(3E,5R,6R,7E)-1,1,8-tribromo-5,6-dichloro-2,6-dimethylocta-1,3,7-triene

Details

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Internal ID 7963891c-702e-4920-b942-ff521fde6f5c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ketene acetals
IUPAC Name (3E,5R,6R,7E)-1,1,8-tribromo-5,6-dichloro-2,6-dimethylocta-1,3,7-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H11Br3Cl2/c1-7(9(12)13)3-4-8(14)10(2,15)5-6-11/h3-6,8H,1-2H3/b4-3+,6-5+/t8-,10-/m1/s1
InChI Key KFRMUOXPJSGGJS-ARGRFEAMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H11Br3Cl2
Molecular Weight 441.80 g/mol
Exact Mass 439.77674 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.08
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,5R,6R,7E)-1,1,8-tribromo-5,6-dichloro-2,6-dimethylocta-1,3,7-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.6130 61.30%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.6038 60.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5604 56.04%
P-glycoprotein inhibitior - 0.9461 94.61%
P-glycoprotein substrate - 0.8807 88.07%
CYP3A4 substrate - 0.5275 52.75%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8100 81.00%
CYP3A4 inhibition - 0.6870 68.70%
CYP2C9 inhibition - 0.7070 70.70%
CYP2C19 inhibition - 0.6639 66.39%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition - 0.7941 79.41%
CYP2C8 inhibition - 0.8667 86.67%
CYP inhibitory promiscuity - 0.7231 72.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7217 72.17%
Carcinogenicity (trinary) Non-required 0.4966 49.66%
Eye corrosion - 0.5633 56.33%
Eye irritation - 0.6662 66.62%
Skin irritation + 0.7218 72.18%
Skin corrosion + 0.6038 60.38%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6184 61.84%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7802 78.02%
skin sensitisation + 0.7608 76.08%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.7319 73.19%
Nephrotoxicity + 0.7163 71.63%
Acute Oral Toxicity (c) III 0.7793 77.93%
Estrogen receptor binding - 0.5719 57.19%
Androgen receptor binding - 0.8825 88.25%
Thyroid receptor binding + 0.5975 59.75%
Glucocorticoid receptor binding + 0.6019 60.19%
Aromatase binding - 0.6656 66.56%
PPAR gamma - 0.5911 59.11%
Honey bee toxicity - 0.5632 56.32%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9404 94.04%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.85% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.58% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 84.84% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.90% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.02% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 82.12% 92.51%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.36% 97.29%

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 23247408
LOTUS LTS0158513
wikiData Q105140527