iPPI-DB

Inhibitors of Protein-Protein Interaction Database

Compound 2000

Identifiers

  • Canonical SMILES: 
    Cc1onc(c1C(=O)N1CCN(CC1)c1ccc(cc1Cl)N(=O)=O)-c1ccccc1
  • IUPAC name: 
    1-(2-chloro-4-nitrophenyl)-4-(5-methyl-3-phenyl-1,2-oxazole-4-carbonyl)piperazine
  • InChi: 
    InChI=1S/C21H19ClN4O4/c1-14-19(20(23-30-14)15-5-3-2-4-6-15)21(27)25-11-9-24(10-12-25)18-8-7-16(26(28)29)13-17(18)22/h2-8,13H,9-12H2,1H3
  • InChiKey: 
    OWXBJAPOSQSWAO-UHFFFAOYSA-N

External links


2863945
CHEMBL2032324
NUZ

External search

Bibliography (1)

Publication Name
Gerritz S. W., Cianci C., Kim S., Pearce B. C., Deminie C., Discotto L., McAuliffe B., Minassian B. F., Shi S., Zhu S., Zhai W., Pendri A., Li G., Poss M. A., Edavettal S., McDonnell P. A., Lewis H. A., Maskos K., Mortl M., Kiefersauer R., Steinbacher S., Baldwin E. T., Metzler W., Bryson J., Healy M. D., Philip T., Zoeckler M., Schartman R., Sinz M., Leyva-Grado V. H., Hoffmann H.-H., Langley D. R., Meanwell N. A., Krystal M.. . Inhibition of influenza virus replication via small molecules that induce the formation of higher-order nucleoprotein oligomers Proceedings of the National Academy of Sciences. 1

Pharmacological data

Biochemical tests Cellular tests PK tests Cytotoxicity tests
1 3 0 0

Targets

PPI family Best activity Diseases MMoA
Influenza NP 6.82 influenza Stabilization
Physicochemical filters
Descriptor Lipinski's RO5 Veber Pfizer's 3/75
Compliance
MW 426.11 g/mol
HBA 8
HBD 0
HBA + HBD 8
AlogP 4.15
TPSA 95.40
RB 4
Radar chart
PCA : iPPI-DB chemical space
PCA : Correlation circle
Efficiencies: iPPI-DB biplot LE versus LLE
Summary
Bibliographic ressources Biochemical tests Cellular tests PK tests Cytotoxicity tests
1 1 3 0 0
Pharmacological data
Bibliography Name Target Competition Assay type Assay name Cell line Activity type Activity
10.1073/pnas.1107906108 1 Q1K9H2
Q1K9H2
Cellular assay Antiviral H1N1 A/WSN/33 MDBK pEC50 (half maximal effective concentration, -log10) 6.77
10.1073/pnas.1107906108 1 Q1K9H2
Q1K9H2
Cellular assay Antiviral H1N1 A/Solomon Islands/3/2006 MDBK pEC50 (half maximal effective concentration, -log10) 5.31
10.1073/pnas.1107906108 1 Q1K9H2
Q1K9H2
Cellular assay Antiviral H5N1 A/Gull_PA/4175/83 MDBK pEC50 (half maximal effective concentration, -log10) 6.82
10.1073/pnas.1107906108 1 Q1K9H2
Q1K9H2
Biochemical assay H1N1 A/WSN polymerase pIC50 (half maximal inhibitory concentration, -log10) 5.60
Ta Structure Name Drugbank ID
0.5689 Cloxacillin DB01147
0.5639 Dicloxacillin DB00485
0.5622 Oxacillin DB00713
0.5470 Flucloxacillin DB00301
0.5153 Leflunomide DB01097
0.4229 Valdecoxib DB00580
0.4192 5-(5-CHLORO-2,4-DIHYDROXYPHENYL)-N-ETHYL-4-(4-METHOXYPHENYL)ISOXAZOLE-3-CARBOXAMIDE DB06964
0.4167 Parecoxib DB08439
0.4076 5-(5-chloro-2,4-dihydroxyphenyl)-N-ethyl-4-[4-(morpholin-4-ylmethyl)phenyl]isoxazole-3-carboxamide DB06961
0.4017 Basmisanil DB11877
0.3857 4-chloro-6-{5-[(2-morpholin-4-ylethyl)amino]-1,2-benzisoxazol-3-yl}benzene-1,3-diol DB07601
0.3855 Cilofexor DB15168
0.3750 AUY922 DB11881
0.3706 N-[4-(2-CHLOROPHENYL)-1,3-DIOXO-1,2,3,6-TETRAHYDROPYRROLO[3,4-C]CARBAZOL-9-YL]FORMAMIDE DB07226
0.3700 PX-102 DB15416