Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > Osalmid

Osalmid

pharmaceutical raw materials
Osalmid structure

Osalmid 

structure
  • CAS No:

    526-18-1

  • Formula:

    C13H11NO3

  • Chemical Name:

    Osalmid

  • 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

  • Categories:

    Organic Chemistry  >  Amides

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).

Osalmid Basic Attributes

229.23

229.23

208-385-9

89741L759Z

93960

DTXSID0042244

2924299090

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

Safety Information

22-36/37/38-42/43

26-36/37

Xn

P264, P270, P301+P312, P330, P501

H302

Drug Information

4'-hydroxysalicylanilide

Osalmid Use and Manufacturing

Methods of 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.

Uses

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.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Shanxi Zhendong Anxin Biopharmaceutical Co., Ltd.

    China China
    Active
  • Jilin Aodong--Taonan Pharnalentical Company Ltd

    China China
    Active
  • Yangzhou NO.3 Pharmacitical Manufacture Co., Ltd.

    China China
    Active

Recommended Suppliers of Osalmid

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.