Nom du produit:4,6-dichloro-1H-pyrazolo[3,4-b]pyridine

IUPAC Name:4,6-dichloro-1H-pyrazolo[3,4-b]pyridine

CAS:2105905-46-0
Formule moléculaire:C6H3Cl2N3
Pureté:95%+
Numéro de catalogue:CM325579
Poids moléculaire:188.01

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CM325579-1g in stock Ōij
CM325579-5g in stock ijŌǸ

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Détails du produit

N° CAS:2105905-46-0
Formule moléculaire:C6H3Cl2N3
Point de fusion:-
Code SMILES:ClC1=CC(Cl)=C2C(NN=C2)=N1
Densité:
Numéro de catalogue:CM325579
Poids moléculaire:188.01
Point d'ébullition:
N° Mdl:
Stockage:Keep in a tight container and store at 2°C~8°C for long term and which can be kept in a tight container at ambient temperature f

Category Infos

Pyrazolopyridines
Over the past few years, many pyrazole fused-ring systems, especially with applications in medicinal chemistry, have been published. These include general structures such as pyrazoline, pyrazoline, pyrazoquinoline, pyrazoloisoquinoline, pyrazoline, pyrazolopyrazine, pyrazolopyrazine, pyranopyrazole, pyrano Pyrazoles, pyrazolotriazines and pyrazole fused phosphorus rings.

Column Infos

Quemliclustat
Data from a phase 1b study of Quemliclustat-based regimens showed promising overall survival in treatment-naïve metastatic pancreatic cancer. Median Overall Survival was 15.7 months for all patients treated with 100 mg quemliclustat-based regimens in the ARC-8 study, which exceeds the historical benchmark data for chemotherapy alone.
Quemliclustat is an investigational, potent and selective small molecule CD73 inhibitor. CD73 is the primary enzymatic producer of immunosuppressive adenosine in the tumor microenvironment, and high CD73 expression is associated with significantly poorer prognosis in several tumor types. Quemliclustat has been shown to block the production of adenosine. Once the immunosuppressive effects of adenosine are removed, activation of antitumor immune cells may be restored, resulting in cancer cell death.