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AZD1305 is a novel, potent, and selective small molecule inhibitor of the fibroblast growth factor receptor (FGFR) family, which plays a crucial role in various cellular processes, including cell proliferation, differentiation, and survival. This chemical has shown promise in the treatment of various cancers, particularly those driven by FGFR gene alterations, such as lung, bladder, and breast cancers. AZD1305 works by binding to the ATP-binding site of the FGFR kinase domain, thereby inhibiting the activation of downstream signaling pathways and ultimately leading to the suppression of tumor growth and survival. Its high selectivity for FGFR over other kinases minimizes off-target effects, potentially reducing the risk of adverse side effects. Clinical trials are underway to evaluate the safety and efficacy of AZD1305 in patients with FGFR-altered tumors, making it a promising candidate for targeted cancer therapy.

872045-91-5

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872045-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872045-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,0,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 872045-91:
(8*8)+(7*7)+(6*2)+(5*0)+(4*4)+(3*5)+(2*9)+(1*1)=175
175 % 10 = 5
So 872045-91-5 is a valid CAS Registry Number.

872045-91-5Downstream Products

872045-91-5Relevant academic research and scientific papers

NEW PHYSICAL FORM OF N,N′- DISUBSTITUTED OXABISPIDINES

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Page/Page column 35-36, (2010/11/25)

There is provided a crystalline material consisting essentially of a compound of formula I, wherein R1 to R4, A, B and D have meanings given in the description, which crystalline material is characterised in that is has surface area

PROCESS FOR THE PREPARATION OF N,N′- DISUBSTITUTED OXABISPIDINES

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Page/Page column 56-59, (2010/11/25)

There is provided a process for the preparation of a sulfonic acid salt of formula I, or a solvate thereof, which process comprises hydrogenating a sulfonic acid salt of formula II,. or a solvate thereof; in the presence of a solvent system consisting essentially of water, a C3-5 secondary alkyl alcohol and no more than 15% v/v of another organic solvent, wherein the sulfonic acid salt of formula I is optionally, without isolation, converted to a compound of formula IX, or a pharmaceutically-acceptable derivative thereof, wherein R1, R2, R3, R6, R7, R8, A, B and D have meanings given in the description.

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