(±)-Pranoprofen
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(±)-Pranoprofen
structure -
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CAS No:
52549-17-4
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Formula:
C15H13NO3
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Chemical Name:
(±)-Pranoprofen
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Synonyms:
5H-[1]Benzopyrano[2,3-b]pyridine-7-acetic acid,α-methyl-;α-Methyl-5H-[1]benzopyrano[2,3-b]pyridine-7-acetic acid;Y 8004;2-(5H-[1]-Benzopyrano[2,3-b]pyridin-7-yl)propionic acid;Pranoprofen;Niflan;α-Methyl-5H-[1]benzopyrano[2,3-b]pyridine-7-ylacetic acid;(±)-Pranoprofen;(RS)-Pranoprofen;dl-Pranoprofen;Oftalar;2-(5H-Chromeno[2,3-b]pyridin-7-yl)propanoic acid;103813-86-1
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CAS No:
Description
Pranoprofen is a non-steroidal anti-inflammatory drug used in ophthalmology. Target: PGE2Pranoprofen 0.1% was found to be as effective as diclofenac sodium 0.1% in reducing inflammation and pain after strabismus surgery. Pranoprofen could be used as a safe and effective anti-inflammatory alternative for the treatment of inflammation following strabismus surgery [1]. pranoprofen has efficacy equivalent to a moderate-potency corticosteroid with a better safety profile. It should be conside
Pranoprofen is a pyridochromene.
(±)-Pranoprofen Basic Attributes
255.27
255.27
1308068-626-2
759832
DTXSID1023497
S01BC09|S - Sensory organs
2934999090
Characteristics
59.4
2.7
1.3±0.1 g/cm3
182-183 °C
465.7°C at 760 mmHg
235.5±25.4 °C
1.628
LD50 in male mice, rats (mg/kg): 447.3, 87.3 orally (Edanaga)
Safety Information
UN 2811 6.1 / PGIII
DJ3100950
P301 + P310 + P330
H301
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P301+P310, P321, P330, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Drug Information
Agents that increase uric acid excretion by the kidney (URICOSURIC AGENTS), decrease uric acid production (antihyperuricemics), or alleviate the pain and inflammation of acute attacks of gout. (See all compounds classified as Gout Suppressants.)|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.)
2-(5H-(1)benzopyrano(2,3-b)pyridin-7-yl)propionic acid
Computed Properties
Molecular Weight:255.27
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:255.08954328
Monoisotopic Mass:255.08954328
Topological Polar Surface Area:59.4
Heavy Atom Count:19
Complexity:346
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Extract from the above information
Registered Holders
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Wuhan Leadpharm Pharmaceutical Technology Co., Ltd.
Active
China
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Gansu Haotian PharmaTech Co., Ltd.
Active
China
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Shijiazhuang Lonzeal Pharmaceuticals Co., Ltd.
Active
China
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