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1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, 6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-3-[(1-pyrrolidinylcarbonyl)thio]-, (4-nitrophenyl)methyl ester, (4R,5S,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192884-06-3

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192884-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192884-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,8,8 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 192884-06:
(8*1)+(7*9)+(6*2)+(5*8)+(4*8)+(3*4)+(2*0)+(1*6)=173
173 % 10 = 3
So 192884-06-3 is a valid CAS Registry Number.

192884-06-3Downstream Products

192884-06-3Relevant academic research and scientific papers

Novel dithiocarbamate carbapenems with anti-MRSA activity

Ohtake, Norikazu,Imamura, Hideaki,Jona, Hideki,Kiyonaga, Hideo,Shimizu, Aya,Moriya, Minoru,Sato, Hiroki,Nakano, Masato,Ushijima, Ryosuke,Nakagawa, Susumu

, p. 1089 - 1101 (2007/10/03)

A new series of 1β-methyl carbapenems, in which a disubstituted-aminothiocarbonylthio moiety was attached to the C-2 position of the carbapenem nucleus, were prepared and evaluated for anti-MRSA activity. These derivatives showed good in vitro antibacterial activity against high-level MRSA, and the finding of good affinity for PBP-2' supported these results. Some of the compounds having favorable protein-binding affinity showed excellent in vivo anti-MRSA activity. Copyright (C) 1998 Elsevier Science Ltd.

Novel dithiocarbamate carbapenems with anti-MRSA activity

Ohtake, Norikazu,Imamura, Hideaki,Kiyonaga, Hideo,Jona, Hideki,Ogawa, Masayuki,Okada, Shigemitsu,Shimizu, Aya,Moriya, Minoru,Sato, Hiroki,Tominaga, Yushin,Yamada, Koji,Nakano, Masato,Ushijima, Ryosuke,Nakagawa, Susumu

, p. 1617 - 1622 (2007/10/03)

A new series of carbapenems, in which disubstituted- aminothiocarbonylthio moiety, directly attached to the C-2 position, were prepared and evaluated for their antibacterial potency. These analogs showed potent activity against high-level MRSA. Among them

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