Venlafaxine hydrochloride
CAS No. 99300-78-4
Venlafaxine hydrochloride( Wy 45030 )
Catalog No. M16910 CAS No. 99300-78-4
Venlafaxine hydrochloride is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
|
| 5MG | 30 | In Stock |
|
| 10MG | 48 | In Stock |
|
| 25MG | 68 | In Stock |
|
| 100MG | 91 | In Stock |
|
| 200MG | 155 | In Stock |
|
| 500MG | 259 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameVenlafaxine hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionVenlafaxine hydrochloride is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class.
-
DescriptionVenlafaxine hydrochloride is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class.
-
In Vitro——
-
In VivoAnimal Model:Male Sprague-Dawley rats weighing 180-230 grams Dosage:10, 30, 100 mg/kg Administration:IP; one hour prior to p-chloramphetamine hydrochloride (p-CA; 10 mg/kg; i.p.)Result:Dose-dependently blocked the depletion of norepinephrine levels in rat hypothalamus induced by 6-OHDA (intracerebroventricularly; 50 μg/rat; one hour later), with ED50 values of 12 and 94 mg/kg i.p., respectively.
-
SynonymsWy 45030
-
PathwayEndocrinology/Hormones
-
Target5-HT Receptor
-
Recptor5-HT
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number99300-78-4
-
Formula Weight313.86
-
Molecular FormulaC17H28CLNO2
-
Purity>98% (HPLC)
-
SolubilityEthanol: 55.5 mg/mL (176.83 mM); Water: 55.5 mg/mL (176.83 mM); DMSO: 55.5 mg/mL (176.83 mM)
-
SMILESOC1(C(C2=CC=C(OC)C=C2)CN(C)C)CCCCC1.[H]Cl
-
Chemical Name1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol hydrochloride
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Peptide 401
Peptide 401 is an antimicrobial peptide (AMP) derived from the venom of bees and wasps. Peptide 401 induces mast cell degranulation, activating histamine release from peritoneal mast cells. Additionally, peptide 401 exhibits some anti-inflammatory activity, decreasing paw edema in animal models.
-
GR 125743
GR 125743 is a novel antagonist of 5-HT1B/1D receptor.GR-125743, a new radiolabelled derivative of a compound that exhibits selective antagonistic properties with respect to the serotonin human (h5-HT1D) and human (h5-HT1B) receptors.?The compound has been characterized for its ability to label the cloned h5-HT1D and h5-HT1B receptors.?
-
Lafutidine
Lafutidine, a newly developed histamine H(2)-receptor antagonist, inhibits gastric acid secretion.
Cart
sales@molnova.com