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N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)

    Cas No: 1454586-90-3

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  • 1454586-90-3 Structure
  • Basic information

    1. Product Name: N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)
    2. Synonyms: N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)
    3. CAS NO:1454586-90-3
    4. Molecular Formula:
    5. Molecular Weight: 586.783
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1454586-90-3.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: N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)(1454586-90-3)
    11. EPA Substance Registry System: N,N',N,N'-([1,1'-biphenyl]-3,3',5,5'-tetrayltetrakis(methylene))tetrakis(1-(1H-pyrrol-2-yl)methanamine)(1454586-90-3)
  • 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: 1454586-90-3(Hazardous Substances Data)

1454586-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1454586-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,5,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1454586-90:
(9*1)+(8*4)+(7*5)+(6*4)+(5*5)+(4*8)+(3*6)+(2*9)+(1*0)=193
193 % 10 = 3
So 1454586-90-3 is a valid CAS Registry Number.

1454586-90-3Downstream Products

1454586-90-3Relevant articles and documents

Binding Studies on a Library of Induced-Fit Synthetic Carbohydrate Receptors with Mannoside Selectivity

Palanichamy, Kalanidhi,Bravo, M. Fernando,Shlain, Milan A.,Schiro, Frank,Naeem, Yasir,Marianski, Mateusz,Braunschweig, Adam B.

, p. 13971 - 13982 (2018)

Synthetic carbohydrate receptors could serve as agents for disease detection, drug delivery, or even therapeutics, however, they are rarely used for these applications because they bind weakly and with a preference towards the all-equatorial glucosides that are not prevalent on the cell surface. Herein the binding of 8 receptors with 5 distinct octyloxy pyranosides, which was measured by mass spectrometry and by 1H NMR titrations in CD2Cl2 at 298 K, is reported, providing binding affinities that vary from ≈101–104 m?1. Although the receptors are promiscuous, 1 shows selectivity for β-Man at a ratio of 103:1 β-Man:β-Gal, receptors 2–4 and 6 have preference for α-Man, 5 is selective for β-Gal, and 10 prefers α-Glc (Man=mannose; Gal=galactose, Glc=glucose). A variety of 1D and 2D NMR, and computational techniques were used to determine the thermodynamic binding parameters (ΔHo and ΔSo) and the structure of the host–guest complex, revealing that dimeric receptor 10 binds β-Man with increased enthalpy, but a larger entropic penalty than 1. The first-principles modelling suggests that 10?β-Man forms an inclusion-type complex where the glycan engages both monomeric subunits of 10 through H-bonding and C?H???π interactions. Like natural glycan-binding proteins, these receptors bind pyranosides by accessing multivalent and cooperative interactions, and these studies suggest a new approach towards biomimetic synthetic carbohydrate receptors, where conformational flexibility and promiscuity are incorporated into design.

Anti-Zika Activity of a Library of Synthetic Carbohydrate Receptors

Palanichamy, Kalanidhi,Joshi, Anjali,Mehmetoglu-Gurbuz, Tugba,Bravo, M. Fernando,Shlain, Milan A.,Schiro, Frank,Naeem, Yasir,Garg, Himanshu,Braunschweig, Adam B.

, p. 4110 - 4119 (2019)

Zika virus (ZIKV), a mosquito-borne flavivirus, is a global health concern because of its association with severe neurological disorders. Currently, there are no antiviral therapies that have been specifically approved to treat ZIKV, and there is an urgent need to develop effective anti-ZIKV agents. Here, we report anti-ZIKV activity of 16 synthetic carbohydrate receptors (SCRs) that inhibit ZIKV infection in Vero and HeLa cells. Using a ZIKV reporter virus particle-based infection assay, our data demonstrates these SCRs are highly potent with IC50s as low as 0.16 μM and negligible toxicity at several-fold higher concentrations. Time-of-addition studies showed that these SCRs inhibit the early stages of the virus infection, which is consistent with the proposed mode of action, where the SCRs likely inhibit binding between the virus and cell-surface glycans, thereby preventing viral entry into the cells and, as such, this study demonstrates a potential new strategy against ZIKV.

CARBOHYDRATE-SELECTIVE RECEPTORS

-

, (2014/03/25)

The present invention is directed to a new class of synthetic carbohydrate receptor compounds comprising Formula I as described herein : (I). Other aspects of the present invention relate to pharmaceutical compositions and pharmaceutical delivery vehicles

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