Pentamidine

CAT:
804-HY-B0537-01
Size:
5 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Pentamidine - image 1

Pentamidine

  • Description:

    Pentamidine (MP-601205) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities[1][2][3][4].
  • Product Name Alternative:

    MP-601205
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Antibiotic; Bacterial; Fungal; Parasite; Phosphatase
  • Type:

    Reference compound
  • Related Pathways:

    Anti-infection; Metabolic Enzyme/Protease
  • Applications:

    COVID-19-immunoregulation
  • Field of Research:

    Cancer; Infection
  • Assay Protocol:

    https://www.medchemexpress.com/pentamidine.html
  • Purity:

    97.19
  • Solubility:

    DMSO : 3.3 mg/mL (ultrasonic; warming; adjust pH to 6 with 1 M HCl; heat to 60°C)
  • Smiles:

    N=C (C1=CC=C (OCCCCCOC2=CC=C (C (N) =N) C=C2) C=C1) N
  • Molecular Formula:

    C19H24N4O2
  • Molecular Weight:

    340.42
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [2]Nguewa, P.A., et al., Pentamidine is an antiparasitic and apoptotic drug that selectively modifies ubiquitin. Chem Biodivers, 2005. 2 (10) : p. 1387-400.|[3]Sands M, et al. Pentamidine: a review. Rev Infect Dis. 1985 Sep-Oct;7 (5) :625-34.|[4]David C. Bean, et al. Pentamidine: a drug to consider re-purposing in the targeted treatment of multi-drug resistant bacterial infections? J Lab Precis Med 2017;2:49.|[1]Pathak MK, et al. Pentamidine is an inhibitor of PRL phosphatases with anticancer activity. Mol Cancer Ther. 2002 Dec;1 (14) :1255-64.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, protect from light)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • Isoform:

    Leishmania; Trypanosoma
  • Citation 01:

    Biochem Biophys Res Commun. 2019 Sep 17;517 (2) :221-226.|BMC Womens Health. 2022 Nov 24;22 (1) :470.|Drug Des Devel Ther. 2021 Jul 1;15:2857-2868.|Immunity. 2023 Feb 14;56 (2) :272-288.e7.|Int J Mol Sci. 2023 Sep 7;24 (18) :13812.|Microbiol Spectr. 2023 Jun 15;11 (3) :e0313822.|Molecules. 2020 Apr 23;25 (8) :1980.|Cell Rep Methods. 2023 Oct 23;3 (10) :100599.
  • CAS Number:

    100-33-4