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GSK1838705A

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Products Intro: Product Name:GSK1838705A
CAS:1116235-97-2
Purity:98% HPLC LCMS Package:10G;20G
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Products Intro: Product Name:GSK1838705A
CAS:1116235-97-2
Purity:99.63% Package:1mg;34USD|5mg;77USD|10mg;133USD Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:GSK1838705A
CAS:1116235-97-2
Purity:99% Package:10kg 25kg 200 kilograms per barrel Remarks:good
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Products Intro: Product Name:GSK1838705A
CAS:1116235-97-2
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer
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Products Intro: Product Name:GSK1838705
CAS:1116235-97-2
Purity:99% Package:5KG;1KG Remarks:GSK1838705

GSK1838705A manufacturers

  • GSK1838705A
  • GSK1838705A pictures
  • $34.00 / 1mg
  • 2026-05-11
  • CAS:1116235-97-2
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  • Purity: 99.89%
  • Supply Ability: 10g
GSK1838705A Basic information
Product Name:GSK1838705A
Synonyms:GSK1838705;GSK1838705A;2-[[2-[[1-[(Dimethylamino)ethanoyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide;2-[[2-[[1-[2-(Dimethylamino)acetyl]-2,3-dihydro-5-methoxy-1H-indol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide;2-(2-(1-(2-(dimethylamino)acetyl)-5-methoxyindolin-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-6-fluoro-N-methylbenzamide;2-[[2-[[1-[(Dimethylamino)ethanoyl]-5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide GSK1838705A;2-[[2-[[1-[2-(Dimethylamino)acetyl]-2,3-dihydro-5-methoxy-1H-indol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methy;CS-236
CAS:1116235-97-2
MF:C27H29FN8O3
MW:532.57
EINECS:
Product Categories:Inhibitors
Mol File:1116235-97-2.mol
GSK1838705A Structure
GSK1838705A Chemical Properties
density 1.399
storage temp. -20°C
solubility DMSO: soluble20mg/mL, clear
form powder
pka13.27±0.50(Predicted)
color white to light brown
InChIKeyHZTYDQRUAWIZRE-UHFFFAOYSA-N
SMILESC(NC)(=O)C1=C(F)C=CC=C1NC1N=C(NC2=CC3=C(C=C2OC)CCN3C(CN(C)C)=O)N=C2NC=CC2=1
Safety Information
WGK Germany 3
Storage Class11 - Combustible Solids
MSDS Information
GSK1838705A Usage And Synthesis
UsesGSK 1838705 is a potent IR and IGF1R inhibitor; also inhibits anaplastic lymphoma kinase (ALK).
DefinitionChEBI: 2-[[2-[[1-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-2,3-dihydroindol-6-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amino]-6-fluoro-N-methylbenzamide is an organooxygen compound and an organonitrogen compound. It is functionally related to an alpha-amino acid.
Biological Activitygsk1838705a is a small-molecule kinase inhibitor that inhibits igf-ir and the insulin receptor with ic50s of 2.0 and 1.6 nmol/l, respectively.igf-1r is a transmembrane receptor which is activated by insulin-like growth factor 1 and by a related hormone igf-2. this protein plays important role in the regulation of development. the insulin receptor is also a transmembrane receptor that is activated by insulin, igf-1 and igf2. this receptor is involved in insulin signaling pathway and plays an essential role in the regulation of glucose homeostasis.gsk1838705a obstructs the in vitro expansion of cell lines got from strong and hematologic malignancies, including numerous myeloma and ewing's sarcoma, and hinders the development of human tumor xenografts in vivo. in spite of the inhibitory impact of gsk1838705a on insulin receptor, insignificant effects on glucose homeostasis were seen at efficacious dosages. gsk1838705a represses the anaplastic lymphoma kinase (alk), which drives the distorted development of anaplastic substantial cell lymphomas, some neuroblastomas, and a subset of non–small cell lung growths.gsk1838705a restrains alk, with an ic50 value of 0.5 nm, furthermore, causes complete relapse of alk-ward tumors in vivo at very-endured measurements. gsk1838705a arrives for a promising antitumor agent for helpful use in human growth.
in vivo

GSK1838705A shows robust antitumor activity in animal xenograft models. Tumor types likely to respond to GSK1838705A include multiple myeloma and Ewing's sarcoma, as well as ALK-driven tumors (e.g., ALCL, NSCLC, and neuroblastoma). A single oral dose of GSK1838705A at 0.1 and 0.3 mg/kg results in 35% and 65% inhibition of IGF-IR phosphorylation, respectively, whereas doses ≥1 mg/kg results in complete inhibition of ligand-induced IGF-IR phosphorylation[1].

storageStore at -20°C
references[1]. sabbatini p, et al. gsk1838705a inhibits the insulin-like growth factor-1 receptor and anaplastic lymphoma kinase and shows antitumor activity in experimental models of human cancers. mol cancer ther. 2009 oct;8(10):2811-20.
GSK1838705A Preparation Products And Raw materials
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