N-cyclooctyl-6-(trifluoromethyl)benzo[b]selenophene-2-carboxamide

ID: ALA5287728

Max Phase: Preclinical

Molecular Formula: C18H20F3NOSe

Molecular Weight: 402.32

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(NC1CCCCCCC1)c1cc2ccc(C(F)(F)F)cc2[se]1

Standard InChI:  InChI=1S/C18H20F3NOSe/c19-18(20,21)13-9-8-12-10-16(24-15(12)11-13)17(23)22-14-6-4-2-1-3-5-7-14/h8-11,14H,1-7H2,(H,22,23)

Standard InChI Key:  CHOUVPFHAJYJNK-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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    2.3266    1.4038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7755   -0.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4568   -1.7156    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1703   -1.3023    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA5287728

    ---

Associated Targets(non-human)

Mycobacterium tuberculosis variant bovis (1746 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 402.32Molecular Weight (Monoisotopic): 403.0662AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Tan YJ, Li M, Gunawan GA, Nyantakyi SA, Dick T, Go ML, Lam Y..  (2021)  Amide-Amine Replacement in Indole-2-carboxamides Yields Potent Mycobactericidal Agents with Improved Water Solubility.,  12  (5.0): [PMID:34055215] [10.1021/acsmedchemlett.0c00588]

Source