ChemicalBook >> CAS DataBase List >>Quinagolide

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
Molecular Weight:
395.56
MDL Number:
MFCD07799967
MOL File:
87056-78-8.mol
MSDS File:
SDS
Last updated:2025-04-17 18:22:24
Product description Number Pack Size Price
QUINAGOLIDE 95.00% API0005294 5MG $498.04

Quinagolide Properties

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)
FDA UNII 80Q9QWN15M
ATC code G02CB04

Pharmacokinetic data

Protein binding 90%
Excreted unchanged in urine Very little
Volume of distribution 100 Litres
Biological half-life 17

Quinagolide price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0005294 QUINAGOLIDE 95.00% 87056-78-8 5MG $498.04 2021-12-16 Buy
Product number Packaging Price Buy
API0005294 5MG $498.04 Buy

Quinagolide Chemical Properties,Uses,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

87056-65-3
87056-78-8
Synthesis of Quinagolide from (+/-)-(3α,4aα,10aβ)-1,2,3,4,4a,5,10,10a-octahydro-6-methoxy-3-(methoxycarbonyl)benzoquinoline

Quinagolide Preparation Products And Raw materials

Raw materials

Preparation Products

Quinagolide Suppliers

Global( 17)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 20582 58
BOC Sciences 16314854226 info@bocsci.com United States 9923 65
Hefei Molake Biotechnology Co., Ltd. 0551-66336380 18956014586 983438788@qq.com China 2384 58
Guangzhou Juntang Technology Co., Ltd 020-36607679 13502246435 sales@dmstandards.com China 10945 58
TargetMol Chemicals Inc. 4008200310 15002144251 marketing@tsbiochem.com China 24955 58
Shanghai Yimiao Pharmaceutical Technology Co., Ltd. 18502785028 1605896178@qq.com China 214 58
TLC Pharmaceutical Standards Ltd. 18012923235 chinasales04@tlcstandards.com.cn China 8143 58
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