Wuensch, Erich et al. published their patent in 1977 |CAS: 53838-27-0

The Article related to leucine motiline, peptide motiline, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.COA of Formula: C10H19NO4

On April 7, 1977, Wuensch, Erich; Wendlberger, Gerhard; Jaeger, Ernst published a patent.COA of Formula: C10H19NO4 The title of the patent was L-Leucine-13-motiline. And the patent contained the following:

H-Phe-Val-Pro-Ile-Phe-Thr-Tyr-Gly-Glu-Leu-Gln-Arg-Leu-Glu-Glu-Lys-Glu-Arg-Asn-Lys-Gly-Gln-OH (I), 13-L-leucine-motiline, was prepared by peptide fragment condensations. Thus, Z-Asn-Lys(BOC)-OH (Z = PhCH2O2C, BOC = Me3CO2C) and H-Gly-Gln-OCMe3 were prepared and coupled together by dicyclohexylcarbodiimide (DCC) in the presence of N-hydroxysuccinimide (HOSu) to give the protected tetrapeptide. The latter was Z-deblocked by hydrogenation and then coupled to Z-Arg(Z2)-OC6H4NO2-4 to give the protected pentapeptide which was hydrogenated and treated with HBr to give H-Arg-Asn-Lys(BOC)-Gly-Gln-OCMe3.2HBr (II), the protected 18-22 sequence of I. Z-Glu(OCMe3)-Glu(OCMe3)-Lys(BOC)-Glu(OCMe3)-OH (III), the 14-17 sequence, Z-Arg(Z2)-Leu-OH (IV), the 12-13 sequence, Z-Glu(OCMe3)-Leu-Gln-OH (V), the 9-11 sequence, H-Thr(CMe3)-Tyr(CMe3)-Gly-OH (VI), the 6-8 sequence, and BOC-Phe-Val-Pro-Ile-Pro-OH (VII), the 1-5 sequence, were also prepared II was coupled to III by DCC-HOSu to give the protected 14-22 sequence which was Z-deblocked and coupled to IV by DCC-HOSu to give the protected 12-22 sequence. The latter was Z-deblocked and coupled to V by DCC-HOSu to give the protected 9-11 sequence which was Z-deblocked and coupled to the protected 1-8 sequence to give the protected 1-22 sequence. The latter was deblocked with CF3CO2H to give I. The protected 1-8 sequence was prepared by coupling VI to VII by the HOSu active ester. The experimental process involved the reaction of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate(cas: 53838-27-0).COA of Formula: C10H19NO4

The Article related to leucine motiline, peptide motiline, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.COA of Formula: C10H19NO4

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Brownstein, Michael J. et al. published their patent in 2019 |CAS: 53838-27-0

The Article related to azetidinone preparation brain injury, Heterocyclic Compounds (One Hetero Atom): 4-Membered Rings and other aspects.Application In Synthesis of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

On March 21, 2019, Brownstein, Michael J. published a patent.Application In Synthesis of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate The title of the patent was Preparation of azetidinone derivatives for use in treating brain injury. And the patent contained the following:

Title compounds I [A = CO2H, ester, or amide; B = OH, SH, CO2H, ester, or amide; R1 = H or alkyl; R2 = H, halo, CN, alkyl, alkoxy, etc.; R3 = amino, amido, acylamido, (un)substituted ureido, etc.; R4 = alkyl, (un)substituted aryl, arylalkyl, etc.], and their pharmaceutically acceptable salts, are prepared and disclosed for use in treating brain injurys. Thus, e.g., II was prepared by a multistep procedure (preparation given). Select I were evaluated in V1a binding assays, e.g., II demonstrated an IC50 value of 0.49 nM. The experimental process involved the reaction of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate(cas: 53838-27-0).Application In Synthesis of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

The Article related to azetidinone preparation brain injury, Heterocyclic Compounds (One Hetero Atom): 4-Membered Rings and other aspects.Application In Synthesis of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Zhao, Shilin et al. published their research in Industrial & Engineering Chemistry Research in 2018 |CAS: 517-23-7

The Article related to cellulose hemicellulose lignin biomass pyrolysis, Cellulose, Lignin, Paper, and Other Wood Products: General and other aspects.COA of Formula: C6H8O3

On April 18, 2018, Zhao, Shilin; Liu, Meng; Zhao, Liang; Zhu, Lingli published an article.COA of Formula: C6H8O3 The title of the article was Influence of Interactions among Three Biomass Components on the Pyrolysis Behavior. And the article contained the following:

Pyrolysis experiments between 25 and 800° for three main components (cellulose, hemicellulose, and lignin) mixed in different proportions were conducted on a thermogravimetric analyzer (TGA) and pyrolysis-gas chromatog./mass spectrometer (Py-GC/MS). The interactions between the three main components during the pyrolysis of biomass were explored from two aspects, namely thermogravimetric properties and pyrolysis products. The results indicate that interactions existed among the three biomass components in the co-pyrolysis process. The presence of lignin significantly reduces the pyrolysis rate of cellulose and inhibits the formation of sugars (mainly levoglucosan) in the pyrolysis of cellulose and hemicellulose. However, the existence of cellulose or hemicellulose greatly promotes the pyrolysis of lignin to produce phenolic compounds This finding is meaningful for the application of biomass pyrolysis. The experimental process involved the reaction of 3-Acetyldihydrofuran-2(3H)-one(cas: 517-23-7).COA of Formula: C6H8O3

The Article related to cellulose hemicellulose lignin biomass pyrolysis, Cellulose, Lignin, Paper, and Other Wood Products: General and other aspects.COA of Formula: C6H8O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Brownstein, Michael J. et al. published their patent in 2015 |CAS: 53838-27-0

The Article related to azetidinone preparation neurodegenerative disease, Heterocyclic Compounds (One Hetero Atom): 4-Membered Rings and other aspects.Reference of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

On October 1, 2015, Brownstein, Michael J. published a patent.Reference of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate The title of the patent was Preparation of substituted azetidinone derivatives for use in the treatment of neurodegenerative diseases. And the patent contained the following:

Title compounds I [A = carboxylic acid, ester, or amide; D = carboxylic acid, ester, amide, alc., or thiol; R1 = H or alkyl; R2 = H, CN, halo, alkyl, etc.; R3 = (un)substituted amino, amido, acylamido, etc.], and their pharmaceutically acceptable salts, are prepared and disclosed for use in the treatment of neurodegenerative diseases. Thus, e.g., II was prepared by a multistep procedure (preparation given). Select I were evaluated in Via receptor binding assays, e.g., II demonstrated an IC50 value of 2.92 nM. The experimental process involved the reaction of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate(cas: 53838-27-0).Reference of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

The Article related to azetidinone preparation neurodegenerative disease, Heterocyclic Compounds (One Hetero Atom): 4-Membered Rings and other aspects.Reference of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Moroder, Luis et al. published their research in International Journal of Peptide & Protein Research in 1977 |CAS: 53838-27-0

The Article related to cytochrome c undecapeptide pentadecapeptide synthesis, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.COA of Formula: C10H19NO4

Moroder, Luis; Borin, Gianfranco; Filippi, Bruno; Stivanello, Diego; Marchiori, Fernando published an article in 1977, the title of the article was Studies on cytochrome c. XII. Synthesis of the protected undecapeptide (sequence 66-76) and pentadecapeptide (sequence 66-80) of horse heart cytochrome c.COA of Formula: C10H19NO4 And the article contains the following content:

Z-Glu-Tyr-Leu-Glu-Asn-Pro-Lys(TFA)-Lys(TFA)-Tyr-Ile-Pro-NHNH2 (I; Z = PhCH2O2C, TFA = CF3CO), the protected 66-76 fragment of horse heart cytochrome c was prepared by coupling Z-Glu(OCMe3)-Tyr-Leu-Glu(OCMe3)-NHNH2 (II) to H-Asn-Pro-Lys(TFA)-Lys(TFA)-Tyr(CMe3)-Ile-Pro-NHNHCO2CMe3 by the azide method and partially deblocking the resulting undecapeptide with CF3CO2H. I was coupled to H-Gly-Thr(CMe3)-Lys(TFA)-Met-NHNHCO2Me3 (III) by the azide method to give the corresponding protected pentadecapeptide which was the protected 66-80 fragment of cytochrome c. II and III were prepared by conventional stepwise peptide couplings. The experimental process involved the reaction of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate(cas: 53838-27-0).COA of Formula: C10H19NO4

The Article related to cytochrome c undecapeptide pentadecapeptide synthesis, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.COA of Formula: C10H19NO4

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Wuensch, Erich et al. published their patent in 1974 |CAS: 53838-27-0

The Article related to motilin norleucine analog, stomach motilin norleucine analog, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.Name: (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

On October 17, 1974, Wuensch, Erich; Wendlberger, Gerhard; Jaeger, Ernst; Scharf, Regine; Deimer, Karl H.; Stocker, Hans published a patent.Name: (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate The title of the patent was Norleucine-13-motiline. And the patent contained the following:

Phe-Val-Pro-Ile-Phe-Thr-Tyr-Gly-Glu-Leu-Glu-Arg-Nle-Glu-Glu-Lys-Glu-Arg-Asn-Lys-Gly-Gln (I) was prepared by successive coupling and deblocking of Arg(HBr)-Asn-Lys(CO2CMe3)-Gly-Gln-OCMe3.HBr, PhCH2O2C-Glu(OCMe3)-Glu(OCMe3)-Lys-(CO2CMe3)-Glu(OCMe3)-OH, PhCH2O2C-Arg[δ,ω – (CO2CH2Ph)2]Nle-OH, PhCH2O2C-Glu(OCMe3)-Leu-Gln-OH, Thr(CMe3)-Tyr(CMe3)-Gly-OH, and Me3CO2C-Phe-Val-Pro-Ile-Phe-OH, which were prepared by standard coupling methods. I, after purification on ion exchange resin, had 90% of the activity of naturally occurring motilin. The experimental process involved the reaction of (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate(cas: 53838-27-0).Name: (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

The Article related to motilin norleucine analog, stomach motilin norleucine analog, Synthesis of Amino Acids, Peptides, and Proteins: Peptides and other aspects.Name: (S)-5-tert-Butyl 1-methyl 2-aminopentanedioate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Sun, Guanqing et al. published their research in Progress in Organic Coatings in 2021 |CAS: 2358-84-1

The Article related to acrylate photopolymerization shrinkage stress rheol property, Coatings, Inks, and Related Products: Epoxy Resin Coatings and other aspects.Computed Properties of 2358-84-1

On June 30, 2021, Sun, Guanqing; Wu, Xingyi; Liu, Ren published an article.Computed Properties of 2358-84-1 The title of the article was A comprehensive investigation of acrylates photopolymerization shrinkage stress from micro and macro perspectives by real time MIR-photo-rheology. And the article contained the following:

The acrylate photocuring system with the high curing rate are widely used in various industries. However, the rapid polymerization kinetics can cause the surge of resin viscosity and the gel point can be reached in advance. This can results in the restriction of mol. chain movement and internal stress release is thus hindered during the photopolymerization Finally, it usually leads to the poor performance of UV-cured materials with lower double bond conversion and large volume shrinkage and shrinkage stress. In order to understand the relationship between properties and polymerization process, this paper employed the combined technique of the mid-IR spectrometer and photo-rheometer to monitor the acrylate free radical photopolymerization process. The effects of curing conditions (curing temperature, radiant intensity and sample thickness) and system compositions (diluent functionality, diluent segment length) on the rheol. properties and chem. conversion of materials were fully investigated. Finally, a standard protocol is established to evaluate the reactivity, mech. properties and volume shrinkage of the photocuring system. Simultaneously, the double bond conversion of the reaction system can be achieved through calculation of peak area of IR absorption. A complex nonlinear relationship between the storage modulus, shrinkage stress and double bond conversion is established. The experimental process involved the reaction of Oxybis(ethane-2,1-diyl) bis(2-methylacrylate)(cas: 2358-84-1).Computed Properties of 2358-84-1

The Article related to acrylate photopolymerization shrinkage stress rheol property, Coatings, Inks, and Related Products: Epoxy Resin Coatings and other aspects.Computed Properties of 2358-84-1

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ji, Xiaoyue et al. published their research in Journal of Food Processing and Preservation in 2020 |CAS: 123-25-1

The Article related to chinese fermented soybean curd volatile component hsspme gcms, Food and Feed Chemistry: Dairy Products (Including Butter) and other aspects.COA of Formula: C8H14O4

Ji, Xiaoyue published an article in 2020, the title of the article was Investigation of the volatile components in commercial sufu (Chinese fermented soybean curd) based on HS-SPME/GC-MS combined with multivariate statistical analysis.COA of Formula: C8H14O4 And the article contains the following content:

Volatile flavor substances in com. sufu samples of different brands were investigated by headspace solid-phase microextraction (HS-SPME) coupled with gas chromatog.-mass spectrometry (GC-MS). Principal component anal. and cluster anal. of volatile substances for evaluating and distinguishing between nine com. sufu samples were carried out. The results were that a total of 36-six volatiles were identified successfully in nine different brands of sufu, including 7 alcs., 22 esters, and 6 other organic compounds Sufu can be classified into five categories by cluster anal. according to the types and contents of volatiles, and it was determined that the predominant source of difference among volatiles was the difference of esters. Meanwhile, the principal component score plot described the differences and classifications of sufu samples. It was noted that types and contents of volatiles can reflect the sufu taste and analyzing the volatile organic components in sufu provides us with valuable information. HS-SPME-GC/MS combined with multivariate statistical anal. was developed to comprehensively compare volatile components in nine brands of com. sufu with large market share in China. The anal. results indicated that there were obvious differences in the types and contents of volatile components. In this study, the difference in volatile components between the nine brands of sufu was studied and the source of some certain chem. substances were traced to explain for the special sufu flavor. This feasible method may be used as a reference for further research on the flavor of sufu and may help formulators, who are trying to improve the taste and quality of food products. The experimental process involved the reaction of Diethyl succinate(cas: 123-25-1).COA of Formula: C8H14O4

The Article related to chinese fermented soybean curd volatile component hsspme gcms, Food and Feed Chemistry: Dairy Products (Including Butter) and other aspects.COA of Formula: C8H14O4

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xie, Haopu et al. published their research in New Journal of Chemistry in 2020 |CAS: 517-23-7

The Article related to thermally healable polyurethane tailored dynamic crosslinking motif, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.Related Products of 517-23-7

Xie, Haopu; Sheng, Dekun; Zhou, Yan; Xu, Shaobin; Wu, Haohao; Tian, Xinxin; Sun, Yinglu; Liu, Xiangdong; Yang, Yuming published an article in 2020, the title of the article was Thermally healable polyurethane with tailored mechanical performance using dynamic crosslinking motifs.Related Products of 517-23-7 And the article contains the following content:

Materials with self-healing abilities have gained tremendous attention in recent years but combing excellent mech. performance and splendid self-healing capacity into a single polymer material is still a great challenge. In this study, a self-healing polyurethane (SHP) material was prepared by constructing a dynamic crosslinked network via quadruple hydrogen bonds formed from 5-(2-hydroxyethyl)-6-methyl-2-aminouracil (UPy). The mech. properties of the materials could be conveniently tuned by adjusting the dynamic crosslinked d. The optimal sample, SHP-75, has excellent mech. performance, showing high tensile strength (27.02 MPa), excellent stretchability (1300%), and prominent toughness (111.37 MJ m-3). Despite such great mech. properties, SHP-75 exhibited superior self-healing abilities and could fully obtain its initial mech. strength after repairing at 80°C for 24 h. A self-healing conductive electrode was further constructed to demonstrate its application prospects in the field of sensing. The experimental process involved the reaction of 3-Acetyldihydrofuran-2(3H)-one(cas: 517-23-7).Related Products of 517-23-7

The Article related to thermally healable polyurethane tailored dynamic crosslinking motif, Plastics Manufacture and Processing: Preparation Of Resins and other aspects.Related Products of 517-23-7

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Obata, Shunsuke et al. published their research in Biochemistry in 2018 |CAS: 79642-50-5

The Article related to hairpin pyrrole imidazole polyamide dimer dna transition g quadruplex, General Biochemistry: Nucleic Acids and Their Constituents and other aspects.Formula: C13H14N2O8

On February 6, 2018, Obata, Shunsuke; Asamitsu, Sefan; Hashiya, Kaori; Bando, Toshikazu; Sugiyama, Hiroshi published an article.Formula: C13H14N2O8 The title of the article was G-Quadruplex Induction by the Hairpin Pyrrole-Imidazole Polyamide Dimer. And the article contained the following:

The G-quadruplex (G4) is one type of higher-order structure of nucleic acids and is thought to play important roles in various biol. events such as regulation of transcription and inhibition of DNA replication. Pyrrole-imidazole polyamides (PIPs) are programmable small mols. that can sequence-specifically bind with high affinity to the minor groove of double-stranded DNA (dsDNA). Herein, we designed head-to-head hairpin PIP dimers and their target dsDNA in a model G4-forming sequence. Using an electrophoresis mobility shift assay and transcription arrest assay, we found that PIP dimers could induce the structural change to G4 DNA from dsDNA through the recognition by one PIP dimer mol. of two duplex-binding sites flanking both ends of the G4-forming sequence. This induction ability was dependent on linker length. This is the first study to induce G4 formation using PIPs, which are known to be dsDNA binders. The results reported here suggest that selective G4 induction in native sequences may be achieved with PIP dimers by applying the same design strategy. The experimental process involved the reaction of Bis(2,5-dioxopyrrolidin-1-yl) glutarate(cas: 79642-50-5).Formula: C13H14N2O8

The Article related to hairpin pyrrole imidazole polyamide dimer dna transition g quadruplex, General Biochemistry: Nucleic Acids and Their Constituents and other aspects.Formula: C13H14N2O8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics