1-Chloro-3-(chloromethyl)-7-methylocta-2,6-diene

Details

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Internal ID 5f7fd247-88a9-4cbd-839a-ec0d44d5850a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 1-chloro-3-(chloromethyl)-7-methylocta-2,6-diene
SMILES (Canonical) CC(=CCCC(=CCCl)CCl)C
SMILES (Isomeric) CC(=CCCC(=CCCl)CCl)C
InChI InChI=1S/C10H16Cl2/c1-9(2)4-3-5-10(8-12)6-7-11/h4,6H,3,5,7-8H2,1-2H3
InChI Key RUYDNRFMMYEACM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16Cl2
Molecular Weight 207.14 g/mol
Exact Mass 206.0629059 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.14
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Chloro-3-(chloromethyl)-7-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 + 0.9850 98.50%
Caco-2 + 0.8325 83.25%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4494 44.94%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7914 79.14%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.9208 92.08%
CYP3A4 substrate - 0.5922 59.22%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate - 0.7574 75.74%
CYP3A4 inhibition - 0.9709 97.09%
CYP2C9 inhibition - 0.8894 88.94%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition - 0.7161 71.61%
CYP2C8 inhibition - 0.9704 97.04%
CYP inhibitory promiscuity - 0.7950 79.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5213 52.13%
Carcinogenicity (trinary) Non-required 0.4238 42.38%
Eye corrosion + 0.8138 81.38%
Eye irritation - 0.5178 51.78%
Skin irritation + 0.7511 75.11%
Skin corrosion - 0.6362 63.62%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5586 55.86%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.8260 82.60%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.7747 77.47%
Acute Oral Toxicity (c) III 0.7325 73.25%
Estrogen receptor binding - 0.8843 88.43%
Androgen receptor binding - 0.9213 92.13%
Thyroid receptor binding - 0.8448 84.48%
Glucocorticoid receptor binding - 0.7011 70.11%
Aromatase binding - 0.8543 85.43%
PPAR gamma - 0.6531 65.31%
Honey bee toxicity - 0.8426 84.26%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9834 98.34%

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 84.59% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 83.63% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.43% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.40% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.20% 96.95%
CHEMBL2581 P07339 Cathepsin D 81.59% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.34% 92.08%

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 72725967
LOTUS LTS0054834
wikiData Q105245885