JKE-1674
CAS No. 2421119-60-8
JKE-1674 ( —— )
Catalog No. M28123 CAS No. 2421119-60-8
JKE-1674 is an inhibitor of glutathione peroxidase 4 (GPX4). JKE-1674 is an active metabolite of the GPX4 inhibitor ML-210.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 102 | Get Quote |
|
10MG | 165 | Get Quote |
|
25MG | 335 | Get Quote |
|
50MG | 537 | Get Quote |
|
100MG | 860 | Get Quote |
|
200MG | 1152 | Get Quote |
|
500MG | 1701 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameJKE-1674
-
NoteResearch use only, not for human use.
-
Brief DescriptionJKE-1674 is an inhibitor of glutathione peroxidase 4 (GPX4). JKE-1674 is an active metabolite of the GPX4 inhibitor ML-210.
-
DescriptionJKE-1674 is an inhibitor of glutathione peroxidase 4 (GPX4). JKE-1674 is an active metabolite of the GPX4 inhibitor ML-210.(In Vitro):JKE-1674 reduces the viability of LOX-IMVI cancer cells with an EC50 of 0.03 μM and in a panel of additional cancer cell lines. JKE-1674 is completely rescued by ferroptosis inhibitors.(In Vivo):JKE-1674 (50?mg/kg; p.o.) could be detected in the serum of mice dosed orally with the compound.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorIL-5
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2421119-60-8
-
Formula Weight451.3
-
Molecular FormulaC20H20Cl2N4O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(C(C[N+]([O-])=O)=NO)N1CCN(C(C2=CC=C(Cl)C=C2)C3=CC=C(Cl)C=C3)CC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ian D Pavord, From DREAM to REALITI-A and beyond: Mepolizumab for the treatment of eosinophil-driven diseases. Allergy. 2022 Mar;77(3):778-797.
molnova catalog
related products
-
19-Oxocinobufotalin
19-Oxocinobufotalin 3-adipoylarginine ester shows significant inhibition effect against human hepatocellular carcinoma cell line SMMC-7721 in vitro.
-
Boc-NH-PEG12-NH2
Boc-NH-PEG12-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
-
SN6
SN 6 is a selective Na+/Ca2+ exchanger (NCX) inhibitor?(IC50s of NCX1: 2.9 μM NCX2: 16 μM NCX3: 8.6 μM).