boronomethanaminium chloride

ID: ALA2035304

Chembl Id: CHEMBL2035304

PubChem CID: 122163886

Max Phase: Preclinical

Molecular Formula: CH7BClNO2

Molecular Weight: 74.88

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: Boronomethanaminium Chloride

Canonical SMILES:  Cl.NCB(O)O

Standard InChI:  InChI=1S/CH6BNO2.ClH/c3-1-2(4)5;/h4-5H,1,3H2;1H

Standard InChI Key:  RXWWNBVDVWZOQN-UHFFFAOYSA-N

Associated Targets(non-human)

dac D-alanyl-D-alanine carboxypeptidase (132 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: 74.88Molecular Weight (Monoisotopic): 75.0492AlogP: #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. Zervosen A, Bouillez A, Herman A, Amoroso A, Joris B, Sauvage E, Charlier P, Luxen A..  (2012)  Synthesis and evaluation of boronic acids as inhibitors of Penicillin Binding Proteins of classes A, B and C.,  20  (12): [PMID:22579615] [10.1016/j.bmc.2012.04.018]

Source