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 UTC 2023
by
admin
on
Sat Dec 16 10:04:47 UTC 2023
|
| Record UNII |
7GL8K930U6
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
9888428
Created by
admin on Sat Dec 16 10:04:47 UTC 2023 , Edited by admin on Sat Dec 16 10:04:47 UTC 2023
|
PRIMARY | |||
|
500214-53-9
Created by
admin on Sat Dec 16 10:04:47 UTC 2023 , Edited by admin on Sat Dec 16 10:04:47 UTC 2023
|
PRIMARY | |||
|
7GL8K930U6
Created by
admin on Sat Dec 16 10:04:47 UTC 2023 , Edited by admin on Sat Dec 16 10:04:47 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> INHIBITOR |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
