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(S)-9-Benzyloxy-11-hydroxy-5-oxo-2,3,11,11a-tetrahydro-1H,5H-benzo[e]pyrrolo[1,2-a][1,4]diazepine-10-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125299-57-2

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125299-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125299-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,9 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125299-57:
(8*1)+(7*2)+(6*5)+(5*2)+(4*9)+(3*9)+(2*5)+(1*7)=142
142 % 10 = 2
So 125299-57-2 is a valid CAS Registry Number.

125299-57-2Relevant academic research and scientific papers

A tricyclic pyrrolobenzodiazepine produced by Klebsiella oxytoca is associated with cytotoxicity in antibiotic-associated hemorrhagic colitis

Tse, Herman,Gu, Qiangshuai,Sze, Kong-Hung,Chu, Ivan K.,Kao, Richard Y.-T.,Lee, Kam-Chung,Lam, Ching-Wan,Yang, Dan,Shing-Chiu Tai, Sherlock,Ke, Yihong,Chan, Elaine,Chan, Wan-Mui,Dai, Jun,Leung, Sze-Pui,Leung, Suet-Yi,Yuen, Kwok-Yung

, p. 19503 - 19520 (2017)

Cytotoxin-producing Klebsiella oxytoca is the causative agent of antibiotic-associated hemorrhagic colitis (AAHC). Recently, the cytotoxin associated with AAHC was identified as tilivalline, a known pentacyclic pyrrolobenzodiazepine (PBD) metabolite produced by K. oxytoca. Although this assertion of tilivalline’s role in AAHC is supported by evidence from animal experiments, some key aspects of this finding appear to be incompatible with toxicity mechanisms of known PBD toxins. We therefore hypothesized that K. oxytoca may produce some other uncharacterized cytotoxins. To address this question, we investigated whether tilivalline alone is indeed necessary and sufficient to induce cytotoxicity or whether K. oxytoca also produces other cytotoxins. LC-MS- and NMR-based metabolomic analy-ses revealed the presence of an abundant tricyclic PBD, provisionally designated kleboxymycin, in the supernatant of toxigenic K. oxytoca strains. Moreover, by generating multiple mutants with gene deletions affecting tilivalline biosynthesis, we show that a tryptophanase-deficient, tilivalline-negative K. oxytoca mutant induced cytotoxicity in vitro similar to tilivalline-positive K. oxytoca strains. Furthermore, synthetic kleboxymycin exhibited greater than 9-fold higher cytotoxicity than tilivalline in TC50 cell culture assays. We also found that the biosynthetic pathways for kleboxymycin and tilivalline appear to overlap, as tilivalline is an indole derivative of kleboxymycin. In summary, our results indicate that tilivalline is not essential for inducing cytotoxicity observed in K. oxytoca-associated AAHC and that kleboxymycin is a tilivalline-related bacterial metabolite with even higher cytotoxicity.

STEREOSELECTIVE SYNTHESIS OF TILIVALLINE

Nagasaka, Tatsuo,Koseki, Yuji,Hamaguchi, Fumiko

, p. 1871 - 1872 (2007/10/02)

Tilivalline (1b) was easily synthesized by converting lactam 3b to the acyliminium precursor 5b followed by stereoselectively introducing indole from the less hindered side of 5b.

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