Cart
sales@molnova.com
Pravadoline
CAS No. 92623-83-1
Pravadoline( WIN 48098-6 | WIN48098-6 | WIN-48098-6 | Pravadoline )
Catalog No. M27394 CAS No. 92623-83-1
Pravadoline is a cannabinoid receptor agonist. Pravadoline inhibited the PGs synthesis in mouse brain and displayed antinociceptive activity in rodents subjected to a variety of thermal, chemical, and mechanical nociceptive stimuli.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 393 | Get Quote |
|
| 10MG | 581 | Get Quote |
|
| 25MG | 888 | Get Quote |
|
| 50MG | 1242 | Get Quote |
|
| 100MG | 1674 | Get Quote |
|
| 500MG | 3348 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NamePravadoline
-
NoteResearch use only, not for human use.
-
Brief DescriptionPravadoline is a cannabinoid receptor agonist. Pravadoline inhibited the PGs synthesis in mouse brain and displayed antinociceptive activity in rodents subjected to a variety of thermal, chemical, and mechanical nociceptive stimuli.
-
DescriptionPravadoline is a cannabinoid receptor agonist. Pravadoline inhibited the PGs synthesis in mouse brain and displayed antinociceptive activity in rodents subjected to a variety of thermal, chemical, and mechanical nociceptive stimuli.
-
In Vitro——
-
In Vivo——
-
SynonymsWIN 48098-6 | WIN48098-6 | WIN-48098-6 | Pravadoline
-
PathwayGPCR/G Protein
-
TargetCannabinoid Receptor
-
RecptorADC Cytotoxin
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number92623-83-1
-
Formula Weight378.472
-
Molecular FormulaC23H26N2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCOc1ccc(cc1)C(=O)c1c(C)n(CCN2CCOCC2)c2ccccc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Puthenveetil S, et al. Natural Product Splicing Inhibitors: A New Class of Antibody-Drug Conjugate (ADC) Payloads. Bioconjug Chem. 2016;27(8):1880-1888.
molnova catalog
related products
-
WIN 55,212-2 mesylat...
WIN 55,212-2 mesylate (WIN 55212-2) is a potent cannabinoid receptor agonist with Ki of 62.3 and 3.3 nM for human recombinant CB1 and CB2 receptors, respectively.
-
Repertaxin
Reparixin is a potent inhibitor of both CXCL8 receptors?CXCR1/2, it inhibits weakly?CXCR2-mediated cell migration (IC50=100 nM), whereas it strongly blocks?CXCR1-mediated chemotaxis (IC50=1 nM).
-
PSNCBAM-1
PSNCBAM-1 is a CB1 receptor negative allosteric modulator (EC50 = 0.1 μM) with hypophagic effects in vivo. PSNCBAM-1 can be used for obesity studies.
