N-(3-(2-amino-1H-imidazol-4-yl)allyl)-1H-indole-2-carboxamide

ID: ALA3261430

Chembl Id: CHEMBL3261430

PubChem CID: 90675942

Max Phase: Preclinical

Molecular Formula: C15H15N5O

Molecular Weight: 281.32

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Nc1nc(/C=C/CNC(=O)c2cc3ccccc3[nH]2)c[nH]1

Standard InChI:  InChI=1S/C15H15N5O/c16-15-18-9-11(19-15)5-3-7-17-14(21)13-8-10-4-1-2-6-12(10)20-13/h1-6,8-9,20H,7H2,(H,17,21)(H3,16,18,19)/b5-3+

Standard InChI Key:  LCRLPZUQHUDMCT-HWKANZROSA-N

Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA1 Tclin Voltage-gated potassium channel subunit Kv1.1 (248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA2 Tclin Voltage-gated potassium channel subunit Kv1.2 (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA3 Tclin Voltage-gated potassium channel subunit Kv1.3 (1067 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA4 Tclin Voltage-gated potassium channel subunit Kv1.4 (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA5 Tclin Voltage-gated potassium channel subunit Kv1.5 (1353 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA6 Tclin Voltage-gated potassium channel subunit Kv1.6 (20 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus mutans (2687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna1 Voltage-gated potassium channel subunit Kv1.1 (34 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna2 Potassium voltage-gated channel subfamily A member 2 (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna3 Voltage-gated potassium channel subunit Kv1.3 (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna4 Voltage-gated potassium channel subunit Kv1.4 (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna5 Potassium voltage-gated channel subfamily A member 5 (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcna6 Potassium voltage-gated channel subfamily A member 6 (27 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Kcnh1 Potassium voltage-gated channel subfamily H member 1 (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 281.32Molecular Weight (Monoisotopic): 281.1277AlogP: 1.92#Rotatable Bonds: 4
Polar Surface Area: 99.59Molecular Species: BASEHBA: 3HBD: 4
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.52CX LogP: 1.37CX LogD: 0.36
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.59Np Likeness Score: 0.01

References

1. Hodnik Ž, Łoś JM, Žula A, Zidar N, Jakopin Ž, Łoś M, Sollner Dolenc M, Ilaš J, Węgrzyn G, Peterlin Mašič L, Kikelj D..  (2014)  Inhibition of biofilm formation by conformationally constrained indole-based analogues of the marine alkaloid oroidin.,  24  (11): [PMID:24755428] [10.1016/j.bmcl.2014.03.094]
2. Tomasic T, Nabergoj D, Vrbek S, Zidar N, Jakopin Z, Zula A, Hodnik Z, Jukic M, Anderluh M, Ilas J, Dolenc MS, Peluso J, Ubeaud-Sequier G, Muller CD, Masic LP, Kikelj D.  (2015)  Analogues of the marine alkaloids oroidin, clathrodin, and hymenidin induce apoptosis in human HepG2 and THP-1 cancer cells,  (1): [10.1039/C4MD00286E]
3. 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]

Source