KH-176
CAS No. 1541170-75-5
KH-176( Sonlicromanol | KH176 )
Catalog No. M12178 CAS No. 1541170-75-5
KH-176 (KH176, Sonlicromanol) is a smal molecule ROS-redox modulator.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 873 | Get Quote |
|
| 50MG | 1782 | Get Quote |
|
| 100MG | 2250 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameKH-176
-
NoteResearch use only, not for human use.
-
Brief DescriptionKH-176 (KH176, Sonlicromanol) is a smal molecule ROS-redox modulator.
-
DescriptionKH-176 (KH176, Sonlicromanol) is a smal molecule ROS-redox modulator, effectively reduces increased cellular ROS levels and protects OXPHOS deficient primary cells against redox perturbation by targeting the Thioredoxin/Peroxiredoxin system; significantly improves rotarod and gait performance and reduces the degeneration of retinal ganglion cells in Ndufs4 -/- mice, shows therapeutic effects in mammalian model of Leigh Disease.
-
In Vitro——
-
In VivoSonlicromanol (KH176, 10 mg/kg, ip, twice daily) has promising, but independent and nonadditive, properties for the pharmacological treatment of CI-deficiency-related mitochondrial diseases. Animal Model:Ndufs4?/? mice.Dosage:10 mg/kg.Administration:Twice daily by intraperitoneal injection.Result:Increased lifespan of Ndufs4?/? mice similar as KH176 and Clofibrate single treatment.
-
SynonymsSonlicromanol | KH176
-
PathwayApoptosis
-
TargetAdenosine Receptor
-
RecptorAdenosine Receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1541170-75-5
-
Formula Weight332.444
-
Molecular FormulaC19H28N2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC1=C(O)C(C)=C2CC[C@@](C)(C(N[C@@H]3CCCNC3)=O)OC2=C1C
-
Chemical Name(2S)-6-hydroxy-2,5,7,8-tetramethyl-N-[(3R)-piperidin-3-yl]-3,4-dihydro-2H-1-benzopyran-2-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. de Haas R, et al. Sci Rep. 2017 Sep 15;7(1):11733.
2. Koene S, et al. Orphanet J Rare Dis. 2017 Oct 16;12(1):163.
3. Beyrath J, et al. Sci Rep. 2018 Apr 26;8(1):6577.
molnova catalog
related products
-
Istradefylline
A potent and highly selective A2A receptor antagonist with Ki of 2.2 nM.
-
Naftopidil hydrochlo...
Naftopidil hydrochloride is a selective alpha1-adrenoceptor antagonist with Ki of 3.7 nM, 20 nM and 1.2 nM for the cloned human α1a-adrenoceptor, α1b-adrenoceptor and α1d-adrenoceptor, respectively.
-
AB928
AB928 is a dual antagonist of the A2aR and A2bR adenosine receptors leads to greater immune activation and reduced tumor growth when combined with chemotherapy.
Cart
sales@molnova.com