1,1-Dibromo-3-chloroacetone

Details

Top
Internal ID caaf9f18-6b65-4b05-be1d-a9c88adf35f2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-haloketones > Alpha-chloroketones
IUPAC Name 1,1-dibromo-3-chloropropan-2-one
SMILES (Canonical) C(C(=O)C(Br)Br)Cl
SMILES (Isomeric) C(C(=O)C(Br)Br)Cl
InChI InChI=1S/C3H3Br2ClO/c4-3(5)2(7)1-6/h3H,1H2
InChI Key GNWZITBRPXAMSE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H3Br2ClO
Molecular Weight 250.31 g/mol
Exact Mass 249.82187 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
1578-18-3
2-Propanone, 1,1-dibromo-3-chloro-
dibromo-3-chloropropone
1,1-Dibromo-3-chloropropanone
SCHEMBL7749250
1,1-Dibromo-3-chloroacetone #
DTXSID40339301
GNWZITBRPXAMSE-UHFFFAOYSA-N
1,1-Dibromo-3-chloro-2-propanone
AKOS040756906
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1,1-Dibromo-3-chloroacetone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 - 0.5886 58.86%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7738 77.38%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.9805 98.05%
CYP3A4 substrate - 0.7164 71.64%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7940 79.40%
CYP3A4 inhibition - 0.9412 94.12%
CYP2C9 inhibition - 0.8594 85.94%
CYP2C19 inhibition - 0.5616 56.16%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition + 0.6311 63.11%
CYP2C8 inhibition - 0.9916 99.16%
CYP inhibitory promiscuity - 0.8068 80.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6972 69.72%
Carcinogenicity (trinary) Non-required 0.6319 63.19%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9840 98.40%
Skin irritation + 0.8927 89.27%
Skin corrosion + 0.9861 98.61%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7909 79.09%
Micronuclear - 0.8026 80.26%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.5704 57.04%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6313 63.13%
Acute Oral Toxicity (c) II 0.7221 72.21%
Estrogen receptor binding - 0.7896 78.96%
Androgen receptor binding - 0.8336 83.36%
Thyroid receptor binding - 0.8321 83.21%
Glucocorticoid receptor binding - 0.8174 81.74%
Aromatase binding - 0.9082 90.82%
PPAR gamma - 0.7086 70.86%
Honey bee toxicity - 0.8443 84.43%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6852 68.52%
Fish aquatic toxicity - 0.7975 79.75%

Targets

Top

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 90.78% 96.09%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.41% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.01% 96.95%

Plants that contains it

Top
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

Top
PubChem 555292
NPASS NPC28840