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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7701 | Boc-NH-PEG3 | PROTAC Linker 10 | Others , PROTAC Linker |
Boc-NH-PEG3 (PROTAC Linker 10) is a PEG derivative containing a hydroxyl group and Boc-protected amino group, and is a PROTAC linker. | |||
T14413 | Azido-PEG10-alcohol | Others , PROTAC Linker | |
Azido-PEG10-alcohol is a PEG-based PROTAC linker that can be used in PROTAC synthesis[1]. | |||
T17694 | Br-C10-methyl ester | Others , PROTAC Linker | |
Br-C10-methyl ester, a PROTAC linker characterized by its alkyl/ether composition, plays a crucial role in the synthesis of a series of PROTACs (MS432). This compound incorporates a dual-ligand system connected via a lin... | |||
T17881 | (S,R,S)-AHPC-C10-NH2 | VH032-C10-NH2 | Others , Ligand for E3 Ligase |
(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. | |||
T18661 | (S,R,S)-AHPC-C10-NH2 dihydrochloride | VH032-C10-NH2 dihydrochloride,VH032-linker 10,VH032 amide-alkylC10-amine | Others , Ligand for E3 Ligase |
(S,R,S)-AHPC-C10-NH2 dihydrochloride (VH032-linker 10) is a synthesized E3 ligase ligand-linker conjugate incorporating the (S,R,S)-AHPC based VHL ligand and a linker[1]. | |||
T13999 | (10-BRomodecyl)phosphonic acid | Others | |
(10-BRomodecyl)phosphonic acid is an alkyl chain-derived PROTAC linker suitable for PROTAC synthesis [1]. | |||
T17901 | CIAP1 Ligand-Linker Conjugates 10 | E3 ligase Ligand-Linker Conjugates 47 | Others |
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 PROT... | |||
T15120 | Diethyl 10-bromodecylphosphonate | Others | |
Diethyl 10-bromodecylphosphonate is an alkyl-based PROTAC linker utilized for the synthesis of PROTACs[1]. | |||
T18515 | Palbociclib-propargyl | PROTAC CDK6 ligand 1 | Others |
Palbociclib-propargyl, a PROTAC ligand targeting the protein CDK6, connects to the CRBN ligand through a PEG linker to form PROTAC CP-10. CP-10 exhibits a potent DC50 value of 2.1 nM against CDK6[1]. | |||
T14000 | [10-(Diethoxy-phosphoryl)-decyl]-phosphonic acid | Others | |
The compound [10-(diethoxy-phosphoryl)-decyl]-phosphonic acid is a suitable alkyl chain-based PROTAC linker for the synthesis of PROTACs [1]. | |||
T16583 | Propargyl-PEG1-acid | Others | |
Propargyl-PEG1-acid, a PEG-based PROTAC linker, enables the synthesis of BTK-CRBN PROTACs, specifically Ibrutinib-based PROTAC 4 and PROTAC 5. At a concentration of 10 μM, PROTAC 5 facilitates the degradation of BTK and ... | |||
T18682 | SJFδ | Others | |
SJFδ is a 10-atom linker PROTAC. SJFδ degrades p38δ with a DC50 of 46.17 nM, but does not degrade p38α, p38β, or p38γ[1]. | |||
T15834 | M-PEG10-alcohol | Decaethylene glycol monomethyl ether | Others |
m-PEG10-alcohol, also known as Decaethylene glycol monomethyl ether, is a non-cleavable 10 unit PEG ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. Additionally, m-PEG10-alcohol serves as a PE... | |||
T17904 | Pomalidomide-PEG1-C2-N3 | E3 ligase Ligand-Linker Conjugates 50,Cereblon Ligand-Linker Conjugates 13 | Others |
Pomalidomide-PEG1-C2-N3 is a compound that has been synthesized as a conjugate of an E3 ligase ligand-linker. This compound incorporates the cereblon ligand based on Pomalidomide and a 1-unit PEG linker, which are common... | |||
T71919 | Boc-10-Aminodecanoic acid | ||
Boc-10-Aminodecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Boc-10-Aminodecanoic acid is an alkane chain with terminal carboxlic acid and Boc-protected amino g... | |||
T18601 | Desmethyl-QCA276 | PROTAC BRD4-binding moiety 4 | Others |
Desmethyl-QCA276, the QCA276-based moiety, binds to cereblon ligand via a linker to form PROTAC to degrade BET. QCA276 is a BET inhibitor with an IC50 of 10 nM, and with a Ki of 2.3 nM[1]. | |||
T18680 | SD-36 | Others | |
SD-36, a potent and efficacious PROTAC STAT3 degrader (Kd=~50 nM), exhibits high specificity for STAT3 over other STAT members. It effectively targets both wild-type and mutated STAT3 proteins in cells, inhibiting their ... | |||
T41146 | ND1-YL2 | ND1-YL2 | |
ND1-YL2 is a peptide-based PROTAC®Degrader of steroid receptor co-activator 1 (SRC-1; also known as nuclear receptor coactivator 1, NCOA1). ND1-YL2 is composed of a stapled peptide that binds SRC-1 (YL2) joined by a link... | |||
T83856 | AP-1 | ||
AP-1, a miniaturized proteolysis-targeting chimera (PROTAC) incorporating an anaplastic lymphoma kinase (ALK) ligand connected to (±)-thalidomide via an ultrashort linker, effectively degrades ALK fusion proteins such as... |