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BBI-503 (BB-503) is a small molecule inhibitor specifically designed to target cancer stem cells by inhibiting the STAT3 signaling pathway, which is crucial for the self-renewal and survival of these cells. This targeted approach has the potential to prevent tumor growth and recurrence, making BBI-503 a promising candidate in the fight against various solid tumors.

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  • 1129403-56-0 Structure
  • Basic information

    1. Product Name: BBI-503(BB-503)
    2. Synonyms: BBI-503(BB-503);BBI-503;Amcasertib (BBI503);QDWKGEFGLQMDAM-UHFFFAOYSA-N
    3. CAS NO:1129403-56-0
    4. Molecular Formula: C31H33N5O2S
    5. Molecular Weight: 539.69102
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1129403-56-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.246±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 11.99±0.20(Predicted)
    10. CAS DataBase Reference: BBI-503(BB-503)(CAS DataBase Reference)
    11. NIST Chemistry Reference: BBI-503(BB-503)(1129403-56-0)
    12. EPA Substance Registry System: BBI-503(BB-503)(1129403-56-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1129403-56-0(Hazardous Substances Data)

1129403-56-0 Usage

Uses

Used in Oncology:
BBI-503 (BB-503) is used as an anti-cancer agent for its ability to target and inhibit the STAT3 signaling pathway in cancer stem cells, thereby preventing tumor growth and recurrence. In preclinical studies, it has demonstrated promising anti-cancer activity against a variety of solid tumors, including breast, lung, and colon cancer.
Used in Clinical Trials:
BBI-503 (BB-503) is currently being investigated in clinical trials for the treatment of advanced solid tumors. It is being evaluated both as a standalone therapy and in combination with other anti-cancer agents to enhance the overall effectiveness of cancer treatment.
Used in Drug Development:
As a small molecule inhibitor, BBI-503 (BB-503) serves as a valuable asset in the development of targeted cancer therapies. Its ability to specifically target cancer stem cells and inhibit the STAT3 signaling pathway makes it a promising candidate for further research and development in the field of oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 1129403-56-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,9,4,0 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1129403-56:
(9*1)+(8*1)+(7*2)+(6*9)+(5*4)+(4*0)+(3*3)+(2*5)+(1*6)=130
130 % 10 = 0
So 1129403-56-0 is a valid CAS Registry Number.

1129403-56-0Downstream Products

1129403-56-0Relevant articles and documents

Treatment of non-alcoholic fatty liver disease

-

, (2021/07/06)

The invention provides novel methods of treating or preventing nonalcoholic fatty liver disease (NAFLD) including non-alcoholic steatohepatitis (NASH) in a mammal including a human.

Treatment of obesity

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, (2021/07/06)

The invention provides novel methods of treating or preventing obesity or overweight and closely associated comorbidities therewith in a mammalian subject including human.

HETEROCYCLIC SUBSTITUTED-3-HETEROARYLIDENYL-2-INDOLINONE DERIVATIVE

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Paragraph 0390; 0391; 0392; 0393, (2014/09/30)

Disclosed is a compound represented by formula (1) or a pharmacologically acceptable salt thereof. (In the formula, R1 is optionally substituted heteroaryl etc.; R2 is hydrogen etc.; R3 and R4 are each independently hydrogen etc., R5 is the following group: (wherein Y is optionally substituted five membered heteroaryl etc., R9a is optionally substituted aryl etc., R9b and R9c are each dependently hydrogen etc., and m is the integral 0 etc.) etc.; R6 is hydrogen etc.; and R7 is hydrogen etc.

COMPOSITIONS OF KINASE INHIBITORS AND THEIR USE FOR TREATMENT OF CANCER AND OTHER DISEASES RELATED TO KINASES

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Page/Page column 46-47, (2009/04/25)

The present invention relates to novel thiazole-substituted indolin-2-ones as inhibitors of CSCPK and related kinases; to methods of inhibiting cancer stem cells by using a kinase inhibitor; to pharmaceutical compositions containing such compounds; and to

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