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135727-85-4

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135727-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135727-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135727-85:
(8*1)+(7*3)+(6*5)+(5*7)+(4*2)+(3*7)+(2*8)+(1*5)=144
144 % 10 = 4
So 135727-85-4 is a valid CAS Registry Number.

135727-85-4Downstream Products

135727-85-4Relevant articles and documents

Short self-assembling peptides with a urea bond: A new type of supramolecular peptide hydrogel materials

Tsutsumi, Hiroshi,Tanaka, Kunifumi,Chia, Jyh Yea,Mihara, Hisakazu

, (2021)

There is an increasing need to develop short self-assembling peptides (SAPs) that can form hydrogels for cell engineering and biomedical applications. In this study, we proposed new short self-assembling peptides with a symmetric structure via a urea bond

Synthesis and evaluation of macrocyclic amino acid derivatives for tumor imaging by gallium-68 positron emission tomography

Shetty, Dinesh,Jeong, Jae Min,Ju, Chang Hwan,Kim, Young Ju,Lee, Ji-Youn,Lee, Yun-Sang,Lee, Dong Soo,Chung, June-Key,Lee, Myung Chul

, p. 7338 - 7347 (2010)

68Ga PET imaging in clinical oncology represents a notable development because the availability of 68Ga is not dependent on a cyclotron. Furthermore, labeled amino acid derivatives have been proven to be useful for the imaging many t

Synthesis of the unnatural amino acid Nα-Nε-(ferrocene-1-acetyl)-l-lysine: A novel organometallic nuclease

Gellett, Amanda M.,Huber, Paul W.,Higgins, Pamela J.

, p. 2959 - 2962 (2008)

The synthesis of a new unnatural amino acid, Nα-Nε-(ferrocene-1-acetyl)-l-lysine, was achieved by coupling a ferroceneacetic acid molecule onto the side chain amine of a lysine. The structure of the compound provides options for inco

METHODS OF PREPARING N6-((2-AZIDOETHOXY)CARBONYL)LYSINE

-

Paragraph 0436; 0438, (2021/07/02)

Disclosed herein are methods of preparing N6-((2-azidoethoxy)carbonyl)lysine, N6-((2-azidoethoxy)carbonyl)-L-lysine, and N6-((2-azidoethoxy)carbonyl)-D-lysine. Also disclosed herein are the compounds tert-butyl N2-(tert-butoxycarbonyl)-N6-((2-chloroethoxy)carbonyl)-L-lysinate and tertbutyl N6-((2-azidoethoxy)carbonyl)-N2-(tert-butoxycarbonyl)-L-lysinate, and uses thereof.

Antitumor agents 7. Synthesis, antiproliferative activity and molecular modeling of new L-lysine-conjugated pyridophenoxazinones as potent DNA-binding ligands and topoisomerase IIα inhibitors

Pedatella, Silvana,Cerchia, Carmen,Manfra, Michele,Cioce, Anna,Bolognese, Adele,Lavecchia, Antonio

, (2019/12/24)

A series of L-lysine-conjugated pyridophenoxazinones 2–5 and 2′-5′ were designed and synthesized for developing compounds with multimodal anticancer potentialities. All compounds inhibited the proliferation of a panel of human liquid and solid neoplastic

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