8-Chloro-6-(chloromethyl)-1-methoxy-2-methylocta-2,6-diene

Details

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Internal ID 3056e5d3-fd69-4c29-b65e-8f0a53e587e2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 8-chloro-6-(chloromethyl)-1-methoxy-2-methylocta-2,6-diene
SMILES (Canonical) CC(=CCCC(=CCCl)CCl)COC
SMILES (Isomeric) CC(=CCCC(=CCCl)CCl)COC
InChI InChI=1S/C11H18Cl2O/c1-10(9-14-2)4-3-5-11(8-13)6-7-12/h4,6H,3,5,7-9H2,1-2H3
InChI Key AVDWIYGWRDQSPX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18Cl2O
Molecular Weight 237.16 g/mol
Exact Mass 236.0734706 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Chloro-6-(chloromethyl)-1-methoxy-2-methylocta-2,6-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.8804 88.04%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.5440 54.40%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9186 91.86%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6547 65.47%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.8272 82.72%
CYP3A4 substrate + 0.5150 51.50%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9744 97.44%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.8178 81.78%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.7500 75.00%
CYP2C8 inhibition - 0.8263 82.63%
CYP inhibitory promiscuity - 0.8924 89.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5751 57.51%
Carcinogenicity (trinary) Danger 0.4235 42.35%
Eye corrosion + 0.5372 53.72%
Eye irritation - 0.5624 56.24%
Skin irritation - 0.5924 59.24%
Skin corrosion - 0.8855 88.55%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4463 44.63%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.7684 76.84%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.8257 82.57%
Acute Oral Toxicity (c) III 0.6458 64.58%
Estrogen receptor binding - 0.8066 80.66%
Androgen receptor binding - 0.8777 87.77%
Thyroid receptor binding - 0.7789 77.89%
Glucocorticoid receptor binding - 0.4924 49.24%
Aromatase binding - 0.7738 77.38%
PPAR gamma - 0.6860 68.60%
Honey bee toxicity - 0.7501 75.01%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9303 93.03%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL2664 P23526 Adenosylhomocysteinase 88.72% 86.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.38% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.52% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.34% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.92% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 72732361
LOTUS LTS0088851
wikiData Q104919381