Aspisol
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Aspisol
structure -
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CAS No:
62952-06-1
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Formula:
C9H8O4.C6H14N2O2
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Chemical Name:
Aspisol
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Synonyms:
Lysine,2-(acetyloxy)benzoate (1:1);DL-Lysine,mono[2-(acetyloxy)benzoate];Lysine,mono[2-(acetyloxy)benzoate];Benzoic acid,2-(acetyloxy)-,compd. with DL-lysine (1:1);Benzoic acid,2-(acetyloxy)-,compd. with lysine (1:1);Aspisol;Acetylsalicylic acid DL-lysine salt;Venopirin;Aspirisine;Lysine acetylsalicylate;Acetylsalicylic acid lysine salt;DL-Lysine acetylsalicylate;Egicalm;Solpirin;Aspegic;Aspirin lysine salt;Vetalgine;Cogla;Laboprin;Acelysin;Atselizin;Acetylsalicylic acid dl-lysine salt;Quinvet;Lysine monosalicylate acetate;Vetalgina;Aspidol;Lysal;Aspirin DL-lysine;LAS;Delgesic;Acelysine;Asalis;Aspirin-dl-lysine;DL-Lysine aspirin salt;o-Acetylsalicylic acid D,L-lysine salt;2,6-diaminohexanoic acid compound with 2-acetoxybenzoic acid (1:1);Lysini racemici acetylsalicylase;97598-63-5;98806-35-0;107032-89-3;123445-32-9;34220-70-7;50641-50-4;51024-94-3;77337-52-1;92520-58-6;145607-63-2
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CAS No:
Characteristics
153
2.23800
Crystalline solid
1.1829 (rough estimate)
155 °C
321.4ºC at 760 mmHg
131.2ºC
-20°C Freezer
LD50 orl-rat: 4350 mg/kg IYKEDH 13,1128,82
Drug Information
Compounds capable of relieving pain without the loss of CONSCIOUSNESS. (See all compounds classified as Analgesics.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes. (See all compounds classified as Cyclooxygenase Inhibitors.)|Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system. (See all compounds classified as Platelet Aggregation Inhibitors.)
acetylsalicylic acid lysinate
Aspisol Use and Manufacturing
Non-steroidal anti-inflammatory drugs (NSAIDs) may inhibit cancer growth. Water soluble, injectable aspirin derivative.Analgesic; antipyretic; anti-inflammatory.
Computed Properties
Molecular Weight:326.34
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:326.14778643
Monoisotopic Mass:326.14778643
Topological Polar Surface Area:157
Heavy Atom Count:23
Complexity:312
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It can inhibit cyclooxygenase, reduce the synthesis of prostaglandins, and has antipyretic, analgesic and anti-inflammatory effects. After intravenous injection, it takes effect quickly, with high blood concentration, about 1.8 times that of oral administration, and is immediately metabolized to salicylic acid, whose concentration rises rapidly. After intramuscular injection of this product, the effective blood concentration can be maintained for 36 to 120 minutes.
Registered Holders
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Shaanxi Xiyue Pharmaceutical (Fufeng) Co., Ltd.
Active
China
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Hainan Huluwa Pharmaceutical Group Co., Ltd.
Active
China
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China Resources Double-Crane Pharmaceutical Co., Ltd.
Active
China
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