Salvinorin a

Code: S8071-1MG D2-231

Not available outside of the UK & Ireland.

Application

Salvinorin A was administered to rats to study effects on lactic acid-stimulated stretching.1

Biochem/physiol Actions

Salv...


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Your Price
$241.76 1MG
Discontinued

Not available outside of the UK & Ireland.

Application

Salvinorin A was administered to rats to study effects on lactic acid-stimulated stretching.1

Biochem/physiol Actions

Salvinorin A is a potent, non-nitrogenous κ opioid selective receptor agonist. Salvinorin A is isolated from Salvia divinorum. Salvinorin A displays high affinity at both native (Ki=4.3 nm) and cloned (Ki=16 nm) κ -opioid receptors. Preliminary studies suggest that Salvanorin A is chemically unique among the psychtropic drugs and does not bind to any known receptor.

Features and Benefits

This compound is featured on the Opioid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

assay≥98% (HPLC)
colorwhite
drug controlregulated under CDSA - not available from Sigma-Aldrich Canada
formsolid
Gene Informationhuman ... OPRD1(4985), OPRK1(4986), OPRM1(4988)rat ... Oprk1(29335)
InChI keyOBSYBRPAKCASQB-AGQYDFLVSA-N
InChI1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16-,17-,19-,22-,23-/m0/s1
Quality Level100
SMILES string[H][C@@]12CC[C@@]3(C)[C@@H](C[C@H](OC(C)=O)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c4ccoc4)C(=O)OC
solubilityethanol: ~3 mg/mL, DMSO: ≥10 mg/mL
storage conditionprotect from light
storage temp.−20°C
Cas Number83729-01-5
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