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(8beta,10xi)-2-bromo-6-methyl-8-(1H-1,2,4-triazol-1-ylmethyl)ergoline is a chemical compound derived from ergoline, characterized by the presence of a bromine atom, a methyl group, and a 1H-1,2,4-triazol-1-ylmethyl group. With a molecular formula of C18H18BrN5O and a molar mass of 397.27 g/mol, (8beta,10xi)-2-bromo-6-methyl-8-(1H-1,2,4-triazol-1-ylmethyl)ergoline is significant in research and pharmaceutical applications, particularly for the development of medications targeting the central nervous system.

160730-57-4

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160730-57-4 Usage

Uses

Used in Pharmaceutical Applications:
(8beta,10xi)-2-bromo-6-methyl-8-(1H-1,2,4-triazol-1-ylmethyl)ergoline is used as a key compound in the development of medications for central nervous system disorders. Its investigation into potential effects on dopamine receptors makes it a promising candidate for therapeutic agents for conditions such as Parkinson's disease and schizophrenia.
Used in Neuroscience Research:
In the field of neuroscience, (8beta,10xi)-2-bromo-6-methyl-8-(1H-1,2,4-triazol-1-ylmethyl)ergoline is utilized as a research tool to study the brain and its functions. Its interaction with dopamine receptors provides valuable insights into the underlying mechanisms of various neurological conditions and aids in the development of novel treatment strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 160730-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,7,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160730-57:
(8*1)+(7*6)+(6*0)+(5*7)+(4*3)+(3*0)+(2*5)+(1*7)=114
114 % 10 = 4
So 160730-57-4 is a valid CAS Registry Number.

160730-57-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aR,9R)-5-bromo-7-methyl-9-(1,2,4-triazol-1-ylmethyl)-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:160730-57-4 SDS

160730-57-4Downstream Products

160730-57-4Relevant academic research and scientific papers

Synthesis and structure-activity relationships of new (5R,8S,10R)-ergoline derivatives with antihypertensive of dopaminergic activity

Ohno,Koumori,Adachi,Mizukoshi,Nagasaka,Ichihara

, p. 2042 - 2048 (2007/10/02)

A series of new (5R,8S,10R)-ergoline derivatives was synthesized, and their antihypertensive and dopaminergic activities were evaluated in conscious spontaneously hypertensive rats and in rats with unilateral 6-hydroxydopamine-induced lesions of the substantia nigra, respectively. (5R,8S,10R)-6-Methyl-8-ergolinemethanols, prepared from the corresponding ergolinecarboxylates, were converted to the tosylates, which were treated with various five-membered heterocycles containing nitrogen atoms to afford the new ergolines. (5R,8S,10R)-8-(1-Imidazolylmethyl)-6-methylergoline (5a, BAM-2101) and (5R,8S,10R)-2-bromo-6-methyl-8-(1,2,4-triazol-1-ylmethyl)ergoline (7c, BAM-2202) exhibited potent antihypertensive activities. The maximum falls of systolic blood presure after oral administration of 5a and 7c at 3 mg/kg were 95 and 132 mmHg, respectively, while those of cianergoline, bromocriptine mesylate, hydralazine, and nifedipine at the same dose were 40, 37, 47, and 49 mmHg, respectively. The durations of significant antihypertensive effects of these compounds except nifedipine were more than 7 h. None of the ergolines exhibited potent dopaminergic activity. Structure-activity relationships are discussed.

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