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Deltarasin

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CAS:1440898-61-2
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CAS:1440898-61-2
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Deltarasin manufacturers

  • Deltarasin
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  • $38.00 / 2mg
  • 2025-09-11
  • CAS:1440898-61-2
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  • Purity: 99.40%
  • Supply Ability: 10g
  • Deltarasin
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  • 2025-01-03
  • CAS:1440898-61-2
  • Min. Order: 5mg
  • Purity: 99% HPLC
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  • Deltarasin
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  • $1.00 / 1KG
  • 2019-07-06
  • CAS:1440898-61-2
  • Min. Order: 1G
  • Purity: 98%
  • Supply Ability: 100KG
Deltarasin Basic information
Product Name:Deltarasin
Synonyms:Deltarasin;Deltarasin-HCl;2-[4-[(2S)-2-(2-Phenyl-1H-benzimidazol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylmethyl)-1H-benzimidazole;1H-Benzimidazole,2-[4-[(2S)-2-(2-phenyl-1H-benzimidazol-1-yl)-2-(4-piperidinyl)ethoxy]phenyl]-1-(phenylmethyl)-;deltarasine;Deltarasin USP/EP/BP;(S)-1-benzyl-2-(4-(2-(2-phenyl-1H-benzo[d]imidazol-1-yl)-2-(piperidin-4-yl)ethoxy)phenyl)-1H-benzo[d]imidazole;Deltarasin,Phosphodiesterase (PDE),inhibit,Inhibitor,Ras
CAS:1440898-61-2
MF:C40H37N5O
MW:603.75
EINECS:
Product Categories:Inhibitors;API
Mol File:1440898-61-2.mol
Deltarasin Structure
Deltarasin Chemical Properties
Boiling point 824.3±75.0 °C(Predicted)
density 1.23±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form solid
pka10.35±0.10(Predicted)
color White
Water Solubility H2O: 2mg/mL, clear
CAS DataBase Reference1440898-61-2
Safety Information
MSDS Information
Deltarasin Usage And Synthesis
UsesDeltarasin is an inhibitior of KRAS-PDEδ which has been shown to impair oncogenic signalling.
Biological Activitythe kras oncogene product is considered a major target in anticancer drug discovery. interfering with binding of mammalian pdeδ to kras by means of small molecules provides a novel opportunity to suppress oncogenic ras signalling by altering its localization to endomembranes. deltarasin is an inhibitor of the kras-pdeδ interaction to impair oncogenic kras signalling.
in vitrowithin a minute, 5 mm of deltarasin completely inhibited pdeδ-kras interaction and released the insolubilized mcitrine-rheb/kras6q to the endomembrane system. this showed that deltarasin interfered with the binding of kras to pdeδ in cells and thereby inhibited its solubilization [1].
in vivoa clear dose-dependent reduction in panc-tu-i tumour growth rate could be observed in deltarasin treated mice with respect to the vehicle-injected controls, where the growth of tumours in mice that were treated with 10mg kg/1 bid deltarasin was almost completely blocked [1].
references[1] zimmermann g, papke b, ismail s, vartak n, chandra a, hoffmann m, hahn sa, triola g, wittinghofer a, bastiaens pi, waldmann h. small molecule inhibition of the kras-pdeδ interaction impairs oncogenic kras signalling. nature. 2013;497(7451):638-42.
Deltarasin Preparation Products And Raw materials
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