ChemicalBook--->CAS DataBase List--->199854-00-7

199854-00-7

199854-00-7 Structure

199854-00-7 Structure
IdentificationBack Directory
[Name]

O-ACETYLSALICYLHYDROXAMIC ACID
[CAS]

199854-00-7
[Synonyms]

ACSHA
O-ASHA
AcSHA, O-ASHA
O-ACETYLSALICYLHYDROXAMIC ACID
N-(ACETYLOXY)-2-HYDROXY BENZAMIDE
Acetic Acid (2-Hydroxybenzoyl)azanyl Ester
[Molecular Formula]

C9H9NO4
[MDL Number]

MFCD05863976
[MOL File]

199854-00-7.mol
[Molecular Weight]

195.17
Chemical PropertiesBack Directory
[Appearance]

Cyrstalline Solid
[storage temp. ]

Store at -20°C
[solubility ]

≤25mg/ml in ethanol;50mg/ml in DMSO;30mg/ml in dimethyl formamide
[form ]

Solid
[color ]

Cyrstalline
Hazard InformationBack Directory
[Chemical Properties]

Cyrstalline Solid
[Uses]

An irreversible, non-selective inhibitor of COX-1 and COX-2.
[Biological Activity]

o-acetyl salicylhydroxamic acid (o-asha) is an irreversible, non-selective inhibitor of cox-1 and cox-2 [1].cyclooxygenase (cox) is the key enzyme required for the conversion of arachidonic acid to prostaglandins. cyclooxygenase enzymes have been involved in diverse physiological situations and disease processes ranging from inflammation to cancer. until now, two cyclooxygenase isoforms have been identified, cox-1 and cox-2. the cox-1 enzyme is produced constitutively (i.e., gastric mucosa) and cox-2 is inducible (i.e., sites of inflammation) [2].o-acetyl salicylhydroxamic acid (o-asha) inhibited the activity of ovine cox-1 in a time-dependent and irreversible manner with a 50% b/b0 value of approximately 4.5 mm [1]. o-acetyl salicylhydroxamic acid was a novel acetylating agent. o-acetyl salicylhydroxamic acid inhibited pge2 synthesis in vivo and blocked the cyclooxygenase activity of pghs in vitro. o-acetyl salicylhydroxamic acid elicited its effects via acetylation of ser-529 in the cyclooxygenase active site [1].
[References]

[1] loll p j, sharkey c t, o'connor s j, et al. o-acetylsalicylhydroxamic acid, a novel acetylating inhibitor of prostaglandin h2 synthase: structural and functional characterization of enzyme-inhibitor interactions[j]. molecular pharmacology, 2001, 60(6): 1407-1413.
[2] dubois r n, abramson s b, crofford l, et al. cyclooxygenase in biology and disease[j]. the faseb journal, 1998, 12(12): 1063-1073.
199854-00-7 suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 010-82848833 400-666-7788
Website: http://www.jkchemical.com
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 821-50328103-801 18930552037
Website: https://www.chemicalbook.com/ShowSupplierProductsList13285/0.htm
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Website: www.shchemsky.com
Company Name: Shanghai TaoSu Biochemical Technology Co., Ltd.  
Tel: 021-33632979
Website: www.tsbiochem.com
Company Name: Shenzhen Polymeri Biochemical Technology Co., Ltd.  
Tel: +86-400-002-6226
Website: www.rrkchem.com
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Website: http://www.med-bio.cn/
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Website: http://www.energy-chemical.com
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Website: http://www.efebio.com
Company Name: ApexBio Technology  
Tel: + 1-832-696-8203
Website: www.apexbt.com
Company Name: BOC Sciences  
Tel: 16314854226
Website: www.bocsci.com
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Website: www.caymanchem.com
Company Name: CLEARSYNTH LABS LTD.  
Tel: +91-22-45045900
Website: www.clearsynth.com
Company Name: United States Biological  
Tel: 800.520.3011 or 781.639.5092
Website: www.usbio.net
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161
Website: www.zzsrm.com
Company Name: Toronto Research Chemicals  
Tel: +1 (416) 665-9696
Website: www.trc-canada.com
Company Name: Medical Isotopes  
Tel: 1-(603) 635-1722
Website: www.medicalisotopes.com
Company Name: Advanced Technology & Industrial Co., Ltd.  
Tel: (852) 23902293
Website: www.advtechind.com
Tags:199854-00-7 Related Product Information