2-(1-Chloro-2-hydroxyethyl)-4,4-dimethylcyclohexa-2,5-dienone

Details

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Internal ID d8ef29de-e604-43f3-815f-1f8e760fa09d
Taxonomy Organohalogen compounds > Halohydrins > Chlorohydrins
IUPAC Name 2-(1-chloro-2-hydroxyethyl)-4,4-dimethylcyclohexa-2,5-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13ClO2/c1-10(2)4-3-9(13)7(5-10)8(11)6-12/h3-5,8,12H,6H2,1-2H3
InChI Key WMIMRGFYQPHFQY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H13ClO2
Molecular Weight 200.66 g/mol
Exact Mass 200.0604073 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1-Chloro-2-hydroxyethyl)-4,4-dimethylcyclohexa-2,5-dienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8589 85.89%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8251 82.51%
OATP2B1 inhibitior - 0.8616 86.16%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8702 87.02%
P-glycoprotein inhibitior - 0.9612 96.12%
P-glycoprotein substrate - 0.9371 93.71%
CYP3A4 substrate - 0.5547 55.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8759 87.59%
CYP3A4 inhibition - 0.8372 83.72%
CYP2C9 inhibition - 0.8125 81.25%
CYP2C19 inhibition - 0.5790 57.90%
CYP2D6 inhibition - 0.8744 87.44%
CYP1A2 inhibition - 0.7422 74.22%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.7373 73.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5673 56.73%
Carcinogenicity (trinary) Non-required 0.6789 67.89%
Eye corrosion - 0.7884 78.84%
Eye irritation + 0.6479 64.79%
Skin irritation + 0.5250 52.50%
Skin corrosion - 0.6041 60.41%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6150 61.50%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5508 55.08%
skin sensitisation + 0.7743 77.43%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7249 72.49%
Acute Oral Toxicity (c) III 0.5928 59.28%
Estrogen receptor binding - 0.8398 83.98%
Androgen receptor binding - 0.8868 88.68%
Thyroid receptor binding - 0.7539 75.39%
Glucocorticoid receptor binding - 0.8402 84.02%
Aromatase binding - 0.8640 86.40%
PPAR gamma - 0.6767 67.67%
Honey bee toxicity - 0.9432 94.32%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8513 85.13%

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 89.66% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.39% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.24% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.53% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 85.46% 83.82%
CHEMBL2581 P07339 Cathepsin D 84.67% 98.95%
CHEMBL4208 P20618 Proteasome component C5 81.15% 90.00%

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 13985280
LOTUS LTS0050584
wikiData Q105308606