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92451-00-8

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92451-00-8 Usage

General Description

O-((N-succinimidyl)succinyl-aminoethyl) is a chemical compound commonly used in bioconjugation reactions to label proteins, peptides, or other biomolecules. It contains a succinimide group, which allows for the formation of stable amide bonds with amino groups on the biomolecules. O-((N-SUCCINIMIDYL)SUCCINYL-AMINOETHYL)& is often used in the production of antibody-drug conjugates (ADCs), where it serves as a linker between the antibody and the drug molecule. Its succinyl-aminoethyl group provides flexibility and stability in the resulting bioconjugates, making it a valuable tool in the field of chemical biology and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 92451-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92451-00:
(7*9)+(6*2)+(5*4)+(4*5)+(3*1)+(2*0)+(1*0)=118
118 % 10 = 8
So 92451-00-8 is a valid CAS Registry Number.

92451-00-8 Well-known Company Product Price

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  • Aldrich

  • (712531)  O-[(N-Succinimidyl)succinyl-aminoethyl]-O′-methylpolyethyleneglycol  750

  • 92451-00-8

  • 712531-250MG

  • 909.09CNY

  • Detail
  • Aldrich

  • (41214)  O-[(N-Succinimidyl)succinyl-aminoethyl]-O′-methylpolyethyleneglycol2′000  

  • 92451-00-8

  • 41214-1G-F

  • 4,496.31CNY

  • Detail

92451-00-8Downstream Products

92451-00-8Relevant articles and documents

Hybrids of Small-Molecule CD4 Mimics with Polyethylene Glycol Units as HIV Entry Inhibitors

Kobayakawa, Takuya,Tsuji, Kohei,Konno, Kiju,Himeno, Ai,Masuda, Ami,Yang, Tingting,Takahashi, Kohei,Ishida, Yusuke,Ohashi, Nami,Kuwata, Takeo,Matsumoto, Kaho,Yoshimura, Kazuhisa,Sakawaki, Hiromi,Miura, Tomoyuki,Harada, Shigeyoshi,Matsushita, Shuzo,Tamamura, Hirokazu

supporting information, p. 1481 - 1496 (2021/02/27)

CD4 mimics are small molecules that inhibit the interaction of gp120 with CD4. We have developed several CD4 mimics. Herein, hybrid molecules consisting of CD4 mimics with a long alkyl chain or a PEG unit attached through a self-cleavable linker were synthesized. In anti-HIV activity, modification with a PEG unit appeared to be more suitable than modification with a long alkyl chain. Thus, hybrid molecules of CD4 mimics, with PEG units attached through an uncleavable linker, were developed and showed high anti-HIV activity and low cytotoxicity. In investigation of pharmacokinetics in a rhesus macaque, a hybrid compound had a more effective PK profile than that of the parent compound, and intramuscular injection was a more useful administration route to maintain the high blood concentration of the CD4 mimic than intravenous injection. The presented hybrid molecules of CD4 mimics with a PEG unit would be practically useful when combined with a neutralizing antibody.

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