9月
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-mPEG (MW 2kDa)；化合物 T17751DBCO-mPEG (MW 2kDa) (2024/9/1)
简介：dbco-mpeg (mw 2kda) is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-mPEG (MW 20kDa)；化合物 T17750DBCO-mPEG (MW 20kDa) (2024/9/1)
简介：dbco-mpeg (mw 20kda) is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
GSK503；化合物GSK503GSK503 (2024/9/1)
简介：gsk-503, a potent ezh2 inhibitor, has potential antitumor activity.
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-mPEG (MW 10kDa)；化合物 T17749DBCO-mPEG (MW 10kDa) (2024/9/1)
简介：dbco-mpeg (mw 10kda) is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
DBCO-CONH-S-S-NHS ester；化合物 T17748DBCO-CONH-S-S-NHS ester (2024/9/1)
简介：dbco-conh-s-s-nhs ester is a disulfide-linked adc linker employed for the synthesis of antibody-drug conjugates (adcs)[1].
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-C3-PEG4-NH-Boc；化合物 T17747DBCO-C3-PEG4-NH-Boc (2024/9/1)
简介：dbco-c3-peg4-nh-boc is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
DBCO-C3-PEG4-amine；化合物 T17746DBCO-C3-PEG4-amine (2024/9/1)
简介：dbco-c3-peg4-amine is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-C2-PEG4-NH-Boc；化合物 T17745DBCO-C2-PEG4-NH-Boc (2024/9/1)
简介：dbco-c2-peg4-nh-boc is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-C2-PEG4-amine；化合物 T17744DBCO-C2-PEG4-amine (2024/9/1)
简介：dbco-c2-peg4-amine is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
DBCO-C-PEG1；化合物 T17743DBCO-C-PEG1 (2024/9/1)
简介：dbco-c-peg1 is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
DBCO-Biotin；DBCO-生物素Azadibenzocyclooctyne-Biotin conjugate；Azadibenzocyclooctyne-Biotin conjugate (2024/9/1)
简介：dbco-biotin (azadibenzocyclooctyne-biotin conjugate) is a protac linker based on the alkyl chain.
Cys-mcMMAD；化合物 T17741Cys-mcMMAD (2024/9/1)
简介：cys-mcmmad is a drug-linker conjugate for adc. mmad is a potent tubulin inhibitor.
Cyclooctyne-O-PFP ester；化合物 T17740Cyclooctyne-O-PFP ester (2024/9/1)
简介：cyclooctyne-o-pfp ester is a used as an adc cytotoxin, which connects antibody and linker[1].
英国雷尼绍M2三坐标测针 (2024/9/1)
简介：红宝石是一种ji为坚硬的材料，因此测球的磨损甚微。它还具有较低密度，使测尖的质量min，从而避免了因设备运行或振动而引起测头的误触发。
Intepirdine；化合物SB 742457RVT-101|||SB 742457|||GSK-742457；RVT-101|||SB 742457|||GSK-742457 (2024/9/1)
简介：intepirdine (gsk-742457) is a highly selective 5-ht6 receptor antagonist, used in trials studying the treatment of alzheimer´s disease.
Cy5-PEG6-NHS ester；化合物 T17739Cy5-PEG6-NHS ester (2024/9/1)
简介：cy5-peg6-nhs ester (chloride) is a peg-based protac linker utilized for protacs[1] synthesis.
Cy5-PEG6-acid；化合物 T17738Cy5-PEG6-acid (2024/9/1)
简介：cy5-peg6-acid is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
Cy5-PEG5-azide；化合物 T17737Cy5-PEG5-azide (2024/9/1)
简介：cy5-peg5-azide is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
Cy5-PEG5-amine hydrochloride；化合物 T17736Cy5-PEG5-amine hydrochloride (2024/9/1)
简介：cy5-peg5-amine (hydrochloride) is a peg-derived protac linker employed for protac synthesis[1].
Cy5-PEG4-acid；化合物 T17735Cy5-PEG4-acid (2024/9/1)
简介：cy5-peg4-acid (chloride) serves as a peg-based protac linker, suitable for synthesizing protacs[1].
Cy5-PEG3-azide；化合物 T17734Cy5-PEG3-azide (2024/9/1)
简介：cy5-peg3-azide is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
ATRA-hydroxyimino；化合物 T17733CRABP-II ligand 1；CRABP-II ligand 1 (2024/9/1)
简介：atra-hydroxyimino, also known as crabp-ii ligand 1, is a chemical compound derived from retinoic acid (atra). this compound binds to the ciap1 ligand, specifically bestatin, through a linker, resulting in the formation of a complex called sniper. the purpose of this complex is to degrade crabp-ii within imr-32 cells[1].
CL2A；化合物 T17732CL2A|||CL-2A|||CL2A；CL2A|||CL-2A|||CL2A (2024/9/1)
简介：cl2a is a ph-sensitive, cleavable peg8- and triazole-containing pabc-peptide-mc linker, characterized by its ability to induce a bystander effect. it forms a disulfide bond with an antibody at a cysteine residue. labetuzumab govitecan utilizes this linker for its drug conjugation[1].
MSN交谈
