HU-210
- CAS No.
- 112830-95-2
- Chemical Name:
- HU-210
- Synonyms
- HU-210;HU-210 (solution);HU-210/112830-95-2;HU-210 DEA Schedule I;HU-210 (Spice Cannabinoid);HU-210 (exempt preparation);HU 210 (100μg/mL in Methanol);11-OH-Δ8-THC-1,1-dimethylheptyl;(-)-11-OH-Δ8-THC-1,1-dimethylheptyl;(6aR)-6aβ,7,10,10aα-Tetrahydro-6,6-dimethyl-1-hydroxy-3-(1,1-dimethylheptyl)-6H-dibenzo[b,d]pyran-9-methanol
- CBNumber:
- CB9151488
- Molecular Formula:
- C25H38O3
- Molecular Weight:
- 386.57
- MOL File:
- 112830-95-2.mol
- MSDS File:
- SDS
- Modify Date:
- 2023/6/8 9:03:07
SAFETY
Risk and Safety Statements
| Symbol(GHS) |    GHS02,GHS06,GHS08 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H225-H301+H311+H331-H370 | |||||||||
| Precautionary statements | P210-P260-P280-P301+P310-P311 | |||||||||
| Hazard Codes | F,T | |||||||||
| Risk Statements | 11-23/24/25-39/23/24/25 | |||||||||
| Safety Statements | 7-16-36/37-45 | |||||||||
| RIDADR | UN1230 - class 3 - PG 2 - Methanol, solution | |||||||||
| WGK Germany | 3 | |||||||||
| HS Code | 29329990 | |||||||||
| NFPA 704 |
|
HU-210 Chemical Properties,Uses,Production
Description
HU-210 (exempt preparation) (Item No. 90083) is an analytical reference standard categorized as a synthetic cannabinoid. HU-210 is regulated as a Schedule I compound in the United States. HU-210 (exempt preparation) (Item No. 90083) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.
Chemical Properties
liquid
Uses
A synthetic agonist analog of ?9-Tetrahydro Cannabinol (T293200), which is the primary psychoactive component of marijuana. HU-210 is a potent central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptor agonist. It binds to neuroblastoma cell membrane CB1 receptors with about the same affinity as CP-55940. Controlled Substance.
Biological Activity
A highly potent cannabinoid receptor agonist (K i values are 0.061 and 0.52 nM at cloned human CB 1 and CB 2 receptors respectively). Induces spatial memory deficits and suppresses hippocampal firing rates in rats. Also displays agonist activity at GPR55 (EC 50 = 26 nM). Also available as part of the Cannabinoid Receptor Agonist Tocriset™ .