Cart
sales@molnova.com
Ibutamoren
CAS No. 159634-47-6
Ibutamoren( L 163191 | L-163191 | L163191 | MK-677 | MK 677 | MK677 )
Catalog No. M27226 CAS No. 159634-47-6
Ibutamoren is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 71 | In Stock |
|
| 10MG | 115 | In Stock |
|
| 25MG | 178 | In Stock |
|
| 50MG | 268 | In Stock |
|
| 100MG | 394 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameIbutamoren
-
NoteResearch use only, not for human use.
-
Brief DescriptionIbutamoren is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin.
-
DescriptionIbutamoren is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It also alters the metabolism of body fat and so may have an application in the treatment of obesity.
-
In Vitro——
-
In Vivo——
-
SynonymsL 163191 | L-163191 | L163191 | MK-677 | MK 677 | MK677
-
PathwayOthers
-
TargetOther Targets
-
RecptorSARS-CoV
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number159634-47-6
-
Formula Weight528.67
-
Molecular FormulaC27H36N4O5S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC(C)(N)C(=O)N[C@H](COCc1ccccc1)C(=O)N1CCC2(CN(c3ccccc23)S(C)(=O)=O)CC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
γ-2-MSH (41-58), ami...
Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.
-
Fulvotomentoside A b
Fulvotomentoside A (Decaisoside E) is a triterpenoid saponin compound isolated from the flowers of Lonicera fulvotomentosa Hsu et S.C. Cheng.
-
2-Phenylethyl-beta-g...
2-Phenylethyl b-D-glucopyranoside is a useful organic compound for research related to life sciences.
