1,1-Dibromo-3,3-dichloroprop-1-ene

Details

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Internal ID 0afd6488-a925-46ef-9553-da04258ad04a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ketene acetals
IUPAC Name 1,1-dibromo-3,3-dichloroprop-1-ene
SMILES (Canonical) C(=C(Br)Br)C(Cl)Cl
SMILES (Isomeric) C(=C(Br)Br)C(Cl)Cl
InChI InChI=1S/C3H2Br2Cl2/c4-2(5)1-3(6)7/h1,3H
InChI Key YSDOFDQKYXYIPZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C3H2Br2Cl2
Molecular Weight 268.76 g/mol
Exact Mass 267.78798 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,1-Dibromo-3,3-dichloroprop-1-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.7380 73.80%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5317 53.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9168 91.68%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9938 99.38%
CYP3A4 substrate - 0.7554 75.54%
CYP2C9 substrate - 0.5452 54.52%
CYP2D6 substrate - 0.7747 77.47%
CYP3A4 inhibition - 0.8656 86.56%
CYP2C9 inhibition - 0.7337 73.37%
CYP2C19 inhibition - 0.6672 66.72%
CYP2D6 inhibition - 0.9286 92.86%
CYP1A2 inhibition - 0.6109 61.09%
CYP2C8 inhibition - 0.9643 96.43%
CYP inhibitory promiscuity - 0.6847 68.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7617 76.17%
Carcinogenicity (trinary) Warning 0.4648 46.48%
Eye corrosion + 0.7734 77.34%
Eye irritation + 0.9251 92.51%
Skin irritation + 0.8546 85.46%
Skin corrosion + 0.9255 92.55%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7889 78.89%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.8750 87.50%
skin sensitisation + 0.6329 63.29%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.6885 68.85%
Acute Oral Toxicity (c) II 0.7414 74.14%
Estrogen receptor binding - 0.8802 88.02%
Androgen receptor binding - 0.8719 87.19%
Thyroid receptor binding - 0.7519 75.19%
Glucocorticoid receptor binding - 0.8740 87.40%
Aromatase binding - 0.9087 90.87%
PPAR gamma - 0.8551 85.51%
Honey bee toxicity + 0.6226 62.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9236 92.36%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.35% 94.45%

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 13538081
NPASS NPC302854
LOTUS LTS0089913
wikiData Q105359529