(6S,7S)-7-{2-(2-Amino-thiazol-4-yl)-2-[(E)-methoxyimino]-acetylamino}-3-[(E)-3-(1-methyl-1H-tetrazol-5-ylsulfanyl)-propenyl]-8-oxo-4-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid

ID: ALA70608

PubChem CID: 44311485

Max Phase: Preclinical

Molecular Formula: C18H19N9O5S3

Molecular Weight: 537.61

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/CSc3nnnn3C)SC[C@H]12)c1csc(N)n1

Standard InChI:  InChI=1S/C18H19N9O5S3/c1-26-18(22-24-25-26)33-5-3-4-10-13(16(30)31)27-9(7-34-10)12(15(27)29)21-14(28)11(23-32-2)8-6-35-17(19)20-8/h3-4,6,9,12H,5,7H2,1-2H3,(H2,19,20)(H,21,28)(H,30,31)/b4-3+,23-11+/t9-,12+/m1/s1

Standard InChI Key:  UOQZPQDYPLRCQK-CPBVFGTBSA-N

Molfile:  

     RDKit          2D

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  2  5  1  0
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M  END

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: 537.61Molecular Weight (Monoisotopic): 537.0671AlogP: -0.31#Rotatable Bonds: 9
Polar Surface Area: 190.81Molecular Species: ACIDHBA: 14HBD: 3
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 2.93CX Basic pKa: 3.53CX LogP: -0.76CX LogD: -3.52
Aromatic Rings: 2Heavy Atoms: 35QED Weighted: 0.16Np Likeness Score: -1.08

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