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Catalog | name | Description | price |
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R-R-0423 | Cyclo(L-Leu-trans-4-hydroxy-L-Pro) | Cyclo(L-Leu-trans-4-hydroxy-L-Pro)/CAS:115006-86-5 is a cyclic dipeptide that is composed of two amino acids: L-Leucine and trans-4-hydroxy-L-Proline. It is a cyclic form of a dipeptide that has been the subject of scientific research due to its potential therapeutic applications. | price> |
R-GDZ003 | 1-Pyrenebutyric acid-PEG1000-Crgd | 1-Pyrenebutyric acid-poly(ethylene glycol)-cRGD,1-Pyrenebutyric acid-PEG1000-cRGD from ruixi.Ruixi is a biotechnology company.Our company focuses on the production and sales of scientific research level drug delivery and drug nano targeting products. At present, our products mainly include synthetic phospholipids,PEG derivatives,block copolymers, nano gold, magnetic nanoparticles,mesoporous silica, reactive fluorescent dyes,fluorescent quantum dots,click chemistry and macrocyclic ligands. | price> |
R-XASYS-00424 | (Rac)-Plevitrexed,cas:153538-08-0 | (Rac)-Plevitrexed(C26H25FN8O4,532.53) is a racemate of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS). | price> |
R-R-0424 | Cyclo(Hpro-Leu) | Cyclo(Hpro-Leu)/CAS:1016899-93-6 is a cyclic peptide derived from the amino acid leucine and is a member of the cyclic peptide family. It is a potent inhibitor of the enzyme cyclooxygenase-2 (COX-2), which is involved in inflammation and pain. It has been studied extensively for its potential therapeutic applications in various diseases, including cancer, inflammation, and pain. | price> |
R-GDZ004 | Dihydrolipoic acid(DHLA)-PEG-NH2 | Dihydrolipoic acid-poly(ethylene glycol)-Amine,Dihydrolipoic acid(DHLA)-PEG-NH2 from ruixi. Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers,but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes. | price> |
R-XASYS-00425 | BAY-218,cas:2162982-11-6 | BAY-218 (AHR antagonist ) is an aryl hydrocarbon receptor (AHR) antagonist. BAY-218 has AHR inhibitory activity with an IC50 of 39.9 μM in in U87 glioblastoma cells. BAY-218 can be used for the research of cancer or conditions with dysregulated immune responses. | price> |
R-R-0425 | CTTHWGFTLC, CYCLIC | CTTHWGFTLC, CYCLIC/CTT, MMP-2/MMP-9 Inhibitor III/CAS 244082-19-7 from ruixi. Disulfide bond is a protein that regulates muscle cell assembly and interactions. Disulfide bonds are formed by the oxidation of two cysteine molecules, which can be found in the extracellular matrix (ECM). The protein is an important regulator of metalloproteinases, which are enzymes that regulate ECM turnover. When disulfide bond lacks, it causes a deficiency in collagen production. Disulfide bond also has interactions with MMP-2, which plays a role in the regulation of arteriosclerosis and genetic disorders such as muscular dystrophy. | price> |
R-GDZ005 | Dihydrolipoic acid(DHLA)-PEG-cooh | Dihydrolipoic acid-poly(ethylene glycol)-Carboxyl,Dihydrolipoic acid(DHLA)-PEG-cooh from ruixi.Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers,but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes | price> |
R-XASYS-00426 | (S)-Crizotinib,cas:1374356-45-2 | (S)-Crizotinib(C21H22Cl2FN5O,450.3) is an inhibitor of muT homolog (MTH1; IC50 = 72 nM).It is selective for MTH1 over a panel of 456 kinases at 1 µM. (S)-Crizotinib (30 µM) induces oxidative DNA damage and apoptosis in SGC-7901 and BGC-823 human gastric cancer cells. | price> |
R-R-0426 | N-Bromoacetyl--alanine | N-Bromoacetyl-β-alanine (CAS 89520-11-6)/N-Bromoacetyl--alanine/UUN20116/3-(2-bromoacetamido)propanoic acid is a compound containing a bromide group and a terminal carboxylic acid. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. | price> |
R-GDZ006 | Dihydrolipoic acid(DHLA)-PEG-NHS | Dihydrolipoic acid-poly(ethylene glycol)-N-hydroxylsuccinimide,Dihydrolipoic acid(DHLA)-PEG-NHS from ruixi.Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers,but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes. | price> |
R-XASYS-00427 | (S)-ML753286,cas:1699720-85-8 | (S)-ML753286(C20H25N3O3,335) is a research tool that activates the receptor and cell biology. It is an activator of Ligand and Receptor, which can be used in Cell Biology, Antibody, Ion channels, High purity, Protein interactions, Pharmacology and Peptides. The chemical formula of (S)-ML753286 is C17H22N2O3 with a molecular weight of 288.32 g/mol. | price> |
R-R-0427 | Tetrazine-biotin/CAS:1714123-51-9 | Tetrazine-biotin/CAS:1714123-51-9 is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Tetrazine-biotin is a click chemistry reagent, itcontains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups. | price> |
R-GDZ007 | Dihydrolipoic acid(DHLA)-PEG-Mal | Dihydrolipoic acid-poly(ethylene glycol)-Maleimide,Dihydrolipoic acid(DHLA)-PEG-Mal from ruixi.Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers,but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes. | price> |
R-XASYS-00428 | (S)-Rasagiline mesylate,cas:202464-88-8 | (S)-Rasagiline (TVP1022) mesylate(C13H17NO3S,267.34) is the S-isomer of rasagiline, which is an anti-Parkinson drug, appears to have the same neuroprotective activity as the R-isomer, but is 1000-fold less active as an MAO-B inhibitor. | price> |
R-R-0428 | Azide-C2-SS-C2-biotin | Azide-SS-biotin/Azide-C2-SS-C2-biotin/CAS NO:1620523-64-9 is a cleavable biotinylation reagent for labeling alkyne-containing biomolecules using click chemistry. The azide group reacts with alkynes, DBCO or BCN reagent to form a stable triazole linkage. | price> |
R-GDZ008 | Dihydrolipoic acid(DHLA)-PEG-Alkyne | Dihydrolipoic acid(DHLA)-PEG-Alkyne,Dihydrolipoic acid-poly(ethylene glycol)-Alkyne from ruixi.Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers,but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes. | price> |
R-XASYS-00429 | (S,R,S)-AHPC-PEG1-N3,cas:2101200-09-1 | (S,R,S)-AHPC-PEG1-N3 is a synthesized E3 ligase ligand-linker conjugate. (S,R,S)-AHPC-PEG1-N3 incorporates the (S,R,S)-AHPC based VHL ligand and 1-unit PEG linker used in PROTAC technology. | price> |
R-R-0429 | Tetrazine-diazo-PEG4-biotin | Tetrazine-diazo-PEG4-biotin is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Tetrazine-diazo-PEG4-biotin is a click chemistry reagent, itcontains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups. | price> |
R-GDZ009 | Dihydrolipoic acid(DHLA)-PEG-Folate | Dihydrolipoic acid-poly(ethylene glycol)-Folic acid,Dihydrolipoic acid(DHLA)-PEG-Folate from ruixi.Dihydrolipoic acid is an organic compound formed by hydrogenation of lipoic acid.It is a carboxylic acid with two sulfhydryl groups.There are two kinds of enantiomers, but only the R-type enantiomer has biological activity.The conversion between lipoic acid and dihydrolipoic acid occurs in many biochemical processes. | price> |