Cart
sales@molnova.com
Norharmane
CAS No. 244-63-3
Norharmane( —— )
Catalog No. M18299 CAS No. 244-63-3
Norharmane is a natural β-carboline first isolated from plants of the Zygophyllaceae family.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | 28 | In Stock |
|
| 500MG | 41 | In Stock |
|
| 1G | 57 | In Stock |
|
Biological Information
-
Product NameNorharmane
-
NoteResearch use only, not for human use.
-
Brief DescriptionNorharmane is a natural β-carboline first isolated from plants of the Zygophyllaceae family.
-
DescriptionNorharmane is a natural β-carboline first isolated from plants of the Zygophyllaceae family.
-
In Vitro——
-
In VivoAnimal Model:Male NMRI mice (22-25?g)Dosage:0, 2.5, 5 and 10?mg/kg Administration:IP, onceResult:Elicited an anxiety- and antidepressant-like behavior, and decreased locomotor activity.
-
Synonyms——
-
PathwayMAPK/ERK Signaling
-
TargetJNK
-
RecptorDNA
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number244-63-3
-
Formula Weight168.2
-
Molecular FormulaC11H8N2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 11 mg/mL (65.40 mM)
-
SMILESc12ccccc1c1ccncc1[nH]2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Jamali., et al. Inhibitory effect of Rosa rugosa tea extract on the formation of heterocyclic amines in meat patties at different temperatures. Molecules 21(2), 173 (2016).
molnova catalog
related products
-
GSK2879552 2HCl
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
-
GNE-617
GNE-617, a specific NAMPT inhibitor(IC50=5 nM), shows potency in xenograft models of cancer.
-
JIP-1 (153-163)
Peptide inhibitor of c-Jun N-terminal kinase (JNK), based on residues 153-163 of JNK-interacting protein-1 (JIP-1). Binds to JNK with affinity in the micromolar range and minimally inhibits p38 and ERK.
