1,3,6-Heptatriene, 2,5,6-trimethyl-

Details

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Internal ID d65f5e2b-5f26-4c8e-b14c-e44c9961af90
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (3E)-2,5,6-trimethylhepta-1,3,6-triene
SMILES (Canonical) CC(C=CC(=C)C)C(=C)C
SMILES (Isomeric) CC(/C=C/C(=C)C)C(=C)C
InChI InChI=1S/C10H16/c1-8(2)6-7-10(5)9(3)4/h6-7,10H,1,3H2,2,4-5H3/b7-6+
InChI Key PSZBPDGPFVFTSW-VOTSOKGWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2,5,6-Trimethyl-1,3,6-heptatriene
PSZBPDGPFVFTSW-VOTSOKGWSA-N
42123-66-0
2,5,6-Trimethyl-hepta-1,3,6-triene
Hepta-1,3,6-triene, 2,5,6-trimethyl
(3E)-2,5,6-Trimethyl-1,3,6-heptatriene

2D Structure

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2D Structure of 1,3,6-Heptatriene, 2,5,6-trimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.6329 63.29%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.5604 56.04%
OATP2B1 inhibitior - 0.8701 87.01%
OATP1B1 inhibitior + 0.9544 95.44%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9189 91.89%
P-glycoprotein inhibitior - 0.9707 97.07%
P-glycoprotein substrate - 0.9746 97.46%
CYP3A4 substrate - 0.6911 69.11%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8047 80.47%
CYP3A4 inhibition - 0.8791 87.91%
CYP2C9 inhibition - 0.9181 91.81%
CYP2C19 inhibition - 0.8606 86.06%
CYP2D6 inhibition - 0.9272 92.72%
CYP1A2 inhibition - 0.8662 86.62%
CYP2C8 inhibition - 0.9841 98.41%
CYP inhibitory promiscuity - 0.7183 71.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7083 70.83%
Carcinogenicity (trinary) Warning 0.5616 56.16%
Eye corrosion + 0.9516 95.16%
Eye irritation + 0.9619 96.19%
Skin irritation + 0.8061 80.61%
Skin corrosion - 0.9232 92.32%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6498 64.98%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8933 89.33%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.6914 69.14%
Nephrotoxicity + 0.6442 64.42%
Acute Oral Toxicity (c) III 0.4685 46.85%
Estrogen receptor binding - 0.8867 88.67%
Androgen receptor binding - 0.8701 87.01%
Thyroid receptor binding - 0.8343 83.43%
Glucocorticoid receptor binding - 0.9384 93.84%
Aromatase binding - 0.7806 78.06%
PPAR gamma - 0.8899 88.99%
Honey bee toxicity - 0.8064 80.64%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9094 90.94%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 80.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.78% 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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5352486
NPASS NPC125034