Product Information
Applications
Biological Information
Primary Targetk opioid receptor
Primary Target K<sub>i</sub>4.3 nM
Purity≥98% by HPLC
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity Standard Handling
Storage ≤ -70°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications

Documentation

Salvinorin A - CAS 83729-01-5 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

References

Reference overview
Roth, B. et al., 2002. PNAS. 99, 11934.
Valdés III., j., et al., 1984. J. Organic Chem. 49, 4716.
Ortega, A., et al., 1982. J. of Chem. Society, Perkins Transactions I. 2505.
Data Sheet

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision31-October-2013 JSW
Synonymsκ-opioid Receptor Agonist, Salvinorin A, Divinorin A
DescriptionA highly potent and selective non-alkaloid positive allosteric modulator of Κ-opioid receptors (Ki = 4.3 nM and 16 nM for native and cloned κ-opioid receptors, respectively). Also acts as a D2DR partial agonist (Ki = 5-10 nM). Used in studies of addition.
FormWhite solid
CAS number83729-01-5
Chemical formulaC₂₃H₂₈O₈
Structure formulaStructure formula
Purity≥98% by HPLC
SolubilityDMSO (50 mM) or Ethanol (10 mM)
Storage ≤ -70°C
Protect from light
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Standard Handling
ReferencesRoth, B. et al., 2002. PNAS. 99, 11934.
Valdés III., j., et al., 1984. J. Organic Chem. 49, 4716.
Ortega, A., et al., 1982. J. of Chem. Society, Perkins Transactions I. 2505.

Related Products & Applications

Categories

Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Neurochemicals > Agonists