10-Acetyloxydeca-2,8-dien-4,6-diynyl acetate

Details

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Internal ID 1e5184de-da22-4bc9-8600-5a468ca68e99
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 10-acetyloxydeca-2,8-dien-4,6-diynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O4/c1-13(15)17-11-9-7-5-3-4-6-8-10-12-18-14(2)16/h7-10H,11-12H2,1-2H3
InChI Key DADBEGIQJYIBBH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Acetyloxydeca-2,8-dien-4,6-diynyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9665 96.65%
Caco-2 - 0.6156 61.56%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7719 77.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6872 68.72%
P-glycoprotein inhibitior - 0.8926 89.26%
P-glycoprotein substrate - 0.9767 97.67%
CYP3A4 substrate - 0.5948 59.48%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8808 88.08%
CYP3A4 inhibition - 0.8728 87.28%
CYP2C9 inhibition - 0.8748 87.48%
CYP2C19 inhibition - 0.8872 88.72%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.8408 84.08%
CYP2C8 inhibition - 0.9663 96.63%
CYP inhibitory promiscuity - 0.8300 83.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5360 53.60%
Carcinogenicity (trinary) Non-required 0.7100 71.00%
Eye corrosion + 0.8967 89.67%
Eye irritation - 0.5582 55.82%
Skin irritation + 0.8253 82.53%
Skin corrosion + 0.5814 58.14%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4826 48.26%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5678 56.78%
skin sensitisation + 0.8130 81.30%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7646 76.46%
Acute Oral Toxicity (c) II 0.4275 42.75%
Estrogen receptor binding - 0.5782 57.82%
Androgen receptor binding - 0.6916 69.16%
Thyroid receptor binding - 0.5072 50.72%
Glucocorticoid receptor binding - 0.7361 73.61%
Aromatase binding - 0.5060 50.60%
PPAR gamma - 0.6427 64.27%
Honey bee toxicity - 0.8450 84.50%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7355 73.55%
Fish aquatic toxicity + 0.9586 95.86%

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 93.80% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.28% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 83.04% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.06% 96.00%

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.
Erigeron filifolius
Felicia filifolia

Cross-Links

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PubChem 162987135
LOTUS LTS0102361
wikiData Q104973410