GSK3186899

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Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:GSK3186899
CAS:1972617-87-0
Purity:98.35% Package:1mg;148USD|5mg;323USD|10mg;491USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Zhejiang J&C Biological Technology Co.,Limited
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Products Intro: Product Name:GSK3186899
CAS:1972617-87-0
Purity:99% Package:5KG;1KG Remarks:GSK3186899
Company Name: Zibo Hangyu Biotechnology Development Co., Ltd
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Products Intro: Product Name:GSK3186899
CAS:1972617-87-0
Company Name: HANGZHOU LEAP CHEM CO., LTD.
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Products Intro: Product Name:GSK3186899(DDD-853651)
CAS:1972617-87-0
Purity:0 Package:1g; 5g; 25g; 1kg; 5kg; 25kg Remarks:0
Company Name: Qingdao IniKem BioPharmaTech Co.,Ltd  
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Products Intro: Product Name:GSK3186899
CAS:1972617-87-0
Purity:98% HPLC Package:50mg/;100mg/;250mg/;500mg/;1g/;5g/

GSK3186899 manufacturers

  • GSK3186899
  • GSK3186899 pictures
  • $148.00 / 1mg
  • 2025-11-10
  • CAS:1972617-87-0
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  • Purity: 99.61%
  • Supply Ability: 10g
GSK3186899 Basic information
Product Name:GSK3186899
Synonyms:GSK3186899;DDD-853651;1-Propanesulfonamide, 3,3,3-trifluoro-N-[trans-4-[[3-[(2S)-2-methyl-4-morpholinyl]-1H-pyrazolo[3,4-d]pyrimidin-6-yl]amino]cyclohexyl]-;3,3,3-Trifluoro-N-[trans-4-[[3-[(S)-2-methylmorpholino]-1H-pyrazolo[3,4-d]pyrimidin-6-yl]amino]cyclohexyl]propane-1-sulfonamide;GSK3186899(DDD-853651)
CAS:1972617-87-0
MF:C19H28F3N7O3S
MW:491.53
EINECS:
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Mol File:1972617-87-0.mol
GSK3186899 Structure
GSK3186899 Chemical Properties
storage temp. Store at -20°C
solubility Soluble in DMSO
form Solid
color Off-white to light yellow
Safety Information
MSDS Information
GSK3186899 Usage And Synthesis
DescriptionGSK3186899, also known as DDD-853651, is a CDC2-related kinase 12 inhibitor (CRK12), with an EC50 of 1.4 μM. GSK3186899 is an candidate for the Treatment of Visceral Leishmaniasis.
UsesGSK3186899 (DDD-853651) is an inhibitor of cdc-2-related kinase 12 (CRK12), with an EC50 of 1.4 μM for L. donovani in an intra-macrophage assay.
in vivo

In the mouse model of infection, GSK3186899 demonstrates comparable activity to the front-line drug miltefosine, reducing parasite levels by 99% when dosed orally twice a day for 10 days at 25 mg/kg. The efficacy of treatment is dependent on dose, frequency, and duration (10 days better than 5). The non-clinical safety data for GSK3186899 suggests a suitable therapeutic window for progression into regulatory preclinical studies. Non-GLP preclinical assessment of cardiovascular effects and genotoxicity does not reveal any issues that would prevent further development. In addition, there are no notable adverse effects in a rat seven-day repeat-dose oral toxicity study with respect to clinical chemistry and histopathology at all doses tested. Both the in vivo efficacy and safety profile of GSK3186899 support progression to definitive safety studies[1].

IC 50Leishmania
References[1] Wyllie S, et al. Cyclin-dependent kinase 12 is a drug target for visceral leishmaniasis. Nature. 2018 Aug;560(7717):192-197. DOI:10.1038/s41586-018-0356-z
GSK3186899 Preparation Products And Raw materials
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