LW6
CAS No. 934593-90-5
LW6( CAY10585 | CAY-10585 | CAY 10585 | LW6 )
Catalog No. M17673 CAS No. 934593-90-5
LW6 is a novel HIF-1 inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 35 | In Stock |
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| 5MG | 57 | In Stock |
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| 10MG | 82 | In Stock |
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| 25MG | 174 | In Stock |
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| 50MG | 282 | In Stock |
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| 100MG | 425 | In Stock |
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| 500MG | 888 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameLW6
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NoteResearch use only, not for human use.
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Brief DescriptionLW6 is a novel HIF-1 inhibitor.
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DescriptionCAY10585, also known as LW6, was first identified and reported by a group scientists from Korea. LW8 was found to inhibits the accumulation of HIF-1alpha. LW6 decreased HIF-1alpha protein expression without affecting HIF-1beta expression. It was further found that LW8 promoted the degradation of wild type HIF-1alpha, but not of a DM-HIF-1alpha with modifications of P402A and P564A, at hydroxylation sites in the oxygen-dependent degradation domain (ODDD). LW6 did not affect the activity of prolyl hydroxylase (PHD), but induced the expression of von Hippel-Lindau (VHL), which interacts with prolyl-hydroxylated HIF-1alpha for proteasomal degradation. In the presence of LW8, knockdown of VHL did not abolish HIF-1alpha protein accumulation, indicating that LW8 degraded HIF-1alpha via regulation of VHL expression. In mice carrying xenografts of human colon cancer HCT116 cells, LW8 demonstrated strong anti-tumor efficacy in vivo and caused a decrease in HIF-1alpha expression in frozen-tissue immunohistochemical staining. These data suggest that LW8 may be valuable in the development of a HIF-1alpha inhibitor for cancer treatment.
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In VitroLW6 affects the stability of the HIF-1α protein. LW6 promotes the degradation of wild type HIF-1α, but not of a DM-HIF-1α with modifications of P402A and P564A, at hydroxylation sites in the oxygen-dependent degradation domain. LW6 induces the expression of von Hippel-Lindau (VHL), which interacts with prolyl-hydroxylated HIF-1α for proteasomal degradation. In the presence of LW6, knockdown of VHL does not abolish HIF-1α protein accumulation, indicating that LW6 degraded HIF-1α via regulation of VHL expression. In MDCKII-BCRP cells overexpressing BCRP, LW6 enhances significantly the cellular accumulation of mitoxantrone, a BCRP substrate. LW6 also down-regulates BCRP expression at concentrations of 0.1-10 μM. LW6 inhibits the expression of HIF 1α induced by hypoxia in A549 cells at 20 μM, independently of the von Hippel Lindau protein. LW6 induces hypoxia selective apoptosis together with a reduction in the mitochondrial membrane potential.
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In VivoIn mice carrying xenografts of human colon cancer HCT116 cells, LW6 demonstrates strong anti-tumor efficacy in vivo and causes a decrease in HIF-1α expression in frozen-tissue immunohistochemical staining.
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SynonymsCAY10585 | CAY-10585 | CAY 10585 | LW6
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PathwayOthers
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TargetOther Targets
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RecptorHIF-1
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number934593-90-5
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Formula Weight435.52
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Molecular FormulaC26H29NO5
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 33 mg/mL; 75.77 mM
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SMILESO=C(OC)C1=CC=C(O)C(NC(COC2=CC=C(C3(C4)CC5CC4CC(C5)C3)C=C2)=O)=C1
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Chemical Namemethyl 3-(2-(4-(adamantan-1-yl)phenoxy)acetamido)-4-hydroxybenzoate
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.Naik R, et al. J Med Chem. 2014 Nov 26;57(22):9522-38.
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