| Name | [3-(nitrooxymethyl)phenyl] 2-acetyloxybenzoate |
|---|---|
| Synonyms |
m-NO-ASA
3-nitrooxyphenyl acetylsalicylate 2-Acetoxybenzoate-2-(1-nitroxymethyl)phenyl ester Nitroaspirin, 10 mM in DMSO 3-(NitroxyMethyl)phenyl 2-acetoxybenzoate NO-ASA nitroaspirin 2-AcetyloxybenzoicAcid3-NitrooxymethylphenylEster 2-(ACETYLOXY)-3-[(NITROOXY)METHYL]PHENYL ESTER, BENZOIC ACID Benzoic acid, 2-(acetyloxy)-, 3-[(nitrooxy)methyl]phenyl ester NO-ASPIRIN 1 Nitric oxide-releasing aspirin Ncx 4016 Inhibitor,Cyclooxygenase,Nitroaspirin,inhibit,NCX4016,NCX-4016,COX,Apoptosis C102148 m-NO-aspirin |
| Description | Nitroaspirin (NCX 4016) is a nitric oxide (NO) donor and a nitro-derivative of Aspirin, which combines with Nitroaspirin to inhibit cyclooxygenase. Nitroaspirin (NCX 4016) has antithrombotic and anti-platelet properties and acts as a direct and irreversible inhibitor of COX-1. Nitroaspirin (NCX 4016) causes significant induction of cell cycle arrest and apoptosis in Cisplatin-resistant human ovarian cancer cells via down-regulation of EGFR/PI3K/STAT3 signaling and modulation of Bcl-2 family proteins[1][2][3][4]. |
|---|---|
| Related Catalog | |
| Target |
COX-1 |
| References |
| Density | 1.347g/cm3 |
|---|---|
| Boiling Point | 499.3ºC at 760mmHg |
| Melting Point | 61-62ºC |
| Molecular Formula | C16H13NO7 |
| Molecular Weight | 331.27700 |
| Flash Point | 214.3ºC |
| Exact Mass | 331.06900 |
| PSA | 107.65000 |
| LogP | 3.06260 |
| Vapour Pressure | 4.21E-10mmHg at 25°C |
| Index of Refraction | 1.58 |
| Storage condition | -20°C |
|
~84%
175033-36-0 |
| Literature: Nicox S.A. Patent: US6696591 B1, 2004 ; Location in patent: Page column 5-6 ; |
|
~%
175033-36-0 |
| Literature: Chiroli, Valerio; Benedini, Francesca; Ongini, Ennio; Del Soldato, Piero European Journal of Medicinal Chemistry, 2003 , vol. 38, # 4 p. 441 - 446 |
|
~%
175033-36-0 |
| Literature: Chiroli, Valerio; Benedini, Francesca; Ongini, Ennio; Del Soldato, Piero European Journal of Medicinal Chemistry, 2003 , vol. 38, # 4 p. 441 - 446 |
|
~%
175033-36-0 |
| Literature: Chiroli, Valerio; Benedini, Francesca; Ongini, Ennio; Del Soldato, Piero European Journal of Medicinal Chemistry, 2003 , vol. 38, # 4 p. 441 - 446 |
| Precursor 4 | |
|---|---|
| DownStream 0 | |