Weight | 249.423 g/mol |
---|---|
Formula | C15H23NS |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
TENOCYCLIDINE (21500-98-1, 1867-65-8)
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- In vitro biological efficiency of tenocyclidine - TCP and its adamantane derivative TAMORF (Toxicology in Vitro, 2006)
- Tenocyclidine treatment in soman-poisoned rats : intriguing results on genotoxicity versus protection (Acta Biochimica Polonica, 2008)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCC(CC1)(C2=CC=CS2)N3CCCCC3
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InChIKeyJUZZEWSCNBCFRL-UHFFFAOYSA-N
- Pubchem - TENOCYCLIDINE
- Wikipedia - tenocyclidine
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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