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 | In Stock |
|
| 10MG | 581 | In Stock |
|
| 25MG | 888 | In Stock |
|
| 50MG | 1242 | In Stock |
|
| 100MG | 1674 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 3348 | In Stock |
|
| 1G | Get Quote | In Stock |
|
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
-
Hemopressin (human, ...
Bioactive endogenous peptide substrate for endopeptidase 24.15 (ep24.15), neurolysin (ep24.16) and ACE. Ki values are 27.76, 3.43 and 1.87 μM respectively. Potent hypotensive in vivo. Also acts as a selective CB1 receptor inverse agonist. Displays antinociceptive activity in vivo.
-
N-Oleoyl glycine
N-Oleoyl glycine, a lipoamino acid, was able to promote 3T3-L1 adipogenesis through the activation of CB1 receptor and the enhancement of insulin-mediated Akt signaling pathway.
-
AM-630
A potent and selective inverse agonist for the cannabinoid receptor CB2 with Ki of 32.1 nM, 165-fold selectivity over CB1.
