8-Bromo-1,3,4,7-tetrachloro-3,7-dimethylocta-1,5-diene

Details

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Internal ID c3152cc5-e212-4294-a622-d0352652a130
Taxonomy Organohalogen compounds > Vinyl halides > Vinyl chlorides
IUPAC Name 8-bromo-1,3,4,7-tetrachloro-3,7-dimethylocta-1,5-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13BrCl4/c1-9(14,7-11)4-3-8(13)10(2,15)5-6-12/h3-6,8H,7H2,1-2H3
InChI Key JQUYRIQWDHGFCY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13BrCl4
Molecular Weight 354.90 g/mol
Exact Mass 353.89252 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.29
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 8-Bromo-1,3,4,7-tetrachloro-3,7-dimethylocta-1,5-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.8283 82.83%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.4932 49.32%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.8958 89.58%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6635 66.35%
P-glycoprotein inhibitior - 0.9490 94.90%
P-glycoprotein substrate - 0.8793 87.93%
CYP3A4 substrate - 0.5431 54.31%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.8051 80.51%
CYP3A4 inhibition - 0.7829 78.29%
CYP2C9 inhibition - 0.7984 79.84%
CYP2C19 inhibition - 0.6697 66.97%
CYP2D6 inhibition - 0.8947 89.47%
CYP1A2 inhibition - 0.7274 72.74%
CYP2C8 inhibition - 0.8440 84.40%
CYP inhibitory promiscuity - 0.7936 79.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6836 68.36%
Carcinogenicity (trinary) Non-required 0.5412 54.12%
Eye corrosion + 0.9227 92.27%
Eye irritation - 0.8970 89.70%
Skin irritation + 0.8162 81.62%
Skin corrosion + 0.6355 63.55%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6269 62.69%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.7647 76.47%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6957 69.57%
Acute Oral Toxicity (c) III 0.8335 83.35%
Estrogen receptor binding - 0.6617 66.17%
Androgen receptor binding - 0.8857 88.57%
Thyroid receptor binding - 0.5397 53.97%
Glucocorticoid receptor binding + 0.5541 55.41%
Aromatase binding - 0.6979 69.79%
PPAR gamma - 0.7764 77.64%
Honey bee toxicity + 0.6469 64.69%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9408 94.08%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 96.42% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.93% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 83.81% 94.73%
CHEMBL2581 P07339 Cathepsin D 83.35% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 82.64% 87.45%
CHEMBL1907 P15144 Aminopeptidase N 82.20% 93.31%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.90% 97.23%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.39% 92.29%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.65% 92.88%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.46% 96.09%

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 135526
LOTUS LTS0191514
wikiData Q105133701