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C9847

Cyclothiazid

AMPA glutamate receptor blocker, powder

Synonym(e):

6-Chlor-3,4-dihydro-3-(2-norbornen-5-yl)-2H-1,2-4-benzothiadiazin-7-sulfonamid-1,1-dioxid

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PackungsgrößeSKUVerfügbarkeitPreis
10 mg
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€ 119,00
25 mg
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€ 283,00

Über diesen Artikel

Empirische Formel (Hill-System):
C14H16ClN3O4S2
CAS-Nummer:
Molekulargewicht:
389.88
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352125
EC Number:
218-859-7
MDL number:
Form:
powder
Quality level:

€ 119,00


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Produktname

Cyclothiazid,

form

powder

Quality Level

originator

Eli Lilly

storage temp.

2-8°C

SMILES string

[H][C@@]12CC(C3Nc4cc(Cl)c(cc4S(=O)(=O)N3)S(N)(=O)=O)[C@@]([H])(C1)C=C2

InChI

1S/C14H16ClN3O4S2/c15-10-5-11-13(6-12(10)23(16,19)20)24(21,22)18-14(17-11)9-4-7-1-2-8(9)3-7/h1-2,5-9,14,17-18H,3-4H2,(H2,16,19,20)/t7-,8+,9?,14?/m0/s1

InChI key

BOCUKUHCLICSIY-QJWLJZLASA-N

General description

Cyclothiazide is a benzothiadiazine, which has a similar structure to diazoxide.[1]

Application

Cyclothiazide has been used as a α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) desensitization blocker to study the effects of γ2 on receptor desensitization.[2]

Biochem/physiol Actions

Blocks the rapid desensitization of the AMPA glutamate receptors and markedly prolongs the decay time of the evoked excitatory post-synaptic current.

Features and Benefits

This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Glutamate Receptors (Ion Channel Family) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Eli Lilly. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Dieser Artikel
D9035C4911SML2047
form

powder

form

powder

form

powder

form

powder

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

-

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

storage temp.

2-8°C

originator

Eli Lilly

originator

Schering Plough

originator

-

originator

-

Gene Information

human ... CA1(759), CA4(762), GRIA1(2890), GRIA2(2891), GRIA3(2892), GRIA4(2893)
rat ... Gria1(50592)

Gene Information

human ... KCNA1(3736), KCNJ11(3767), KCNJ8(3764), KCNMA1(3778)
mouse ... Kcnj1(56379), Kcnj11(16514)
rat ... Gria1(50592), Kcna1(24520), Kcnj1(24521), Kcnj11(83535), Kcnj8(25472)

Gene Information

human ... CA1(759), CA4(762), SLC12A3(6559)

Gene Information

-


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Lagerklasse

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Helle Hald et al.
Journal of molecular biology, 391(5), 906-917 (2009-07-14)
Ionotropic glutamate receptors (iGluRs) mediate fast excitatory neurotransmission. Upon glutamate application, 2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid receptors undergo rapid and almost complete desensitization that can be attenuated by positive allosteric modulators. The molecular mechanism of positive allosteric modulation has been elucidated previously by
L O Trussell et al.
Neuron, 10(6), 1185-1196 (1993-06-01)
We have investigated the role of AMPA receptor desensitization during transmission at a calyceal synapse. Cyclothiazide blocked the rapid desensitization of AMPA receptors and markedly prolonged the decay time of the evoked excitatory postsynaptic current (PSC). This effect was greater
Craig S Walker et al.
Current biology : CB, 19(11), 900-908 (2009-06-02)
Ionotropic glutamate receptors (iGluRs) are glutamate-gated ion channels that mediate excitatory neurotransmission in the central nervous system. Based on both molecular and pharmacological criteria, iGluRs have been divided into two major classes, the non-NMDA class, which includes both AMPA and



Global Trade Item Number

SKUGTIN
C9847-25MG04061833531259
C9847-10MG04061833531242

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