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5,6-Dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione is a heterocyclic chemical compound characterized by the presence of both nitrogen and oxygen atoms in its ring structure. 5,6-DIHYDRO-1H-IMIDAZO[4,5-D]PYRIDAZINE-4,7-DIONE possesses potential medicinal properties and has been the subject of research for its therapeutic applications. Its unique chemical structure and properties make it a molecule of interest for further exploration in the fields of medicine and chemical synthesis.

6293-09-0

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6293-09-0 Usage

Uses

Used in Pharmaceutical Industry:
5,6-Dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione is used as a therapeutic agent for its potential medicinal properties. Its heterocyclic structure and the presence of nitrogen and oxygen atoms in the ring contribute to its potential as a pharmaceutical candidate.
Used in Chemical Synthesis:
5,6-Dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione is utilized in the synthesis of other organic compounds. Its unique chemical structure allows it to serve as a building block or intermediate in the creation of various chemical products, expanding its applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 6293-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6293-09:
(6*6)+(5*2)+(4*9)+(3*3)+(2*0)+(1*9)=100
100 % 10 = 0
So 6293-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N4O2/c10-4-2-3(7-1-6-2)5(11)9-8-4/h1-3H,(H,6,7)

6293-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dihydro-1H-imidazo[4,5-d]pyridazine-4,7-dione

1.2 Other means of identification

Product number -
Other names 5,6-Dihydro-1H,4H-pyrrolo[3,2,1-ij]chinolin-2-on

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:6293-09-0 SDS

6293-09-0Relevant academic research and scientific papers

1-Amino-4-benzylphthalazines as orally bioavailable smoothened antagonists with antitumor activity

Miller-Moslin, Karen,Peukert, Stefan,Jain, Rishi K.,McEwan, Michael A.,Karki, Rajesh,Llamas, Luis,Yusuff, Naeem,He, Feng,Li, Yanhong,Sun, Yingchuan,Dai, Miao,Perez, Lawrence,Michael, Walter,Sheng, Tao,Lei, Huangshu,Zhang, Rui,Williams, Juliet,Bourret, Aaron,Ramamurthy, Arun,Yuan, Jing,Guo, Ribo,Matsumoto, Melissa,Vattay, Anthony,Maniara, Wieslawa,Amaral, Adam,Dorsch, Marion,Kelleher III, Joseph F.

experimental part, p. 3954 - 3968 (2010/01/16)

Abnormal activation of the Hedgehog (Hh) signaling pathway has been linked to several types of human cancers, and the development of small-molecule inhibitors of this pathway represents a promising route toward novel anticancer therapeutics. A cell-based screen performed in our laboratories identified a new class of Hh pathway inhibitors, 1-amino-4-benzylphthalazines, that act via antagonism of the Smoothened receptor. A variety of analogues were synthesized and their structure-activity relationships determined. This optimization resulted in the discovery of high affinity Smoothened antagonists, one of which was further profiled in vivo. This compound displayed a good pharmacokinetic profile and also afforded tumor regression in a genetic mouse model of medulloblastoma.

ORGANIC COMPOUNDS AND THEIR USES

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Page/Page column 117, (2008/12/07)

The present disclosure relates to compounds relating to the diagnosis and treatment of pathologies relating to the Hedgehog pathway, including but not limited to tumor formation, cancer, neoplasia, and non-malignant hyperproliferative disorders; specifically relating to compounds of formula (I).

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