Osalmid
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Osalmid
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CAS No:
526-18-1
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Formula:
C13H11NO3
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Chemical Name:
Osalmid
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Synonyms:
Benzamide,2-hydroxy-N-(4-hydroxyphenyl)-;Salicylanilide,4′-hydroxy-;2-Hydroxy-N-(4-hydroxyphenyl)benzamide;Driol;Driol-Labaz;Enidran;N-(p-Hydroxyphenyl)salicylamide;4′-Hydroxysalicylanilide;Oxaphenamide;Salmidochol;p-Hydroxyphenylsalicylamide;PHPS;p′-Hydroxysalicylanilide;N′-Salicyloyl-p-aminophenol;N-(4-Hydroxyphenyl)salicylamide;Osalmid;Osalmide;Auxobil;Bilene;Oxaphenamid;Dribazil;L 1718;Bilocol;Li Dan Feng;WR 17456;Fumispore;Oksafenamide;Saryuurin;Jestmin;Kanochol;Yoshicol;NSC 93960
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CAS No:
Description
Osalmid is a ribonucleotide reductase small subunit M2 (RRM2) targeting compound; suppresses ribonucleotide reductase activity with an IC50 of 8.23 μM.
Osalmid is an organic molecular entity.|Osalmid is under investigation in clinical trial NCT03670173 (Safety and Efficacy Assessments of Osalmid in Multiple Myeloma).
Characteristics
69.6
2.9
1.4±0.1 g/cm3
179 °C
350.8°C at 760 mmHg
165.9±23.7 °C
1.711
LD50 oral in rat: 6702mg/kg
Osalmid Use and Manufacturing
General procedure: To the reaction vessel were added 0.07 mol of p-aminophenol, 0.076 mol of 2-hydroxy-benzamide and 80 ml of ethyl acetate, and the stirring rate was controlled at150rpm, slowly adding stannous chloride 0.031mol, the solution becomes darker color, add finished slowly heated to 170 , the reaction 6h, 2.1kPa vacuum distillationDistill part of ethyl acetate, lower the temperature of the solution to 38 , pour the reactant into 500ml mass fraction of 23percent sodium bisulfite solution, Adding water 33percent oxalic acid solution, adjusting the pH value to 4, precipitating the solid, separating the substance from the solution, Was recrystallized from 87percent ethylenediamine solution to obtain 13.47 g of white solid N-p-hydroxyphenyl salicylamide in 84percent yield.
It is used to treat acute and chronic cholecystitis, gallstone calculi, and at the same time it has a yellowing bile effect
Computed Properties
Molecular Weight:229.23
XLogP3:2.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:229.07389321
Monoisotopic Mass:229.07389321
Topological Polar Surface Area:69.6
Heavy Atom Count:17
Complexity:261
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It increases liver blood flow, improves liver function, and significantly increases the water content in bile. Its choleretic effect is stronger than that of dehydrocholic acid, and it can relax the sphincter of Oddi and lower blood cholesterol.
Registered Holders
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Shanxi Zhendong Anxin Biopharmaceutical Co., Ltd.
Active
China
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Jilin Aodong--Taonan Pharnalentical Company Ltd
Active
China
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Yangzhou NO.3 Pharmacitical Manufacture Co., Ltd.
Active
China
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