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Related to PHENFORMIN HYDROCHLORIDE, H1 receptor antagonists, Pyrrolidines

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Antihistamines (1)
Cyclic compounds (1)
Drugs acting on the nervous system (1)
Drugs acting on the respiratory system (1)
Five-membered rings (1)
Psychoactive drugs (1)
Respiratory system drug (1)

Histapyrrodine (493-80-1, 6113-17-3)  
Domistan  ·  N-phenyl-N-benzyl-1-pyrrolidineethanamine  ·  histapyrrodine hydrochloride

Related Results:
1-Benzylpiperidine (2905-56-8)  
N-benzylpiperidine  ·  1-benzylpiperidine hydrochloride
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".
1-(2-Methoxyphenyl)piperazine (35386-24-4)  
o-methoxyphenylpiperazine  ·  1-(2-methoxyphenyl)piperazine hydrochloride  ·  1-(ortho-methoxyphenyl)piperazine
1-Phenylpiperazine hydrochloride (2210-93-7)  
phenylpiperazine  ·  1-phenylpiperazine  ·  phenylpiperazine monohydrochloride
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-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:
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.
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.
1-Phenylpiperazine dihydrochloride (4004-95-9)  
phenylpiperazine  ·  1-phenylpiperazine  ·  phenylpiperazine monohydrochloride
4-(4'-Fluorobenzyl)piperidine (92822-02-1)  
92822-02-1  ·  4-(4-fluorobenzyl)piperidine
1-(4-Fluorophenyl)piperazine (2252-63-3)  
para-fluoro-phenylpiperazine  ·  p-fluoro-phenylpiperazine  ·  4-fluoro-phenylpiperazine
para-Fluorophenylpiperazine (pFPP, 4-FPP, 4-Fluorophenylpiperazine; Fluoperazine, Flipiperazine) is a piperazine derivative with mildly psychedelic and euphoriant effects. It has been sold as an ingredient in legal recreational drugs known as "Party pills", initially in New Zealand and subsequently in other countries around the world. pFPP has been found in vitro to act mainly as a 5-HT1A receptor agonist, with some additional affinity for the 5-HT2A and 5-HT2C receptors.
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.
Piperazine dihydrochloride (6094-40-2, 142-64-3)  
piperazine  ·  piperazine hexahydrate  ·  piperazine phosphate
TENOCYCLIDINE (21500-98-1, 1867-65-8)  
Tenocyclidine (TCP) was discovered by a team at Parke Davis in the late 1950s. It is a dissociative anesthetic drug with psychostimulant and hallucinogenic effects. It is similar in effects to phencyclidine (PCP) but is considerably more potent.
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H1 receptor antagonists
Pyrrolidines
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