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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891186Generated: October 30, 2026

HCID 11442519, compound → HCID 45263211, compound

https://huagongshe.com/reaction/891186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11442519HCID 11442519—
ReactantHCID 11496753HCID 11496753—
ReactantHCID 11525106HCID 11525106—
ReactantHCID 11547534HCID 11547534—
ReactantHCID 11596668HCID 11596668—
ReactantHCID 131725287HCID 131725287—
ProductHCID 45263211HCID 45263211—

Reaction Steps

As is apparent from the above Tables 1–3, a limited class of N-alkylarylpolyamine compounds (i.e. N-naphthylalkyl, N-anthracenylalkyl and N-pyrenylalkyl) have unique properties of surprising cytotoxicity, unexpected selectivity in killing cancer cells (especially cells with high polyamine transport activity), and/or facilitate the delivery of known toxic agents into cancer cells. As shown in Table 2, the N-(3-Amino-propyl)-N-anthracen-9-ylmethyl-butane-1,4-diamine, trihydrochloride (8d), N-(4-Amino-butyl)-N-anthracen-9-ylmethyl-butane-1,4-diamine, trihydrochloride (8e), N-(4-Amino-butyl)-N-anthracen-9-ylmethyl-pentane-1,5-diamine, trihydrochloride (8g), N-(4-Amino-butyl)-N′-naphthalen-1-ylmethyl-butane-1,4-diamine trihydrochloride (27b), N-(4-Amino-butyl)-N′-pyren-1-ylmethyl-butane-1,4-diamine trihydrochloride (27d), and N-{4-[(Anthracen-9-ylmethyl)-amino]-butyl}-cyclohexane-1,4-diamine trihydrochloride (31) have outstanding selectivity in targeting and killing cells with active polyamine transporters.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001925B1
Source datasetuspto-grants-2006_02
ORD IDord-04e08b1c1c1a4b738fb20761890184da
Source noteuspto-grants-2006_02