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Organoantimony

Organoantimony compounds possess direct bonds between carbon and antimony atoms. Organoantimony compounds commonly have Sb(V) or Sb(III) oxidation states and are studied in organometallic chemistry.

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1

Medchemexpress LLC Benzenemethanol, α-[(1S)-1-aminoethyl]-3-hydroxy-, (αR)-, (2R,3R)-2,3-dihydroxybutanedioate (1:1) | 33402-03-8 | 99.9% | 100 MG
SDP

Metaraminol tartrate is an α-adrenergic agonist and a sympathomimetic amine that directly and indirectly affects adrenergic receptors, with alpha effects being predominant. It acts as a vasopressor agent and is for research use only.

  • α-Adrenergic agonist
  • Sympathomimetic amine
  • Acts as a vasopressor agent
  • High purity: 99.9%

ENCOMPASS_PREFERRED
2

Medchemexpress LLC Budiodarone tartrate | 478941-93-4 | 98.14% | 853.43 | 25 MG
SDP

Budiodarone tartrate (ATI-2042) is a chemical analogue of Amiodarone that acts as an antiarrhythmic agent. It inhibits multiple cardiac ion channels, including potassium, sodium, and calcium channels.

  • Acts as an antiarrhythmic agent
  • Inhibits multiple cardiac ion channels
  • Exhibits balanced potassium, sodium, and calcium channel inhibition
  • Chemical analogue of Amiodarone
  • High purity of 98.14%

ENCOMPASS_PREFERRED
3

Medchemexpress LLC Tolterodine tartrate | 124937-52-6 | 98.6% | C26H37NO7 | 1 ML
SDP

Tolterodine tartrate is a mAChR inhibitor and a substrate for cytochrome P450 enzymes. It competitively binds acetylcholine, which reduces sympathetic excitation and inhibits involuntary bladder muscle contraction. It restores the Nrf2/NF-κB signaling pathway, providing protection against inflammatory response and ferroptosis, and ameliorates LPS-induced reactive oxygen species production and lipid oxidation. This product can be used for research related to urinary tract infections and overactive bladder.

  • Competitively binds acetylcholine
  • Reduces sympathetic excitation
  • Inhibits involuntary bladder muscle contraction
  • Restores Nrf2/NF-κB signaling pathway
  • Provides protection against inflammatory response and ferroptosis
  • Ameliorates LPS-induced reactive oxygen species production and lipid oxidation

ENCOMPASS_PREFERRED
4

Medchemexpress LLC Gemigliptin tartrate | 1374639-74-3 | 99.5% | 639.45 | 5 MG
SDP

Gemigliptin tartrate is a highly selective, reversible, and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor, with an IC50 of 10.3 nM for human recombinant DPP-4. It exhibits potent anti-glycation properties and can be used for the research of advanced glycation end products (AGE)-related diabetic complications. This product is for research use only.

  • Highly selective, reversible, and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor
  • IC50 of 10.3 nM for human recombinant DPP-4
  • Exhibits potent anti-glycation properties
  • Useful for research of advanced glycation end products (AGE)-related diabetic complications
  • Dose-dependently inhibits the formation of AGE-BSA
  • Suppresses the cross-linking of preformed AGE-BSA with rat tail tendon collagen
  • Inhibits AGEs formation and AGE cross-links in vivo
  • Dose-dependently inhibits plasma DPP-4 activity in various animal models

ENCOMPASS_PREFERRED