6-(Chloromethyl)-8-methoxy-2-methylocta-1,6-dien-3-ol

Details

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Internal ID 5dd0cb06-7b1a-453b-ba31-57e7b5a504aa
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 6-(chloromethyl)-8-methoxy-2-methylocta-1,6-dien-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H19ClO2/c1-9(2)11(13)5-4-10(8-12)6-7-14-3/h6,11,13H,1,4-5,7-8H2,2-3H3
InChI Key ORTLPYMSRXBBBT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H19ClO2
Molecular Weight 218.72 g/mol
Exact Mass 218.1073575 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(Chloromethyl)-8-methoxy-2-methylocta-1,6-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.7870 78.70%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5633 56.33%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9290 92.90%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8464 84.64%
P-glycoprotein inhibitior - 0.9647 96.47%
P-glycoprotein substrate - 0.8128 81.28%
CYP3A4 substrate + 0.5324 53.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7324 73.24%
CYP3A4 inhibition - 0.8417 84.17%
CYP2C9 inhibition - 0.9151 91.51%
CYP2C19 inhibition - 0.7910 79.10%
CYP2D6 inhibition - 0.9227 92.27%
CYP1A2 inhibition - 0.7571 75.71%
CYP2C8 inhibition - 0.8933 89.33%
CYP inhibitory promiscuity - 0.9568 95.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5751 57.51%
Carcinogenicity (trinary) Non-required 0.6805 68.05%
Eye corrosion - 0.7032 70.32%
Eye irritation - 0.7211 72.11%
Skin irritation - 0.7333 73.33%
Skin corrosion - 0.9243 92.43%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5056 50.56%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.6701 67.01%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7484 74.84%
Acute Oral Toxicity (c) III 0.6287 62.87%
Estrogen receptor binding - 0.8367 83.67%
Androgen receptor binding - 0.8946 89.46%
Thyroid receptor binding - 0.8132 81.32%
Glucocorticoid receptor binding - 0.4738 47.38%
Aromatase binding - 0.8976 89.76%
PPAR gamma - 0.6539 65.39%
Honey bee toxicity - 0.6669 66.69%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7599 75.99%

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 94.18% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.59% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.24% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.69% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.47% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.05% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 82.61% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.07% 97.25%

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 72740292
LOTUS LTS0007402
wikiData Q105198435