iPPI-DB

Inhibitors of Protein-Protein Interaction Database

Compound 2099

Identifiers

  • Canonical SMILES: 
    CC[C@@H]1NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](CCCNC(=O)[C@H](NC1=O)c1ccccc1)NC(=O)C(C)C
  • IUPAC name: 
    N-[(3R,6S,9S,12R)-9-(3-carbamimidamidopropyl)-6-ethyl-2,5,8,11-tetraoxo-3-phenyl-1,4,7,10-tetraazacyclopentadecan-12-yl]-2-methylpropanamide
  • InChi: 
    InChI=1S/C27H42N8O5/c1-4-18-23(37)35-21(17-10-6-5-7-11-17)26(40)30-14-8-12-19(33-22(36)16(2)3)25(39)34-20(24(38)32-18)13-9-15-31-27(28)29/h5-7,10-11,16,18-21H,4,8-9,12-15H2,1-3H3,(H,30,40)(H,32,38)(H,33,36)(H,34,39)(H,35,37)(H4,28,29,31)/t18-,19+,20-,21+/m0/s1
  • InChiKey: 
    TYRJPXXEXDBARQ-JSXRDJHFSA-N

External links


137630010
CHEMBL4116408

External search

Bibliography (1)

Publication Name
Karatas Hacer, Li Yangbing, Liu Liu, Ji Jiao, Lee Shirley, Chen Yong, Yang Jiuling, Huang Liyue, Bernard Denzil, Xu Jing, Townsend Elizabeth C., Cao Fang, Ran Xu, Li Xiaoqin, Wen Bo, Sun Duxin, Stuckey Jeanne A, Lei Ming, Dou Yali, Wang Shaomeng. . Discovery of a Highly Potent, Cell-Permeable Macrocyclic Peptidomimetic (MM-589) Targeting the WD Repeat Domain 5 Protein (WDR5)–Mixed Lineage Leukemia (MLL) Protein–Protein Interaction Journal of Medicinal Chemistry. 11

Pharmacological data

Biochemical tests Cellular tests PK tests Cytotoxicity tests
2 0 0 0

Targets

PPI family Best activity Diseases MMoA
WDR5/MLL 7.48 lymphoid leukemia (disease) Inhibition
Physicochemical filters
Descriptor Lipinski's RO5 Veber Pfizer's 3/75
Compliance
MW 558.33 g/mol
HBA 13
HBD 9
HBA + HBD 22
AlogP -1.22
TPSA 209.14
RB 8
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 2 0 0 0
Pharmacological data
Bibliography Name Target Competition Assay type Assay name Cell line Activity type Activity
10.1021/acs.jmedchem.6b01796 11 KMT2A
Q03164 		WDR5
P61964 		Biochemical assay Fluorescence Polarization pIC50 (half maximal inhibitory concentration, -log10) 6.79
10.1021/acs.jmedchem.6b01796 11 KMT2A
Q03164 		WDR5
P61964 		Biochemical assay Fluorescence Polarization pKi (inhibition constant, -log10) 7.48
Ta Structure Name Drugbank ID
0.7353 D-phenylalanyl-N-benzyl-L-prolinamide DB07143
0.7333 CR665 DB05155
0.7076 D-phenylalanyl-N-(3-methylbenzyl)-L-prolinamide DB07133
0.7064 D-phenylalanyl-N-{4-[amino(iminio)methyl]benzyl}-L-prolinamide DB07005
0.6931 1-[(2R)-2-aminobutanoyl]-N-(4-carbamimidoylbenzyl)-L-prolinamide DB06947
0.6931 D-leucyl-N-(4-carbamimidoylbenzyl)-L-prolinamide DB06996
0.6818 D-phenylalanyl-N-(3-fluorobenzyl)-L-prolinamide DB07027
0.6810 Neocitrullamon DB13396
0.6765 (S)-N-(4-carbamimidoylbenzyl)-1-(2-(cyclopentylamino)ethanoyl)pyrrolidine-2-carboxamide DB06845
0.6757 D-phenylalanyl-N-(3-chlorobenzyl)-L-prolinamide DB06919
0.6735 Antineoplaston A10 DB11702
0.6733 1-butanoyl-N-(4-carbamimidoylbenzyl)-L-prolinamide DB06929
0.6733 N-(4-carbamimidoylbenzyl)-1-(4-methylpentanoyl)-L-prolinamide DB06936
0.6635 (S)-N-(4-carbamimidoylbenzyl)-1-(2-(cyclohexylamino)ethanoyl)pyrrolidine-2-carboxamide DB06850
0.6635 N-cyclooctylglycyl-N-(4-carbamimidoylbenzyl)-L-prolinamide DB06858