4-Hydroxyisoleucine
CAS No. 781658-23-9
4-Hydroxyisoleucine( 4-?Hydroxy-?L-?isoleucine )
Catalog No. M20779 CAS No. 781658-23-9
4-Hydroxyisoleucine has antidepressant-like antidyslipidemic and antihyperglycemic effects.?It displays an insulinotropic activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 54 | In Stock |
|
| 5MG | 77 | In Stock |
|
| 10MG | 138 | In Stock |
|
| 25MG | 249 | In Stock |
|
| 50MG | 373 | 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 Name4-Hydroxyisoleucine
-
NoteResearch use only, not for human use.
-
Brief Description4-Hydroxyisoleucine has antidepressant-like antidyslipidemic and antihyperglycemic effects.?It displays an insulinotropic activity.
-
Description4-Hydroxyisoleucine has antidepressant-like antidyslipidemic and antihyperglycemic effects.?It displays an insulinotropic activity.
-
In VitroCell Viability Assay Cell Line:RAW264.7 macrophages and 3 T3-L1 adipocytes Concentration:0-20 μM Incubation Time:6 h Result:Didn’t affect the cell viability.Cell Migration Assay Cell Line:RAW264.7 macrophages and 3 T3-L1 adipocytes Concentration:20 μM Incubation Time:24 h Result:Inhibited the migration of RAW264.7 macrophages in 3 T3-L1 adipocytes.Western Blot Analysis Cell Line:L6-GLUT4mycConcentration:25 μM Incubation Time:16 h Result:Increased the AKT (Ser-473) phosphorylation.
-
In VivoAnimal Model:Fructose-fed rat Dosage:50 mg/kg Administration:Oral gavage (p.o.), daily, 8 weeksResult:Decreased the levels of glucose and ALT.Reduced 80% of fructosehe-induced AST release to 151 ± 45 U/mL.Animal Model:Type 2 diabetic rat Dosage:50 mg/kg Administration:i.g., daily, 14 days Result:Restored the level of HDL-cholesterol to levels comparable to controls.Animal Model:Male C57BL/6 mice Dosage:50-200 mg/kg Administration: Oral gavage (p.o.), 8 weeks Result:Decreases the body weights of mice in a dose-dependent manner.Decreased blood glucose levels and fasting plasma insulin content in mice.Decreased the expression of TLR4, inhibited the phosphorylation of JNK, and increased the production of IκB-α.Animal Model:Type 1 diabetic ratDosage:50 mg/kg Administration: i.g., daily, 14 days Result:Improved appearance and heavy ocular vascularization.Reduced the blood glucose from 500 mg/dl to 330 mg/dl.Decreased the levels of lipid markers (TG, LDL and HDL) and uric acid.
-
Synonyms4-?Hydroxy-?L-?isoleucine
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number781658-23-9
-
Formula Weight147.17
-
Molecular FormulaC6H13NO3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?H2O : 100 mg/mL (679.49 mM)
-
SMILESCC(O)[C@H](C)[C@H](N)C(=O)O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Risuteganib hydrochl...
Risuteganib hydrochloride is an anti-integrin that downregulates oxidative stress and restores homeostasis, and targets three integrin receptors that are implicated in dry age-related macular degeneration (AMD) in order to restore homeostasis in the retina.
-
Pivagabine
Pivagabine is a derivative of hydrophobic 4-aminobutyric acid, with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor function and corticotropin-releasing factor (CRF) concentrations in rat brain.
-
Isoscopoletin
6-Hydroxy-7-methoxycoumarin is a predicted metabolite generated by BioTransformer1 that is produced by the metabolism of 6, 7-dimethoxy-2h-chromen-2-one.
Cart
sales@molnova.com