Dehydroevodiamine
CAS No. 67909-49-3
Dehydroevodiamine( —— )
Catalog No. M18986 CAS No. 67909-49-3
Dehydroevodiamine, a constituent of Evodia rutaecarpa, has various biological effects such as hypotensive, negative chronotropic, ion channel depressant, inhibition of nitric oxide production and cerebral blood flow enhancing activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 33 | In Stock |
|
| 10MG | 46 | In Stock |
|
| 25MG | 73 | In Stock |
|
| 50MG | 105 | In Stock |
|
| 100MG | 154 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDehydroevodiamine
-
NoteResearch use only, not for human use.
-
Brief DescriptionDehydroevodiamine, a constituent of Evodia rutaecarpa, has various biological effects such as hypotensive, negative chronotropic, ion channel depressant, inhibition of nitric oxide production and cerebral blood flow enhancing activities.
-
DescriptionDehydroevodiamine, a constituent of Evodia rutaecarpa, has various biological effects such as hypotensive, negative chronotropic, ion channel depressant, inhibition of nitric oxide production and cerebral blood flow enhancing activities.
-
In VitroDehydroevodiamine (0-50 μM; 2 hours) inhibits iNOS and COX-2 expressionand prevents degradation of IκB-α in LPS induced RAW 264.7 macrophages. Dehydroevodiamine (0-50 μM; 2 hours) inhibits a LPS-induced increase in the iNOS and COX-2 mRNA expression.Western Blot Analysis Cell Line:RAW 264.7 macrophage cells Concentration:10 μM, 30 μM, 50 μM Incubation Time:pretreated 2 hours Result:Reduced iNOS and COX-2 expression and increased IκB-α expression.RT-PCR Cell Line:RAW 264.7 macrophage cells Concentration:10 μM, 30 μM, 50 μM Incubation Time:pretreated 2 hours Result:Reduced iNOS and COX-2 mRNA expression.
-
In Vivo——
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetDopamine Receptor
-
RecptorOthers
-
Research AreaOthers-Field
-
Indication——
Chemical Information
-
CAS Number67909-49-3
-
Formula Weight301.34
-
Molecular FormulaC19H15N3O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 8.33 mg/mL (27.64 mM)
-
SMILESCN1C2=CC=CC=C2C(=O)N3C1=C4C(=C5C=CC=CC5=N4)CC3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
GSK598809
GSK598809 (GSK-598809) is a potent, selective, CNS penetrant and orally bioavailable dopamine D3 receptor antagonist with pKi of 8.9; displays >100-fold selectivity over D2 and H1 receptors.
-
Tedatioxetine
Tedatioxetine (Lu AA24530) is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI) with antidepressant properties.Tedatioxetine acts as a CYP2D6 substrate.
-
Talquetamab
Talquetamab (JNJ-64407564) is a GPRC5D bispecific antibody for multiple myeloma (MM) that induces T-cell-mediated killing of GPRC5-expressing MM cells through T-cell recruitment and activation, demonstrating antitumor activity.
Cart
sales@molnova.com