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Related to PHENFORMIN HYDROCHLORIDE, H1 receptor antagonists, Ketones

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Antihistamines (1)
Drugs acting on the nervous system (1)
Pharmaceuticals (1)
Psychoactive drugs (1)

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propiomazine (362-29-8)  
Largon
Propiomazine (Largon, Propavan, Indorm, Serentin, Dorevane, Dorevan) is an antihistamine blocking H1 receptors. It is used to treat insomnia, and to produce sleepiness or drowsiness and to relieve anxiety before or during surgery or other procedures and in combination with analgetics also during labor. Propiomazine is a phenothiazine, but is not used as a neuroleptic because it does not block dopamine receptors well.

Related Results:
1-Benzylpiperidine (2905-56-8)  
N-benzylpiperidine  ·  1-benzylpiperidine hydrochloride
1-Phenylpiperazine hydrochloride (2210-93-7)  
phenylpiperazine  ·  1-phenylpiperazine  ·  phenylpiperazine monohydrochloride
1-(2-Methoxyphenyl)piperazine (35386-24-4)  
o-methoxyphenylpiperazine  ·  1-(2-methoxyphenyl)piperazine hydrochloride  ·  1-(ortho-methoxyphenyl)piperazine
2-Propylpiperidine (458-88-8, 3238-60-6)  
coniine  ·  cicutine  ·  conicine
Coniine refers to a poisonous chemical compound, an alkaloid present in and isolable from poison hemlock (Conium maculatum), where its presence has been a source of significant economic, medical, and historico-cultural interest; coniine is also produced by the yellow pitcher plant (Sarracenia flava), and fool's parsley (Aethusa cynapium). Its ingestion and extended exposure are toxic to humans and all classes of livestock; its mechanism of poisoning involves disruption of the peripheral nervous system, with death caused by respiratory paralysis. The biosynthesis of coniine contains as its penultimate step the non-enzymatic cyclisation of 5-oxooctylamine to γ-coniceine, a Schiff base differing from coniiine only by its carbon-nitrogen double bond in the ring.
1-Benzhydrylpiperazine (841-77-0)  
norcyclizine  ·  norcyclizine oxalate (1:2)  ·  norcyclizine oxalate (1:1)
1-(Diphenylmethyl)piperazine, also known as benzhydrylpiperazine, is a chemical compound and piperazine derivative. It features a piperazine ring with a benzhydryl (diphenylmethyl) group bound to one of the nitrogens.
1-PHENYLPIPERAZINE (92-54-6)  
phenylpiperazine  ·  phenylpiperazine monohydrochloride  ·  phenylpiperazine dihydrobromide
1-Phenylpiperazine is a simple chemical compound featuring a phenyl group bound to a piperazine ring. The suffix ‘-piprazole’ is sometimes used in the names of drugs to indicate they belong to this class. A number of phenylpiperazine derivatives are drugs, including: Pharmaceuticals: Research chemicals: Designer drugs:
Piperazine dihydrochloride (6094-40-2, 142-64-3)  
piperazine  ·  piperazine hexahydrate  ·  piperazine phosphate
15532-75-9 (15532-75-9)  
TFMPP  ·  1-(m-trifluoromethylphenyl)piperazine  ·  1-(3-trifluoromethylphenyl)piperazine
3-Trifluoromethylphenylpiperazine (TFMPP) is a recreational drug of the piperazine chemical class. Usually in combination with its analogue benzylpiperazine (BZP), it is sold as an alternative to the illicit drug MDMA ("Ecstasy") under the name "Legal X".
PIPERAZINE HYDROCHLORIDE (6091-62-9, 6094-40-2, 7542-23-6, 142-64-3)  
piperazine  ·  piperazine hexahydrate  ·  piperazine phosphate
cloperastine (3703-76-2)  
1-(2-((4-chloro-alpha-phenylbenzyl)oxy)ethyl)piperidine  ·  cloperastine hydrochloride
Cloperastine (INN) or cloperastin, also known as cloperastine hydrochloride (JAN) (brand names Hustazol, Nitossil, Seki) and cloperastine fendizoate (or hybenzoate), is an antitussive and antihistamine that is marketed as a cough suppressant in Japan, Hong Kong, and in some European countries. It was first introduced in 1972 in Japan, and then in Italy in 1981. The precise mechanism of action of cloperastine is not fully clear, but several different biological activities have been identified for the drug, of which include: ligand of the σ1 receptor (Ki = 20 nM) (likely an agonist), GIRK channel blocker (described as "potent"), antihistamine (Ki = 3.8 nM for the H1 receptor), and anticholinergic.
QUINUCLIDINE (100-76-5)  
Quinuclidine is an organic compound and a bicyclic amine and used as a catalyst and a chemical building block. It is a strong base with pKa of the conjugate acid of 11.0. This is due to greater availability of the nitrogen lone pair.
zafirlukast (107753-78-6)  
Zafirlukast is an orally administered leukotriene receptor antagonist (LTRA) used for the chronic treatment of asthma. While zafirlukast is generally well-tolerated, headache and stomach upset often occur. Some rare side effects can occur, which can be life-threatening, such as liver failure.
1-(3-Chlorophenyl)piperazine (6640-24-0)  
m-CPP  ·  1-(3-chlorophenyl)piperazine dihydrochloride  ·  m-chlorophenylpiperazine
meta-Chlorophenylpiperazine (mCPP) is a psychoactive drug of the phenylpiperazine class. It was initially developed in the late-1970s and used in scientific research before being sold as a designer drug in the mid-2000s. It has been detected in pills touted as legal alternatives to illicit stimulants in New Zealand and pills sold as "ecstasy" in Europe and the United States.
diphenylpyraline (147-20-6)  
diphenylpyraline hydrochloride  ·  diphenylpyraline maleate (2:1)  ·  Lergobine
Diphenylpyraline (DPP; sold as Allergen, Arbid, Belfene, Diafen, Hispril, Histyn, Lergobine, Lyssipol, Mepiben, Neargal) is a first-generation antihistamine with anticholinergic effects of the diphenylpiperidine class. It is marketed in Europe for the treatment of allergies. DPP has also been found to act as a dopamine reuptake inhibitor and produces hyperactivity in rodents.
1-Benzylpiperazine (2759-28-6)  
1-benzylpiperazine hydrochloride  ·  1-benzylpiperazine tartrate  ·  1-benzylpiperazine dihydrochloride
Benzylpiperazine (BZP) is a recreational drug with euphoriant and stimulant properties. The effects produced by BZP are comparable to those produced by amphetamine. Adverse effects have been reported following its use including acute psychosis, renal toxicity and seizures.
Piperazine phosphate (14538-56-8, 1951-97-9)  
piperazine  ·  piperazine hexahydrate  ·  piperazine hydrochloride
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H1 receptor antagonists
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