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GSK1904529A

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Products Intro: Product Name:GSK1904529A
CAS:1089283-49-7
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:1089283-49-7
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CAS:1089283-49-7
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Products Intro: Product Name:GSK1904529A
CAS:1089283-49-7
Purity:99% Package:10kg 25kg 200 kilograms per barrel Remarks:good

GSK1904529A manufacturers

  • GSK1904529A
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  • $34.00
  • 2026-07-27
  • CAS:1089283-49-7
  • Purity: 99.96%
  • Supply Ability: 10g
  • GSK1904529A
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  • $1.10
  • 2025-06-25
  • CAS:1089283-49-7
  • Min. Order: 1g
  • Purity: 99.0% min
  • Supply Ability: 100 tons min
GSK1904529A Basic information
Product Name:GSK1904529A
Synonyms:CS-29;GSK1904529A;GSK-1904529A;GSK 1904529A;GSK 4529;GSK1904529A;GSK1904529A : IGF-IR, IGF-IIR inhibitor;N-(2,6-Difluorophenyl)-5-[3-[2-[[5-ethyl-2-(methyloxy)-4-[4-[4-(methylsulfonyl)-1-piperazinyl]-1-piperidinyl]phenyl]amino]-4-pyrimidinyl]imidazo[1,2-a]pyridin-2-yl]-2-(methyloxy)benzamide;N-(2,6-difluorophenyl)-5-(3-(2-(5-ethyl-2-methoxy-4-(4-(4-(methylsulfonyl)piperazin-1-yl)piperidin-1-yl)phenylamino)pyrimidin-4-yl)H-imidazo[1,2-a]pyridin-2-yl)-2-methoxybenzamide;N-(2,6-Difluorophenyl)-5-[3-[2-[[5-ethyl-2-(methyloxy)-4-[4-[4-(methylsulfonyl)-1-piperazinyl]-1-piperidinyl]phenyl]amino]-4-pyrimidinyl]imidazo[1,2-a]pyridin-2-yl]-2-(methyloxy)benzamide GSK 1904529A
CAS:1089283-49-7
MF:C44H47F2N9O5S
MW:851.96
EINECS:
Product Categories:Inhibitors
Mol File:1089283-49-7.mol
GSK1904529A Structure
GSK1904529A Chemical Properties
density 1.39
storage temp. Store at -20°C
solubility ≥42.6 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
form solid
pka11.12±0.70(Predicted)
color Light yellow to yellow
InChIKeyMOSKATHMXWSZTQ-UHFFFAOYSA-N
SMILESC(NC1=C(F)C=CC=C1F)(=O)C1=CC(C2=C(C3C=CN=C(NC4=CC(CC)=C(N5CCC(N6CCN(S(C)(=O)=O)CC6)CC5)C=C4OC)N=3)N3C(=N2)C=CC=C3)=CC=C1OC
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
GSK1904529A Usage And Synthesis
UsesA selective inhibitor of IGF-1R and IR with IC50s of 27 nM and 25 nM, respectively.
UsesGSK 1904529A is a small-molecule inhibitor of the insulin-like growth factor-I receptor tyrosine kinase.
DefinitionChEBI: N-(2,6-difluorophenyl)-5-[3-[2-[5-ethyl-2-methoxy-4-[4-(4-methylsulfonyl-1-piperazinyl)-1-piperidinyl]anilino]-4-pyrimidinyl]-2-imidazo[1,2-a]pyridinyl]-2-methoxybenzamide is a member of benzamides.
Biological Activitygsk1904529a is a small-molecule inhibitor of the insulin-like growth factor-i receptor (igf-ir) with ic50 value of 27 nm 1.gsk1904529a is a reversible and atp-competitive inhibitor with ki value of 1.6 nm. in nih-3t3/lisn cells, gsk1904529a potently inhibited phosphorylation of igf-ir with ic50 value of 22 nm. it also demonstrated to be a selective inhibitor since it showed poor inhibitory activity against 45 other serine/threonine and tyrosine kinases. when treated with whole-cell extracts, gsk1904529a significantly inhibited the ligand-induced phosphorylation of igf-ir and decreased phosphorylation of downstream signaling including akt, irs-1 and erk at concentrations > 0.01μm. gsk1904529a suppressed cell proliferation in a variety of tumor cells. the ic50 values for nci-h929, tc-71, sk-n-mc, colo 205, mcf7 and prec are 81, 35, 43, 124, 137 and 68 nm, respectively. in colo 205, mcf-7, and nci-h929 cells, gsk1904529a treatment resulted in cell accumulation in g1 and decrease in s and g2-m phases. moreover, in nih-3t3/lisn xenograft model, once daily administration of gsk1904529a at 30 mg/kg inhibited 56% of tumor growth 1.
in vivo

GSK1904529A (30 mg/kg; p.o. once or twice daily for 21 d) has antitumor activity in mice[1].
GSK1904529A (1-30 mg/kg; a single p.o.) decreases IGF-I-induced IGF-IR phosphorylation in a dose-dependent manner in mice[1].
GSK1904529A (30 mg/kg; p.o. once or twice daily for 21 d) has no significant alterations in the blood glucose levels in mice[1].

Animal Model:Female athymic nu/nu CD-1 mice are bring NIH-3T3/LISN tumor[1]
Dosage:30 mg/kg
Administration:P.o. once or twice daily for 21 d
Result:Resulted in 56% (once daily) and 98% (twice daily) inhibition of tumor growth.
No significant decrease in body weight on the once-daily schedule.
Observed 11-13% of body weight loss, and recovered to near baseline 6 days after the cessation of treatment in twice-daily group.
targetIGF1R
references1. sabbatini p, rowand j l, groy a, et al. antitumor activity of gsk1904529a, a small-molecule inhibitor of the insulin-like growth factor-i receptor tyrosine kinase. clinical cancer research, 2009, 15(9): 3058-3067.
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