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Pyrido[3,4-d]pyridazin-4(3H)-one is a heterocyclic chemical compound characterized by a unique fused pyridazine and pyridine ring structure. It possesses potential pharmacological properties and has been the subject of research for its diverse biological activities, making it a promising candidate for various therapeutic applications in the pharmaceutical and medicinal chemistry fields.

40511-70-4

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40511-70-4 Usage

Uses

Used in Pharmaceutical Industry:
Pyrido[3,4-d]pyridazin-4(3H)-one is used as a lead compound for the development of new drugs due to its potential biological activities, including antibacterial, antifungal, anti-inflammatory, and antitumor properties. Its diverse pharmacological profile makes it a valuable asset in the discovery and design of novel therapeutic agents.
Used in Antibacterial Applications:
Pyrido[3,4-d]pyridazin-4(3H)-one is used as an antibacterial agent for its ability to target and inhibit the growth of various bacterial pathogens. Its unique chemical structure allows it to interact with specific bacterial targets, making it a potential candidate for the development of new antibiotics to combat drug-resistant infections.
Used in Antifungal Applications:
Pyrido[3,4-d]pyridazin-4(3H)-one is used as an antifungal agent for its potential to treat fungal infections by inhibiting the growth and proliferation of fungi. Its heterocyclic nature enables it to target specific fungal enzymes or pathways, offering a new approach to combat fungal diseases.
Used in Anti-inflammatory Applications:
Pyrido[3,4-d]pyridazin-4(3H)-one is used as an anti-inflammatory agent for its potential to modulate inflammatory responses and alleviate symptoms associated with inflammation. Its ability to target specific inflammatory mediators or pathways may contribute to the development of new treatments for various inflammatory disorders.
Used in Antitumor Applications:
Pyrido[3,4-d]pyridazin-4(3H)-one is used as an antitumor agent for its potential to inhibit tumor growth and progression. Its unique chemical structure allows it to target specific molecular pathways involved in cancer development, making it a promising candidate for the development of new anticancer drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 40511-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40511-70:
(7*4)+(6*0)+(5*5)+(4*1)+(3*1)+(2*7)+(1*0)=74
74 % 10 = 4
So 40511-70-4 is a valid CAS Registry Number.

40511-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3H-pyrido[3,4-d]pyridazin-4-one

1.2 Other means of identification

Product number -
Other names 4-Oxo-3,4-dihydropyrido<3,4-d>pyridazin

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:40511-70-4 SDS

40511-70-4Upstream product

40511-70-4Downstream Products

40511-70-4Relevant academic research and scientific papers

Tetrahydropyrido[d]pyridazinones - Promising scaffolds for drug discovery

Yaremenko, Anatoliy G.,Volochnyuk, Dmitriy M.,Shelyakin, Vyacheslav V.,Grygorenko, Oleksandr O.

, p. 6799 - 6803 (2013)

An approach to the synthesis of all possible tetrahydropyrido[d] pyridazinones has been developed. The method relies on the catalytic hydrogenation of the corresponding aromatic counterparts, which were obtained by cyclization of the relevant dibromomethyl-substituted pyridinecarboxylates with hydrazine. The synthetic schemes include 4-5 steps starting from commercially available materials. The tetrahydropyrido[d]pyridazinone scaffolds are combinations of a saturated heterocycle (piperidine) and a privileged aromatic heterocycle (pyridazinone); hence they are promising starting points for the design in medicinal chemistry.

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