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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
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. | |||
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... | |||
T18669L | (S,R,S)-AHPC-Me-C10-NH2 hydrochloride | Ligand for E3 Ligase | |
(S,R,S)-AHPC-Me-C10-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate incorporating a VHL ligand and a linker. | |||
T39378 | Thalidomide-O-C10-NH2 | Thalidomide-O-C10-NH2 | |
Thalidomide-O-C10-NH2 is a synthetic E3 ligase ligand-linker conjugate combining a cereblon ligand derived from Thalidomide with a linker crucial for PROTAC technology. | |||
T40892 | Bromo-C10-OBn | Bromo-C10-OBn | |
Bromo-C10-OBn is a PROTAC linker that can be used in the synthesis of PROTACs. | |||
T38756 | Thiol-C10-amide-PEG8 | Thiol-C10-amide-PEG8 | |
Thiol-C10-amide-PEG8 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 sys... | |||
T41010 | Maleimide-C10-NHS ester | Maleimide-C10-NHS ester | |
Maleimide-C10-NHS ester is an alkyl/ether-based linker for PROTAC synthesis. | |||
T20499 | Norchlorcyclizine | C10,C-10,C 10 | Others |
Norchlorcyclizine (C-10) is a partially selective NPR-B inhibitor. It also is an inhibitor of human tyrosyl-DNA phosphodiesterase 1. | |||
T37739 | N-decanoyl-L-Homoserine lactone | C10-HSL,N-decanoyl-L-Homoserine lactone | Reactive Oxygen Species , Antibacterial |
N-decanoyl-L-Homoserine lactone (C10-HSL) is an N-acyl-homoserine lactone (AHL) produced by Pseudomonas cremoris strain ND07.N-decanoyl-L-homoserine lactone inhibits the growth of primary roots of Arabidopsis thaliana.N-... | |||
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]. | |||
T18806 | Thalidomide-NH-C10-COOH | Others | |
Thalidomide-NH-C10-COOH (compound 6b) is a synthetic E3 ligase ligand-linker conjugate. This compound combines the Thalidomide-based von Hippel-Lindau (VHL) ligand with a linker commonly employed in PROTAC technology. [1... | |||
T17547 | Biotin-C10-NHS Ester | Others | |
Biotin-C10-NHS Ester is an alkyl/ether-based linker compound utilized in the synthesis of PROTACs[1]. | |||
T15930 | M-PEG8-C10-phosphonic acid | Others | |
m-PEG8-C10-phosphonic 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-proteaso... | |||
T18669 | (S,R,S)-AHPC-Me-C10-NH2 | Others | |
(S,R,S)-AHPC-Me-C10-NH2 is a chemical compound consisting of a synthesized E3 ligase ligand-linker conjugate that incorporates both a VHL ligand and a linker. This compound, (S,R,S)-AHPC-Me-C10-NH2, finds application in ... | |||
T18668 | (S,R,S)-AHPC-Me-C10-Br | Others | |
(S,R,S)-AHPC-Me-C10-Br is a chemically synthesized conjugate that functions as a ligand-linker for E3 ligases. This compound incorporates a VHL E3 ligase linker and MS432, derived from the MEK1/2 inhibitor PD0325901[1]. | |||
T74366 | 6BrCaQ-C10-TPP | ||
6BrCaQ-C10-TPP, a potent inhibitor of the mitochondrial heat shock protein TRAP1, exhibits antiproliferative activity against various human cancer cells, with an IC50 range of 0.008-0.30 μM. Additionally, it induces dist... | |||
T77957 | Thalidomide-5-O-C10-NH2 hydrochloride | ||
Thalidomide-5-O-C10-NH2 hydrochloride, a Thalidomide-based cereblon ligand, facilitates the recruitment of CRBN protein and, when linked to a protein ligand, forms PROTACs [1]. | |||
T77980 | Pomalidomide-5-C10-NH2 hydrochloride | ||
Pomalidomide-5-C10-NH2 hydrochloride, a Pomalidomide-derived cereblon (CRBN) ligand, facilitates the recruitment of CRBN protein. This compound can be tethered to a protein ligand via a linker to construct a PROTAC [1]. | |||
T77984 | Thalidomide-NH-C10-NH2 hydrochloride | ||
Thalidomide-NH-C10-NH2 hydrochloride, a thalidomide-derived cereblon ligand, facilitates CRBN protein recruitment and, when conjugated with a linker, forms PROTACs [1]. | |||
T81722 | N-(3-Oxodecanoyl)-L-homoserine lactone | 3-Oxo-C10-HSL | |
N-(3-Oxodecanoyl)-L-homoserine lactone (3-Oxo-C10-HSL) functions as a bacterial quorum-sensing signal autoinducer [1]. |