2-(3,5-Dibromo-1,6-dihydroxy-4-oxocyclohex-2-en-1-yl)acetonitrile

Details

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Internal ID 194c5794-830e-4966-86ac-e872747aa589
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 2-(3,5-dibromo-1,6-dihydroxy-4-oxocyclohex-2-en-1-yl)acetonitrile
SMILES (Canonical) C1=C(C(=O)C(C(C1(CC#N)O)O)Br)Br
SMILES (Isomeric) C1=C(C(=O)C(C(C1(CC#N)O)O)Br)Br
InChI InChI=1S/C8H7Br2NO3/c9-4-3-8(14,1-2-11)7(13)5(10)6(4)12/h3,5,7,13-14H,1H2
InChI Key WHLPZHXHZAAZBP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7Br2NO3
Molecular Weight 324.95 g/mol
Exact Mass 324.87722 g/mol
Topological Polar Surface Area (TPSA) 81.30 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,5-Dibromo-1,6-dihydroxy-4-oxocyclohex-2-en-1-yl)acetonitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9858 98.58%
Caco-2 - 0.8651 86.51%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8000 80.00%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8438 84.38%
P-glycoprotein inhibitior - 0.9761 97.61%
P-glycoprotein substrate - 0.9421 94.21%
CYP3A4 substrate - 0.5447 54.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8151 81.51%
CYP3A4 inhibition - 0.6965 69.65%
CYP2C9 inhibition - 0.7424 74.24%
CYP2C19 inhibition - 0.7942 79.42%
CYP2D6 inhibition - 0.9043 90.43%
CYP1A2 inhibition - 0.7612 76.12%
CYP2C8 inhibition - 0.9423 94.23%
CYP inhibitory promiscuity - 0.8354 83.54%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7561 75.61%
Carcinogenicity (trinary) Non-required 0.4890 48.90%
Eye corrosion - 0.9484 94.84%
Eye irritation - 0.5416 54.16%
Skin irritation - 0.6191 61.91%
Skin corrosion - 0.9037 90.37%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7130 71.30%
Micronuclear + 0.5239 52.39%
Hepatotoxicity + 0.8014 80.14%
skin sensitisation - 0.5522 55.22%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6584 65.84%
Acute Oral Toxicity (c) III 0.5938 59.38%
Estrogen receptor binding - 0.7404 74.04%
Androgen receptor binding - 0.7993 79.93%
Thyroid receptor binding - 0.6440 64.40%
Glucocorticoid receptor binding - 0.6986 69.86%
Aromatase binding - 0.8548 85.48%
PPAR gamma - 0.5519 55.19%
Honey bee toxicity - 0.8237 82.37%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.3637 36.37%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.56% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.64% 91.11%
CHEMBL1871 P10275 Androgen Receptor 92.28% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.31% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.61% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.35% 95.56%

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 74051641
LOTUS LTS0052434
wikiData Q105305412