CID 163106474

Details

Top
Internal ID 356977ea-e818-4970-9ee6-d935820328fa
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Hydropyrimidines
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C45H78N6O5/c1-4-6-7-8-9-10-11-12-13-14-15-16-23-39(41-47-30-20-31-50(41)33-36(52)26-29-46)54-42(53)40-38-25-24-35-32-44(27-18-17-22-37(5-2)56-44)48-43(51(35)38)49-45(40)28-19-21-34(3)55-45/h17,22,34-40,52H,4-16,18-21,23-33,46H2,1-3H3,(H,48,49)/t34-,35+,36-,37+,38-,39+,40-,44-,45-/m1/s1
InChI Key WSZFUIXQILMXEW-RADRGRJTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C45H78N6O5
Molecular Weight 783.10 g/mol
Exact Mass 782.60336961 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.74
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 21

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 163106474

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8779 87.79%
Caco-2 - 0.8391 83.91%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.6143 61.43%
OATP2B1 inhibitior - 0.5780 57.80%
OATP1B1 inhibitior + 0.8460 84.60%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9018 90.18%
P-glycoprotein inhibitior + 0.7387 73.87%
P-glycoprotein substrate + 0.8339 83.39%
CYP3A4 substrate + 0.7297 72.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8118 81.18%
CYP3A4 inhibition - 0.6035 60.35%
CYP2C9 inhibition - 0.7884 78.84%
CYP2C19 inhibition - 0.7646 76.46%
CYP2D6 inhibition - 0.8751 87.51%
CYP1A2 inhibition - 0.8360 83.60%
CYP2C8 inhibition + 0.7494 74.94%
CYP inhibitory promiscuity - 0.8830 88.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5921 59.21%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.9126 91.26%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.9098 90.98%
Ames mutagenesis - 0.5837 58.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5353 53.53%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5699 56.99%
skin sensitisation - 0.8399 83.99%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5642 56.42%
Acute Oral Toxicity (c) III 0.5471 54.71%
Estrogen receptor binding + 0.7557 75.57%
Androgen receptor binding + 0.7244 72.44%
Thyroid receptor binding + 0.5473 54.73%
Glucocorticoid receptor binding + 0.6085 60.85%
Aromatase binding + 0.6261 62.61%
PPAR gamma + 0.6453 64.53%
Honey bee toxicity - 0.7072 70.72%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6537 65.37%
Fish aquatic toxicity + 0.7661 76.61%

Targets

Top

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 99.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.87% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.11% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.84% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 96.31% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 95.86% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 93.72% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 93.20% 95.50%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 92.75% 91.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.27% 91.11%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 88.66% 98.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.60% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.79% 82.69%
CHEMBL4588 P22894 Matrix metalloproteinase 8 87.23% 94.66%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.00% 96.21%
CHEMBL2094135 Q96BI3 Gamma-secretase 85.62% 98.05%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.64% 99.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.51% 90.08%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.87% 96.90%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.83% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.10% 93.03%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 82.87% 97.64%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.54% 90.71%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.32% 97.50%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.47% 96.47%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 163106474
LOTUS LTS0211097
wikiData Q105312226