Ponalrestat
CAS No. 72702-95-5
Ponalrestat( ICI 128436 | MK-538 | Ponalrestat )
Catalog No. M15783 CAS No. 72702-95-5
ponalrestat, an aldose reductase inhibitor, activates lipoprotein lipase (LPL) activity in the adipose tissue and alleviates the cachectic symptoms induced by B16 melanoma in mice
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 38 | 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 NamePonalrestat
-
NoteResearch use only, not for human use.
-
Brief Descriptionponalrestat, an aldose reductase inhibitor, activates lipoprotein lipase (LPL) activity in the adipose tissue and alleviates the cachectic symptoms induced by B16 melanoma in mice
-
Descriptionponalrestat, an aldose reductase inhibitor, activates lipoprotein lipase (LPL) activity in the adipose tissue and alleviates the cachectic symptoms induced by B16 melanoma in mice.
-
In Vitro——
-
In VivoAnimal Model:Adult female Sprague-Dawley ratsDosage:10, 50 mg/kg Administration:Orally; daily; 8 weeks Result:Reduced sorbitol accumulation.
-
SynonymsICI 128436 | MK-538 | Ponalrestat
-
PathwayEndocrinology/Hormones
-
TargetReductase
-
RecptorAldose reductase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number72702-95-5
-
Formula Weight391.19
-
Molecular FormulaC17H12BrFN2O3
-
Purity>98% (HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESO=C(O)CC1=NN(CC2=CC=C(Br)C=C2F)C(C3=C1C=CC=C3)=O
-
Chemical Name2-(3-(4-bromo-2-fluorobenzyl)-4-oxo-3,4-dihydrophthalazin-1-yl)acetic acid
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Pekiner C, McLean WG. Br J Pharmacol. 1990 Dec;101(4):978-80.
molnova catalog
related products
-
Isoliquiritigenin
Isoliquiritigenin, an anti-tumor flavonoid from the root of Glycyrrhiza glabra, inhibits aldose reductase with an IC50 of 320 nM.
-
PHA767491 HCl
PHA-767491 is an effective ATP-competitive dual Cdc7/CDK9 inhibitor (IC50: 10/34 nM).
-
CH5138303
CH5138303 is an orally available Hsp90 inhibitor with Kd of 0.48 nM.
Cart
sales@molnova.com