(10R)-10-[(Z)-(2-imino-3-methyl-5-oxoimidazolidin-4-ylidene)methyl]-1,3,6,8-tetrazatricyclo[6.3.1.04,12]dodeca-4(12),6-diene-2,5-dione

Details

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Internal ID 5ab00f62-8110-40c4-866e-761a89478889
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones > Hypoxanthines
IUPAC Name (10R)-10-[(Z)-(2-imino-3-methyl-5-oxoimidazolidin-4-ylidene)methyl]-1,3,6,8-tetrazatricyclo[6.3.1.04,12]dodeca-4(12),6-diene-2,5-dione
SMILES (Canonical) CN1C(=CC2CN3C=NC(=O)C4=C3N(C2)C(=O)N4)C(=O)NC1=N
SMILES (Isomeric) CN1/C(=C\[C@@H]2CN3C=NC(=O)C4=C3N(C2)C(=O)N4)/C(=O)NC1=N
InChI InChI=1S/C13H13N7O3/c1-18-7(9(21)17-12(18)14)2-6-3-19-5-15-10(22)8-11(19)20(4-6)13(23)16-8/h2,5-6H,3-4H2,1H3,(H,16,23)(H2,14,17,21)/b7-2-/t6-/m1/s1
InChI Key BNXDXEIAWGCYRM-USZBSYLJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H13N7O3
Molecular Weight 315.29 g/mol
Exact Mass 315.10798730 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -1.60
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (10R)-10-[(Z)-(2-imino-3-methyl-5-oxoimidazolidin-4-ylidene)methyl]-1,3,6,8-tetrazatricyclo[6.3.1.04,12]dodeca-4(12),6-diene-2,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 - 0.5903 59.03%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7709 77.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7049 70.49%
P-glycoprotein inhibitior - 0.8384 83.84%
P-glycoprotein substrate - 0.5134 51.34%
CYP3A4 substrate + 0.5518 55.18%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.8843 88.43%
CYP3A4 inhibition + 0.7629 76.29%
CYP2C9 inhibition - 0.7443 74.43%
CYP2C19 inhibition - 0.6949 69.49%
CYP2D6 inhibition - 0.9010 90.10%
CYP1A2 inhibition - 0.6437 64.37%
CYP2C8 inhibition - 0.8310 83.10%
CYP inhibitory promiscuity - 0.8532 85.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6313 63.13%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.9926 99.26%
Skin irritation - 0.7760 77.60%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6529 65.29%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.8604 86.04%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6402 64.02%
Acute Oral Toxicity (c) III 0.5606 56.06%
Estrogen receptor binding + 0.5555 55.55%
Androgen receptor binding + 0.5759 57.59%
Thyroid receptor binding + 0.6186 61.86%
Glucocorticoid receptor binding + 0.5685 56.85%
Aromatase binding + 0.6443 64.43%
PPAR gamma - 0.5504 55.04%
Honey bee toxicity - 0.8990 89.90%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8561 85.61%

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 95.68% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 95.09% 94.75%
CHEMBL2581 P07339 Cathepsin D 94.73% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.28% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.05% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 90.94% 98.59%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.90% 89.34%
CHEMBL230 P35354 Cyclooxygenase-2 90.36% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.25% 94.45%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.31% 90.08%
CHEMBL3401 O75469 Pregnane X receptor 85.45% 94.73%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.01% 86.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.55% 99.23%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.53% 82.38%
CHEMBL3310 Q96DB2 Histone deacetylase 11 83.18% 88.56%
CHEMBL3524 P56524 Histone deacetylase 4 82.41% 92.97%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.48% 86.33%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 81.46% 98.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.39% 97.09%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 80.17% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.16% 95.89%

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 162914546
LOTUS LTS0017125
wikiData Q104939084