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Sedatives

Prepared by reduction of 4-nitrophenol or 4-nitrosophenoi. Can be diazotized and used as a first component in azo-dyes. Chief outlet is for sulphur dyes in which it is fused with sodium polysulphides. L/sed as a photographic developer. [Pg.30]

White crystals, m.p. 191°C. A barbituric acid derivative. The sodium salt is administered orally as a sedative. [Pg.51]

C10H16N2O3. White crystalline powder, m.p. I22-124°C. Prepared by condensing ethyl butylethylmalonate with urea. It is used as a sedative and hypnotic. [Pg.72]

CifiHijClNj. White plates m.p. 125 C. Diazepam is one of several benzodiazepines which are very widely used as minor tranquillizers for allaying anxiety, as hypnotics or, in sufficiently high dosage given intravenously, as pre-anaesthetic sedatives. [Pg.132]

Obtained as a syrup from plants of the Solanaceae family. Intensely poisonous, its action resembles that of atropine. Sedative in small doses. [Pg.213]

C12H12N2O3. White crystals, m.p. 174°C. Prepared by condensing the ethyl ester of phenylethylmalonic acid with urea. It is a more active hypnotic than barbitone. It and its sodium salt - soluble phenobarbitone - are used as sedatives and in treating epilepsy. [Pg.303]

Vapour Pressure Base Sed. and Water Teperature Salinity... [Pg.238]

To operate the MPI or LPI equipment at stable and reprodncable inspection conditions modern units are equipped with a monitoring and control system called "Quality Assurance Package" (termed QAP). The QAP System is ba.sed on an industrial PC with a bus system and field sensors. It ensures that process parameters important for the reproducability of the MPI or LPI are controlled an held between defined limits by a central computer system. It can be adapted to any old system, as well as integrated into new systems. [Pg.628]

In order to be able to reduce prices, even more and more test- and measurement systems are integrated on PC-boards. The powerful and inexpensive PC eomponents can be directly u.sed for these (virtual) instruments. The limited dimensions of the PC boards require a reduction to the absolute necessity of the electronic components. Analogue signal proeessing must carried out by software as far as possible. [Pg.855]

Lead dioxide is slightly soluble in concentrated nitric acid and concentrated sulphuric acid, and it dissolves in fused alkalis. It therefore has amphoteric properties, although these are not well characteri.sed since it is relatively inert. [Pg.194]

Notes and Comments. Further improvements in efficiency were achieved by implementing the method on computers with highly parallel architecture. SISM performs in parallel as LFV which means the speed up Is gained due to longer time stop wliidi cun be u.sed by SISM [20]. [Pg.345]

Tiiinpiiraiiii (3 is handled the sanii way in Langavin dynamics as it iisin molecular dynamics. High tern peraLurc runs m ay he n sed to overcome poten lial cnergy barriers. Cooling a system to a low tern -peratnre in steps may result in a different stable conformation than would be round by direct geometry optimization. [Pg.94]

Although in teraetion s between vicinal I 4 atom s arc n om in ally treated as non bonded interactions, triost of the force fields treat these somewhat differently from normal 1 5 and greater non-bonded interactions. HyperCbern allows each of these 1 4 non-bonded interactions to be scaled down by a scale factor < 1.0 with AMBHR or OPI-S. bor HIO+ the electrostatic may be scaled and different param eters rn ay be ti sed for I 4 van dcr Waals interactions, fh e. AMBHR force field, for exam pie, n orrn a lly uses a seal in g factor of 0.5 for both van der Waals an d electrostatic interactions. [Pg.182]

When a specific value above is n ot hn own, the rule of Pauling (the van der Waals radius is approximately 0.76 A larger than the cova-len t radiiis) is u sed. [Pg.213]

Most simple empirical or semi-empirical molecular orbital methods. including all ofthose ii sed in IlyperCh em, neglect inner sh ell orbitals and electrons and use a minimal basis se.i r>f valence Slater orbitals. [Pg.269]

Chambers C C, G D Hawkins, C J Cramer and D G Tmlilar 1996. Model for Aqueous Solvation Ba sed on Class IC Atomic Charges and First Solvation Shell Effects. Journal of Physical Chemistry 100 16385-16398. [Pg.650]

The salts of monoalkyl sulphates are frequently encountered as commercial detergents (for example, dreft, gardinol and pentrone ) they are usually sodium salts, the alkyl components contain 12 or more carbon atoms, and give colloidal solutions. They are hydrol3 sed by boiling with dilute sodium hydroxide solution ... [Pg.1079]

However, in the reaction of 1-alkenylboranes with aryl- or 1-alkenyi iodides. 2-aryl-l-alkenes 648 are obtained as the main products. When Pd metal produced from Pd(OAc)2 as a catalyst and EtjN as a weak bu.se are u.sed. abnormal products are formed. On the other hand, normal products 649 are obtained by using NaOH[5l7]. [Pg.221]

CHjCiMeljCHjCO-U.sed as indicators in the titration of strong acids or strong bases... [Pg.159]

CYlionic nicthine dye u.sed to 1002 ohtaln positive colored image in an Ag-free photobleaching process... [Pg.162]

A much more serious drawback to using chiral drugs as racemic mixtures is illustrated by thalidomide briefly employed as a sedative and antinausea drug in Europe during the period 1959-1962 The desired properties are those of (/ ) thalidomide (S) Thalido mide however has a very different spectrum of bio logical activity and was shown to be responsible for over 2000 cases of serious birth defects in children born to women who took it while pregnant... [Pg.296]


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Abstinence syndrome (withdrawal sedative-hypnotic

Alcohol, sedative effects

Amnesia, sedative-hypnotics producing

Anesthesia sedative-hypnotics causing

Anticonvulsants sedative-hypnotics

Antidepressant drugs (antidepressants sedative

Antihistamines sedative effects

Antihistaminics sedative side effects

Antipsychotic drugs antipsychotics sedatives

Antipsychotics sedative effects

Antiseizure drugs sedative-hypnotics

Anxiolytic effect, sedatives

Anxiolytics and Sedatives

Anxiolytics sedatives

Anxiolytics, sedatives, hypnotics, and antipsychotics

Barbiturate sedative-hypnotics pharmacologic effects

Barbiturates sedative-hypnotics

Basilicum polystachyon for sedative in convulsions and

Benzodiazepine derivatives sedative effects

Benzodiazepine sedative-hypnotics clinical pharmacology

Benzodiazepine sedative-hypnotics currently used drugs

Benzodiazepine sedative-hypnotics pharmacologic effects

Benzodiazepine sedative-hypnotics receptor interactions

Benzodiazepines sedative-hypnotics

Biological sedative effect

Bupropion Sedatives

Central nervous system sedatives/tranquillizers

Central nervous system with sedative-hypnotics

Chlorpheniramine, sedative

Cimetidine sedative effect

Clonidine sedative effects

Crocus sativus for sedative in convulsions

Dependence sedative-hypnotics

Dependence with sedative-hypnotics

Diphenhydramine, sedative

Diphenhydramine, sedative properties

Ethanol, sedative effects

Flumazenil, a benzodiazepine receptor antagonist, is used to reverse the sedative effects of benzodiazepines after anesthesia

HYPNOTICS, SEDATIVES, ANTICONVULSANTS, AND ANXIOLYTICS

Halogenated sedative-hypnotics

Haloperidol sedative effects

Herbal Sedatives and Anxiolytics

Heterocyclic sedative-hypnotics

Histamine receptor antagonists) sedative effects

Hypnosis sedative-hypnotics causing

Hypnotics, Sedatives And Tranquilizers

Iridoids sedative activity

Major sedatives

Medullary depression sedative-hypnotics causing

Moxonidine Sedatives

Nervous system drugs sedative-hypnotics

Non-barbiturate sedatives

Nonbarbiturate Sedatives and Hypnotics — Benzodiazepine Derivatives

Nonbarbiturate sedatives

Nonbenzodiazepine sedative-hypnotics

Overdose sedative-hypnotic drug

Pharmacodynamics sedative-hypnotics

Phenobarbital sedative-hypnotic

Physiologic dependence with sedative-hypnotics

Psychologic dependence with sedative-hypnotics

Residues of Sedative Drugs

SEDS

SEDS

SEDS (Solution Enhanced

SEDS (Solution Enhanced Dispersion with Supercritical

SEDS (Solution Enhanced method

Sed-tox index

Sedation sedative-hypnotics causing

Sedative Expectorants

Sedative Hypnotics estazolam

Sedative Hypnotics flunitrazepam

Sedative Hypnotics flurazepam

Sedative Hypnotics midazolam

Sedative Hypnotics quazepam

Sedative Hypnotics temazepam

Sedative Hypnotics trazodone

Sedative Hypnotics triazolam

Sedative Hypnotics zaleplon

Sedative Hypnotics zolpidem

Sedative Hypnotics zopiclone

Sedative activity

Sedative agent

Sedative agents phenothiazines

Sedative agents receptors

Sedative and hypnotic drugs

Sedative belladonna

Sedative calamus

Sedative catnip

Sedative drugs, combined prescribing

Sedative effect medications

Sedative effects

Sedative effects of antihistamines

Sedative hypnotic drugs

Sedative hypnotic drugs actions

Sedative hypnotics, acute actions

Sedative in convulsions

Sedative in epilepsy

Sedative jasmine

Sedative lavender

Sedative medications

Sedative medications dependence

Sedative medications interaction with other drugs

Sedative orange

Sedative passion flower

Sedative salt

Sedative thyme

Sedative valerian root

Sedative, opioid

Sedative-Hypnotic and Antianxiety Agents

Sedative-hypnotic agents

Sedative-hypnotic agents antipsychotics

Sedative-hypnotic agents barbiturates

Sedative-hypnotic agents benzodiazepines

Sedative-hypnotic agents common drugs

Sedative-hypnotic agents nonbenzodiazepines

Sedative-hypnotic agents pharmacokinetics

Sedative-hypnotic and anxiolytic

Sedative-hypnotic and anxiolytic agents

Sedative-hypnotic drugs abuse

Sedative-hypnotic drugs adverse effects

Sedative-hypnotic drugs alcohol

Sedative-hypnotic drugs barbiturates

Sedative-hypnotic drugs benzodiazepines

Sedative-hypnotic drugs chronic abuse effects

Sedative-hypnotic drugs effects

Sedative-hypnotic drugs ethanol

Sedative-hypnotic drugs family

Sedative-hypnotic drugs mechanism

Sedative-hypnotic drugs pharmacodynamics

Sedative-hypnotic drugs toxicity

Sedative-hypnotic drugs withdrawal from

Sedative-hypnotic effects

Sedative-hypnotic-anxiolytics

Sedative-hypnotics

Sedative-hypnotics Benzodiazepines Glutethimide

Sedative-hypnotics abuse

Sedative-hypnotics classification

Sedative-hypnotics coma caused

Sedative-hypnotics confusion caused

Sedative-hypnotics currently used drugs

Sedative-hypnotics delirium caused

Sedative-hypnotics evaluation

Sedative-hypnotics history

Sedative-hypnotics hypertension caused

Sedative-hypnotics hypotension caused

Sedative-hypnotics hypothermia caused

Sedative-hypnotics pharmacology

Sedative-hypnotics toxicity

Sedative-hypnotics withdrawal from

Sedatives 1,3-thiazines

Sedatives Ambien

Sedatives abuse

Sedatives adverse effects

Sedatives and Tranquilizers

Sedatives and hypnotics

Sedatives antimuscarinics

Sedatives antipsychotics

Sedatives benzodiazepines

Sedatives chlordiazepoxide

Sedatives confirmation

Sedatives definition

Sedatives detection

Sedatives essential

Sedatives herbal medicines

Sedatives interaction

Sedatives lorazepam

Sedatives miscellaneous

Sedatives overdose

Sedatives physicochemical properties

Sedatives pregnancy

Sedatives risks

Sedatives sample preparation

Sedatives warfarin interactions

Sedatives, Hypnotics, and Analgesics

Sedatives, Hypnotics, and Antipsychotics

Sedatives, Hypnotics, and Tranquillizers

Sedatives, tranquilizer addiction

Sedatives/hypnotics adverse effects

Sedatives/hypnotics clinical profile

Sedatives/tranquillizers

Sedatives/tranquillizers benzodiazepines (diazepam

Side effects, sedative

Skeletal muscle relaxants sedative-hypnotics

Sleep Sedative-hypnotics

Sleep disorders, sedative-hypnotics

Special Consideration of Sedative-Hypnotic and Antianxiety Agents in Rehabilitation

Study Sedative-Hypnotic Drugs

Subject sedative medications

Substance abuse sedative-hypnotics

Terfenadine, sedative properties

Therapeutic withdrawal, with sedative-hypnotics

Tolerance to sedative-hypnotics

Tolerance with sedative-hypnotics

Tolerance, drug sedative-hypnotics

Tranquilizers, minor (sedative-hypnotic

Uterine sedative

Withania somnifera as sedative in epilepsy

Withdrawal state sedative-hypnotic

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