2,4,6-Trimethyl-1,3,6-heptatriene

Details

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Internal ID 8fedbb5f-ed28-4517-a5ce-e997812f4b3f
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (3E)-2,4,6-trimethylhepta-1,3,6-triene
SMILES (Canonical) CC(=C)CC(=CC(=C)C)C
SMILES (Isomeric) CC(=C)C/C(=C/C(=C)C)/C
InChI InChI=1S/C10H16/c1-8(2)6-10(5)7-9(3)4/h6H,1,3,7H2,2,4-5H3/b10-6+
InChI Key ZHGQAJFRWAXWEK-UXBLZVDNSA-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 4.70
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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24648-33-7
(3E)-2,4,6-trimethylhepta-1,3,6-triene
2,4,6-Trimethyl-1,3,6-heptadiene
NSC157588
ZHGQAJFRWAXWEK-UXBLZVDNSA-N
AKOS006274072
NSC-157588
(3E)-2,4,6-Trimethyl-1,3,6-heptatriene #

2D Structure

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2D Structure of 2,4,6-Trimethyl-1,3,6-heptatriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.8653 86.53%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Nucleus 0.4747 47.47%
OATP2B1 inhibitior - 0.8652 86.52%
OATP1B1 inhibitior + 0.9291 92.91%
OATP1B3 inhibitior + 0.9413 94.13%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9440 94.40%
P-glycoprotein inhibitior - 0.9713 97.13%
P-glycoprotein substrate - 0.9318 93.18%
CYP3A4 substrate - 0.6540 65.40%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.8902 89.02%
CYP2C9 inhibition - 0.9129 91.29%
CYP2C19 inhibition - 0.8836 88.36%
CYP2D6 inhibition - 0.9180 91.80%
CYP1A2 inhibition - 0.8122 81.22%
CYP2C8 inhibition - 0.9883 98.83%
CYP inhibitory promiscuity - 0.6671 66.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6783 67.83%
Carcinogenicity (trinary) Warning 0.5790 57.90%
Eye corrosion + 0.8812 88.12%
Eye irritation + 0.9703 97.03%
Skin irritation + 0.7874 78.74%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7393 73.93%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.9188 91.88%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.6090 60.90%
Acute Oral Toxicity (c) III 0.7632 76.32%
Estrogen receptor binding - 0.9082 90.82%
Androgen receptor binding - 0.9029 90.29%
Thyroid receptor binding - 0.7878 78.78%
Glucocorticoid receptor binding - 0.8679 86.79%
Aromatase binding - 0.7296 72.96%
PPAR gamma - 0.8245 82.45%
Honey bee toxicity - 0.8564 85.64%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity + 0.9586 95.86%

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 93.11% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.59% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 5368777
NPASS NPC28933