(3Z)-6-methylhepta-3,5-dien-2-one

Details

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Internal ID 1dfc17fe-8d20-4b97-b320-38d2657cb96e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (3Z)-6-methylhepta-3,5-dien-2-one
SMILES (Canonical) CC(=CC=CC(=O)C)C
SMILES (Isomeric) CC(=C/C=C\C(=O)C)C
InChI InChI=1S/C8H12O/c1-7(2)5-4-6-8(3)9/h4-6H,1-3H3/b6-4-
InChI Key KSKXSFZGARKWOW-XQRVVYSFSA-N
Popularity 14 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 2.00
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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6-Methyl-3,5-heptadienone-2
6-Methyl-hepta-3,5-diene-2-one
6-methyl-(E)-3,5-heptadien-2-one
CHEBI:89984
FEMA 3363
KSKXSFZGARKWOW-XQRVVYSFSA-
KSKXSFZGARKWOW-XQRVVYSFSA-N
(Z)-6-Methyl-3,5-heptadien-2-one
Q27162192
InChI=1/C8H12O/c1-7(2)5-4-6-8(3)9/h4-6H,1-3H3/b6-4-

2D Structure

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2D Structure of (3Z)-6-methylhepta-3,5-dien-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 + 0.9944 99.44%
Caco-2 + 0.9272 92.72%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4824 48.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9407 94.07%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8998 89.98%
P-glycoprotein inhibitior - 0.9906 99.06%
P-glycoprotein substrate - 0.9856 98.56%
CYP3A4 substrate - 0.6696 66.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8763 87.63%
CYP3A4 inhibition - 0.9546 95.46%
CYP2C9 inhibition - 0.8991 89.91%
CYP2C19 inhibition - 0.8431 84.31%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.8181 81.81%
CYP2C8 inhibition - 0.9902 99.02%
CYP inhibitory promiscuity - 0.6440 64.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5983 59.83%
Carcinogenicity (trinary) Non-required 0.5338 53.38%
Eye corrosion + 0.9565 95.65%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8622 86.22%
Skin corrosion + 0.6706 67.06%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7879 78.79%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.7199 71.99%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7471 74.71%
Acute Oral Toxicity (c) III 0.8148 81.48%
Estrogen receptor binding - 0.9686 96.86%
Androgen receptor binding - 0.9661 96.61%
Thyroid receptor binding - 0.9004 90.04%
Glucocorticoid receptor binding - 0.8376 83.76%
Aromatase binding - 0.9122 91.22%
PPAR gamma - 0.9559 95.59%
Honey bee toxicity - 0.9012 90.12%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.3998 39.98%

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 94.60% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.29% 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.
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Crocus sativus

Cross-Links

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PubChem 12510894
NPASS NPC47768