Trans-N1-Ethyl-N4-[2-[4-(ethylamino)butylaminomethyl]cyclopropylmethyl]-1,4-butanediamine tetrahydrochloride, with CAS number 306292-64-8, is a synthetic organic compound characterized by its complex molecular structure, which includes multiple amine groups and a cyclopropyl moiety. This compound is typically classified as a tetrahydrochloride salt, indicating that it is a quaternary ammonium compound with four chloride ions associated with the amine functionalities. Its structure suggests potential applications in pharmacology, particularly in the development of drugs targeting specific receptors or pathways due to the presence of the ethyl and butylamine side chains, which may enhance its biological activity. The compound's solubility in water is likely high due to the presence of multiple amine groups, which can engage in hydrogen bonding. Additionally, the stereochemistry indicated by "trans" suggests specific spatial arrangements that may influence its interaction with biological targets. Overall, this compound's unique characteristics make it a subject of interest in medicinal chemistry and related fields.

trans-N1-Ethyl-N4-[2-[4-(ethylamino)butylaminomethyl]cyclopropylmethyl]-1,4-butanediamine tetrahydrochloride

306292-64-8: Trans-N1-Ethyl-N4-[2-[4-(ethylamino)butylaminomethyl]cyclopropylmethyl]-1,4-butanediamine tetrahydrochloride, with CAS number 306292-64-8, is a synthetic organic compound characterized by its complex molecular structure, which includes multiple amine groups and a cyclopropyl moiety. This compound is typically classified as a tetrahydrochloride salt, indicating that it is a quaternary ammonium compound with four chloride ions associated with the amine functionalities. Its structure suggests potential applications in pharmacology, particularly in the development of drugs targeting specific receptors or pathways due to the presence of the ethyl and butylamine side chains, which may enhance its biological activity. The compound's solubility in water is likely high due to the presence of multiple amine groups, which can engage in hydrogen bonding. Additionally, the stereochemistry indicated by "trans" suggests specific spatial arrangements that may influence its interaction with biological targets. Overall, this compound's unique characteristics make it a subject of interest in medicinal chemistry and related fields.

<p>CGC 11093: A polyamine analog inhibiting human prostate tumor growth in mice; may help regress choroidal neovascularization.</p>

CAS 306292-64-8

trans-N1-Ethyl-N4-[2-[4-(ethylamino)butylaminomethyl]cyclopropylmethyl]-1,4-butanediamine tetrahydrochloride

CGC 11093

Ref: TM-T69479