ChemicalBook
Chinese Japanese Germany Korea

Suprofen

Suprofen
Suprofen structure
CAS No.
40828-46-4
Chemical Name:
Suprofen
Synonyms
r25061;Suprol;TN 762;Anemet;Srendam;maldocil;Suprocil;Topalgic;Profenal;Profenol
CBNumber:
CB2496867
Molecular Formula:
C14H12O3S
Formula Weight:
260.30828
MOL File:
40828-46-4.mol

Suprofen Properties

Melting point:
278°C
Boiling point:
373.57°C (rough estimate)
Density 
1.2959 (rough estimate)
refractive index 
1.5050 (estimate)
storage temp. 
-20°C Freezer
pka
3.91(at 25℃)
Water Solubility 
soluble
CAS DataBase Reference
40828-46-4(CAS DataBase Reference)

SAFETY

RIDADR  3249
HazardClass  6.1(b)
PackingGroup  III
Toxicity LD50 (7 days post-drug) in mice, rats, guinea pigs, dogs (mg/kg): 590, 353, 280, 160 orally (Niemegeers)

Suprofen price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21350 Suprofen ≥98% 40828-46-4 5mg $49 2018-11-19 Buy
Cayman Chemical 21350 Suprofen ≥98% 40828-46-4 10mg $93 2018-11-19 Buy
Cayman Chemical 21350 Suprofen ≥98% 40828-46-4 25mg $221 2018-11-19 Buy
Cayman Chemical 21350 Suprofen ≥98% 40828-46-4 50mg $343 2018-11-19 Buy

Suprofen Chemical Properties,Uses,Production

Description

Suprofen is an arylpropionic acid analgesic/antiinflammatory agent with close structural resemblance to ketoprofen. It is more potent in many assays than indomethacin and ketoprofen and appears better tolerated.

Chemical Properties

Off-White to Light-Brown

Originator

Janssen (Belgium)

Uses

Prostaglandin biosynthesis inhibitor. Analgesic

Uses

Bridged pseudopelletierine derivative; specific serotonin (5HT3) receptor antagonist. Antiemetic.

Definition

ChEBI: An aromatic ketone that is thiophene substituted at C-2 by a 4-(1-carboxyethyl)benzoyl group.

brand name

Profenal (Alcon);Algiamida;Algiasdi;Bordol;Erdol;Masterfen;Sufenid;Supranol;Surfex;MALDOCIL.

Veterinary Drugs and Treatments

Suprofen is a non-steroidal anti-inflammatory agent similar to flurbiprofen. Suprofen and flurbiprofen are phenylalkanoic acids that inhibit the cyclo-oxygenase enzymes responsible for conversion of arachadonic acid from cell membranes into various prostaglandins. These prostaglandins mediate certain aspects of ocular inflammation including disruption of the blood-aqueous barrier, uveal vasodilation, increases in intraocular pressure, and leakage of white blood cells and protein from uveal vessels into the aqueous humor. Prostaglandins cause iris sphincter constriction (miosis) independent of cholinergic mechanisms. Suprofen can inhibit this intraocular miosis and may also be useful in the management of uveal inflammation (usually in addition to topical steroids).

Suprofen Preparation Products And Raw materials

Raw materials

Preparation Products


Suprofen Suppliers

Global( 75)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Mainchem Co., Ltd.
+86-0592-6210733
+86-0592-6210733 sales@mainchem.com CHINA 32451 55
Sangel Pharmaceutical & Chemical Factory +86 571 85773987 +86 13505717485
+86 571 85773986 1610413282@qq.com China 62 58
J & K SCIENTIFIC LTD. 400-666-7788 +86-10-82848833
+86-10-82849933 jkinfo@jkchemical.com;market6@jkchemical.com China 96815 76
Chemsky(shanghai)International Co.,Ltd. 021-50135380
shchemsky@sina.com China 32363 50
Richest Group Limited +86 21 5017 5386/3175 7285/86/87/88/89
+86 21 6085 3086 info@richest-group.com China 13930 57
BOC Sciences
info@bocsci.com United States 10507 65
Wuhan Fortuna Chemical Co., Ltd +86-27-59207852 85767163
+86-27-59524646 info@fortunachem.com China 2613 58
Dalian Meilun Biotech Co., Ltd. 0411-66771943;0411-66771942
0411-66771945 sales@meilune.com China 4062 58
Beijing HuaMeiHuLiBiological Chemical 010-56205725;010-86181995
010-65763397 waley188@sohu.com China 12342 58
Haoyuan Chemexpress Co., Ltd. 86-21-58998985
(86) 21-58955996 apisales@chemexpress.com.cn China 7560 61

40828-46-4(Suprofen)Related Search:


  • 1H-Indole-3-carboxylic acid(2α,6α,8α,9αβ)-octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester
  • Dolasetron Methanesulformte
  • MDL-73147EF:Anzemet
  • 2-[4-(Thiophene-2-carbonyl)phenyl]propanoic acid
  • a-Methyl-p-(2-thenoyl)phenylacetic acid
  • 2-[4-(thiophene-2-carbonyl)phenyl]propionic acid
  • Suprofen (200 mg)
  • α-Methyl-4-(2-thienylcarbonyl)benzeneacetic Acid
  • para-(2-Thenoyl) hydratropic acid
  • Maldocil,Masterfen,Supranol,Supro,
  • (+-)-2-(p-(2-thenoyl)phenyl)propionicacid
  • alpha-methyl-4-(2-thienylcarbonyl)-benzeneaceticaci
  • alpha-methyl-4-(2-thienylcarbonyl)benzeneaceticacid
  • maldocil
  • p-(2-thenoyl)-hydratropicaci
  • p-(2-thenoyl)hydratropicacid
  • r25061
  • a-Methyl-4-(2-thienylcarbonyl)benzeneacetic Acid
  • Masterfen
  • Srendam
  • Sulprotin
  • Suprocil
  • Suprol
  • Sutoprofen
  • Topalgic
  • DOLASETRON(FREE BASE)
  • Benzeneacetic acid, a-methyl-4-(2-thienylcarbonyl)- (9CI)
  • NSC 303611
  • Profenal
  • Profenol
  • Racemic suprofen
  • Sulproltin
  • TN 762
  • 2-(4-Thiophen-2-ylcarbonylphenyl)propanoic acid
  • Suprofen
  • -
  • 40828-46-4
  • Heterocyclic Compounds
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Inhibitors
  • BENZENEACETICACID,A-METHYL-4-(2-THIENYLCARBONYL)
  • Anemet
  • MDL 73147
  • Octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl Ester 1H-Indole-3-carboxylic Acid Stereoisomer
  • 115956-12-0
  • 115952-12-2
Copyright 2017 © ChemicalBook. All rights reserved