6-(dibromomethyl)-2-(1,2-dichloropropan-2-yl)-5-methyl-3,6-dihydro-2H-pyran

Details

Top
Internal ID c46d2f87-daae-4443-8352-5e63628d9b43
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name 6-(dibromomethyl)-2-(1,2-dichloropropan-2-yl)-5-methyl-3,6-dihydro-2H-pyran
SMILES (Canonical) CC1=CCC(OC1C(Br)Br)C(C)(CCl)Cl
SMILES (Isomeric) CC1=CCC(OC1C(Br)Br)C(C)(CCl)Cl
InChI InChI=1S/C10H14Br2Cl2O/c1-6-3-4-7(10(2,14)5-13)15-8(6)9(11)12/h3,7-9H,4-5H2,1-2H3
InChI Key FVPHWLFPVMYUFV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14Br2Cl2O
Molecular Weight 380.93 g/mol
Exact Mass 379.87680 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.44
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-(dibromomethyl)-2-(1,2-dichloropropan-2-yl)-5-methyl-3,6-dihydro-2H-pyran

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.7190 71.90%
Blood Brain Barrier + 0.9771 97.71%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5675 56.75%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9134 91.34%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9279 92.79%
P-glycoprotein inhibitior - 0.9342 93.42%
P-glycoprotein substrate - 0.8699 86.99%
CYP3A4 substrate + 0.5186 51.86%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7608 76.08%
CYP3A4 inhibition + 0.5155 51.55%
CYP2C9 inhibition - 0.6496 64.96%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8788 87.88%
CYP1A2 inhibition - 0.5650 56.50%
CYP2C8 inhibition - 0.8868 88.68%
CYP inhibitory promiscuity + 0.5091 50.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5889 58.89%
Carcinogenicity (trinary) Non-required 0.5561 55.61%
Eye corrosion - 0.7768 77.68%
Eye irritation - 0.8496 84.96%
Skin irritation - 0.5585 55.85%
Skin corrosion - 0.7461 74.61%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6492 64.92%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.6321 63.21%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6785 67.85%
Estrogen receptor binding - 0.7213 72.13%
Androgen receptor binding - 0.7245 72.45%
Thyroid receptor binding - 0.5333 53.33%
Glucocorticoid receptor binding - 0.7152 71.52%
Aromatase binding - 0.8227 82.27%
PPAR gamma - 0.6082 60.82%
Honey bee toxicity - 0.8354 83.54%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9436 94.36%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.70% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 95.17% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.89% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.84% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.57% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.17% 89.62%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.85% 93.56%

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.
There are no matching plants.

Cross-Links

Top
PubChem 76319758
LOTUS LTS0139043
wikiData Q105002681