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ID: ALA2323440
Max Phase: Preclinical
Molecular Formula: C22H40Cl2N4
Molecular Weight: 360.59
Molecule Type: Small molecule
Associated Items:
ID: ALA2323440
Max Phase: Preclinical
Molecular Formula: C22H40Cl2N4
Molecular Weight: 360.59
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C[n+]1ccn(CCCCCCCCCCCCCCn2cc[n+](C)c2)c1.[Cl-].[Cl-]
Standard InChI: InChI=1S/C22H40N4.2ClH/c1-23-17-19-25(21-23)15-13-11-9-7-5-3-4-6-8-10-12-14-16-26-20-18-24(2)22-26;;/h17-22H,3-16H2,1-2H3;2*1H/q+2;;/p-2
Standard InChI Key: ZRNKZXKKLUPHME-UHFFFAOYSA-L
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 360.59 | Molecular Weight (Monoisotopic): 360.3242 | AlogP: 4.32 | #Rotatable Bonds: 15 |
Polar Surface Area: 17.62 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: -2.09 | CX LogD: -2.09 |
Aromatic Rings: 2 | Heavy Atoms: 26 | QED Weighted: 0.33 | Np Likeness Score: -0.14 |
1. Gao Y, Vlahakis JZ, Szarek WA, Brockhausen I.. (2013) Selective inhibition of glycosyltransferases by bivalent imidazolium salts., 21 (5): [PMID:23375091] [10.1016/j.bmc.2012.12.034] |
2. Kocev A, Melamed J, Wang S, Kong X, Vlahakis JZ, Xu Y, Szarek WA, Brockhausen I.. (2020) Inhibition of bacterial growth and galactosyltransferase activity of WbwC by α, ω-bis(3-alkyl-1H-imidazolium)alkane salts: Effect of varying carbon content., 28 (11): [PMID:32312486] [10.1016/j.bmc.2020.115494] |
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