Heptan-2-one, 3,3-dibromo-1-iodo-

Details

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Internal ID 99f2de61-366d-4f0e-9960-f294b6b0a795
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-haloketones
IUPAC Name 3,3-dibromo-1-iodoheptan-2-one
SMILES (Canonical) CCCCC(C(=O)CI)(Br)Br
SMILES (Isomeric) CCCCC(C(=O)CI)(Br)Br
InChI InChI=1S/C7H11Br2IO/c1-2-3-4-7(8,9)6(11)5-10/h2-5H2,1H3
InChI Key JJBPIIXVRZGUKZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C7H11Br2IO
Molecular Weight 397.87 g/mol
Exact Mass 397.82009 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Heptan-2-one, 3,3-dibromo-1-iodo-
3,3-dibromo-1-iodo-heptan-2-one
DTXSID50203387
1-iodo-3,3-dibromo-2-heptanone

2D Structure

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2D Structure of Heptan-2-one, 3,3-dibromo-1-iodo-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9854 98.54%
Caco-2 + 0.8497 84.97%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6968 69.68%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.8571 85.71%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9101 91.01%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.9130 91.30%
CYP3A4 substrate - 0.6595 65.95%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7839 78.39%
CYP3A4 inhibition - 0.9247 92.47%
CYP2C9 inhibition - 0.8151 81.51%
CYP2C19 inhibition - 0.8368 83.68%
CYP2D6 inhibition - 0.9042 90.42%
CYP1A2 inhibition + 0.7506 75.06%
CYP2C8 inhibition - 0.9369 93.69%
CYP inhibitory promiscuity - 0.8549 85.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5011 50.11%
Carcinogenicity (trinary) Non-required 0.7161 71.61%
Eye corrosion + 0.9362 93.62%
Eye irritation + 0.9245 92.45%
Skin irritation + 0.5568 55.68%
Skin corrosion - 0.6063 60.63%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6997 69.97%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.7556 75.56%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5964 59.64%
Acute Oral Toxicity (c) III 0.6523 65.23%
Estrogen receptor binding - 0.9380 93.80%
Androgen receptor binding - 0.7362 73.62%
Thyroid receptor binding - 0.7692 76.92%
Glucocorticoid receptor binding - 0.8836 88.36%
Aromatase binding - 0.9062 90.62%
PPAR gamma - 0.8459 84.59%
Honey bee toxicity - 0.9945 99.45%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5268 52.68%
Fish aquatic toxicity + 0.9052 90.52%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.78% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.34% 85.94%
CHEMBL2581 P07339 Cathepsin D 94.05% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.18% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 85.64% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.44% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.11% 96.95%

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 185779
LOTUS LTS0254961
wikiData Q83076764