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(E)-N-(3-(2-amino-1H-imidazol-4-yl)allyl)-4-chloro-5-methyl-1H-pyrrole-2-carboxamide ID: ALA4202870
Chembl Id: CHEMBL4202870
PubChem CID: 145978207
Max Phase: Preclinical
Molecular Formula: C12H14ClN5O
Molecular Weight: 279.73
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Cc1[nH]c(C(=O)NC/C=C/c2c[nH]c(N)n2)cc1Cl
Standard InChI: InChI=1S/C12H14ClN5O/c1-7-9(13)5-10(17-7)11(19)15-4-2-3-8-6-16-12(14)18-8/h2-3,5-6,17H,4H2,1H3,(H,15,19)(H3,14,16,18)/b3-2+
Standard InChI Key: LCCRCPRIAOYATR-NSCUHMNNSA-N
Associated Targets(Human) 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: 279.73Molecular Weight (Monoisotopic): 279.0887AlogP: 1.73#Rotatable Bonds: 4Polar Surface Area: 99.59Molecular Species: BASEHBA: 3HBD: 4#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 8.52CX LogP: 1.16CX LogD: 0.14Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.69Np Likeness Score: 0.07
References 1. Zidar N, Žula A, Tomašič T, Rogers M, Kirby RW, Tytgat J, Peigneur S, Kikelj D, Ilaš J, Mašič LP.. (2017) Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels., 139 [PMID:28802123 ] [10.1016/j.ejmech.2017.08.015 ]