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Bromocriptine mesylate

Bromocriptine mesylate Structure
CAS No.
22260-51-1
Chemical Name:
Bromocriptine mesylate
Synonyms
BCT;BRC;Bromocryptine mesylate;Bromocriptine-13C-d3 Mesylate;Bromocriptine Mesylate (150 mg);Bagren;cb-154;Pravidel;Serono-Bagren;CB-154 mesylate
CBNumber:
CB4335584
Molecular Formula:
C33H44BrN5O8S
Molecular Weight:
750.7
MOL File:
22260-51-1.mol
MSDS File:
SDS
Modify Date:
2023/9/26 16:29:58

Bromocriptine mesylate Properties

Melting point 192-196° (dec)
alpha D20 +95° (c = 1 in methanol-methylene chloride)
storage temp. 2-8°C
solubility H2O: 0.8 mg/mL
form solid
pka 4.90(at 25℃)
color white
optical activity [α]20/D +95°, c = 1 in methanol: methylene chloride (1:1)(lit.)
Merck 13,1400
BRN 4115238
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months
InChIKey NOJMTMIRQRDZMT-JGYCFGIMSA-N
CAS DataBase Reference 22260-51-1(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H410
Precautionary statements  P273-P301+P312+P330
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  22-24/25-36
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
RTECS  KE1595000
3-10
HS Code  29396900
Toxicity LD50 in mice, rats, rabbits (mg/kg): 190, 72, 12.5 i.v. (Parkes)
NFPA 704
0
2 0

Bromocriptine mesylate price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) B2134 2-Bromo-α-ergocryptine methanesulfonate salt solid 22260-51-1 25MG ₹9190.43 2022-06-14 Buy
Sigma-Aldrich(India) B2134 2-Bromo-α-ergocryptine methanesulfonate salt solid 22260-51-1 100MG ₹24735.13 2022-06-14 Buy
Sigma-Aldrich(India) B2134 2-Bromo-α-ergocryptine methanesulfonate salt solid 22260-51-1 250MG ₹48864.05 2022-06-14 Buy
Product number Packaging Price Buy
B2134 25MG ₹9190.43 Buy
B2134 100MG ₹24735.13 Buy
B2134 250MG ₹48864.05 Buy

Bromocriptine mesylate Chemical Properties,Uses,Production

Description

Bromocriptine is a dopamine receptor agonist (Kis = 1,659, 12.2, 12.2, 59.7, and 1,691 nM for dopamine D1, D2, D3, D4, and D5 receptors, respectively). It also binds to the serotonin (5-HT) receptor subtypes 5-HT1A and 5-HT1D (Kis = 12.9 and 10.7 nM, respectively), as well as α1-adrenergic receptors (Kis = 1.12-4.17 nM). Bromocriptine (5 mg/kg) restores locomotor activity, without inducing dyskinesia, in a macaque model of Parkinson’s disease induced by MPTP. Formulations containing bromocriptine have been used in the treatment of Parkinson''s disease, hyperprolactinemia-associated dysfunctions, and acromegaly.

Chemical Properties

Solid

Uses

Dopamine receptor agonist; derivative of the ergotoxin group of ergot alkaloids. Prolactin inhibitor; antiparkinsonian.

General Description

Bromocriptine mesylate,(6aR,9R)-5-bromo-N-((2R,5S,10aS,10bS)-10b-hydroxy-5-isobutyl-2-isopropyl-3,6-dioxooctahydro-2H-oxazolo[3,2-a]pyrrolo[2,1c]pyrazin-2-yl)-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide methanesulfonate(Parlodel), is a white solid soluble in ethanol and slightly solublein water (pKa’s=6.6 and 15). Bromocriptine is rapidlyabsorbed after oral administration and it has low systemicbioavailability because of its extensive first-pass metabolism.Bromocriptine enters the brain quickly with a half-lifefor uptake into the brain of approximately 0.3 hours; 8% ofthe drug crosses the BBB.The metabolites are excreted primarilyin the bile and feces. The high first-pass hepatic metabolismimplies an increased risk of drug interactions.Concomitant administration with the DA antagonists, metoclopramide,or domperidone may aggravate parkinsoniansymptoms and induce extrapyramidal side effects (EPS).Other drugs that may interact with bromocriptine are highlyplasma protein–bound drugs (e.g., warfarin, increased dyskinesiacaused by bromocriptine); macrolides antibacterials(enhanced dopaminergic effects); and caffeine (elevation inplasma bromocriptine concentrations). The combination oflevodopa/AADC inhibitors with bromocriptine permits a reductionof the dose of levodopa. Thus, the side effects oflevodopa are decreased, resulting in a more continuous stimulationof DA receptors.

Biological Activity

Selective D 2 -like dopamine receptor agonist (K i values are ~ 8, ~ 5, ~ 290, ~ 440 and ~ 450 nM for D 2 , D 3 , D 4 , D 1 and D 5 receptors respectively).

Bromocriptine mesylate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 264)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Astitva Chemicals 08048262675 Gujarat, India 90 58 Inquiry
Global Chem Asia Pacific 91-9849161572 Hyderabad, India 255 58 Inquiry
Maas Pharma Chemicals +91-9958666224 Delhi, India 1607 58 Inquiry
Dr. Ashavin's Lab Services(OPC) Private Limited 91--9855611075 Punjab, India 3 58 Inquiry
Aaditya Pharmachem 91-8037401177 Maharashtra, India 9 58 Inquiry

Bromocriptine mesylate Spectrum

(5'A)-2-BROMO-12'-HYDROXY-2'-(1-METHYLETHYL)-5'-(2-METHYLPROPYL)ERGOTAMAN-3',6',18-TRIONE MESYLATE (+)-BROMOCRIPTINE MESYLATE BROMOCRIPTINE MESYLATE (+)-BROMOCRIPTINE METHANESULFONATE BROMOCRIPTINE METHANESULPHONATE BROMOCRYPTINE MESYLATE METHANESULFONATE SALT (+)-2-BROMO-12'-HYDROXY-2'-(1-METHYLETHYL)-5'-(2-METHYLPROPYL)-ERGOTAMAN-3',6',18-TRIONE METHANESULFONATE (+)-2-bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)ergotaman-3',6'-18-trione methanesulfonate salt 2-BROMO-12'-HYDROXY-2'-(1-METHYLETHYL)-5'-(2-METHYL-PROPYL)ERGOTAMAN-3',6',18-TRIONE-METHANESULFONATE 2-BROMOERGOCRYPTINE MONOMETHANESULFONATE SALT 2-BROMO-ALPHA-ERGOCRYPTINE METHANESULFONATE 2-BROMO-ALPHA-ERGOCRYPTINE METHANESULFONATE SALT (+)-Bromocriptine methanesulfonate salt, Bromocriptine mesylate salt, (+)-2-Bromo-12μ-hydroxy-2μ-(1-methylethyl)-5μ-(2-methylpropyl)ergotaman-3μ,6μ-18-trione methanesulfonate salt Ergotaman-3,6,18-trione, 2-bromo-12-hydroxy-2-(1-methylethyl)-5-(2-methylpropyl)-, (5.alpha.)-, monomethanesulfonate (salt) 2-bromo-α-ergocryptine methanesulfonate salt BROMOCRIPTINEMESYLATE,USP Bagren Ergocryptine, 2-bromo-, monomethanesulfonate (salt) (8CI) Ergotaman-3',6',18-trione, 2-bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)-, (5'α)-, monomethanesulfonate (salt) (9CI) Pravidel 2-Bromo-α-ergocryptine methanesulfonate salt,(+)-2-Bromo-12′-hydroxy-2′-(1-methylethyl)-5′-(2-methylpropyl)ergotaman-3′,6′-18-trione methanesulfonate salt, (+)-Bromocriptine methanesulfonate salt, Bro 2-BroMo α-Ergocryptine Mesylate (5'alpha)-2-Bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)ergotaman-3',6', 18-trione mesylate Serono-Bagren (5'α)-2-BroMo-12'-hydroxy-2'-(1-Methylethyl)-5'-(2-Methylpropyl)ergotaMan-3',6',18-trione Methanesulfonate (6aR,9R)-5-broMo-N-((2R,5S,10aS,10bS)-10b-hydroxy-5-isobutyl-2-isopropyl-3,6-dioxooctahydro-2H-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl)-7-Methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxaMide Methanesulfonate (+)-Bromocriptine methanesulfonate salt Bromocriptine mesylate salt Bromocriptin mesylate 2-bromo-alpha-ergocryptinemesylate 2-bromo-alpha-ergocryptinmethanesulfonate 2-bromo-alpha-ergokryptine-mesilate bromocriptinemesilate bromocryptinemethanesulfonate cb-154 2-bromo-A-ergocryptine methanesulfonate salt 2-bromo-12'-hydroxy-5'alpha-isobutyl-2'-isopropylergotaman-3',6',18-trione monomethanesulphonate Bromocriptine mesylate EP Bromocriptine mesilate CRS Bromocriptine mesilate for system suitability CRS CB-154 mesylate Bromocriptine mesylate USP/EP/BP Bromocriptine mesyla High Quality Bromocriptine Mesylate Powder CAS?22260-51-1 Bromocriptine Mesylate (CB-154) TIANFU-CHEM CAS NO.22260-51-1 Bromocriptine mesylate Bromocriptine Mesylate (1076501) Bromocriptine-13C-d3 Mesylate Bromocriptine Mesylate (150 mg) Bromocryptine mesylate BRC BCT 2-Bromo α-Ergocryptine Mesylate 22260-51-1 C32H40BrN5O5CH4O3S C33H44BrN5O8S C32H40BrN5O5CH3SO3H C32H40N5O5BRCH4SO3