Pharmacology and mechanism of action Indications Side effects Contraindications and precautions Interactions Preparations References
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dehydroemetine

Pharmacology and mechanism of action Indications Side effects Contraindications and precautions Interactions Preparations References
Product Name
dehydroemetine
CAS No.
4914-30-1
Chemical Name
dehydroemetine
Synonyms
BT 436;Mebadin;Dametin;Ro 1-9334/19;dehydroemetine;2,3-DEHYDROEMETINE;dehydroemetine USP/EP/BP;Dehydroemetine hydrochloride;4H-Benzo[a]quinolizine, 3-ethyl-1,6,7,11b-tetrahydro-9,10-dimethoxy-2-[[(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-isoquinolinyl]methyl]-, (11bS)-;(11bS)-2-[[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-3-ethyl-9,10-dimethoxy-4,6,7,11b-tetrahydro-1H-pyrido[2,1-a]isoquinoline
CBNumber
CB9942510
Molecular Formula
C29H38N2O4
Formula Weight
478.62
MOL File
4914-30-1.mol
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dehydroemetine Property

Melting point:
94-96°
alpha 
D -183°
Boiling point:
604.7±55.0 °C(Predicted)
Density 
1.19±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
pka
8.86±0.40(Predicted)
form 
Solid
color 
Off-white to light yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0016158
Product name
DEHYDROEMETINE
Purity
95.00%
Packaging
5MG
Price
$504.48
Updated
2021/12/16
ChemScene
Product number
CS-0081294
Product name
Dehydroemetine
Purity
98.60%
Packaging
5mg
Price
$650
Updated
2021/12/16
ChemScene
Product number
CS-0081294
Product name
Dehydroemetine
Purity
98.60%
Packaging
10mg
Price
$980
Updated
2021/12/16
ChemScene
Product number
CS-0081294
Product name
Dehydroemetine
Purity
98.60%
Packaging
50mg
Price
$2800
Updated
2021/12/16
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dehydroemetine Chemical Properties,Usage,Production

Pharmacology and mechanism of action

Dehydroemetine, is a derivative of emetine and has similar pharmacological properties, but it is considered to be less toxic. Dehydroemetine acts against Entamoeba histolytica in tissue and has little effect on amoeba confined to the lumen of the bowel. It has a direct amoebicidal effect in vitro by interfering with the mRNA translocation along the ribosome, which causes inhibition of protein synthesis [1].

Indications

Serious intestinal amoebiasis and amoebic hepatitis with liver abscess. Dehydroemetine is usually given with chloroquine. It is only indicated when other safer drugs are not available or contraindicated.

Side effects

Side effects are similar to those caused by emetine, but they are milder and less frequent. They are largely gastrointestinal, cardiac and neuromuscular reactions. Gastrointestinal reactions include nausea, vomiting, and abdominal pain. Neuromuscular effects are generalized muscle weakness, muscle pain and stiffness of the limbs and neck. Cardiac effects include fall in blood pressure, tachycardia and ECG changes of T-wave flattening or inversion [2,3]. The injection of dehydroemetine is painful and the formation of an abscess is common [2].

Contraindications and precautions

Patients with heart, muscle, or neurological diseases or in poor general condition should be treated with great caution. Dehydroemetine should always be given under medical supervision. Strenuous exercise should be forbidden until 4–5 weeks after completion of therapy[4]. Dehydroemetine should not be given earlier than 1.5–2 months after emetine treatment because of cardiotoxicity.
Previous recommendations to use a contact amoebicide (e.g. di-iodohydroxyquinoline) together with an oral drug preparation can no longer be supported. The hydroxyquinolines have been withdrawn from most markets because of their potential risk of inducing subacute myelo-optic neuropathy (SMON).

Interactions

There have been no reports.

Preparations

Available as dehydroemetine hydrochloride: 100 mg salt equals 87 mg base.
• Dehydroemetine® (Roche) Ampoules 30 mg/ml, ampoules 60 mg/2 ml.

References

1. Westwood JT, Wagenaar EB (1983). Chinese hamster cells can be reversibly blocked before mitosis with the protein synthesis inhibitor Emetine. J Cell Sci, 59, 257–268.
2. Salem HH, Abd-Rabbo H (1964). Clinical trials with dehydroemetine dihydrochloride in the treatment of acute amoebiasis. J Trop Med Hyg, 67, 137–141.
3. Powell SW, Wilmot AJ, McLeod IN et al. (1965). Dehydroemetine in the treatment of amoebic liver abcess. Ann Trop Med Parasitol, 59, 208–209.
4. Wilmot AJ (1962). Clinical Amoebiasis (Oxford: Blackwell Scientific Publications).

Definition

ChEBI: Dehydroemetine is a pyridoisoquinoline which was developed in response to the cardiovascular toxicity associated with emetine and results from the dehydrogenation of the heterotricylic ring of emetine. It is an antiprotozoal agent and displays antimalarial, antiamoebic, and antileishmanial properties. It has a role as an antiprotozoal drug, an antimalarial and an antileishmanial agent. It is a member of isoquinolines, an aromatic ether and a pyridoisoquinoline. It derives from a hydride of an emetan.

Pharmaceutical Applications

The synthetic racemic derivative of the plant alkaloid emetine. Formulated as the hydrochloride for intramuscular administration. Like the parent compound, emetine, it inhibits E. histolytica at concentrations of 1–10 mg/L in vitro, but it is more active than the parent in animal models. Drugresistance in E. histolytica is rare.
No human pharmacokinetic data are available. A halflife of 2 days, compared with 5 days for emetine, has been reported. There is selective tissue binding and accumulation in the liver, lung, spleen and kidney.
It is considerably less toxic than emetine, possibly because it is more rapidly eliminated. Nevertheless, nausea, vomiting, diarrhea and abdominal cramps frequently occur. Neuromuscular effects have also been reported. More serious cardiotoxic effects can lead to electrocardiogram (EGG) changes, tachycardia and a drop in blood pressure.
It was formerly used as a second-line treatment in severe intestinal or hepatic amebiasis, but is no longer recommended for use.

dehydroemetine Preparation Products And Raw materials

Raw materials

Preparation Products

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dehydroemetine Suppliers

Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12306
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32063
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
23225
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 15801484223;
Email
psaitong@jm-bio.com
Country
China
ProdList
29774
Advantage
58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd
Tel
17691182729 18161915376
Email
1046@dideu.com
Country
China
ProdList
10007
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24648
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11974
Advantage
58
Henan Tianfu Chemical Co.,Ltd.
Tel
+86-0371-55170693 +86-19937530512
Fax
0371-55170693
Email
info@tianfuchem.com
Country
China
ProdList
21638
Advantage
55
SHANGHAI KEAN TECHNOLOGY CO., LTD.
Tel
+8613817748580
Fax
021-50175322
Email
cooperation@kean-chem.com
Country
China
ProdList
40066
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52925
Advantage
58
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View Lastest Price from dehydroemetine manufacturers

Dideu Industries Group Limited
Product
dehydroemetine 4914-30-1
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons Min
Release date
2021-06-17

4914-30-1, dehydroemetineRelated Search:


  • dehydroemetine
  • Dehydroemetine hydrochloride
  • BT 436
  • Dametin
  • Mebadin
  • Ro 1-9334/19
  • (11bS)-2-[[(1R)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-3-ethyl-9,10-dimethoxy-4,6,7,11b-tetrahydro-1H-pyrido[2,1-a]isoquinoline
  • 2,3-DEHYDROEMETINE
  • 4H-Benzo[a]quinolizine, 3-ethyl-1,6,7,11b-tetrahydro-9,10-dimethoxy-2-[[(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-isoquinolinyl]methyl]-, (11bS)-
  • dehydroemetine USP/EP/BP
  • 4914-30-1