1,6-Heptadien-4-one, 2,5,5-trimethyl-

Details

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Internal ID 51981084-6c60-40b4-9c7e-a819f51d1c2a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 2,5,5-trimethylhepta-1,6-dien-4-one
SMILES (Canonical) CC(=C)CC(=O)C(C)(C)C=C
SMILES (Isomeric) CC(=C)CC(=O)C(C)(C)C=C
InChI InChI=1S/C10H16O/c1-6-10(4,5)9(11)7-8(2)3/h6H,1-2,7H2,3-5H3
InChI Key UHZJRKGDIXMHFS-UHFFFAOYSA-N
Popularity 33 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
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 1,6-Heptadien-4-one, 2,5,5-trimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.6359 63.59%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4011 40.11%
OATP2B1 inhibitior - 0.8642 86.42%
OATP1B1 inhibitior + 0.9394 93.94%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9353 93.53%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.9520 95.20%
CYP3A4 substrate - 0.6210 62.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7993 79.93%
CYP3A4 inhibition - 0.8380 83.80%
CYP2C9 inhibition - 0.8514 85.14%
CYP2C19 inhibition - 0.7524 75.24%
CYP2D6 inhibition - 0.9260 92.60%
CYP1A2 inhibition - 0.7299 72.99%
CYP2C8 inhibition - 0.9749 97.49%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6183 61.83%
Carcinogenicity (trinary) Non-required 0.5141 51.41%
Eye corrosion + 0.7927 79.27%
Eye irritation + 0.9891 98.91%
Skin irritation + 0.8548 85.48%
Skin corrosion - 0.8240 82.40%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6259 62.59%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation + 0.9676 96.76%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7505 75.05%
Acute Oral Toxicity (c) III 0.6780 67.80%
Estrogen receptor binding - 0.9357 93.57%
Androgen receptor binding - 0.8943 89.43%
Thyroid receptor binding - 0.8350 83.50%
Glucocorticoid receptor binding - 0.8688 86.88%
Aromatase binding - 0.8410 84.10%
PPAR gamma - 0.8679 86.79%
Honey bee toxicity - 0.8677 86.77%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity + 0.8634 86.34%

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 92.81% 83.82%
CHEMBL2581 P07339 Cathepsin D 88.37% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.29% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.83% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 84.09% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.64% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.55% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.22% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.80% 94.33%

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.
Artemisia annua

Cross-Links

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PubChem 12308603
NPASS NPC107159