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  • 1252660-82-4 Structure
  • Basic information

    1. Product Name: C35H49N5O5
    2. Synonyms:
    3. CAS NO:1252660-82-4
    4. Molecular Formula:
    5. Molecular Weight: 619.805
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1252660-82-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C35H49N5O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C35H49N5O5(1252660-82-4)
    11. EPA Substance Registry System: C35H49N5O5(1252660-82-4)
  • 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: 1252660-82-4(Hazardous Substances Data)

1252660-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1252660-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,2,6,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1252660-82:
(9*1)+(8*2)+(7*5)+(6*2)+(5*6)+(4*6)+(3*0)+(2*8)+(1*2)=144
144 % 10 = 4
So 1252660-82-4 is a valid CAS Registry Number.

1252660-82-4Upstream product

1252660-82-4Downstream Products

1252660-82-4Relevant articles and documents

Design and synthesis of Hsp90 inhibitors: Exploring the SAR of Sansalvamide A derivatives

Sellers, Robert P.,Alexander, Leslie D.,Johnson, Victoria A.,Lin, Chun-Chieh,Savage, Jeremiah,Corral, Ricardo,Moss, Jason,Slugocki, Tim S.,Singh, Erinprit K.,Davis, Melinda R.,Ravula, Suchitra,Spicer, Jamie E.,Oelrich, Jenna L.,Thornquist, Andrea,Pan, Chung-Mao,McAlpine, Shelli R.

, p. 6822 - 6856 (2010)

Utilizing the structure-activity relationship we have developed during the synthesis of the first two generations and mechanism of action studies that point to the interaction of these molecules with the key oncogenic protein Hsp90, we report here the design of 32 new Sansalvamide A derivatives and their synthesis. Our new structures, designed from previously reported potent compounds, were tested for cytotoxicity on the HCT116 colon cancer cell line, and their binding to the biological target was analyzed using computational studies involving blind docking of derivatives using Autodock. Further, we show new evidence that our molecules bind directly to Hsp90 and modulate Hsp90's binding with client proteins. Finally, we demonstrate that we have integrated good ADME properties into a new derivative.

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