Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

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'That Obscure Object of Desire': in systemic lupus erythematosus B-cell activating factor/B-lymphocyte stimulator is targeted both by the immune system and by physicians.Adenosine receptors are not involved in theophylline-induced seizures.Purinergic system in psychiatric diseases.

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P2860

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

Item

http://www.wikidata.org/entity/Q48899794

description

1990 nî lūn-bûn

@nan

1990年の論文

@ja

1990年学术文章

@wuu

1990年学术文章

@zh

1990年学术文章

@zh-cn

1990年学术文章

@zh-hans

1990年学术文章

@zh-my

1990年学术文章

@zh-sg

1990年學術文章

@yue

1990年學術文章

@zh-hant

name

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@en

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@nl

type

Item

label

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@en

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@nl

prefLabel

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@en

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@nl

P1476

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

@en

P2093

Anderson SM

http://www.w3.org/2001/XMLSchema#string

Daly JW

http://www.w3.org/2001/XMLSchema#string

Weir RL

http://www.w3.org/2001/XMLSchema#string

P2860

Non-xanthine heterocycles: activity as antagonists of A1- and A2-adenosine receptors

Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

Enhancement of the binding of 3H-diazepam to rat brain membranes in vitro by SQ 20009, A novel anxiolytic, gamma-aminobutyric acid (GABA) and muscimol.

The role of hormone receptors and GTP-regulatory proteins in membrane transduction.

Carbamazepine and carbamazepine-10, 11-epoxide concentrations in human brain.

Two distinct adenosine-sensitive sites on adenylate cyclase.

Adenosine receptors and behavioral actions of methylxanthines

PACPX--a substituted xanthine--antagonizes both the A1 and A2 subclasses of the P1-purinoceptor: antagonism of the A2 subclass is competitive but antagonism of the A1 subclass is not

Adenosine inhibits epileptiform activity arising in hippocampal area CA3.

Adenosine receptors in brain membranes: binding of N6-cyclohexyl[3H]adenosine and 1,3-diethyl-8-[3H]phenylxanthine

P304

503-512

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1528-1157.1990.TB06098.X

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

1990-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

2401242

http://www.w3.org/2001/XMLSchema#string

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

about

P2860

P2860

Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698