NSC 262266: structure given in first source
ID Source | ID |
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PubMed CID | 6438713 |
MeSH ID | M0197228 |
Synonym |
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73387-70-9 |
nsc 262666 |
1,4-diazoniabicyclo(2.2.1)heptane, 1,4-bis(2-chloroethyl)-,(z)-2-butenedioate (1:2) |
1,4-diazoniabicyclo(2.2.1)heptane, 1,4-bis(2-chloroethyl)-, (z)-2-butenedioate (1:2) |
1,4-bis(2-chloroethyl)-1,4-diazoniabicyclo(2.2.1)heptane (z)-2-butenedioate (1:2) |
nsc 262664 |
nsc 262266 |
2-butenedioic acid, (z)-, ion(1-), 1,4-bis(2-chloroethyl)-1,4-diazoniabicyclo(2.2.1)heptane (2:1) |
1,4-bis(2-chloroethyl)-1,4-diazoniabicyclo[2.2.1]heptane;(z)-4-hydroxy-4-oxobut-2-enoate |
Excerpt | Reference | Relevance |
---|---|---|
"Cardiotoxicity, a side-effect that can occur after treatment with an anticancer drug, has severe clinical implications." | ( In vitro screening of antitumour agents for cardiotoxicity by means of isolated mouse left atria. Bast, A; Haenen, GR; van Acker, FA; van Acker, SA; van der Vijgh, WJ, ) | 0.13 |
Excerpt | Relevance | Reference |
---|---|---|
"We investigated the antitumoral activity of Dabis Maleate given on different dosage schedules and as continuous infusion in a murine reticular cell sarcoma M5076 (M5) and in a subline made resistant to cyclophosphamide and other nitrogen mustards (M5/CTX)." | ( Antitumor activity of 1,4-bis (2'-chloroethyl)-1,4-diazabicyclo-[2.2.1] heptane dimaleate (Dabis Maleate) in M5076 and its subline resistant to cyclophosphamide M5/CTX. D'Incalci, M; Filippeschi, S; Hendricks, H; Tagliabue, G, 1992) | 0.28 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (20.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (80.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |