Cart
sales@molnova.com
HIF-PHD-IN-3
CAS No. 794582-71-1
HIF-PHD-IN-3( —— )
Catalog No. M36622 CAS No. 794582-71-1
HIF-PHD-IN-3 is a potent hiPSC-CM cardioprotective scaffold with potential inhibitory effects on HIF-PHD, regulates heme oxygenase-1, and can be used to study anaemia.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 29 | In Stock |
|
| 25MG | 41 | In Stock |
|
| 50MG | 57 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameHIF-PHD-IN-3
-
NoteResearch use only, not for human use.
-
Brief DescriptionHIF-PHD-IN-3 is a potent hiPSC-CM cardioprotective scaffold with potential inhibitory effects on HIF-PHD, regulates heme oxygenase-1, and can be used to study anaemia.
-
DescriptionHIF-PHD-IN-3 (compound 4) is a potent hiPSC-CM cardioprotective scaffold. HIF-PHD-IN-3 can induce upregulation of heme oxygenase-1.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorReactive Oxygen Species
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number794582-71-1
-
Formula Weight327.42
-
Molecular FormulaC16H13N3OS2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(NC1=NC(=CS1)C=2N=CC=CC2)CSC=3C=CC=CC3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Kirby RJ, et, al. Discovery of Novel Small-Molecule Inducers of Heme Oxygenase-1 That Protect Human iPSC-Derived Cardiomyocytes from Oxidative Stress. J Pharmacol Exp Ther. 2018 Jan;364(1):87-96.?
molnova catalog
related products
-
(-)-Maackiain
(-)-Maackiain, a phytoalexin, which is an anti-allergic compound that suppresses the up-regulation of the histamine H1 receptor (H1R) gene.
-
Cefpodoxime (free ac...
Cefpodoxime (free acid) is an oral, third-generation cephalosporin antibiotic. It is active against most Gram-positive and Gram-negative organisms, except Pseudomonas aeruginosa, Enterococcus, and Bacteroides fragilis.
-
LDC-4297 HCl
LDC4297 is a potent and selective CDK7 inhibitor with an IC50 of 0.13 nM.
