1-{5-[(E)-2-((6S,7S)-7-{2-(2-Amino-thiazol-4-yl)-2-[(E)-methoxyimino]-acetylamino}-2-carboxy-8-oxo-4-thia-1-aza-bicyclo[4.2.0]oct-2-en-3-yl)-vinyl]-furan-2-ylmethyl}-pyridinium

ID: ALA3559428

PubChem CID: 118753752

Max Phase: Preclinical

Molecular Formula: C25H22N6O6S2

Molecular Weight: 566.62

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CO/N=C(/C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(/C=C/c3ccc(C[n+]4ccccc4)o3)SC[C@H]12)c1csc(N)n1

Standard InChI:  InChI=1S/C25H22N6O6S2/c1-36-29-19(16-12-39-25(26)27-16)22(32)28-20-17-13-38-18(21(24(34)35)31(17)23(20)33)8-7-14-5-6-15(37-14)11-30-9-3-2-4-10-30/h2-10,12,17,20H,11,13H2,1H3,(H3-,26,27,28,32,34,35)/b8-7+,29-19+/t17-,20+/m1/s1

Standard InChI Key:  APIGEWVKOBSGIO-VCTKVYEWSA-N

Molfile:  

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M  CHG  2  15   1  32  -1
M  END

Alternative Forms

  1. Parent:

    ALA3559428

    ---

Associated Targets(non-human)

Staphylococcus sp. (496 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterobacteriaceae (669 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

Biocomponents

Calculated Properties

Molecular Weight: 566.62Molecular Weight (Monoisotopic): 566.1042AlogP: 0.12#Rotatable Bonds: 9
Polar Surface Area: 167.06Molecular Species: ACIDHBA: 11HBD: 2
#RO5 Violations: 2HBA (Lipinski): 12HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 2.92CX Basic pKa: 3.53CX LogP: -3.67CX LogD: -3.34
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.16Np Likeness Score: -0.31

References

1. Aszodi J, Bonnet A, Chantot J, Costerousse G, Didierlaurent S, Teutsch G.  (1993)  Vinylogous vs arylogous isocephems,  (11): [10.1016/S0960-894X(01)80930-6]

Source