(1E,3R,4S,5E,7R)-1,8-dibromo-3,4,7-trichloro-3,7-dimethylocta-1,5-diene

Details

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Internal ID 540aaf5a-e1db-49da-8b17-868283546e27
Taxonomy Organohalogen compounds > Vinyl halides > Vinyl bromides
IUPAC Name (1E,3R,4S,5E,7R)-1,8-dibromo-3,4,7-trichloro-3,7-dimethylocta-1,5-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13Br2Cl3/c1-9(14,7-12)4-3-8(13)10(2,15)5-6-11/h3-6,8H,7H2,1-2H3/b4-3+,6-5+/t8-,9+,10+/m0/s1
InChI Key XSMHHESOHBEVBV-MPMRZOORSA-N
Popularity 2 references 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 4.50
Atomic LogP (AlogP) 5.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1E,3R,4S,5E,7R)-1,8-dibromo-3,4,7-trichloro-3,7-dimethylocta-1,5-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.7735 77.35%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4932 49.32%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6882 68.82%
P-glycoprotein inhibitior - 0.9456 94.56%
P-glycoprotein substrate - 0.8754 87.54%
CYP3A4 substrate - 0.5462 54.62%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition - 0.7829 78.29%
CYP2C9 inhibition - 0.7984 79.84%
CYP2C19 inhibition - 0.6697 66.97%
CYP2D6 inhibition - 0.8947 89.47%
CYP1A2 inhibition - 0.7274 72.74%
CYP2C8 inhibition - 0.8766 87.66%
CYP inhibitory promiscuity - 0.7936 79.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6836 68.36%
Carcinogenicity (trinary) Non-required 0.5412 54.12%
Eye corrosion + 0.9227 92.27%
Eye irritation - 0.9039 90.39%
Skin irritation + 0.8162 81.62%
Skin corrosion + 0.6355 63.55%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5863 58.63%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7262 72.62%
skin sensitisation + 0.7647 76.47%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6744 67.44%
Acute Oral Toxicity (c) III 0.8335 83.35%
Estrogen receptor binding - 0.6897 68.97%
Androgen receptor binding - 0.9044 90.44%
Thyroid receptor binding - 0.5803 58.03%
Glucocorticoid receptor binding + 0.5984 59.84%
Aromatase binding - 0.7415 74.15%
PPAR gamma - 0.7849 78.49%
Honey bee toxicity - 0.4750 47.50%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9408 94.08%

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 94.39% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.38% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.20% 96.77%
CHEMBL2581 P07339 Cathepsin D 83.77% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.08% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 80.74% 93.31%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.37% 97.23%

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 163009442
LOTUS LTS0138198
wikiData Q105341095