(E,3R,4R,6R,7S)-1,7-dibromo-4,8-dichloro-3,7-dimethyloct-1-ene-3,6-diol

Details

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Internal ID 6378f6f9-7923-4f46-a286-bf9bd03e24fd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (E,3R,4R,6R,7S)-1,7-dibromo-4,8-dichloro-3,7-dimethyloct-1-ene-3,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16Br2Cl2O2/c1-9(12,6-13)8(15)5-7(14)10(2,16)3-4-11/h3-4,7-8,15-16H,5-6H2,1-2H3/b4-3+/t7-,8-,9-,10-/m1/s1
InChI Key BNEHRLDXDDBGIG-ZCFOMSGHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16Br2Cl2O2
Molecular Weight 398.94 g/mol
Exact Mass 397.88736 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,3R,4R,6R,7S)-1,7-dibromo-4,8-dichloro-3,7-dimethyloct-1-ene-3,6-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.6621 66.21%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7012 70.12%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9128 91.28%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6876 68.76%
P-glycoprotein inhibitior - 0.9400 94.00%
P-glycoprotein substrate - 0.8691 86.91%
CYP3A4 substrate - 0.5473 54.73%
CYP2C9 substrate - 0.8103 81.03%
CYP2D6 substrate - 0.7758 77.58%
CYP3A4 inhibition - 0.7392 73.92%
CYP2C9 inhibition - 0.7590 75.90%
CYP2C19 inhibition - 0.6199 61.99%
CYP2D6 inhibition - 0.8702 87.02%
CYP1A2 inhibition - 0.7129 71.29%
CYP2C8 inhibition - 0.8332 83.32%
CYP inhibitory promiscuity - 0.8374 83.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.6021 60.21%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.7426 74.26%
Eye irritation - 0.9882 98.82%
Skin irritation - 0.5121 51.21%
Skin corrosion - 0.6845 68.45%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6048 60.48%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6868 68.68%
skin sensitisation + 0.7212 72.12%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5564 55.64%
Acute Oral Toxicity (c) III 0.8286 82.86%
Estrogen receptor binding + 0.5413 54.13%
Androgen receptor binding - 0.8455 84.55%
Thyroid receptor binding + 0.5702 57.02%
Glucocorticoid receptor binding + 0.5506 55.06%
Aromatase binding - 0.7154 71.54%
PPAR gamma - 0.6153 61.53%
Honey bee toxicity - 0.8361 83.61%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8409 84.09%

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 92.69% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 92.06% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.29% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.82% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.15% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.73% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 80.41% 93.31%

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 101205293
LOTUS LTS0202019
wikiData Q104938746