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glucametacin

Product Name
glucametacin
CAS No.
52443-21-7
Chemical Name
glucametacin
Synonyms
glucometacin;glucametacin;2-[[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetylamino]-2-deoxy-D-glucose;2-[[2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetyl]amino]-2-deoxy-D-glucose;D-Glucose, 2-[[2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetyl]amino]-2-deoxy-
CBNumber
CB5885480
Molecular Formula
C25H27ClN2O8
Formula Weight
518.94
MOL File
52443-21-7.mol
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glucametacin Property

Melting point:
>160°C (dec.)
Boiling point:
793.7±60.0 °C(Predicted)
Density 
1.44
storage temp. 
Refrigerator, under inert atmosphere
solubility 
DMSO (Slightly)
form 
Solid
pka
13.05±0.20(Predicted)
color 
White to Pale Yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0016190
Product name
GLUCAMETACIN
Purity
95.00%
Packaging
250MG
Price
$329.7
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
18649
Product name
Glucametacin
Packaging
5mg
Price
$950
Updated
2021/12/16
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glucametacin Chemical Properties,Usage,Production

Description

Glucametacin is used to treat inflammatory and degenerative arthropathy. The compound is well tolerated with significantly less gastrointestinal distress than indomethacin. Glucametacin does not appear to be metabolized to indomethacin.

Originator

Glucametacin,Shanghai Lansheng Corporation

Uses

A nonsteroidal antiinflammatory analgesic. An indomethacin conjugates with D-glucosamine was prepared for reducing ulcerogenic potency, increasing the bioavailability of indomethacin and exerting the coordinative effects on osteoarthritis.

Manufacturing Process

125 g (75 ml) thionyl chloride were added to 30 g 1-(p-chlorobenzoyl)-2- methyl-5-methoxy-indolyl-3-acetic acid (indometacine) in 200 ml of dry chloroform and heated to reflux for 15 min. The solvent was distilled off and the residue was recrystallized from benzene to give 23 g 1-(p-chlorobenzoyl)- 2-methyl-5-methoxy-indolyl-3-acetyl chloride. MP: 126°-129°C.
43 g d-(+)-glucosamine hydrochloride in 140 ml of cold water, 20 g above prepared acetyl chloride in any inert solvent (chloroform, ethyl acetate, dioxane) and 35 ml 12% NaOH was mixed and stirred for 1hour at a room temperature. Then it was diluted with water and a solid was filtered off, washed and dried in vacuum. 10 volumes (by weight) methanol was added to the obtained dry product, filtered off and dried in vacuum. Yield of 1-(pchlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid monohydrate glucosamide 20 g. Glucametacine was obtained as a powder. MP: about 218°C (with decomposition).

Therapeutic Function

Antiinflammatory, Analgesic, Antipyretic

Trade name

Euminex (Asta Medica, Spain), Teoremin (Labofarma/Degussa, Brazil).

Synthesis

glucametacin is prepared by acylation of d-glucosamine with indomethacin acid chloride (prepared from indomethacin and thionyl chloride) in the presence of sodium hydroxide.

glucametacin Preparation Products And Raw materials

Raw materials

Preparation Products

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glucametacin Suppliers

Hangzhou Yuhao Chemical Technology Co., Ltd
Tel
0571-82693216
Fax
+86-571-82880190
Email
info@yuhaochemical.com
Country
China
ProdList
9387
Advantage
52
CONIER CHEM AND PHARMA LIMITED
Tel
+8618523575427
Email
sales@conier.com
Country
China
ProdList
49374
Advantage
58
Hangzhou Jinghao Biotechnology Co., LTD
Tel
17513242016 17513242016
Fax
QQ:1576861551
Email
1576861551@qq.com
Country
China
ProdList
2803
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11974
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Country
China
ProdList
19699
Advantage
58
Watson Biotechnology Co.,Ltd
Tel
+86-18186686046 +86-18186686046
Fax
+86-27-59524646
Email
sales01@watsonbiotech.cn
Country
China
ProdList
5853
Advantage
58
Lanospharma Laboratories Co.,Ltd
Tel
--
Fax
--
Email
sales@lanospharma.com
Country
China
ProdList
6329
Advantage
56

52443-21-7, glucametacinRelated Search:


  • glucametacin
  • glucometacin
  • 2-[[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetylamino]-2-deoxy-D-glucose
  • 2-[[2-[1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetyl]amino]-2-deoxy-D-glucose
  • D-Glucose, 2-[[2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetyl]amino]-2-deoxy-
  • 52443-21-7
  • C25H27ClN2O8