4-Bromo-6-chloro-1-ethenyl-5,5-dimethylcyclohexene

Details

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Internal ID 8616fda5-2fa1-47fb-ab74-d1b4220a1a2d
Taxonomy Organohalogen compounds > Organochlorides
IUPAC Name 4-bromo-6-chloro-1-ethenyl-5,5-dimethylcyclohexene
SMILES (Canonical) CC1(C(CC=C(C1Cl)C=C)Br)C
SMILES (Isomeric) CC1(C(CC=C(C1Cl)C=C)Br)C
InChI InChI=1S/C10H14BrCl/c1-4-7-5-6-8(11)10(2,3)9(7)12/h4-5,8-9H,1,6H2,2-3H3
InChI Key OJGKICRNORIFDM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14BrCl
Molecular Weight 249.57 g/mol
Exact Mass 247.99674 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL139535
NSC-692988

2D Structure

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2D Structure of 4-Bromo-6-chloro-1-ethenyl-5,5-dimethylcyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.8106 81.06%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5878 58.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9216 92.16%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8854 88.54%
P-glycoprotein inhibitior - 0.9582 95.82%
P-glycoprotein substrate - 0.9541 95.41%
CYP3A4 substrate - 0.5110 51.10%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.7973 79.73%
CYP3A4 inhibition - 0.6890 68.90%
CYP2C9 inhibition - 0.5890 58.90%
CYP2C19 inhibition - 0.5671 56.71%
CYP2D6 inhibition - 0.8950 89.50%
CYP1A2 inhibition - 0.7559 75.59%
CYP2C8 inhibition - 0.9014 90.14%
CYP inhibitory promiscuity - 0.5832 58.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5252 52.52%
Carcinogenicity (trinary) Non-required 0.6446 64.46%
Eye corrosion - 0.5900 59.00%
Eye irritation + 0.8692 86.92%
Skin irritation + 0.6214 62.14%
Skin corrosion - 0.6794 67.94%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5759 57.59%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.7779 77.79%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.7933 79.33%
Nephrotoxicity + 0.7294 72.94%
Acute Oral Toxicity (c) III 0.7724 77.24%
Estrogen receptor binding - 0.7220 72.20%
Androgen receptor binding - 0.7462 74.62%
Thyroid receptor binding - 0.7261 72.61%
Glucocorticoid receptor binding - 0.5823 58.23%
Aromatase binding - 0.9429 94.29%
PPAR gamma - 0.5944 59.44%
Honey bee toxicity - 0.5229 52.29%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7300 73.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.99% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.92% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.97% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 84.81% 94.75%
CHEMBL221 P23219 Cyclooxygenase-1 82.92% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.36% 97.25%
CHEMBL240 Q12809 HERG 80.60% 89.76%
CHEMBL4208 P20618 Proteasome component C5 80.50% 90.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.13% 89.34%

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 392488
LOTUS LTS0234753
wikiData Q105193072