(Z)-1,1,3,4-tetrabromobut-3-en-2-one

Details

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Internal ID 8ef27507-e73d-4d50-b6dc-348696d64644
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Alpha-branched alpha,beta-unsaturated ketones
IUPAC Name (Z)-1,1,3,4-tetrabromobut-3-en-2-one
SMILES (Canonical) C(=C(C(=O)C(Br)Br)Br)Br
SMILES (Isomeric) C(=C(/C(=O)C(Br)Br)\Br)\Br
InChI InChI=1S/C4H2Br4O/c5-1-2(6)3(9)4(7)8/h1,4H/b2-1-
InChI Key QDMHHSIUMQQFCZ-UPHRSURJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H2Br4O
Molecular Weight 385.67 g/mol
Exact Mass 385.67982 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-1,1,3,4-tetrabromobut-3-en-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 + 0.9946 99.46%
Caco-2 + 0.5888 58.88%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5024 50.24%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.9302 93.02%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9250 92.50%
P-glycoprotein inhibitior - 0.9817 98.17%
P-glycoprotein substrate - 0.9906 99.06%
CYP3A4 substrate - 0.7150 71.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.9396 93.96%
CYP2C9 inhibition - 0.8679 86.79%
CYP2C19 inhibition - 0.7460 74.60%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition - 0.5732 57.32%
CYP2C8 inhibition - 0.9781 97.81%
CYP inhibitory promiscuity - 0.7478 74.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7240 72.40%
Carcinogenicity (trinary) Non-required 0.5187 51.87%
Eye corrosion + 0.9918 99.18%
Eye irritation + 0.9564 95.64%
Skin irritation + 0.8546 85.46%
Skin corrosion + 0.9731 97.31%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7894 78.94%
Micronuclear + 0.5074 50.74%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.8453 84.53%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6091 60.91%
Acute Oral Toxicity (c) II 0.7959 79.59%
Estrogen receptor binding - 0.8981 89.81%
Androgen receptor binding - 0.9103 91.03%
Thyroid receptor binding - 0.7818 78.18%
Glucocorticoid receptor binding - 0.9404 94.04%
Aromatase binding - 0.8674 86.74%
PPAR gamma - 0.8275 82.75%
Honey bee toxicity - 0.6602 66.02%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.6774 67.74%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.84% 85.94%

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 23426728
NPASS NPC28936
LOTUS LTS0225837
wikiData Q105218870