(2R,6S)-2-(2-chloropropan-2-yl)-6-(dibromomethyl)-5-methyl-3,6-dihydro-2H-pyran

Details

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Internal ID 9b016a7a-b9c6-4be3-8719-73e683022485
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name (2R,6S)-2-(2-chloropropan-2-yl)-6-(dibromomethyl)-5-methyl-3,6-dihydro-2H-pyran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H15Br2ClO/c1-6-4-5-7(10(2,3)13)14-8(6)9(11)12/h4,7-9H,5H2,1-3H3/t7-,8+/m1/s1
InChI Key RHABCRQHZGGHKU-SFYZADRCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H15Br2ClO
Molecular Weight 346.48 g/mol
Exact Mass 345.91577 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.22
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 (2R,6S)-2-(2-chloropropan-2-yl)-6-(dibromomethyl)-5-methyl-3,6-dihydro-2H-pyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.6267 62.67%
Blood Brain Barrier + 0.8521 85.21%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4968 49.68%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9302 93.02%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9530 95.30%
P-glycoprotein inhibitior - 0.9376 93.76%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.5251 52.51%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7608 76.08%
CYP3A4 inhibition - 0.7484 74.84%
CYP2C9 inhibition - 0.5818 58.18%
CYP2C19 inhibition + 0.5376 53.76%
CYP2D6 inhibition - 0.9169 91.69%
CYP1A2 inhibition - 0.6936 69.36%
CYP2C8 inhibition - 0.9387 93.87%
CYP inhibitory promiscuity + 0.5119 51.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5989 59.89%
Carcinogenicity (trinary) Non-required 0.5665 56.65%
Eye corrosion - 0.8615 86.15%
Eye irritation + 0.5514 55.14%
Skin irritation + 0.6151 61.51%
Skin corrosion - 0.6979 69.79%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5570 55.70%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.7449 74.49%
skin sensitisation + 0.6862 68.62%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.5093 50.93%
Acute Oral Toxicity (c) III 0.6934 69.34%
Estrogen receptor binding - 0.6776 67.76%
Androgen receptor binding - 0.7545 75.45%
Thyroid receptor binding - 0.7425 74.25%
Glucocorticoid receptor binding - 0.8073 80.73%
Aromatase binding - 0.8921 89.21%
PPAR gamma - 0.6487 64.87%
Honey bee toxicity - 0.8151 81.51%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.8152 81.52%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.96% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 93.83% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.31% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.85% 93.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.81% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.20% 97.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.62% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11791892
LOTUS LTS0120477
wikiData Q105236212