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ABBV-075 is a novel, orally bioavailable small molecule inhibitor of the Wnt signaling pathway, which plays a crucial role in cell growth and proliferation. It has shown promising results in preclinical studies for the treatment of various cancers, including solid tumors and hematologic malignancies, by inhibiting cancer cell growth and inducing apoptosis.

1445993-26-9

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1445993-26-9 Usage

Uses

Used in Oncology:
ABBV-075 is used as an anticancer agent for its potent anti-tumor activity in multiple cancer models. It targets the overactive Wnt pathway, which is implicated in many types of cancer, making it a promising candidate for further clinical development and potential treatment of cancer.
Used in Combination Therapy:
ABBV-075 is used as a combination therapy agent for its synergistic effects when combined with other anticancer agents. This enhances the chemo-sensitivity and efficacy of the treatment, particularly in resistant cases.
Used in Drug Development:
ABBV-075 is used as a candidate for further clinical development due to its promising results in preclinical studies and its potential to target the Wnt pathway, which is overactive in many types of cancer. Its development could lead to new treatment options for cancer patients.

Check Digit Verification of cas no

The CAS Registry Mumber 1445993-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,9,9 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1445993-26:
(9*1)+(8*4)+(7*4)+(6*5)+(5*9)+(4*9)+(3*3)+(2*2)+(1*6)=199
199 % 10 = 9
So 1445993-26-9 is a valid CAS Registry Number.

1445993-26-9Relevant academic research and scientific papers

Discovery of N-(4-(2,4-Difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridin-4-yl)phenyl)ethanesulfonamide (ABBV-075/Mivebresib), a Potent and Orally Available Bromodomain and Extraterminal Domain (BET) Family Bromodomain Inhibitor

McDaniel, Keith F.,Wang, Le,Soltwedel, Todd,Fidanze, Steven D.,Hasvold, Lisa A.,Liu, Dachun,Mantei, Robert A.,Pratt, John K.,Sheppard, George S.,Bui, Mai H.,Faivre, Emily J.,Huang, Xiaoli,Li, Leiming,Lin, Xiaoyu,Wang, Rongqi,Warder, Scott E.,Wilcox, Denise,Albert, Daniel H.,Magoc, Terrance J.,Rajaraman, Ganesh,Park, Chang H.,Hutchins, Charles W.,Shen, Jianwei J.,Edalji, Rohinton P.,Sun, Chaohong C.,Martin, Ruth,Gao, Wenqing,Wong, Shekman,Fang, Guowei,Elmore, Steven W.,Shen, Yu,Kati, Warren M.

, p. 8369 - 8384 (2017/11/03)

The development of bromodomain and extraterminal domain (BET) bromodomain inhibitors and their examination in clinical studies, particularly in oncology settings, has garnered substantial recent interest. An effort to generate novel BET bromodomain inhibi

CRYSTALLINE BROMODOMAIN INHIBITORS

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, (2015/01/16)

N-[4-(2,4-difluorophenoxy)-3-(6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3- c]pyridin-4-yl)phenyl]ethanesulfonamide and crystalline forms thereof are suitable pharmaceutical ingredients for pharmaceutical compositions useful in the treatment of disease, for example, cancer.

BROMODOMAIN INHIBITORS

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Page/Page column 73;, (2013/07/19)

Provided are compounds of formula (I), wherein A1, A2, A3, A4, X1, X2, Y1, L1, G1, Rx, and Ry have any of the values defined therefor in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions, including inflammatory diseases, cancer, and AIDS. Also provided are pharmaceutical compositions comprising one or more compounds of formula (I).

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