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S7001

Sigma-Aldrich

Strychnine hemisulfate salt

≥98.0%, suitable for ligand binding assays and NMR

Synonym(s):

Strychnidin-10-one sulfate (2:1)

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About This Item

Linear Formula:
C21H22N2O2 · 1/2H2SO4
CAS Number:
60-41-3
Molecular Weight:
383.45
EC Number:
200-477-7
MDL number:
MFCD00068328
UNSPSC Code:
12352210
PubChem Substance ID:
329824573
NACRES:
NA.26

product name

Strychnine hemisulfate salt,

Assay

≥98.0%

form

powder

technique(s)

NMR: suitable
ligand binding assay: suitable

color

white to off-white

SMILES string

OS(O)(=O)=O.O=C1C[C@@H]2OCC=C3CN4CC[C@@]56[C@@H]4C[C@@H]3[C@@H]2[C@@H]5N1c7ccccc67.O=C8C[C@@H]9OCC=C%10CN%11CC[C@@]%12%13[C@@H]%11C[C@@H]%10[C@@H]9[C@@H]%12N8c%14ccccc%13%14

InChI

1S/2C21H22N2O2.H2O4S/c2*24-18-10-16-19-13-9-17-21(6-7-22(17)11-12(13)5-8-25-16)14-3-1-2-4-15(14)23(18)20(19)21;1-5(2,3)4/h2*1-5,13,16-17,19-20H,6-11H2;(H2,1,2,3,4)/t2*13-,16-,17-,19-,20-,21+;/m00./s1

InChI key

GOOCRIHPADOQAS-ZNUXJMJHSA-N

Related Categories

Biochem/physiol Actions

Convulsant; glycine receptor antagonist not associated with the NMDA receptor.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H300 + H330,H410

Hazard Classifications

Acute Tox. 1 Oral - Acute Tox. 2 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mari Hondo et al.
PloS one, 6(9), e25076-e25076 (2011-09-29)
Glycine, a nonessential amino-acid that acts as an inhibitory neurotransmitter in the central nervous system, is currently used as a dietary supplement to improve the quality of sleep, but its mechanism of action is poorly understood. We confirmed the effects
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Studies have indicated that the metabotropic glutamate receptor 5 (mGluR5) antagonist 6-methyl-2-(phenylethynyl)-pyridine (MPEP) decreases ethanol self-administration, and the same receptor type was also suggested to be involved in the mechanism of action of the anti-craving substance acamprosate. Our previous research

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