(3S,6Z)-8-chloro-6-(chloromethyl)-3-methoxy-2-methylocta-1,6-diene

Details

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Internal ID 1cffb0a6-4df8-4367-93c9-b0a81ececc86
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name (3S,6Z)-8-chloro-6-(chloromethyl)-3-methoxy-2-methylocta-1,6-diene
SMILES (Canonical) CC(=C)C(CCC(=CCCl)CCl)OC
SMILES (Isomeric) CC(=C)[C@H](CC/C(=C/CCl)/CCl)OC
InChI InChI=1S/C11H18Cl2O/c1-9(2)11(14-3)5-4-10(8-13)6-7-12/h6,11H,1,4-5,7-8H2,2-3H3/b10-6-/t11-/m0/s1
InChI Key BEFGZSRQCOTMHP-YAEJEKNGSA-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 3.70
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 (3S,6Z)-8-chloro-6-(chloromethyl)-3-methoxy-2-methylocta-1,6-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.4891 48.91%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5591 55.91%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9170 91.70%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8810 88.10%
P-glycoprotein inhibitior - 0.9489 94.89%
P-glycoprotein substrate - 0.7838 78.38%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9259 92.59%
CYP2C9 inhibition - 0.9177 91.77%
CYP2C19 inhibition - 0.7523 75.23%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition - 0.6992 69.92%
CYP2C8 inhibition - 0.9497 94.97%
CYP inhibitory promiscuity - 0.8138 81.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5049 50.49%
Carcinogenicity (trinary) Non-required 0.6450 64.50%
Eye corrosion + 0.4797 47.97%
Eye irritation - 0.8832 88.32%
Skin irritation - 0.5902 59.02%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4770 47.70%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.6355 63.55%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.7863 78.63%
Acute Oral Toxicity (c) III 0.6654 66.54%
Estrogen receptor binding - 0.8283 82.83%
Androgen receptor binding - 0.8285 82.85%
Thyroid receptor binding - 0.7929 79.29%
Glucocorticoid receptor binding - 0.6365 63.65%
Aromatase binding - 0.7933 79.33%
PPAR gamma - 0.6471 64.71%
Honey bee toxicity + 0.6067 60.67%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8542 85.42%

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 90.85% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.87% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.36% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 84.62% 91.49%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.16% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.55% 99.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.01% 92.29%

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 14486219
LOTUS LTS0114804
wikiData Q104932787