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N-(2,4-difluorophenyl)-2-(N-(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl)-N-methylnicotinamide ID: ALA2288502
PubChem CID: 76334709
Max Phase: Preclinical
Molecular Formula: C20H18F2N6O6S
Molecular Weight: 508.46
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ncccc2C(=O)N(C)c2ccc(F)cc2F)n1
Standard InChI: InChI=1S/C20H18F2N6O6S/c1-28(14-7-6-11(21)9-13(14)22)18(29)12-5-4-8-23-17(12)35(31,32)27-20(30)26-19-24-15(33-2)10-16(25-19)34-3/h4-10H,1-3H3,(H2,24,25,26,27,30)
Standard InChI Key: GXNALWAWNGYLOE-UHFFFAOYSA-N
Molfile:
RDKit 2D
35 37 0 0 0 0 0 0 0 0999 V2000
28.9752 -24.4793 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
29.7924 -24.4780 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
29.3827 -23.7710 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
26.8503 -23.2528 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
26.8492 -24.0723 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5572 -24.4813 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
28.2669 -24.0718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.2641 -23.2492 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.5554 -22.8439 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.9702 -22.8379 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.6795 -23.2438 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
28.9671 -22.0207 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
28.9765 -25.2965 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
29.6849 -25.7040 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.6862 -26.5212 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
30.3919 -25.2943 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
31.1003 -25.7018 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.0972 -26.5185 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
31.8047 -26.9259 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.5128 -26.5162 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.5088 -25.6948 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.8008 -25.2910 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
33.2145 -25.2826 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
33.9242 -25.6875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.8056 -27.7431 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
31.0983 -28.1525 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.3856 -22.8326 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.3847 -23.6490 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.0933 -23.2419 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.7990 -22.8313 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.7963 -22.0133 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.0821 -21.6075 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.3794 -22.0204 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.5020 -21.6011 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
29.6685 -21.6173 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
1 3 2 0
4 5 2 0
5 6 1 0
6 7 2 0
7 8 1 0
8 9 2 0
9 4 1 0
8 10 1 0
10 11 1 0
10 12 2 0
7 1 1 0
1 13 1 0
13 14 1 0
14 15 2 0
14 16 1 0
16 17 1 0
17 18 2 0
18 19 1 0
19 20 2 0
20 21 1 0
21 22 2 0
22 17 1 0
21 23 1 0
23 24 1 0
19 25 1 0
25 26 1 0
11 27 1 0
11 28 1 0
27 29 2 0
29 30 1 0
30 31 2 0
31 32 1 0
32 33 2 0
33 27 1 0
31 34 1 0
33 35 1 0
M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 508.46Molecular Weight (Monoisotopic): 508.0977AlogP: 1.95#Rotatable Bonds: 7Polar Surface Area: 152.71Molecular Species: ACIDHBA: 9HBD: 2#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 2#RO5 Violations (Lipinski): 2CX Acidic pKa: 4.98CX Basic pKa: 2.68CX LogP: 2.72CX LogD: 1.79Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.49Np Likeness Score: -1.77
References 1. MURAI S, HAGA T, SAKASHITA N, NAKAMURA Y, HONDA C, HONZAWA S, KIMURA F, TSUJII Y, NISHIYAMA R. (1995) Synthesis and Herbicidal Activity of Sulfonylureas; SL-950 and Its Related Compounds, 20 (4): [10.1584/jpestics.20.453 ]