Cart
sales@molnova.com
(Iso)-Dehydroemetine
CAS No. 2649-50-5
(Iso)-Dehydroemetine( —— )
Catalog No. M36071 CAS No. 2649-50-5
(Iso)-Dehydroemetine (Dehydroisoemetine, (+/-)-) is a compound with antispasmolytic effect on smooth muscle.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 340 | Get Quote |
|
| 5MG | 273 | Get Quote |
|
| 10MG | 372 | Get Quote |
|
| 25MG | 563 | Get Quote |
|
| 50MG | 742 | Get Quote |
|
| 100MG | 977 | Get Quote |
|
| 200MG | 1293 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product Name(Iso)-Dehydroemetine
-
NoteResearch use only, not for human use.
-
Brief Description(Iso)-Dehydroemetine (Dehydroisoemetine, (+/-)-) is a compound with antispasmolytic effect on smooth muscle.
-
Description(Iso)-Dehydroemetine (Dehydroisoemetine, (+/-)-) is a compound with antispasmolytic effect on smooth muscle.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2649-50-5
-
Formula Weight478.62
-
Molecular FormulaC29H38N2O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC(C=1C[C@]2(C=3C(=CC(OC)=C(OC)C3)CCN2CC1CC)[H])[C@H]4C=5C(=CC(OC)=C(OC)C5)CCN4
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
Butin
Butin is a major biologically active flavonoid isolated from the heartwood of Dalbergia odorifera with oral activity, with strong antioxidant, antiplatelet and anti-inflammatory activities. Butin significantly alleviates myocardial infarction and improves heart function, together with prevents diabetes-induced cardiac oxidative damage in rat.
-
Eptifibatide acetate
Eptifibatide an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class is a cyclic heptapeptide constructed from 6 amino acids and a mercaptopropionyl residue.
-
MSC-4106
MSC-4106, an orally active and potent YAP/TAZ-TEAD inhibitor, disrupts TEAD1 and TEAD3 auto-palmitoylation and demonstrates significant efficacy in the NCI-H226 tumor xenograft model .
