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75250

Sigma-Aldrich

Salvinorin B

≥93.0% (HPLC)

Sinónimos:

(2S,4aR,6aR,7R,9S,10aS,10bR)-2-(3-Furanyl)dodecahydro-9-hydroxy-6a,10b-dimethyl-4,10-dioxo 2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester, Divinorin B

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About This Item

Fórmula empírica (notación de Hill):
C21H26O7
Número de CAS:
92545-30-7
Peso molecular:
390.43
Beilstein/REAXYS Number:
4335292
MDL number:
MFCD16036232
UNSPSC Code:
12352204
PubChem Substance ID:
329766282
NACRES:
NA.83

assay

≥93.0% (HPLC)

form

powder or crystals

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

solubility

chloroform: soluble

storage temp.

−20°C

SMILES string

COC(=O)[C@@H]1C[C@H](O)C(=O)[C@H]2[C@@]1(C)CC[C@H]3C(=O)O[C@@H](C[C@]23C)c4ccoc4

InChI

1S/C21H26O7/c1-20-6-4-12-19(25)28-15(11-5-7-27-10-11)9-21(12,2)17(20)16(23)14(22)8-13(20)18(24)26-3/h5,7,10,12-15,17,22H,4,6,8-9H2,1-3H3/t12-,13-,14-,15-,17-,20-,21-/m0/s1

InChI key

BLTMVAIOAAGYAR-CEFSSPBYSA-N

Categorías relacionadas

Biochem/physiol Actions

Salvinorin B is the major deacetylated metabolite of salvinorin A, a diterpene from Salvia divinorum with reported psychotropic activity, not observed in Salvinorin B.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

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Kenji Tsujikawa et al.
Forensic science international, 180(2-3), 105-109 (2008-09-05)
Two major salvinorins, salvinorin A (SalA) and salvinorin B (SalB), in three Salvia divinorum dried leaf products and nine of its "concentrated extract" products circulated in Japan were determined. These ingredients were extracted twice with acetonitrile and decolored with graphite
Seda Damla Hatipoglu et al.
Phytochemical analysis : PCA, 28(6), 541-549 (2017-07-20)
Salvia, an important and widely available member of Lamiaceae family. Although comparative analysis on secondary metabolites in several Salvia species from Turkey has been reported, their hallucinogenic chemicals have not been screened thoroughly. This study provides LC-MS/MS analysis of 40
Thomas A Munro et al.
Bioorganic & medicinal chemistry, 16(3), 1279-1286 (2007-11-06)
Protection of salvinorin B as standard alkoxyalkyl ethers yielded highly potent kappa opioid receptor agonists. Ethoxymethyl ether 6 is among the most potent and selective kappa agonists reported to date. Fluoroethoxymethyl ether 11 is the first potent, selective fluorinated kappa
Mark S Schmidt et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 818(2), 221-225 (2005-03-01)
Salvinorin A was quantitated in human and rhesus monkey plasma, rhesus monkey cerebrospinal fluid, and human urine by negative ion LC-MS/APCI. The method for Salvinorin A has been fully validated, the LLOQ using FDA guidelines is 2 ng/mL for 0.5
Sanya Aggarwal et al.
Neuroendocrinology, 108(3), 172-189 (2018-12-12)
The medial amygdala (MeA) responds to olfactory stimuli and alters reproductive physiology. However, the neuronal circuit that relays signals from the MeA to the reproductive axis remains poorly defined. This study aimed to test whether MeA kisspeptin (MeAKiss) neurons in
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