(E,E)-3,5-octadien-2-one

Details

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Internal ID 356515db-c618-4279-820d-254c2381965d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (3E,5E)-octa-3,5-dien-2-one
SMILES (Canonical) CCC=CC=CC(=O)C
SMILES (Isomeric) CC/C=C/C=C/C(=O)C
InChI InChI=1S/C8H12O/c1-3-4-5-6-7-8(2)9/h4-7H,3H2,1-2H3/b5-4+,7-6+
InChI Key LWRKMRFJEUFXIB-YTXTXJHMSA-N
Popularity 110 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O
Molecular Weight 124.18 g/mol
Exact Mass 124.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(E,E)-3,5-octadien-2-one
(3E,5E)-octa-3,5-dien-2-one
38284-27-4
30086-02-3
3,5-octadienone
trans, trans-3,5-Octadien-2-one
3E,5E-Octadien-2-one
3,5-(E,E)-Octadien-2-one
trans,trans-3,5-Octadien-2-one
trans-3,trans-5-Octadien-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (E,E)-3,5-octadien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.9250 92.50%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4935 49.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9298 92.98%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8274 82.74%
P-glycoprotein inhibitior - 0.9914 99.14%
P-glycoprotein substrate - 0.9724 97.24%
CYP3A4 substrate - 0.7064 70.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9738 97.38%
CYP2C9 inhibition - 0.9282 92.82%
CYP2C19 inhibition - 0.8792 87.92%
CYP2D6 inhibition - 0.9504 95.04%
CYP1A2 inhibition - 0.6451 64.51%
CYP2C8 inhibition - 0.9810 98.10%
CYP inhibitory promiscuity - 0.6920 69.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6164 61.64%
Eye corrosion + 0.9838 98.38%
Eye irritation + 0.9905 99.05%
Skin irritation + 0.8973 89.73%
Skin corrosion - 0.6653 66.53%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7608 76.08%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.9644 96.44%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5265 52.65%
Acute Oral Toxicity (c) III 0.8887 88.87%
Estrogen receptor binding - 0.9810 98.10%
Androgen receptor binding - 0.9059 90.59%
Thyroid receptor binding - 0.8400 84.00%
Glucocorticoid receptor binding - 0.8465 84.65%
Aromatase binding - 0.8725 87.25%
PPAR gamma - 0.8714 87.14%
Honey bee toxicity - 0.9615 96.15%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.5422 54.22%

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 91.21% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.96% 89.34%
CHEMBL255 P29275 Adenosine A2b receptor 81.09% 98.59%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.84% 99.17%

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.
Atractylodes lancea
Atractylodes macrocephala
Senna alexandrina

Cross-Links

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PubChem 5352876
NPASS NPC190301