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8-benzyl-2-(4-hydroxyphenylmethyl)-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853941-52-3

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853941-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853941-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,9,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 853941-52:
(8*8)+(7*5)+(6*3)+(5*9)+(4*4)+(3*1)+(2*5)+(1*2)=193
193 % 10 = 3
So 853941-52-3 is a valid CAS Registry Number.

853941-52-3Downstream Products

853941-52-3Relevant academic research and scientific papers

NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE

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, (2012/05/20)

An isolated polynucleotide encoding a modified luciferase polypeptide and novel coelenterazine-based substrates. The OgLuc variant polypeptide has at least 60% amino acid sequence identity to SEQ ID NO: 1 and at least one amino acid substitution at a position corresponding to an amino acid in SEQ ID NO: 1. The OgLuc variant polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the corresponding polypeptide of the wild-type Oplophorus luciferase.

NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE

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Page/Page column 67, (2012/05/20)

An isolated polynucleotide encoding a modified luciferase polypeptide and novel coelenterazine- based substrates. The OgLuc variant polypeptide has at least 60% amino acid sequence identity to SEQ ID NO: 1 and at least one amino acid substitution at a position corresponding to an amino acid in SEQ ID NO: 1. The OgLuc variant polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the corresponding polypeptide of the wild-type Oplophorus luciferase.

Novel synthetic route of coelenterazines -2-:Synthesis of various dehydrocoelenterazine analogs

Kondo, Nobuhiro,Kuse, Masaki,Mutarapat, Thumnoon,Thasana, Nopporn,Isobe, Minoru

, p. 843 - 856 (2007/10/03)

The novel synthetic route to introduce varioussubstituents into 5-position of coelenteramine is described. Difficulties, however, are observed in the attempted synthesis of some analogs having labile functional groups. This is due to the strong acid conc. H2SO4 after Suzuki-Miyaura coupling, so that the route was limited only to the synthesis for aminopyrazines having acid-stable functional groups. In this report, we describe alternative success in the deprotection of N-tosyl-animopyrazine triflate before the cross coupling; thus, we obtained the aminopyrazine triflate in high yield. This compound enables us to synthesize various coelenterazine analogs. This triflate was proven to be so important intermediate that the versatile synthesis for coelenterazine and dehydrocoelenterazine analogs was established through Suzuki-Miyaura or Sonogashira coupling.

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