1,1-Dibromo-2-propanone

Details

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Internal ID fbb3d73a-a4d7-41a4-a8aa-a1e763bf9503
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-haloketones
IUPAC Name 1,1-dibromopropan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H4Br2O/c1-2(6)3(4)5/h3H,1H3
InChI Key ZABBFAHZPHMIJC-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4Br2O
Molecular Weight 215.87 g/mol
Exact Mass 215.86084 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1,1-Dibromopropanone
1,1-dibromopropan-2-one
1,1-Dibromo-2-propanone
1,1-Dibromopropanone 1,1-Dibromoacetone
DTXSID9021558
RefChem:71013
DTXCID801558
ZABBFAHZPHMIJC-UHFFFAOYSA-N
867-54-9
dibromopropanone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,1-Dibromo-2-propanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 - 0.6603 66.03%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5853 58.53%
OATP2B1 inhibitior - 0.8655 86.55%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9652 96.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9247 92.47%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9919 99.19%
CYP3A4 substrate - 0.7557 75.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8036 80.36%
CYP3A4 inhibition - 0.9590 95.90%
CYP2C9 inhibition - 0.9251 92.51%
CYP2C19 inhibition - 0.8581 85.81%
CYP2D6 inhibition - 0.9536 95.36%
CYP1A2 inhibition - 0.5921 59.21%
CYP2C8 inhibition - 0.9984 99.84%
CYP inhibitory promiscuity - 0.9128 91.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6953 69.53%
Carcinogenicity (trinary) Non-required 0.6307 63.07%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9779 97.79%
Skin irritation + 0.8667 86.67%
Skin corrosion + 0.9163 91.63%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8209 82.09%
Micronuclear + 0.6674 66.74%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.6356 63.56%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7058 70.58%
Acute Oral Toxicity (c) II 0.5230 52.30%
Estrogen receptor binding - 0.9210 92.10%
Androgen receptor binding - 0.9336 93.36%
Thyroid receptor binding - 0.8414 84.14%
Glucocorticoid receptor binding - 0.9111 91.11%
Aromatase binding - 0.9390 93.90%
PPAR gamma - 0.8668 86.68%
Honey bee toxicity - 0.8828 88.28%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.6494 64.94%

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 89.08% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.77% 98.95%

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 540118
NPASS NPC13580