2-Bromo-1,4-dichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

Details

Top
Internal ID 67b970e7-3dc8-4f5d-a41c-c34484dab839
Taxonomy Organohalogen compounds > Alkyl halides > Cyclohexyl halides
IUPAC Name 2-bromo-1,4-dichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane
SMILES (Canonical) CC1(CC(C(CC1Cl)Br)(C)Cl)C=CCl
SMILES (Isomeric) CC1(CC(C(CC1Cl)Br)(C)Cl)C=CCl
InChI InChI=1S/C10H14BrCl3/c1-9(3-4-12)6-10(2,14)7(11)5-8(9)13/h3-4,7-8H,5-6H2,1-2H3
InChI Key ZXRVNNDUSZKNEH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14BrCl3
Molecular Weight 320.50 g/mol
Exact Mass 317.93445 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.91
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Bromo-1,4-dichloro-5-(2-chloroethenyl)-1,5-dimethylcyclohexane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.7139 71.39%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5318 53.18%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8893 88.93%
P-glycoprotein inhibitior - 0.9482 94.82%
P-glycoprotein substrate - 0.9258 92.58%
CYP3A4 substrate + 0.5492 54.92%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.6314 63.14%
CYP2C9 inhibition - 0.7111 71.11%
CYP2C19 inhibition - 0.6959 69.59%
CYP2D6 inhibition - 0.8879 88.79%
CYP1A2 inhibition - 0.6943 69.43%
CYP2C8 inhibition - 0.8888 88.88%
CYP inhibitory promiscuity - 0.6872 68.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5471 54.71%
Carcinogenicity (trinary) Non-required 0.6178 61.78%
Eye corrosion + 0.5280 52.80%
Eye irritation - 0.9352 93.52%
Skin irritation + 0.5574 55.74%
Skin corrosion - 0.8128 81.28%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5181 51.81%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.8196 81.96%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7145 71.45%
Mitochondrial toxicity - 0.6713 67.13%
Nephrotoxicity + 0.8269 82.69%
Acute Oral Toxicity (c) III 0.6253 62.53%
Estrogen receptor binding - 0.8728 87.28%
Androgen receptor binding - 0.5900 59.00%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6065 60.65%
Aromatase binding - 0.8388 83.88%
PPAR gamma - 0.7226 72.26%
Honey bee toxicity + 0.6283 62.83%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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
CHEMBL284 P27487 Dipeptidyl peptidase IV 95.49% 95.69%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.70% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.65% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.88% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.37% 90.17%
CHEMBL1937 Q92769 Histone deacetylase 2 85.93% 94.75%
CHEMBL301 P24941 Cyclin-dependent kinase 2 85.70% 91.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.39% 85.30%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.14% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.49% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.89% 95.56%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 74051225
LOTUS LTS0255311
wikiData Q105385743