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(6S,9S,12S)-methyl 6-(3-iodo-4-methoxyphenyl)-1 2-(4-methoxy-3-(4,4,5 ,5-tetramethyl-1,3 ,2-dioxaborolan-2-yl)benzyl)-2,2,5 ,9-tetramethyl-4,7, 1 0-trioxo-3-oxa-5 ,8,11-triazatridecan-13-oate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1086702-98-8

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1086702-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1086702-98-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,7,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1086702-98:
(9*1)+(8*0)+(7*8)+(6*6)+(5*7)+(4*0)+(3*2)+(2*9)+(1*8)=168
168 % 10 = 8
So 1086702-98-8 is a valid CAS Registry Number.

1086702-98-8Downstream Products

1086702-98-8Relevant academic research and scientific papers

MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS

-

, (2018/09/12)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.

MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS

-

, (2017/06/12)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.

MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS

-

, (2017/08/01)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.

Intramolecular suzuki-miyaura reaction for the total synthesis of signal peptidase inhibitors, arylomycins A2and B2

Dufour, Jeremy,Neuville, Luc,Zhu, Jieping

supporting information; experimental part, p. 10523 - 10534 (2010/11/04)

Development of the total syntheses of arylomycins A1 and B 2 is detailed. Key features of our approach include 1) formation of 14-membered meta, meta-cyclophane by an intramolecular Suzuki-Miyaura reaction; 2) incorporation of N-Me-4-hydroxyphenylglycine into the cyclization precursor, which avoids the late-stage low-yielding N-methylation step; 3) segment coupling of a fully elaborated peptide side chain to the macrocycle, which makes the synthesis highly convergent. Overall, arylomycin A2 was obtained in 13 steps from L-Tyr for the longest linear sequence, in 13% overall yield. Arylomycin B2 was synthesized in 10 steps from L-3-nitro-Tyr, in 10% overall yield.

Total synthesis of arylomycin A2, a signal peptidase I (SPase I) inhibitor

Dufour, Jeremy,Neuville, Luc,Zhu, Jieping

scheme or table, p. 2355 - 2359 (2009/05/07)

A concise total synthesis of arylomycin A2 has been accomplished featuring a key intramolecular Suzuki-Miyaura reaction for the formation of the 14-membered meta,meta-cyclophane and direct coupling of a fully elaborated peptide side chain with

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