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TAK-441 is a chemical compound developed by Takeda Pharmaceuticals with potential antineoplastic activity, meaning it has the ability to inhibit the maturation and proliferation of malignant cells. It is known for its activity as a Par-1 antagonist, targeting the Protease-activated receptor 1, which is often overexpressed in many types of cancer.

1186231-83-3

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1186231-83-3 Usage

Uses

Used in Oncology:
TAK-441 is used as an antineoplastic agent for its potential to inhibit cancer cell growth. It targets the Par-1 receptor, which is often overexpressed in various cancers, and its suppression can help in managing the disease.
Used in Cancer Treatment Research:
TAK-441 is used as a subject of investigation in the treatment of different types of cancer, including pancreatic cancer. Its role as a Par-1 antagonist makes it a promising candidate for cancer therapy, although there is currently no definitive clinical data confirming its efficacy as a cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 1186231-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,2,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1186231-83:
(9*1)+(8*1)+(7*8)+(6*6)+(5*2)+(4*3)+(3*1)+(2*8)+(1*3)=153
153 % 10 = 3
So 1186231-83-3 is a valid CAS Registry Number.

1186231-83-3Relevant academic research and scientific papers

FUSED HETEROCYCLIC RING DERIVATIVE AND USE THEREOF

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, (2012/07/14)

The present invention provides a fused heterocycle derivative having a strong Smo inhibitory activity, and use thereof. Specially, the present invention relates to a compound represented by the formula wherein each symbol is as defined in the specificatio

Discovery of the investigational drug TAK-441, a pyrrolo[3,2-c]pyridine derivative, as a highly potent and orally active hedgehog signaling inhibitor: Modification of the core skeleton for improved solubility

Ohashi, Tomohiro,Oguro, Yuya,Tanaka, Toshio,Shiokawa, Zenyu,Tanaka, Yuta,Shibata, Sachio,Sato, Yoshihiko,Yamakawa, Hiroko,Hattori, Harumi,Yamamoto, Yukiko,Kondo, Shigeru,Miyamoto, Maki,Nishihara, Mitsuhiro,Ishimura, Yoshimasa,Tojo, Hideaki,Baba, Atsuo,Sasaki, Satoshi

, p. 5507 - 5517 (2012/10/30)

We recently reported the discovery of the novel pyrrolo[3,2-c]quinoline-4- one derivative 1 as a potent inhibitor of Hedgehog (Hh) pathway signaling. However, the PK evaluation of 1 at high dosage (100 mg/kg) revealed the C max value 3.63 μg/mL

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