
GW-803430
CAS No. 515141-51-2
GW-803430( —— )
Catalog No. M33378 CAS No. 515141-51-2
GW-803430 (GW-3430) is an orally active and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist used in the study of obesity.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 88 | In Stock |
![]() ![]() |
5MG | 140 | In Stock |
![]() ![]() |
10MG | 250 | In Stock |
![]() ![]() |
25MG | 514 | In Stock |
![]() ![]() |
50MG | 717 | In Stock |
![]() ![]() |
100MG | 945 | In Stock |
![]() ![]() |
200MG | 1278 | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameGW-803430
-
NoteResearch use only, not for human use.
-
Brief DescriptionGW-803430 (GW-3430) is an orally active and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist used in the study of obesity.
-
DescriptionGW-803430 (GW-3430) is a potent and selective melanin-concentrating hormone receptor 1 (MCH R1) antagonist with a pIC50 of 9.3. GW-803430 is orally active in an animal model of obesity.
-
In VitroGW-803430 demonstrates a potent antagonist activity towards MCH induced MCHR1 receptor with an IC50 value of ~13?nM.
-
In VivoGW-803430 (0.3, 3, and 15 mg/kg; oral administration; once daily) causes a sustained dose-dependent weight loss relative to vehicle controls.GW-803430 is a suitable compound for its good pharmacokinetic properties (bioavailability=31%, t1/2=11 h) and brain penetration (6:1 brain:plasma concentration) in mice.Animal Model:High fat diet-induced obese AKR/J mice Dosage:0.3, 3, and 15 mg/kg Administration:Orally, qd,12 days Result:Caused a sustained dose-dependent weight loss of -6.2%, -12.1%, and -13.1%, respectively, relative to vehicle controls.
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetMCHR
-
RecptorMelanin-concentrating Hormone Receptor (MCHR)
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number515141-51-2
-
Formula Weight481.99
-
Molecular FormulaC25H24ClN3O3S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1C=2SC(=CC2N=CN1C3=CC=C(OCCN4CCCC4)C(OC)=C3)C=5C=CC(Cl)=CC5
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Hertzog DL, et al. The discovery and optimization of pyrimidinone-containing MCH R1 antagonists. Bioorg Med Chem Lett. 2006 Sep 15;16(18):4723-7.?
molnova catalog



related products
-
AZD-1979
A potent, selective melanin concentrating hormone receptor 1 (MCH-R1) antagonist with binding Ki of 12.2 nM.
-
TC-MCH 7c
TC-MCH 7c is an oral, selectable and blood-brain barrier penetrating MCH1R antagonist with IC50 performance of 5.6 nM against hMCH1R, and TC-MCH 7c is a phenylpyridone derivative with MCH1R Ki of 3.4 nM against human. In mice, MCH1R Ki was 3.0 nM.
-
BMS 830216
The the phosphate ester prodrug of BMS 819881, a potent, selective melanin concentrating hormone receptor 1 (MCHR1) inhibitor with Ki of 10.4 nM.