NVP-ADW742 b
CAS No. 475488-23-4
NVP-ADW742 b( ADW | GSK 552602A | ADW742 )
Catalog No. M19445 CAS No. 475488-23-4
NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 103 | In Stock |
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| 5MG | 81 | In Stock |
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| 10MG | 136 | In Stock |
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| 25MG | 282 | In Stock |
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| 50MG | 440 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNVP-ADW742 b
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NoteResearch use only, not for human use.
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Brief DescriptionNVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.
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DescriptionNVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM >16-fold more potent against IGF-1R than InsR; little activity to HER2 PDGFR VEGFR-2 Bcr-Abl and c-Kit.
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In VitroNVP-ADW742 (ADW742; 0.1-10 μM; 72 hours) dose-dependently inhibits serum-induced cell growth in all cell lines. NVP-ADW742 (0.1-9 μM; 20 min) blocks IGF-1-induced phosphorylation of IGF-1R and its known downstream target Akt at submicromolar concentrations. NVP-ADW742 has much higher IC50 values for other kinases (IC50>10 μM for HER2, PDGFR, VEGFR-2, or Bcr-Abl p210; and IC50>5 μM for c-Kit). Cell Viability Assay Cell Line:A panel of cell lines from multiple myeloma (MM), other hematologic malignancies and solid tumors Concentration:0.1, 0.5, 1, 2, 5, 10 μM Incubation Time:72 hours Result:Dose-dependently inhibited serum-induced cell growth in all cell lines.Western Blot Analysis Cell Line:NWT-21 cells Concentration:0.1, 0.3, 1, 3, 9 μM Incubation Time:20 min Result:Blocked IGF-1-induced phosphorylation of IGF-1R and its known downstream target Akt at submicromolar concentrations.
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In VivoNVP-ADW742 (ADW742; 10 mg/kg for IP or 50 mg/kg for orally; twice daily for 19 days) significantly suppresses tumor growth and prolongs the survival of mice. Animal Model:6- to 8-week-old male SCID/NOD mice with diffuse skeletal lesions of luciferase-expressing MM cells Dosage:10 mg/kg (IP) or 50 mg/kg (orally) Administration:IP or orally; twice daily for 19 days Result:Significantly suppressed tumor growth and prolonged the survival of mice.
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SynonymsADW | GSK 552602A | ADW742
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PathwayAngiogenesis
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TargetIGF-1R
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RecptorIGF-1R
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Research Area——
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Indication——
Chemical Information
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CAS Number475488-23-4
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Formula Weight453.58
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Molecular FormulaC28H31N5O
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Purity>98% (HPLC)
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SolubilityDMSO:10 mg/mL (22.04 mM) warmed;Ethanol:3 mg/mL (6.61 mM);Water:<1 mg/mL
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SMILESC1CCN(C1)CC2CC(C2)N3C=C(C4=C3N=CN=C4N)C5=CC(=CC=C5)OCC6=CC=CC=C6
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Chemical Name5-(3-(benzyloxy)phenyl)-7-((1r3r)-3-(pyrrolidin-1-ylmethyl)cyclobutyl)-7H-pyrrolo[23-d]pyrimidin-4-amine
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.Mitsiades CS et al. Cancer Cell 2004 5(3) 221-230.
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