3-Bromo-6-(4-bromo-3-chloro-4-methylcyclohexyl)-2,2,6-trimethyloxane

Details

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Internal ID b65a18e9-cc4d-44fa-80cf-7d7b234f7c8e
Taxonomy Organohalogen compounds > Alkyl halides > Cyclohexyl halides
IUPAC Name 3-bromo-6-(4-bromo-3-chloro-4-methylcyclohexyl)-2,2,6-trimethyloxane
SMILES (Canonical) CC1(C(CCC(O1)(C)C2CCC(C(C2)Cl)(C)Br)Br)C
SMILES (Isomeric) CC1(C(CCC(O1)(C)C2CCC(C(C2)Cl)(C)Br)Br)C
InChI InChI=1S/C15H25Br2ClO/c1-13(2)11(16)6-8-15(4,19-13)10-5-7-14(3,17)12(18)9-10/h10-12H,5-9H2,1-4H3
InChI Key FGWVVJIZZSRMKT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H25Br2ClO
Molecular Weight 416.60 g/mol
Exact Mass 415.99402 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 1
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 3-Bromo-6-(4-bromo-3-chloro-4-methylcyclohexyl)-2,2,6-trimethyloxane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.6932 69.32%
Blood Brain Barrier + 0.9271 92.71%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6732 67.32%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9095 90.95%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8882 88.82%
P-glycoprotein inhibitior - 0.8434 84.34%
P-glycoprotein substrate - 0.8845 88.45%
CYP3A4 substrate + 0.6204 62.04%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.7510 75.10%
CYP3A4 inhibition - 0.8946 89.46%
CYP2C9 inhibition - 0.5868 58.68%
CYP2C19 inhibition - 0.6317 63.17%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.8058 80.58%
CYP2C8 inhibition - 0.7686 76.86%
CYP inhibitory promiscuity - 0.6455 64.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7623 76.23%
Carcinogenicity (trinary) Non-required 0.6234 62.34%
Eye corrosion - 0.9245 92.45%
Eye irritation - 0.8953 89.53%
Skin irritation - 0.7191 71.91%
Skin corrosion - 0.9210 92.10%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5364 53.64%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5283 52.83%
skin sensitisation - 0.6201 62.01%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.8965 89.65%
Acute Oral Toxicity (c) III 0.5292 52.92%
Estrogen receptor binding + 0.6894 68.94%
Androgen receptor binding - 0.6456 64.56%
Thyroid receptor binding + 0.7300 73.00%
Glucocorticoid receptor binding + 0.8251 82.51%
Aromatase binding + 0.5852 58.52%
PPAR gamma - 0.5782 57.82%
Honey bee toxicity - 0.6928 69.28%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9714 97.14%

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 96.66% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.98% 96.61%
CHEMBL204 P00734 Thrombin 90.88% 96.01%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.00% 97.09%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 87.50% 88.84%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.85% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.08% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.81% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.71% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.56% 97.14%
CHEMBL259 P32245 Melanocortin receptor 4 80.43% 95.38%

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 73999905
LOTUS LTS0233093
wikiData Q105155121