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N4159

Sigma-Aldrich

NCS-382 hydrate

solid, ≥98% (HPLC)

Synonym(s):

5,7,8,9-Tetrahydro-5-hydroxy-6H-benzocyclohepten-6-ylidene acetic acid monosodium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C13H13O3Na · xH2O
CAS Number:
1049743-38-5
Molecular Weight:
240.23 (anhydrous basis)
MDL number:
MFCD11046018
UNSPSC Code:
12352202
PubChem Substance ID:
24278588
Pricing and availability is not currently available.

Quality Level

100

Assay

≥98% (HPLC)

form

solid

color

white to off-white

solubility

H2O: 22 mg/mL

SMILES string

O.[Na+].OC1C(\CCCc2ccccc12)=C\C([O-])=O

InChI

1S/C13H14O3.Na.H2O/c14-12(15)8-10-6-3-5-9-4-1-2-7-11(9)13(10)16;;/h1-2,4,7-8,13,16H,3,5-6H2,(H,14,15);;1H2/q;+1;/p-1/b10-8+;;

InChI key

FCHWTCFJPQOCCJ-PIHABLKOSA-M

Biochem/physiol Actions

γ-Hydroxybutyrate (GHB) receptor antagonist; anti­convulsant.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
066K47043V
066K47042
066K47041
125K4705
066K4704

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M Maitre et al.
The Journal of pharmacology and experimental therapeutics, 255(2), 657-663 (1990-11-01)
Administration of gamma-hydroxybutyrate (GHB) to animals induces electroencephalographic and behavioral changes that resemble petit-mal seizures. Furthermore, these GHB-induced electroencephalogram-behavioral changes can be blocked by anticonvulsant drugs, which are specific in their action against petit-mal seizures. These effects of GHB on
M Maitre
Progress in neurobiology, 51(3), 337-361 (1997-02-01)
gamma-Hydroxybutyrate is a metabolite of GABA which is synthesized and accumulated by neurons in brain. This substance is present in micromolar quantities in all brain regions investigated as well as in several peripheral organs. Neuronal depolarization releases gamma-hydroxybutyrate into the

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