3-(Bromomethyl)-2,3,6-trichloro-7-methylocta-1,6-diene

Details

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Internal ID 5ae02303-0459-4ccf-93af-71825872b460
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 3-(bromomethyl)-2,3,6-trichloro-7-methylocta-1,6-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14BrCl3/c1-7(2)9(13)4-5-10(14,6-11)8(3)12/h3-6H2,1-2H3
InChI Key IVWLPIDLFZKNHM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14BrCl3
Molecular Weight 320.50 g/mol
Exact Mass 317.93445 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.42
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 3-(Bromomethyl)-2,3,6-trichloro-7-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 + 0.9833 98.33%
Caco-2 + 0.7951 79.51%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5532 55.32%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9110 91.10%
OATP1B3 inhibitior + 0.9370 93.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5960 59.60%
P-glycoprotein inhibitior - 0.9561 95.61%
P-glycoprotein substrate - 0.8573 85.73%
CYP3A4 substrate - 0.5355 53.55%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.7701 77.01%
CYP3A4 inhibition - 0.8884 88.84%
CYP2C9 inhibition - 0.7912 79.12%
CYP2C19 inhibition - 0.7111 71.11%
CYP2D6 inhibition - 0.8917 89.17%
CYP1A2 inhibition - 0.6914 69.14%
CYP2C8 inhibition - 0.9001 90.01%
CYP inhibitory promiscuity - 0.7463 74.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5053 50.53%
Carcinogenicity (trinary) Non-required 0.5001 50.01%
Eye corrosion + 0.5293 52.93%
Eye irritation + 0.7355 73.55%
Skin irritation + 0.6128 61.28%
Skin corrosion - 0.7521 75.21%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5300 53.00%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6451 64.51%
skin sensitisation + 0.7571 75.71%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7289 72.89%
Nephrotoxicity + 0.6107 61.07%
Acute Oral Toxicity (c) III 0.7416 74.16%
Estrogen receptor binding - 0.7919 79.19%
Androgen receptor binding - 0.7583 75.83%
Thyroid receptor binding - 0.5801 58.01%
Glucocorticoid receptor binding - 0.5161 51.61%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6525 65.25%
Honey bee toxicity - 0.8334 83.34%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9925 99.25%

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
CHEMBL240 Q12809 HERG 95.64% 89.76%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.55% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.85% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.63% 96.09%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 82.27% 94.01%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.92% 91.11%
CHEMBL206 P03372 Estrogen receptor alpha 81.29% 97.64%
CHEMBL2581 P07339 Cathepsin D 80.39% 98.95%

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 4554
LOTUS LTS0272482
wikiData Q105121352