Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H27N5 |
Molecular Weight | 361.4833 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCCNC1=NC=CC2=C(C)C3=C(C=C12)C4=CN=CC=C4N3
InChI
InChIKey=LPHSYQSMAGVYNT-UHFFFAOYSA-N
InChI=1S/C22H27N5/c1-4-27(5-2)12-6-9-24-22-18-13-17-19-14-23-10-8-20(19)26-21(17)15(3)16(18)7-11-25-22/h7-8,10-11,13-14,26H,4-6,9,12H2,1-3H3,(H,24,25)
Pazelliptine (previously known as BD 40 or SR 95225A) was developed as an antitumor drug that binds to the DNA sequence, preferable to G-C rich region and thus produces cellular DNA lesions. This drug was undergoing phase II trials in France for the treatment of cancer. However, this study was discontinued.
Approval Year
PubMed
Title | Date | PubMed |
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Production of protein-associated DNA breaks by 10-[diethylaminopropylamino]-6-methyl-5H-pyrido[3',4':4,5]pyrrolo [2,3-g]isoquinoline in cultured L1210 cells and in isolated nuclei: comparison with other topoisomerase II inhibitors. | 1988 Mar 15 |
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Two-photon ionisation of the antitumor drug pazelliptine (BD40) by 355 nm laser photolysis. | 1993 Dec |
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Spectroscopic study of the interaction of pazelliptine with nucleic acids. | 1997 Oct |
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C582
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C66330
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C024256
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CHEMBL40124
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ACTIVE MOIETY