Details
Stereochemistry | ACHIRAL |
Molecular Formula | C23H23N3O5 |
Molecular Weight | 421.4458 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(OC)C=C2C(=C1)C(=O)N(CCN(C)C)C3=C2C=NC4=CC5=C(OCO5)C=C34
InChI
InChIKey=UVXCXZBZPFCAAJ-UHFFFAOYSA-N
InChI=1S/C23H23N3O5/c1-25(2)5-6-26-22-15-9-20-21(31-12-30-20)10-17(15)24-11-16(22)13-7-18(28-3)19(29-4)8-14(13)23(26)27/h7-11H,5-6,12H2,1-4H3
Molecular Formula | C23H23N3O5 |
Molecular Weight | 421.4458 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Nitro and amino substitution within the A-ring of 5H-8,9-dimethoxy-5-(2-N,N-dimethylaminoethyl)dibenzo[c,h][1,6]naphthyridin-6-ones: influence on topoisomerase I-targeting activity and cytotoxicity. | 2004 Jul 1 |
|
Facile formation of hydrophilic derivatives of 5H-8,9-dimethoxy-5-[2-(N,N-dimethylamino)ethyl]-2,3-methylenedioxydibenzo[c,h] [1,6]naphthyridin-6-one (ARC-111) and its 12-aza analog via quaternary ammonium intermediates. | 2008 Jun 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:04:47 GMT 2023
by
admin
on
Sat Dec 16 10:04:47 GMT 2023
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Record UNII |
7GL8K930U6
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Record Status |
Validated (UNII)
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Record Version |
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500214-53-9
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7GL8K930U6
Created by
admin on Sat Dec 16 10:04:47 GMT 2023 , Edited by admin on Sat Dec 16 10:04:47 GMT 2023
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