4,8-Dibromo-1,1,7-trichloro-3,7-dimethylocta-2,5-diene

Details

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Internal ID ceb8e520-f095-4f7b-820c-4d2274e3d88e
Taxonomy Organohalogen compounds > Organochlorides
IUPAC Name 4,8-dibromo-1,1,7-trichloro-3,7-dimethylocta-2,5-diene
SMILES (Canonical) CC(=CC(Cl)Cl)C(C=CC(C)(CBr)Cl)Br
SMILES (Isomeric) CC(=CC(Cl)Cl)C(C=CC(C)(CBr)Cl)Br
InChI InChI=1S/C10H13Br2Cl3/c1-7(5-9(13)14)8(12)3-4-10(2,15)6-11/h3-5,8-9H,6H2,1-2H3
InChI Key XYWJXYNATGBZQB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H13Br2Cl3
Molecular Weight 399.40 g/mol
Exact Mass 397.84291 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.45
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 4,8-Dibromo-1,1,7-trichloro-3,7-dimethylocta-2,5-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.6952 69.52%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.5306 53.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8907 89.07%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7313 73.13%
P-glycoprotein inhibitior - 0.9720 97.20%
P-glycoprotein substrate - 0.8974 89.74%
CYP3A4 substrate - 0.5093 50.93%
CYP2C9 substrate - 0.5814 58.14%
CYP2D6 substrate - 0.7947 79.47%
CYP3A4 inhibition - 0.7099 70.99%
CYP2C9 inhibition - 0.7427 74.27%
CYP2C19 inhibition - 0.6685 66.85%
CYP2D6 inhibition - 0.8787 87.87%
CYP1A2 inhibition - 0.7771 77.71%
CYP2C8 inhibition - 0.8167 81.67%
CYP inhibitory promiscuity - 0.7081 70.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6736 67.36%
Carcinogenicity (trinary) Non-required 0.4567 45.67%
Eye corrosion + 0.7974 79.74%
Eye irritation - 0.9760 97.60%
Skin irritation + 0.7264 72.64%
Skin corrosion + 0.7333 73.33%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8288 82.88%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.7432 74.32%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6700 67.00%
Acute Oral Toxicity (c) III 0.8407 84.07%
Estrogen receptor binding - 0.7582 75.82%
Androgen receptor binding - 0.7660 76.60%
Thyroid receptor binding - 0.6115 61.15%
Glucocorticoid receptor binding - 0.5657 56.57%
Aromatase binding - 0.7288 72.88%
PPAR gamma - 0.8143 81.43%
Honey bee toxicity + 0.5703 57.03%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9611 96.11%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.07% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 86.10% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.90% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.57% 89.34%
CHEMBL242 Q92731 Estrogen receptor beta 84.39% 98.35%
CHEMBL2581 P07339 Cathepsin D 83.76% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.82% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.63% 91.11%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.28% 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 72966989
LOTUS LTS0070864
wikiData Q105344716