Oxychloroaphine

Modify Date: 2024-01-04 17:51:31

Oxychloroaphine Structure
Oxychloroaphine structure
Common Name Oxychloroaphine
CAS Number 550-89-0 Molecular Weight 223.23000
Density 1.371g/cm3 Boiling Point 526.1ºC at 760 mmHg
Molecular Formula C13H9N3O Melting Point 242ºC
MSDS N/A Flash Point 272ºC

 Use of Oxychloroaphine


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].

 Names

Name phenazine-1-carboxamide
Synonym More Synonyms

 Oxychloroaphine Biological Activity

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].
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.

 Chemical & Physical Properties

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

 Safety Information

HS Code 2933990090

 Synthetic Route

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Oxychloroaphine Structure

Oxychloroaphine

CAS#:550-89-0

Literature: Lasseur;zit.bei Koegl;Postowsky Justus Liebigs Annalen der Chemie, 1930 , vol. 480, p. 280,289,291

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Oxychloroaphine Structure

Oxychloroaphine

CAS#: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

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Oxychloroaphine Structure

Oxychloroaphine

CAS#: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

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Oxychloroaphine Structure

Oxychloroaphine

CAS#:550-89-0

Literature: Toromanoff Annales de Chimie (Cachan, France), 1956 , vol. <13>1, p. 115,142

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Oxychloroaphine Structure

Oxychloroaphine

CAS#:550-89-0

Literature: Toromanoff Annales de Chimie (Cachan, France), 1956 , vol. <13>1, p. 115,142

~%

Oxychloroaphine Structure

Oxychloroaphine

CAS#: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

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Oxychloroaphine Structure

Oxychloroaphine

CAS#: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

 Customs

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%

 Synonyms

α-Amidophenazin
phenazine-1-carboxylic acid amide
PCN
1-Carbamoyl-phenazin
Phenazine-1-carboxamide
Phenazin-1-carbamid
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