Cart
sales@molnova.com
Undecylenoyl phenylalanine
CAS No. 175357-18-3
Undecylenoyl phenylalanine( Sepiwhite msh QD | Sepiwhite msh | Undecylenoylphenylalanine )
Catalog No. M27281 CAS No. 175357-18-3
Undecylenoyl phenylalanine is a novel depigmenting agent, which possibly acts as an alpha-melanocyte-stimulating hormone antagonist, thus inhibiting melaninogenesis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | 27 | In Stock |
|
Biological Information
-
Product NameUndecylenoyl phenylalanine
-
NoteResearch use only, not for human use.
-
Brief DescriptionUndecylenoyl phenylalanine is a novel depigmenting agent, which possibly acts as an alpha-melanocyte-stimulating hormone antagonist, thus inhibiting melaninogenesis.
-
DescriptionUndecylenoyl phenylalanine is a novel depigmenting agent, which possibly acts as an alpha-melanocyte-stimulating hormone antagonist, thus inhibiting melaninogenesis.
-
In Vitro——
-
In Vivo——
-
SynonymsSepiwhite msh QD | Sepiwhite msh | Undecylenoylphenylalanine
-
PathwayGPCR/G Protein
-
TargetMelanocortin Receptor
-
RecptorNF-κB
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number175357-18-3
-
Formula Weight331.456
-
Molecular FormulaC20H29NO3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCCCCCCCC\C=C\C(=O)N[C@@H](Cc1ccccc1)C(O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Mathew B, et, al. Structure-activity relationship (SAR) studies of N-(3-methylpyridin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine (SRI-22819) as NF-?B activators for the treatment of ALS. Eur J Med Chem. 2020 Oct 22;112952.
molnova catalog
related products
-
THIQ
THIQ is a selective melanocortin-4 receptor (MC4R)?agonist (hMC4R and rMC4R with IC50 of 1.2 nM and 0.6 nM , respectively).?
-
HS 024
Highly potent melanocortin MC4 receptor antagonist (Ki values are 0.29, 18.6, 5.45 and 3.29 nM for cloned human MC4, MC1, MC3 and MC5 receptors respectively). Increases food intake, and blocks α-MSH- and MTII-induced hypotension and bradycardia in rats, following central administration in vivo.
-
MCL 0020
Potent and selective melanocortin MC4 receptor antagonist (IC50 values are 11.63, 1115 and > 10 000 nM at MC4, MC3 and MC1 receptors respectively). Significantly reverses stress-induced anorexia but has no effect on food intake in free-feeding rats.
