Quinagolide

Product Name: Quinagolide
CAS No.: 87056-78-8
Chemical Name: Quinagolide
Synonyms: D07217;Norprolac;CV-205-502;Quinagolide;Quinagolide Free Base;Quinagolide (inn/ban);Quinagolide USP/EP/BP;3-(Diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline;(3S,4aS,10aR)-3-(diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline;Sulfamide, N,N-diethyl-N'-[(3R,4aR,10aS)-1,2,3,4,4a,5,10,10a-octahydro-6-hydroxy-1-propylbenzo[g]quinolin-3-yl]-, rel-
CBNumber: CB81179635
Molecular Formula: C20H33N3O3S
Formula Weight: 395.56
MOL File: 87056-78-8.mol

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Quinagolide Property

Melting point:: 122.5-124°
Boiling point:: 539.1±60.0 °C(Predicted)
Density: 1.23±0.1 g/cm3(Predicted)
pka: 10.31±0.40(Predicted)

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation

Product number: API0005294
Product name: QUINAGOLIDE
Purity: 95.00%
Packaging: 5MG
Price: $498.04
Updated: 2021/12/16

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Quinagolide Chemical Properties,Usage,Production

Uses

Quinagolide (CV205-502) is a non-ergot dopamine D(2) receptor agonist that promotes dopamine activity. Quinagolide has shown effectiveness in modulating endocrine function, particularly in inhibiting disorders associated with dopamine deficiency. Quinagolide is used to suppress hyperprolactinemia and corresponding clinical symptoms, showing good efficacy. Quinagolide's biological activity enables its use as an important research compound in drug isolation and analysis[1].

Definition

ChEBI: Quinagolide is an organonitrogen heterocyclic compound and an organic heterotricyclic compound.

Clinical Use

Hyperprolactinaemia

Metabolism

Quinagolide is extensively metabolised. Quinagolide and its N-desethyl analogue are the biologically active but minor components. Their inactive sulphate or glucuronide conjugates represent the major circulating metabolites. Studies performed with 3 H-labelled quinagolide revealed that more than 95% of the drug is excreted as metabolites. About equal amounts of total radioactivity are found in faeces and urine.

References

[1] Chiral Separations by Host-Guest Complexation with Cyclodextrin and Crown Ether in Capillary Zone Electrophoresis

Quinagolide Preparation Products And Raw materials

Raw materials

Preparation Products

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Quinagolide Suppliers

China 6 France 1 India 2 United States 8 Global 17

BOC Sciences

Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Country: United States
ProdList: 12952
Advantage: 65

BOC Sciences

Tel: 16314854226
Email: info@bocsci.com
Country: United States
ProdList: 9923
Advantage: 65

Shanghai Yimiao Pharmaceutical Technology Co., Ltd.

Tel: 18717991116
Fax: -
Email: 1605896178@qq.com
Country: China
ProdList: 250
Advantage: 58

Hefei Molake Biotechnology Co., Ltd.

Tel: 0551-66336380 18956014586
Fax: 055166336380
Email: 983438788@qq.com
Country: China
ProdList: 2297
Advantage: 58

Dideu Industries Group Limited

Tel: +86-29-89586680 +86-15129568250
Email: 1026@dideu.com
Country: China
ProdList: 20284
Advantage: 58

CONIER CHEM AND PHARMA LIMITED

Tel: +8618523575427
Email: sales@conier.com
Country: China
ProdList: 49975
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Guangzhou Juntang Technology Co., Ltd

Tel: 020-36607679 13502246435
Email: sales@dmstandards.com
Country: China
ProdList: 10945
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TargetMol Chemicals Inc.

Tel: 4008200310
Email: marketing@tsbiochem.com
Country: China
ProdList: 24961
Advantage: 58

87056-78-8, QuinagolideRelated Search:

N,N-Diisopropylethylamine Tris(hydroxymethyl)aminomethane Quinhydrone Quinclorac Propyl gallate CHLOROPHOSPHONAZO III 1-Hydroxyethylidene-1,1-diphosphonic acid Pergolide Propyl butyrate Lithium diisopropylamide Pergolide mesylate salt 8-Hydroxyquinoline Quinagolide hydrochloride Quinagolide

3-(Diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline

CV-205-502

Quinagolide

D07217

Quinagolide (inn/ban)

Norprolac

(3S,4aS,10aR)-3-(diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline

Quinagolide USP/EP/BP

Sulfamide, N,N-diethyl-N'-[(3R,4aR,10aS)-1,2,3,4,4a,5,10,10a-octahydro-6-hydroxy-1-propylbenzo[g]quinolin-3-yl]-, rel-

Quinagolide Free Base

87056-78-8

C20H33N3O3S