2,4-Heptadien-6-one

Details

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Internal ID b12e26d9-51e9-49b4-9bb5-78a87857f9e8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (3E,5E)-hepta-3,5-dien-2-one
SMILES (Canonical) CC=CC=CC(=O)C
SMILES (Isomeric) C/C=C/C=C/C(=O)C
InChI InChI=1S/C7H10O/c1-3-4-5-6-7(2)8/h3-6H,1-2H3/b4-3+,6-5+
InChI Key SWGLACWOVFCDQS-VNKDHWASSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O
Molecular Weight 110.15 g/mol
Exact Mass 110.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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3916-64-1
(3E,5E)-hepta-3,5-dien-2-one
3,5-HEPTADIEN-2-ONE
Crotylideneacetone
Crotonylideneacetone
3,5-Heptadienone
18402-90-9
AI3-28327
3,5-Heptadien-2-one, (3E,5E)- (9CI)
SCHEMBL3132513
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4-Heptadien-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8908 89.08%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5208 52.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9432 94.32%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8454 84.54%
P-glycoprotein inhibitior - 0.9923 99.23%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7002 70.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8763 87.63%
CYP3A4 inhibition - 0.9655 96.55%
CYP2C9 inhibition - 0.9562 95.62%
CYP2C19 inhibition - 0.9035 90.35%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.7766 77.66%
CYP2C8 inhibition - 0.9876 98.76%
CYP inhibitory promiscuity - 0.8407 84.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6583 65.83%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion + 0.9942 99.42%
Eye irritation + 0.9965 99.65%
Skin irritation + 0.9106 91.06%
Skin corrosion + 0.6472 64.72%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7627 76.27%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.9130 91.30%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6882 68.82%
Acute Oral Toxicity (c) III 0.8234 82.34%
Estrogen receptor binding - 0.9811 98.11%
Androgen receptor binding - 0.9190 91.90%
Thyroid receptor binding - 0.8782 87.82%
Glucocorticoid receptor binding - 0.8514 85.14%
Aromatase binding - 0.9332 93.32%
PPAR gamma - 0.9462 94.62%
Honey bee toxicity - 0.9296 92.96%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.6311 63.11%

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
CHEMBL4040 P28482 MAP kinase ERK2 91.59% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.20% 96.09%

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.
Tetradium ruticarpum

Cross-Links

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PubChem 643537
NPASS NPC192063