP1A2 inhibition - 0.5248 52.48%
CYP2C8 inhibition - 0.8166 81.66%
CYP inhibitory promiscuity - 0.5657 56.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6551 65.51%
Carcinogenicity (trinary) Non-required 0.5760 57.60%
Eye corrosion + 0.8639 86.39%
Eye irritation - 0.9818 98.18%
Skin irritation + 0.5604 56.04%
Skin corrosion + 0.6061 60.61%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7454 74.54%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6442 64.42%
skin sensitisation + 0.8532 85.32%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5967 59.67%
Acute Oral Toxicity (c) III 0.6657 66.57%
Estrogen receptor binding + 0.7432 74.32%
Androgen receptor binding - 0.7963 79.63%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5616 56.16%
Aromatase binding - 0.5191 51.91%
PPAR gamma - 0.5090 50.90%
Honey bee toxicity - 0.8241 82.41%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9239 92.39%

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 92.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.51% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.44% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.59% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.27% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.31% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.97% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.27% 89.34%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.48% 96.61%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 74051813
LOTUS LTS0152388
wikiData Q105192919