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1-Ethyl-3-[1-(1-methyl-2-oxopyrrolidin-3-yl)-6-(pyridin-3-yl)-1H-pyrrolo[3,2-b]pyridin-3-yl]urea ID: ALA3734950
PubChem CID: 127036094
Max Phase: Preclinical
Molecular Formula: C20H22N6O2
Molecular Weight: 378.44
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CCNC(=O)Nc1cn(C2CCN(C)C2=O)c2cc(-c3cccnc3)cnc12
Standard InChI: InChI=1S/C20H22N6O2/c1-3-22-20(28)24-15-12-26(16-6-8-25(2)19(16)27)17-9-14(11-23-18(15)17)13-5-4-7-21-10-13/h4-5,7,9-12,16H,3,6,8H2,1-2H3,(H2,22,24,28)
Standard InChI Key: ZFKMXFSDIMHLLR-UHFFFAOYSA-N
Molfile:
RDKit 2D
28 31 0 0 0 0 0 0 0 0999 V2000
4.1277 -4.3539 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.6552 -2.9294 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4530 -2.0330 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.1855 -2.6254 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
0.2917 -0.7475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2917 0.7475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0028 1.5132 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3155 0.7475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3155 -0.7475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0028 -1.5132 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1.7138 1.2033 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1.7138 -1.2033 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5889 0.0182 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9144 0.7421 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6168 1.4950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.6204 2.9950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9211 3.7421 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.2185 2.9892 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.2151 1.4892 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.5974 -4.6579 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9752 -5.7969 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1749 2.6315 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3751 3.8801 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3406 5.0280 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.7308 4.4644 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.6243 2.9682 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1776 3.9578 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0517 6.1927 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 2 0
2 4 1 0
5 6 1 0
6 7 2 0
7 8 1 0
8 9 2 0
9 10 1 0
5 10 2 0
12 13 2 0
11 13 1 0
5 12 1 0
6 11 1 0
14 15 1 0
15 16 2 0
16 17 1 0
17 18 2 0
18 19 1 0
14 19 2 0
8 15 1 0
4 12 1 0
20 21 1 0
1 20 1 0
11 22 1 0
22 23 1 0
23 24 1 0
24 25 1 0
25 26 1 0
26 22 1 0
23 27 2 0
24 28 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: 378.44Molecular Weight (Monoisotopic): 378.1804AlogP: 2.64#Rotatable Bonds: 4Polar Surface Area: 92.15Molecular Species: NEUTRALHBA: 5HBD: 2#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 12.02CX Basic pKa: 4.62CX LogP: 0.60CX LogD: 0.60Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.73Np Likeness Score: -1.32
References 1. Zhang J, Yang Q, Cross JB, Romero JA, Poutsiaka KM, Epie F, Bevan D, Wang B, Zhang Y, Chavan A, Zhang X, Moy T, Daniel A, Nguyen K, Chamberlain B, Carter N, Shotwell J, Silverman J, Metcalf CA, Ryan D, Lippa B, Dolle RE.. (2015) Discovery of Azaindole Ureas as a Novel Class of Bacterial Gyrase B Inhibitors., 58 (21): [PMID:26460684 ] [10.1021/acs.jmedchem.5b00961 ]