Cart
sales@molnova.com
Orotirelin
CAS No. 62305-86-6
Orotirelin( —— )
Catalog No. M34676 CAS No. 62305-86-6
Orotirelin(CG 3509), a thyrotropin-releasing hormone analog, reversed pentobarbital-induced sleep time.Orotirelin may be beneficial in animals with focal cerebral ischemia.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 392 | Get Quote |
|
| 5MG | 610 | Get Quote |
|
| 10MG | 867 | Get Quote |
|
| 25MG | 1260 | Get Quote |
|
| 50MG | 1702 | Get Quote |
|
| 100MG | 2250 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameOrotirelin
-
NoteResearch use only, not for human use.
-
Brief DescriptionOrotirelin(CG 3509), a thyrotropin-releasing hormone analog, reversed pentobarbital-induced sleep time.Orotirelin may be beneficial in animals with focal cerebral ischemia.
-
DescriptionOrotirelin(CG 3509), a thyrotropin-releasing hormone analog, reversed pentobarbital-induced sleep time.Orotirelin may be beneficial in animals with focal cerebral ischemia.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number62305-86-6
-
Formula Weight389.37
-
Molecular FormulaC16H19N7O5
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC([C@H](CC1=CN=CN1)NC(=O)C2=CC(=O)NC(=O)N2)(=O)N3[C@H](C(N)=O)CCC3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
6-Chloro-3-indolyl-β...
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
-
D-alpha-Methylbenzyl...
D-alpha-Methylbenzyl isothiocyanate, an antioxidant and a chiral agent, induces phase II enzyme activity.
-
EN106
EN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
