Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H18NO4.Cl |
| Molecular Weight | 383.825 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].COC1=C(OC)C=C2C(=C1)C=[N+](C)C3=C2C=CC4=C3C=C5OCOC5=C4
InChI
InChIKey=QLDAACVSUMUMOR-UHFFFAOYSA-M
InChI=1S/C21H18NO4.ClH/c1-22-10-13-7-17(23-2)18(24-3)8-15(13)14-5-4-12-6-19-20(26-11-25-19)9-16(12)21(14)22;/h4-10H,11H2,1-3H3;1H/q+1;/p-1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. | 1991 Jan-Feb |
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| HIV-1 and HIV-2 reverse transcriptases: a comparative study of sensitivity to inhibition by selected natural products. | 1992 May 29 |
|
| Comparison of in vitro activities of camptothecin and nitidine derivatives against fungal and cancer cells. | 1999 Dec |
|
| Biological activities of nitidine, a potential anti-malarial lead compound. | 2012 Mar 9 |
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13063-04-2
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DTXSID50926842
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146397
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XO8WQL69T8
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25659
Created by
admin on Sat Dec 16 07:53:52 GMT 2023 , Edited by admin on Sat Dec 16 07:53:52 GMT 2023
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
