Research Pharmaceuticals and Intermediates

Pharmaceuticals are useful tools for mechanism of action studies in many ways. Besides being enzyme inhibitors, receptor agonists or antagonists, channel blockers, neurotransmitters themselves, they are used to compare and define other emerging compounds for their prospective applications.

  • Group 1
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  • Group 3
  • Group 4
  • Group 5
  • Group 6
  • Others
  • Group 1

    Structure Details
    Product Name: Ceftriaxone sodium
    Order number: 100995
    CAS: 104376-79-6
    Purity: >=95%
    Appearance: solid
    MF: C18H17N8NaO7S3
    MW: 576.553
    MP: 236 oC

    Description:
    This substance inhibits bacterial cell wall synthesis by binding one or more of the penicillin binding proteins (PBPs).
    Product Name: Penicillin G
    Order number: 100997
    CAS: 61-33-6
    Purity: >=95%
    Appearance: solid
    MF: C16H18N2O4S
    MW: 334.39
    MP: n.a. oC

    Description:
    This substance acts through the inhibition of biosynthesis of cell-wall peptidoglycan, rendering the cell wall osmotically unstable.
    Product Name: Cefotaxime acid
    Order number: 101001
    CAS: 63527-52-6
    Purity: >=95%
    Appearance: solid
    MF: C16H17N5O7S2
    MW: 455.46
    MP: >158 oC

    Description:
    Penicillin binds to PBPs and inhibits bacterial cell wall synthesis.
    Product Name: Cefuroxime sodium
    Order number: 101003
    CAS: 56238-63-2
    Purity: >=95%
    Appearance: solid
    MF: C16H15N4NaO8S
    MW: 446.366
    MP: n.a. oC

    Description:
    The mechanism of action is by inhibition of bacterial cell wall synthesis.
    Product Name: GEO: Penicillin-G-p-Methoxybenzyl ester Sulfoxide
    Order number: 101012
    CAS: 30034-13-0
    Purity: >=95%
    Appearance: solid
    MF: C24H26N2O6S
    MW: 470.54
    MP: n.a. oC

    Description:
    Penicillin G sulfoxide p-methoxybenzyl ester is a penicillin based beta-lactam derivative.
    Product Name: Carbenicillin
    Order number: 101017
    CAS: 4697-36-3
    Purity: >=95%
    Appearance: solid
    MF: C17H18N2O6S
    MW: 378.399
    MP: n.a. oC

    Description:
    This substance interferes in the final cell wall synthesis. The acylation of the penicillin-sensitive transpeptidase C-terminal domain can be achieved by opening the lactam ring.