| Name | phenazine-1-carboxamide |
|---|---|
| Synonyms |
α-Amidophenazin
phenazine-1-carboxylic acid amide PCN 1-Carbamoyl-phenazin Phenazine-1-carboxamide Phenazin-1-carbamid |
| Description | Oxychloroaphine could be isolated from the bacterium Pantoea agglomerans naturally present in soil. Oxychloroaphine has broad-spectrum antifungal activity. Oxychloroaphine has cytotoxicity in a dose-dependent manner and induces apoptosis. Oxychloroaphine can be used in research of cancer[1][2]. |
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| Related Catalog | |
| In Vitro | Oxychloroaphine (1-256 μM; 24 h) has cytotoxicity with IC50 values for A549, HeLa, and SW480 cancer cell lines between 32 and 40 μM[2]. Oxychloroaphine (1-150 μM; A549, HeLa, and SW480 cancer cell lines) causes cell membrane damage, leading to increase apoptosis and leakage of lactate dehydrogenase, and increases production of cytochrome c protein[2]. Oxychloroaphine (32 μM; A549 and SW480 cells) induces cycle arrest at G1 phase and induction of sub-G phase[2]. Oxychloroaphine (48 h; A549 cells) induces downregulation of antiapoptotic Bcl-2 protein and the activation of proapoptotic protein caspase-3 led to the cleavage of PARP[2]. Cell Viability Assay[2] Cell Line: A549, HeLa, and SW480 cancer cell lines Concentration: 1, 2, 4, 8, 16, 32, 64, 128, and 256 μM Incubation Time: 24 hours Result: Inhibited cell proliferative in a dose-dependent manner. |
| Density | 1.371g/cm3 |
|---|---|
| Boiling Point | 526.1ºC at 760 mmHg |
| Melting Point | 242ºC |
| Molecular Formula | C13H9N3O |
| Molecular Weight | 223.23000 |
| Flash Point | 272ºC |
| Exact Mass | 223.07500 |
| PSA | 68.87000 |
| LogP | 2.58220 |
| Index of Refraction | 1.76 |
| HS Code | 2933990090 |
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|
~%
550-89-0 |
| Literature: Lasseur;zit.bei Koegl;Postowsky Justus Liebigs Annalen der Chemie, 1930 , vol. 480, p. 280,289,291 |
|
~%
550-89-0 |
| Literature: Borrero, Nicholas V.; Bai, Fang; Perez, Cristian; Duong, Benjamin Q.; Rocca, James R.; Jin, Shouguang; Huigens Iii, Robert W. Organic and Biomolecular Chemistry, 2014 , vol. 12, # 6 p. 881 - 886 |
|
~%
550-89-0 |
| Literature: Borrero, Nicholas V.; Bai, Fang; Perez, Cristian; Duong, Benjamin Q.; Rocca, James R.; Jin, Shouguang; Huigens Iii, Robert W. Organic and Biomolecular Chemistry, 2014 , vol. 12, # 6 p. 881 - 886 |
|
~%
550-89-0 |
| Literature: Toromanoff Annales de Chimie (Cachan, France), 1956 , vol. <13>1, p. 115,142 |
|
~%
550-89-0 |
| Literature: Toromanoff Annales de Chimie (Cachan, France), 1956 , vol. <13>1, p. 115,142 |
|
~%
550-89-0 |
| Literature: Dufraisse et al. Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1952 , vol. 235, p. 920 Full Text Show Details Koegl; Postowsky Justus Liebigs Annalen der Chemie, 1930 , vol. 480, p. 280,286, 293 |
|
~%
550-89-0 |
| Literature: Borrero, Nicholas V.; Bai, Fang; Perez, Cristian; Duong, Benjamin Q.; Rocca, James R.; Jin, Shouguang; Huigens Iii, Robert W. Organic and Biomolecular Chemistry, 2014 , vol. 12, # 6 p. 881 - 886 |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |