Gomisin N
CAS No. 69176-52-9
Gomisin N( —— )
Catalog No. M21528 CAS No. 69176-52-9
Gomisin N isolated from Schisandra chinensis produces beneficial sedative and hypnotic bioactivity. It has the potential for use in the treatment of allergy and inhibits proliferation and induces apoptosis in cancer.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 85 | In Stock |
|
| 10MG | 123 | In Stock |
|
| 25MG | 203 | In Stock |
|
| 50MG | 302 | In Stock |
|
| 100MG | 447 | In Stock |
|
| 500MG | 1017 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameGomisin N
-
NoteResearch use only, not for human use.
-
Brief DescriptionGomisin N isolated from Schisandra chinensis produces beneficial sedative and hypnotic bioactivity. It has the potential for use in the treatment of allergy and inhibits proliferation and induces apoptosis in cancer.
-
DescriptionGomisin N isolated from Schisandra chinensis produces beneficial sedative and hypnotic bioactivity. It has the potential for use in the treatment of allergy and inhibits proliferation and induces apoptosis in cancer.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayApoptosis
-
TargetApoptosis
-
RecptorApoptosis
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number69176-52-9
-
Formula Weight400.5
-
Molecular FormulaC23H28O6
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (249.71 mM)
-
SMILESCOc1cc2C[C@@H](C)[C@@H](C)Cc3cc4OCOc4c(OC)c3-c2c(OC)c1OC
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Zhang C et al. Gomisin N isolated from Schisandra chinensis augments pentobarbital-induced sleep behaviors through the modification of the serotonergic and GABAergic system. Fitoterapia. 2014 Jul;96:123-30.
molnova catalog
related products
-
2,5-dimethyl Celecox...
2,5-dimethyl Celecoxib is a celecoxib derivative and a targeted inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1), a key enzyme in the PGE2 synthesis pathway of inflammatory mediators.
-
DT2216
DT2216 inhibits various Bcl-XL-dependent leukemias and cancer cells, but is significantly less toxic to platelets.DT2216 is a selective B-cell lymphoma, extremely large (BCL-XL), proteolytic targeting chimera (PROTAC).
-
Fmoc-D-Cha-OH
Fmoc-D-Cha-OH (FDCO) is an apoptotic DNase γ inhibitor that inhibits the release of HMGB1.
Cart
sales@molnova.com