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CAS

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150036-88-7

Verongamine is a monocarboxylic acid amide derivative, specifically N-[2-(1H-imidazol-4-yl)ethyl]propanamide, which is substituted by a hydroxyimino group at position 2 and a 3-bromo-4-methoxyphenyl group at position 3. It is a bromotyrosine derivative isolated from the marine sponge Verongula gigantea and is known for its histamine-H3 antagonist activity.

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  • 150036-88-7 Structure

  • Basic information

    1. Product Name: verongamine
    2. Synonyms: verongamine
    3. CAS NO:150036-88-7
    4. Molecular Formula: C15H17BrN4O3
    5. Molecular Weight: 381.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150036-88-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 1.53g/cm3
    6. Refractive Index: 1.637
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: verongamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: verongamine(150036-88-7)
    11. EPA Substance Registry System: verongamine(150036-88-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 150036-88-7(Hazardous Substances Data)

150036-88-7 Usage

Uses

Used in Pharmaceutical Industry:
Verongamine is used as a histamine-H3 antagonist for its ability to block the histamine-H3 receptors, which play a role in various physiological processes, including the regulation of wakefulness, appetite, and cognitive functions. This application is particularly relevant in the development of drugs targeting conditions such as insomnia, attention deficit hyperactivity disorder (ADHD), and Alzheimer's disease.
Used in Marine Biotechnology:
In the field of marine biotechnology, verongamine is used as a source of bioactive compounds derived from marine organisms. Its unique chemical structure and biological activity make it a valuable candidate for further research and potential development of new therapeutic agents.
Used in Chemical Research:
Verongamine is also used as a research tool in chemical research, particularly in the study of natural products and their interactions with biological systems. Its histamine-H3 antagonist activity provides insights into the structure-activity relationships of related compounds and can aid in the design of novel drugs with improved pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 150036-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,0,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 150036-88:
(8*1)+(7*5)+(6*0)+(5*0)+(4*3)+(3*6)+(2*8)+(1*8)=97
97 % 10 = 7
So 150036-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H17BrN4O3/c1-23-14-3-2-10(6-12(14)16)7-13(20-22)15(21)18-5-4-11-8-17-9-19-11/h2-3,6,8-9,22H,4-5,7H2,1H3,(H,17,19)(H,18,21)/b20-13+

150036-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name verongamine

1.2 Other means of identification

Product number -
Other names Verongamine

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150036-88-7 SDS

150036-88-7Upstream product

150036-88-7Downstream Products

150036-88-7Relevant articles and documents

Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: Synthesis of verongamine and purealidin N

Boehlow,Harburn,Spilling

, p. 3111 - 3118 (2007/10/03)

The oxidation of tyrosine ethyl ester (7) with Na2WO4/H2O2 in ethanol, dimethyldioxirane in acetone, or methyltrioxorhenium/H2O2 in EtOH gave the corresponding tyrosine oxime (8) in high yi

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