1,1-Dibromo-3-iodopropan-2-one

Details

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Internal ID ccaa94db-4c11-4a57-8e59-a103fef81945
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-haloketones
IUPAC Name 1,1-dibromo-3-iodopropan-2-one
SMILES (Canonical) C(C(=O)C(Br)Br)I
SMILES (Isomeric) C(C(=O)C(Br)Br)I
InChI InChI=1S/C3H3Br2IO/c4-3(5)2(7)1-6/h3H,1H2
InChI Key UDPFVNCNMONXIZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C3H3Br2IO
Molecular Weight 341.77 g/mol
Exact Mass 341.75749 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1,1-Dibromo-3-iodo-2-propanone
59227-99-5
1,1-Dibromo-3-iodoacetone
DTXSID90633987
CHEBI:184490

2D Structure

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2D Structure of 1,1-Dibromo-3-iodopropan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.6470 64.70%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7529 75.29%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9429 94.29%
OATP1B3 inhibitior + 0.9545 95.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9405 94.05%
P-glycoprotein inhibitior - 0.9839 98.39%
P-glycoprotein substrate - 0.9893 98.93%
CYP3A4 substrate - 0.7604 76.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7914 79.14%
CYP3A4 inhibition - 0.9261 92.61%
CYP2C9 inhibition - 0.8489 84.89%
CYP2C19 inhibition - 0.7122 71.22%
CYP2D6 inhibition - 0.9216 92.16%
CYP1A2 inhibition + 0.6787 67.87%
CYP2C8 inhibition - 0.9877 98.77%
CYP inhibitory promiscuity - 0.8290 82.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6672 66.72%
Carcinogenicity (trinary) Non-required 0.6439 64.39%
Eye corrosion + 0.9966 99.66%
Eye irritation + 0.9577 95.77%
Skin irritation + 0.8754 87.54%
Skin corrosion + 0.9534 95.34%
Ames mutagenesis + 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8464 84.64%
Micronuclear - 0.6926 69.26%
Hepatotoxicity + 0.7802 78.02%
skin sensitisation - 0.5297 52.97%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5130 51.30%
Acute Oral Toxicity (c) II 0.5502 55.02%
Estrogen receptor binding - 0.9001 90.01%
Androgen receptor binding - 0.8784 87.84%
Thyroid receptor binding - 0.8274 82.74%
Glucocorticoid receptor binding - 0.8078 80.78%
Aromatase binding - 0.9092 90.92%
PPAR gamma - 0.7102 71.02%
Honey bee toxicity - 0.9106 91.06%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.7926 79.26%

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 87.12% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.21% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Ainsliaea dissecta
Platycarphella carlinoides
Pulicaria dysenterica
Uncaria homomalla

Cross-Links

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PubChem 23426733
NPASS NPC109074
LOTUS LTS0159159
wikiData Q82541993