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APOMORPHINE HYDROCHLORIDE

CAS No.
314-19-2
Chemical Name:
APOMORPHINE HYDROCHLORIDE
Synonyms
(r)-id;UPRIMA;TAK251);KW-6500;R(–)-APO;NSC 11442;APL130277;(theta)-id;APL 130277;APL-130277
CBNumber:
CB8357092
Molecular Formula:
C17H18ClNO2
Molecular Weight:
303.78
MDL Number:
MFCD00069236
MOL File:
314-19-2.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

APOMORPHINE HYDROCHLORIDE Properties

Melting point >250℃
storage temp. Store at RT
solubility ≥1.08 mg/mL in EtOH with ultrasonic; ≥12.9 mg/mL in DMSO; ≥5.12 mg/mL in H2O
form solid
FDA UNII 9K13MD7A0D
EPA Substance Registry System Apomorphine hydrochloride (314-19-2)

Pharmacokinetic data

Protein binding 90%
Excreted unchanged in urine <2%
Volume of distribution 2-19(L/kg)
Biological half-life 29.1-36.9 minutes

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H334-H312-H332-H317
Precautionary statements  P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P261-P285-P304+P341-P342+P311-P501
RIDADR  3249
HazardClass  6.1(b)
PackingGroup  III
Toxicity mmo-sat 20 mg/plate MUREAV 137,17,84
NFPA 704
0
2 0

APOMORPHINE HYDROCHLORIDE price More Price(13)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 16094 (-)-Apomorphine (hydrochloride) ≥95% 314-19-2 10mg $25 2021-12-16 Buy
Cayman Chemical 16094 (-)-Apomorphine (hydrochloride) ≥95% 314-19-2 50mg $56 2021-12-16 Buy
Cayman Chemical 16094 (-)-Apomorphine (hydrochloride) ≥95% 314-19-2 100mg $100 2021-12-16 Buy
Tocris 2073 (R)-(-)-Apomorphinehydrochloride ≥99%(HPLC) 314-19-2 50 $107 2021-12-16 Buy
TRC A727548 (R)-(-)-ApomorphineHydrochloride 314-19-2 1mg $45 2021-12-16 Buy
Product number Packaging Price Buy
16094 10mg $25 Buy
16094 50mg $56 Buy
16094 100mg $100 Buy
2073 50 $107 Buy
A727548 1mg $45 Buy

APOMORPHINE HYDROCHLORIDE Chemical Properties,Uses,Production

Originator

Apomorphine hydrochloride,Nastech Pharmaceuticals Company, Inc.

Uses

Emetic.

Uses

(R)-(-)-Apomorphine Hydrochloride is a prototypical dopamine agonist. Potential treatment for Parkinson’s disease.

Manufacturing Process

2 Methods of producing of apomorphine
1. The apomorphine was obtained by dehydratation of morphine at heating to 120°C in the presence phosphoric acid and rendering of HCl gas over reaction mixture.
2. The morphine was converted to β-chloromorphine and then to dichlorodihydrodesoxymorphine at heating to 140°-150°C in the presence hydrochloric acid. Then apomorphine is obtained by dehydratation of dichlorodihydrodesoxymorphine.

brand name

Apokyn (Vernalis).

Therapeutic Function

Emetic, Expectorant, Hypnotic, Antiparkinsonian, Dopamine agonist

General Description

Apomorphine hydrochloride,(6aR)-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolone-10,11-diol hydrochloride (Apokyn), is awhite or off-white powder or crystal soluble in hot water(pKa=8.92). Apormorphine is an aporphine alkaloid of thebenzoquinoline class. Oral apomorphine is poorly absorbedand has a bioavailability of less than 4%. Upon subcutaneousadministration, apomorphine is completely absorbed. Within10 to 20 minutes, the maximum concentration of the drug isdistributed from the blood plasma to the CSF. Other potentialroutes of administration include continuous subcutaneous infusion,intravenous infusion, intranasal spray application,sublingual, and rectal administration.23 The agent is highlylipophilic in nature, allowing for rapid diffusion across theBBB after injection. Apomorphine has a short plasma halflife;however, clinical effects may last from 60 to 90 minutes.Apomorphine displays a significant degree of interpatientvariability in its pharmacokinetic profile. Studies of bothintravenous and subcutaneous injection routes found this variation was not attributable to body weight, age, gender,and duration of PD or L-DOPA dose/duration alone.Apomorphine is extensively metabolized. Hypothesizedroutes include sulfation, N-demethylation, glucuronidation,and oxidation. Subcutaneous injections of apomorphine arerenally and hepatically cleared, with the majority appearingto be renally cleared. Dosage adjustments are needed in bothliver and renal impairment. The activity of apomorphine isbelieved to be caused by stimulation of postsynaptic D1- andD2-type receptors within the caudate/putamen in the brain.Apomorphine is indicated for the acute, intermittent treatmentof hypomobility, “off” episodes (“end-of-dose wearingoff” and unpredictable on/off episodes) associated with advancedPD.

Biological Activity

Prototypical dopamine agonist (pK i values are 6.43, 7.08, 7.59, 8.36 and 7.83 for human recombinant D 1 , D 2L , D 3 , D 4 and D 5 receptors respectively). Produces biphasic effects on locomotor activity, and displays anti-Parkinsonian and neuroprotective actions following systemic administration in vivo .

Clinical Use

Treatment of refractory motor fluctuations in Parkinson’s disease

Safety Profile

Poison by intravenous andintraperitoneal routes. Mutation data reported. When heated to decomposition itemits very toxic fumes of NOx and HCl.

Veterinary Drugs and Treatments

Apomorphine is used primarily as an emetic in dogs, and is considered the emetic of choice for dogs by many clinicians. It is sometimes used in cats, but its use in this species is somewhat controversial.

Drug interactions

Potentially hazardous interactions with other drugs
Antihypertensives: enhanced hypotensive effect.
Domperidone: possible increased risk of ventricular arrhythmias.
5HT3 -receptor antagonists: possibly increased hypotensive effects with ondansetron.
Nitrates: enhanced hypotensive effect.

Metabolism

After subcutaneous injection its fate can be described by a two-compartment model, with a distribution half-life of 5 (±1.1) minutes and an elimination half-life of 33 (±3.9) minutes. Clinical response correlates well with levels of apomorphine in the cerebrospinal fluid. Apomorphine is extensively metabolised in the liver, mainly by conjugation with glucuronic acid or sulfate; the major metabolite is apomorphine sulfate. It is also demethylated to produce norapomorphine. Most of a dose is excreted in urine, mainly as metabolites.

storage

Store at RT

APOMORPHINE HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 56)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569265 +86-18612256290 1056@dideu.com China 3842 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9604 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29525 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8449 60
Beijing Solarbio Science & Tecnology Co., Ltd. 010-50973186 4009686088 3193328036@qq.com China 18352 68
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684 sales@rrkchem.com China 55591 58
Shenzhen Botel Biotechnology Co. Ltd. 0755-22202135 13316968096 1979313431@qq.com China 7516 58

View Lastest Price from APOMORPHINE HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
APOMORPHINE HYDROCHLORIDE pictures 2022-05-12 APOMORPHINE HYDROCHLORIDE
314-19-2
US $1.10 / g 1g 99.0% Min 100 Tons Dideu Industries Group Limited
Apomorphine hydrochloride USP/EP/BP pictures 2021-08-05 Apomorphine hydrochloride USP/EP/BP
US $1.10 / g 1g 0.999 100 Tons min Dideu Industries Group Limited
Apomorphine Hydrochloride pictures 2021-07-20 Apomorphine Hydrochloride
314-19-2
US $1.00-1.00 / KG 1g 99% 50tons Shaanxi Dideu Medichem Co. Ltd
(-)-apomorphiniumhydrochloride (r)-id (theta)-id (-)-APO H CL 4H-Dibenzode,gquinoline-10,11-diol, 5,6,6a,7-tetrahydro-6-methyl-, hydrochloride, (6aR)- Apomorphine hydrochoride g)quinoline-10,11-diol,5,6,6a,7-tetrahydro-6-methyl-4h-dibenzo(dhydr R()-Apomorphine hydrochloride,R(–)-10,11-Dihydroxyaporphine, R(–)-APO NSC 11442 R(–)-APO 6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol hydrochloride 11-diol,6-methyl-6a-beta-noraporphine-1hydrochloride 6a-beta-aporphine-10,11-diol,hydrochloride apomorphinechloride apomorphiniumchloride g)quinoline-10,11-diol,5,6,6a,7-tetrahydro-6-methyl-4h-dibenzo(dhydrochlor g]quinoline-10,11-diol,5,6,6a,7-tetrahydro-6-methyl-4h-dibenzo[dhydrochlor (R)-(-)-APOMORPHINE HYDROCHLORIDE (R)-5,6,6A,7-TETRAHYDRO-6-METHYL-4H-DIBENZO[DE,G]QUINOLINE-10,11-DIOL HYDROCHLORIDE R(-)-10,11-DIHYDROXYAPORPHINE HYDROCHLORIDE UPRIMA APOMORPHINE HCL APOMORPHINE HYDROCHLORIDE APOMORPHINE HYDROCHLORIDE USP/EP/BP Apomorphinhydrochlorid (?)-Apomorphine Apomorphine HCl (APL130277 TAK251) Apomorphine HydrochlorideQ: What is Apomorphine Hydrochloride Q: What is the CAS Number of Apomorphine Hydrochloride Q: What is the storage condition of Apomorphine Hydrochloride Q: What are the applications of Apomorphine Hydrochloride APL 130277 APL130277 APL-130277 KW-6500 314-19-2 C17H18NO2Cl