HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891186Generated: October 30, 2026
HCID 11442519, compound → HCID 45263211, compound
https://huagongshe.com/reaction/891186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11442519 | HCID 11442519 | — |
| Reactant | HCID 11496753 | HCID 11496753 | — |
| Reactant | HCID 11525106 | HCID 11525106 | — |
| Reactant | HCID 11547534 | HCID 11547534 | — |
| Reactant | HCID 11596668 | HCID 11596668 | — |
| Reactant | HCID 131725287 | HCID 131725287 | — |
| Product | HCID 45263211 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001925B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-04e08b1c1c1a4b738fb20761890184da |
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| Source note | uspto-grants-2006_02 |
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