CB1/2 agonist 2

Modify Date: 2025-08-27 19:25:51

CB1/2 agonist 2 Structure
CB1/2 agonist 2 structure
Common Name CB1/2 agonist 2
CAS Number 2772379-97-0 Molecular Weight 417.62
Density N/A Boiling Point N/A
Molecular Formula C26H43NO3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of CB1/2 agonist 2


CB1/2 agonist 2 (compound 23) is a potent non-selective cannabinoid ligand, with Ki values of 3.5 and 1.2 nM, respectively. CB1/2 agonist 2 can behave as a full CB1 agonist and CB2 competitive inverse agonist. CB1/2 agonist 2 shows antinociceptive activity[1].

 Names

Name CB1/2 agonist 2

 CB1/2 agonist 2 Biological Activity

Description CB1/2 agonist 2 (compound 23) is a potent non-selective cannabinoid ligand, with Ki values of 3.5 and 1.2 nM, respectively. CB1/2 agonist 2 can behave as a full CB1 agonist and CB2 competitive inverse agonist. CB1/2 agonist 2 shows antinociceptive activity[1].
Related Catalog
Target

hCB2-R:1.2 nM (Ki)

hCB1-R:3.5 nM (Ki)

In Vitro CB1/2 agonist 2 (compound 23) (1 µM, 24-72 h) exhibits a very low cytotoxic potential in Hep-G2 cells[1]. CB1/2 agonist 2 (0-10 µM) shows a slight but significant inhibition of [35S]GTPγS binding to hCB2-CHO cell membranes, with a mean EC50 of 397.90 nM and a mean Emax value of -17.81%[1]. Cell Cytotoxicity Assay[1] Cell Line: Human hepatoblastoma (Hep-G2) cells Concentration: 1 µM Incubation Time: 24, 48 or 72 h Result: Exhibited a very low cytotoxic potential, as Hep-G2 cell viability was comparable to controls after 24-72 h of treatment.
In Vivo CB1/2 agonist 2 (compound 23) (0-6 mg/kg, IP, once) significantly reduces the late phase of formalin-induced nocifensive behaviour at 6 mg/kg[1]. Animal Model: Male CD-1 outbred mice (40-45 g)[1] Dosage: 0, 1, 3, and 6 mg/kg Administration: IP, once, 10 min before the formalin or saline injection Result: Significantly reduced the late phase of formalin-induced nocifensive behaviour at the highest dose (6 mg/kg, i.p.), whereas no effect was produced by doses of 1 and 3 mg/kg.
References

[1]. Brizzi A, et al. Synthetic bioactive olivetol-related amides: The influence of the phenolic group in cannabinoid receptor activity. Bioorg Med Chem. 2020 Jun 1;28(11):115513.

 Chemical & Physical Properties

Molecular Formula C26H43NO3
Molecular Weight 417.62
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here
Related Compounds: More...
CB1/2 agonist 4
2772949-38-7
CB1/2 agonist 3
2772655-86-2
formaldehyde,2-(2-hydroxyethylamino)ethanol,urea
63528-97-2
(5S)-2,2,3-TRIMETHYL-5-PHENYLMETHYL-4-IMIDAZOLIDINONEMONOHYDROCHLORIDE
278173-23-2
Ethanamine,2-[[(2-chlorophenyl)methyl]thio]-
42416-23-9
Benzene,2-[(2-chloro-2-phenylethyl)sulfonyl]-1,3,5-trimethyl-
30158-42-0
Bis(2,2,2-trifluoro-N-phenylethanehydrazonoyl) disulfide
4454-60-8
1-(2-[(2-PYRIDYLSULFONYL)METHYL]-1,3-THIAZOL-4-YL)ETHAN-1-ONE
54151-73-4
1-(2,2-dichloroethylsulfanyl)ethanone
71172-37-7
4-[3-cyclohexyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]but-2-enoic acid
2172626-66-1
2-[3-cyclopentyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-N-(propan-2-yl)propanamido]acetic acid
2172099-43-1
(2S)-4-[3-cyclopentyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]-2-hydroxybutanoic acid
2171445-84-2
(2R)-2-[3-cyclohexyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid
2648918-51-6
5-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-N-methylbutanamido}pentanoic acid
2171857-23-9
(2S)-2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1,3-thiazol-4-yl]formamido}-3-methoxypropanoic acid
2171270-85-0
(2S)-2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methyl-1,3-thiazol-5-yl]formamido}-3-methoxypropanoic acid
2171253-88-4
(2S)-2-{[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylphenyl]formamido}-3-methoxypropanoic acid
2171198-43-7
2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methoxypropanamido]-5-iodobenzoic acid
2171194-53-7
(2S)-2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5-fluorophenyl]formamido}-3-methoxypropanoic acid
2171275-96-8