Pentamidine dihydrochloride
CAS No. 50357-45-4
Pentamidine dihydrochloride ( MP-601205 dihydrochloride )
Catalog No. M27680 CAS No. 50357-45-4
Pentamidine dihydrochloride is an aromatic diamidine agent with activity against a number of microorganisms including protozoa (Trypanosoma brucei, Leishmania spp., and Babesia spp.) and fungi (Pneumocystis jirovecii).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 45 | Get Quote |
|
10MG | 68 | Get Quote |
|
25MG | 115 | Get Quote |
|
50MG | 173 | Get Quote |
|
100MG | 258 | Get Quote |
|
200MG | 388 | Get Quote |
|
500MG | 642 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
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Product NamePentamidine dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionPentamidine dihydrochloride is an aromatic diamidine agent with activity against a number of microorganisms including protozoa (Trypanosoma brucei, Leishmania spp., and Babesia spp.) and fungi (Pneumocystis jirovecii).
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DescriptionPentamidine dihydrochloride is an aromatic diamidine agent with activity against a number of microorganisms including protozoa (Trypanosoma brucei, Leishmania spp., and Babesia spp.) and fungi (Pneumocystis jirovecii). Pentamidine dihydrochloride is a potent and selective protein tyrosine phosphatases and phosphatase of regenerating liver inhibitor. Pentamidine dihydrochloride inhibits parasite Leishmania infantum with an IC50 of 2.5 μM.(In Vitro):Pentamidine at its therapeutic doses inhibited recombinant PRL phosphatases in vitro and inactivated ectopically expressed PRLs in NIH3T3 transfectants with an effective duration more than 24 h after a pulse cell treatment.(In Vivo):Pentamidine at a tolerable dose markedly inhibited the growth of WM9 human melanoma tumors in nude mice coincident with the induction of tumor cell necrosis and is capable of inactivating ectopically expressed PRL-2 in the cancer cells.
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SynonymsMP-601205 dihydrochloride
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PathwayMetabolic Enzyme/Protease
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TargetPhosphatase
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Recptoraryl hydrocarbon receptor;GSK-3;CDK1/CyclinB;CDK5/p25
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Research Area——
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Indication——
Chemical Information
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CAS Number50357-45-4
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Formula Weight413.3
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Molecular FormulaC19H26Cl2N4O2
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Purity>98% (HPLC)
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Solubility——
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SMILES[Cl-].[Cl-].NC(=[NH2+])c1ccc(OCCCCCOc2ccc(cc2)C(N)=[NH2+])cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Meijer L, et al. GSK-3-selective inhibitors derived from Tyrian purple indirubins. Chem Biol. 2003 Dec;10(12):1255-66.
molnova catalog
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