149577-05-9 Usage
Uses
Used in Pharmaceutical Industry:
m-PEG2-acid is used as a PEGylation agent for improving the pharmacokinetic properties of therapeutic proteins and peptides. The PEGylation process enhances the solubility, stability, and circulation time of these biomolecules in the body, leading to better therapeutic efficacy and reduced immunogenicity.
Used in Drug Delivery Systems:
In the field of drug delivery, m-PEG2-acid is utilized as a key component in the synthesis of polymer-drug conjugates. The stable amide bond formed between the terminal carboxylic acid and primary amine groups of drug molecules allows for the creation of conjugates with controlled release properties, improving the drug's bioavailability and targeting capabilities.
Used in Diagnostics and Imaging:
m-PEG2-acid is employed as a PEGylation agent for enhancing the solubility and stability of imaging agents, such as contrast agents for magnetic resonance imaging (MRI) or optical imaging agents. The increased solubility and circulation time provided by the PEG spacer can lead to better imaging results and reduced side effects.
Used in Biomaterials and Tissue Engineering:
In the realm of biomaterials and tissue engineering, m-PEG2-acid is used as a component in the design of hydrogels and scaffolds. The hydrophilic PEG spacer can improve the biocompatibility, swelling properties, and overall performance of these materials, making them more suitable for various biomedical applications, such as wound healing, drug delivery, and cell culture.
Used in Cosmetics and Personal Care:
In the cosmetics and personal care industry, m-PEG2-acid is used as an ingredient in the formulation of creams, lotions, and other skincare products. The PEGylation process can improve the solubility, stability, and skin permeability of active ingredients, leading to enhanced efficacy and reduced irritation potential.
Check Digit Verification of cas no
The CAS Registry Mumber 149577-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149577-05:
(8*1)+(7*4)+(6*9)+(5*5)+(4*7)+(3*7)+(2*0)+(1*5)=169
169 % 10 = 9
So 149577-05-9 is a valid CAS Registry Number.
149577-05-9Relevant articles and documents
Pyrimido-pyridone compound and application thereof
-
Paragraph 0326; 0328; 0330, (2021/05/08)
The invention provides a pyrimido-pyridone compound with a structure as shown in a formula I, pharmaceutically acceptable salts, stereoisomers, tautomers, N-oxides or prodrug molecules of the pyrimido-pyridone compound and applications thereof. The compound can be used as a protein kinase inhibitor, can effectively inhibit the activity of TTK protein kinase and can inhibit proliferation, migration and invasion of various tumor cells.
2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS
-
Page/Page column 67, (2017/02/09)
The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.
Tumour-specific cytotoxicity and structure-activity relationships of novel 1-[3-(2-methoxyethylthio)propionyl]-3,5-bis(benzylidene)-4-piperidones
Hossain, Mohammad,Das, Umashankar,Umemura, Naoki,Sakagami, Hiroshi,Balzarini, Jan,De Clercq, Erik,Kawase, Masami,Dimmock, Jonathan R.
, p. 2206 - 2214 (2016/04/26)
A series of 1-acyl-3,5-bis(benzylidene)-4-piperidones 3-7 were designed and synthesized as novel cytotoxic agents. These compounds displayed potent cytotoxic properties towards human Molt4/C8, CEM, HSC-2, HSC-3 and HSC-4 neoplasms and also to murine L1210
ONIUM SALT, LIQUID COMPOSITION CONTAINING SAID ONIUM SALT AND CELLULOSE, AND CELLULOSE RECOVERY METHOD
-
Paragraph 0119; 0120; 0121, (2016/02/19)
The invention relates to an onium salt, a liquid composition containing the onium salt and cellulose, and a method for recovering cellulose. The invention makes it possible to provide an onium salt having an extremely high ability to dissolve cellulose at temperatures of 100° C. or lower. It also makes it possible to provide a liquid composition containing this onium salt and cellulose, as a composition suitable for the recovery of cellulose, and a method for recovering cellulose efficiently by using such a liquid composition containing the onium salt and cellulose.