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- Cypenamine (INN, BAN), or cypenamine hydrochloride (USAN), also known as 2-phenylcyclopentylamine, is a psychostimulant drug which was developed by a group at the William S. Merrell Chemical Company in the 1940s. It is currently known only in scientific research and has never been developed for market use. Cypenamine is currently legal throughout the entire world, and though its chemical structure has a vague similarity to certain controlled stimulants like fencamfamine, it is likely that it is too distant for it to be considered an illicit analogue under the United States Federal Analogue Act of the Controlled Substances Act. (en)
- シペナミン(Cypenamine)またはフェニルシクロペンタミン(Phenylcyclopentamine)は、1940年代にWilliam S. Merrill companyで開発された精神刺激薬である。現在では科学研究のみに用いられており、市販向けには開発されていない。シペナミンは世界中のほとんどの国でも合法であり、その化学構造は等の法規制の対象となっている覚醒剤とは漠然とした類似性があるものの、構造の違いが大きすぎるためアメリカ合衆国の規制物質法のにおける違法な構造類似体とはみなせないと考えられている。 (ja)
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- 5117 (xsd:nonNegativeInteger)
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- -trans-2-phenylcyclopentan-1-amine (en)
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- N[C@H]1CCC[C@@H]1C2=CC=CC=C2 (en)
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- VNGYTYNUZHDMPP-UHFFFAOYSA-N (en)
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- Cypenamine (INN, BAN), or cypenamine hydrochloride (USAN), also known as 2-phenylcyclopentylamine, is a psychostimulant drug which was developed by a group at the William S. Merrell Chemical Company in the 1940s. It is currently known only in scientific research and has never been developed for market use. Cypenamine is currently legal throughout the entire world, and though its chemical structure has a vague similarity to certain controlled stimulants like fencamfamine, it is likely that it is too distant for it to be considered an illicit analogue under the United States Federal Analogue Act of the Controlled Substances Act. (en)
- シペナミン(Cypenamine)またはフェニルシクロペンタミン(Phenylcyclopentamine)は、1940年代にWilliam S. Merrill companyで開発された精神刺激薬である。現在では科学研究のみに用いられており、市販向けには開発されていない。シペナミンは世界中のほとんどの国でも合法であり、その化学構造は等の法規制の対象となっている覚醒剤とは漠然とした類似性があるものの、構造の違いが大きすぎるためアメリカ合衆国の規制物質法のにおける違法な構造類似体とはみなせないと考えられている。 (ja)
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- Cypenamine (en)
- シペナミン (ja)
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-Cypenamine_Enantiomers_Structural_Formulae.png?width=300)
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