4-(2-amino-5-oxo-1H-imidazol-4-ylidene)-3-bromo-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one

Details

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Internal ID 7e87c106-db3e-4f83-ad1a-0a969dda69d2
Taxonomy Organoheterocyclic compounds > Pyrroloazepines
IUPAC Name 4-(2-amino-5-oxo-1H-imidazol-4-ylidene)-3-bromo-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10BrN5O2/c12-5-3-15-8-6(5)4(1-2-14-9(8)18)7-10(19)17-11(13)16-7/h3,15H,1-2H2,(H,14,18)(H3,13,16,17,19)
InChI Key BGQVVTJSMBYUHC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10BrN5O2
Molecular Weight 324.13 g/mol
Exact Mass 323.00179 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP -0.50
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-amino-5-oxo-1H-imidazol-4-ylidene)-3-bromo-1,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 - 0.6342 63.42%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4204 42.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7326 73.26%
P-glycoprotein inhibitior - 0.9348 93.48%
P-glycoprotein substrate - 0.7573 75.73%
CYP3A4 substrate - 0.5229 52.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8348 83.48%
CYP3A4 inhibition - 0.5949 59.49%
CYP2C9 inhibition - 0.6866 68.66%
CYP2C19 inhibition - 0.6057 60.57%
CYP2D6 inhibition - 0.8268 82.68%
CYP1A2 inhibition + 0.5130 51.30%
CYP2C8 inhibition - 0.8459 84.59%
CYP inhibitory promiscuity - 0.8137 81.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7522 75.22%
Carcinogenicity (trinary) Non-required 0.5720 57.20%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.9647 96.47%
Skin irritation - 0.7655 76.55%
Skin corrosion - 0.9142 91.42%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6003 60.03%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8364 83.64%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.4880 48.80%
Acute Oral Toxicity (c) III 0.5660 56.60%
Estrogen receptor binding - 0.6962 69.62%
Androgen receptor binding + 0.6327 63.27%
Thyroid receptor binding - 0.5393 53.93%
Glucocorticoid receptor binding + 0.6207 62.07%
Aromatase binding - 0.5451 54.51%
PPAR gamma + 0.6844 68.44%
Honey bee toxicity - 0.8349 83.49%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.5091 50.91%

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 96.73% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 96.59% 85.30%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 94.31% 95.72%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.25% 91.11%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 91.95% 80.96%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 91.25% 83.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.21% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.48% 97.09%
CHEMBL3384 Q16512 Protein kinase N1 87.54% 80.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.28% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 86.93% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.85% 94.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.85% 92.88%
CHEMBL226 P30542 Adenosine A1 receptor 85.71% 95.93%
CHEMBL5443 O00311 Cell division cycle 7-related protein kinase 85.31% 96.11%
CHEMBL3310 Q96DB2 Histone deacetylase 11 85.10% 88.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.87% 93.99%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.85% 96.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.56% 90.08%
CHEMBL1937 Q92769 Histone deacetylase 2 83.27% 94.75%
CHEMBL1829 O15379 Histone deacetylase 3 82.85% 95.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.12% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.96% 99.23%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 81.18% 88.84%
CHEMBL2535 P11166 Glucose transporter 81.10% 98.75%
CHEMBL284 P27487 Dipeptidyl peptidase IV 80.19% 95.69%

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 136350025
LOTUS LTS0130113
wikiData Q104935698