4-Bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

Details

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Internal ID 343c10ac-ebb9-419b-9a11-2b2cbfac29e0
Taxonomy Organohalogen compounds > Organochlorides
IUPAC Name 4-bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane
SMILES (Canonical) CC1(C(CC(C(=CCCl)C1Cl)Br)Cl)C
SMILES (Isomeric) CC1(C(CC(C(=CCCl)C1Cl)Br)Cl)C
InChI InChI=1S/C10H14BrCl3/c1-10(2)8(13)5-7(11)6(3-4-12)9(10)14/h3,7-9H,4-5H2,1-2H3
InChI Key LYWCAYROTMXQAJ-UHFFFAOYSA-N
Popularity 1 reference 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 3.90
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Bromo-2,6-dichloro-3-(2-chloroethylidene)-1,1-dimethylcyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.6490 64.90%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4991 49.91%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8790 87.90%
OATP1B3 inhibitior + 0.9082 90.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8650 86.50%
P-glycoprotein inhibitior - 0.9399 93.99%
P-glycoprotein substrate - 0.8785 87.85%
CYP3A4 substrate + 0.5418 54.18%
CYP2C9 substrate - 0.5957 59.57%
CYP2D6 substrate - 0.7825 78.25%
CYP3A4 inhibition - 0.8279 82.79%
CYP2C9 inhibition - 0.6152 61.52%
CYP2C19 inhibition - 0.5598 55.98%
CYP2D6 inhibition - 0.8812 88.12%
CYP1A2 inhibition - 0.7077 70.77%
CYP2C8 inhibition - 0.7928 79.28%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5352 53.52%
Carcinogenicity (trinary) Non-required 0.6225 62.25%
Eye corrosion - 0.5988 59.88%
Eye irritation + 0.6276 62.76%
Skin irritation + 0.5746 57.46%
Skin corrosion + 0.5500 55.00%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6660 66.60%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.7440 74.40%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7539 75.39%
Nephrotoxicity + 0.6510 65.10%
Acute Oral Toxicity (c) III 0.6100 61.00%
Estrogen receptor binding - 0.7251 72.51%
Androgen receptor binding - 0.7407 74.07%
Thyroid receptor binding - 0.6792 67.92%
Glucocorticoid receptor binding - 0.6151 61.51%
Aromatase binding - 0.8698 86.98%
PPAR gamma - 0.7061 70.61%
Honey bee toxicity - 0.6907 69.07%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.61% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.49% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 89.65% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.57% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.18% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 85.81% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 82.88% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.66% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.55% 94.45%

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 392487
LOTUS LTS0032432
wikiData Q105159634