簡介:nutlin-c1-amido-peg4-c2-n3 is a novel compound that functions as a ligand-linker conjugate for the e3 ligase. it is a synthesized molecule incorporating the mdm2 ligand derived from nutlin 3, and a 4-unit peg linker. this compound is specifically designed for utilization in protac technology.
簡介:ciap1 ligand-linker conjugates 10 comprise of an iap ligand and a protac linker, which facilitates the design of snipers. these conjugates incorporate an iap ligand that interacts with the e3 ubiquitin ligase, and a protac linker. snipers can be developed using ciap1 ligand-linker conjugates 10.
簡介:ciap1 ligand-linker conjugates 8 comprises an iap ligand for the e3 ubiquitin ligase and a protac linker. this compound is specifically utilized for the purpose of sniper design[1].
簡介:fosaprepitant dimeglumine (mk-0517) is the dimeglumine salt form of fosaprepitant, the water-soluble, n-phosphorylated prodrug of aprepitant, with antiemetic activity. upon intravenous administration and rapid conversion to aprepitant, this agent binds selectively to the human substance p/neurokinin 1 (nk1) receptors in the central nervous system (cns). this inhibits receptor binding of the endogenous substance p and prevents substance p-induced emesis.
簡介:ciap1 ligand-linker conjugates 9 feature an iap ligand specifically targeting the e3 ubiquitin ligase, along with a protac linker. it is valuable tools for developing snipers[1].
簡介:ciap1 ligand-linker conjugates 7 is a chemical compound that combines an iap ligand for the e3 ubiquitin ligase with a protac linker. it is utilized in the design of snipers[1].
簡介:ciap1 ligand-linker conjugates 13, containing an iap ligand for the e3 ubiquitin ligase, and a protac linker, are utilized in the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 4 is a chemical compound that comprises an iap ligand specifically designed for the e3 ubiquitin ligase and a protac linker. this compound, ciap1 ligand-linker conjugates 4, has the potential to be utilized in the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 1 is composed of an iap ligand for the e3 ubiquitin ligase and a protac linker. this compound, ciap1 ligand-linker conjugates 1, is particularly useful in the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 3 are chemical compounds comprising an iap ligand designed specifically for the e3 ubiquitin ligase and a protac linker. these conjugates, denoted as ciap1 ligand-linker conjugates 3, find utility in the design of snipers, short for specific and non-genetic iap-dependent protein erasers [1].
簡介:ciap1 ligand-linker conjugates 5 is a chemical compound consisting of an iap ligand that targets the e3 ubiquitin ligase, and a protac linker. this compound, ciap1 ligand-linker conjugates 5, is specifically designed for the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 12 is a chemical compound that combines an iap ligand, which targets the e3 ubiquitin ligase, with a protac linker. this compound, ciap1 ligand-linker conjugates 12, is valuable for creating snipers[1].
簡介:ciap1 ligand-linker conjugates 2 is a chemical compound that combines an iap ligand for the e3 ubiquitin ligase with a protac linker. this compound is particularly useful in the design of snipers [1].
簡介:ciap1 ligand-linker conjugates 2 hydrochloride is a chemical compound that combines an iap ligand, which targets the e3 ubiquitin ligase, with a protac linker. it is utilized in the creation of snipers[1].
簡介:ciap1 ligand-linker conjugates 14 consist of an iap ligand that targets the e3 ubiquitin ligase and a protac linker. these conjugates, known as ciap1 ligand-linker conjugates 14, are used in the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 6 hydrochloride is a compound that combines an iap ligand for the e3 ubiquitin ligase and a protac linker. it is utilized for the purpose of designing snipers[1].
簡介:ciap1 ligand-linker conjugates 15 consists of an iap ligand that targets the e3 ubiquitin ligase, along with a protac linker. this compound, ciap1 ligand-linker conjugates 15, is suitable for the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 15 hydrochloride is a chemical compound that combines an iap ligand for the e3 ubiquitin ligase and a protac linker. this compound is useful in the development of snipers[1].
簡介:ciap1 ligand-linker conjugates 11 is a chemical compound that combines an iap ligand specifically designed for the e3 ubiquitin ligase with a protac linker. this compound, ciap1 ligand-linker conjugates 11, is useful in the development of snipers[1], allowing for the targeted degradation of proteins.
簡介:ciap1 ligand-linker conjugates 11 hydrochloride is a chemical compound consisting of an iap ligand that targets the e3 ubiquitin ligase, along with a protac linker. it is primarily utilized in the development of snipers, a molecular tool for targeted protein degradation[1].
簡介:pomalidomide-peg3-c2-nh2 (cereblon ligand-linker conjugates 5) is a synthesized e3 ligase ligand-linker conjugate incorporating the pomalidomide based cereblon ligand and 3-unit peg linker.
簡介:pomalidomide-peg3-c2-nh2 tfa is a synthesized e3 ligase ligand-linker conjugate that incorporates the pomalidomide based cereblon ligand and 3-unit peg linker used in protac technology.
簡介:(s,r,s)-ahpc-c10-nh2 (vh032-c10-nh2) is a synthesized e3 ligase ligand-linker conjugate, comprising the (s,r,s)-ahpc-based vhl ligand and a linker, designed for bet-targeted protac applications.
簡介:e3 ligase ligand 9 is a compound that serves as a ligand for e3 ubiquitin ligase. it can be linked to the protein ligand through a linker, forming protacs or snipers. these protacs are known to induce the degradation of cancer-promoting proteins through ubiquitination-mediated mechanisms[1].
簡介:tazemetostat (epz6438) is a histone methyltransferase ezh2 inhibitor (ic50=11 nm) that is orally active, selective, and sam-competitive. tazemetostat exhibits antitumor activity and may be used for the treatment of epithelioid sarcoma/follicular lymphoma.
簡介:e3 ligase ligand 8 is a ligand for e3 ubiquitin ligase. the e3 ligase ligand 8 can be linked to protein ligands through linkers to form protacs, which are inducers of ubiquitination-mediated degradation of cancer-promoting proteins.
簡介:lenalidomide-c4-nh2 hydrochloride is a cereblon ligand derived from lenalidomide. it serves as a recruiting agent for the crbn protein. the compound, known as protac (compound 24), can be formed by linking lenalidomide-c4-nh2 hydrochloride to the ligand for the protein. it exhibits inhibitory effects with ic50s of 0.98 nm and 13.7 nm against the growth of rs4;11 and molm-13 acute leukemia cell lines, respectively[1].