
ZINC13466751
CAS No. 117953-17-0
ZINC13466751( —— )
Catalog No. M26522 CAS No. 117953-17-0
ZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 μM).
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 177 | Get Quote |
![]() ![]() |
10MG | 295 | Get Quote |
![]() ![]() |
25MG | 532 | Get Quote |
![]() ![]() |
50MG | 767 | Get Quote |
![]() ![]() |
100MG | 1053 | Get Quote |
![]() ![]() |
500MG | 2115 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameZINC13466751
-
NoteResearch use only, not for human use.
-
Brief DescriptionZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 μM).
-
DescriptionZINC13466751 is a potent HIF-1α/von Hippel-Lindau interaction inhibitor(IC50 = 2.0 μM).
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayAngiogenesis
-
TargetHIF/HIF Prolyl-hydroxylase
-
RecptorCYP2B6| CYP2C19
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number117953-17-0
-
Formula Weight363.421
-
Molecular FormulaC20H21N5O2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 50 mg/mL (137.59 mM)
-
SMILESCC1=NN(C(=O)\C1=N/Nc1ccc(cc1)N1CCOCC1)c1ccccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Vijayabhaskar V, Srivastava P, Rajagopal S. Breaking the sensitivity limitations of cytochrome P450 oxidation product: dansyl chloride derivatisation of 4-OH mephenytoin, a CYP2C19 metabolite and its application to in vitro CYP inhibition assay. J Chromatogr B Analyt Technol Biomed Life Sci. 2015 May 1;989:27-36.
molnova catalog



related products
-
ML228
ML228 (ML-228, CID-46742353) is an activator of the hypoxia inducible factor (HIF) pathway with EC50 of 1.4 uM in HIF-1α nuclear translocation assays.
-
HIF-IN-1
HIF-IN-1 is a potent inhibitor of hypoxia-inducible factor (HIF-1), which is associated with tumor and cancer cell proliferation and inhibits HIF-1α protein aggregation.
-
TP-0463518
TP-0463518 is a novel, highly potent HIF prolyl hydroxylase (PHD) inhibitor.