2-Bromo-1-bromomethyl-1,4-dichloro-5-chloroethenyl-5-methylcyclohexane

Details

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Internal ID 2a1fb337-a594-4156-a0bd-bbedaa389c0e
Taxonomy Organohalogen compounds > Alkyl halides > Cyclohexyl halides
IUPAC Name 2-bromo-1-(bromomethyl)-1,4-dichloro-5-(2-chloroethenyl)-5-methylcyclohexane
SMILES (Canonical) CC1(CC(C(CC1Cl)Br)(CBr)Cl)C=CCl
SMILES (Isomeric) CC1(CC(C(CC1Cl)Br)(CBr)Cl)C=CCl
InChI InChI=1S/C10H13Br2Cl3/c1-9(2-3-13)5-10(15,6-11)7(12)4-8(9)14/h2-3,7-8H,4-6H2,1H3
InChI Key MMMYYEWTEBVZHZ-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 5.20
Atomic LogP (AlogP) 5.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Bromo-1-bromomethyl-1,4-dichloro-5-chloroethenyl-5-methylcyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.6663 66.63%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4733 47.33%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8912 89.12%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8113 81.13%
P-glycoprotein inhibitior - 0.9490 94.90%
P-glycoprotein substrate - 0.8435 84.35%
CYP3A4 substrate + 0.5512 55.12%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.5956 59.56%
CYP2C9 inhibition - 0.7058 70.58%
CYP2C19 inhibition - 0.6125 61.25%
CYP2D6 inhibition - 0.8735 87.35%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8240 82.40%
CYP inhibitory promiscuity - 0.5803 58.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5352 53.52%
Carcinogenicity (trinary) Non-required 0.6077 60.77%
Eye corrosion + 0.6326 63.26%
Eye irritation - 0.9642 96.42%
Skin irritation + 0.5700 57.00%
Skin corrosion + 0.5922 59.22%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8062 80.62%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.7257 72.57%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7821 78.21%
Acute Oral Toxicity (c) III 0.6598 65.98%
Estrogen receptor binding - 0.7956 79.56%
Androgen receptor binding - 0.6152 61.52%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6027 60.27%
Aromatase binding - 0.7071 70.71%
PPAR gamma - 0.7175 71.75%
Honey bee toxicity - 0.5236 52.36%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6700 67.00%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.30% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 96.08% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 94.56% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 94.05% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 88.60% 95.69%
CHEMBL301 P24941 Cyclin-dependent kinase 2 86.99% 91.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.84% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 84.53% 97.79%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.45% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.40% 91.11%

Plants that contains it

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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.
Tragopogon porrifolius

Cross-Links

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PubChem 74051228
LOTUS LTS0139766
wikiData Q105171975