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6bromohexylphosphonic acid
" in TargetMol Product Catalog- Inhibitors & Agonists6580
- Compound Libraries7
- Peptide Products311
- Inhibitory Antibodies31
- Dye Reagents141
- PROTAC Products273
- Natural Products2774
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- Recombinant Protein708
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- Cell Research275
6-Bromohexylphosphonic acid
T14056133345-66-1
6-Bromohexylphosphonic acid, an alkyl chain-based linker, is commonly used in the synthesis of PROTACs (proteolysis targeting chimeras) [1].
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6-Maleimidocapronic acid 
T1406055750-53-3
6-Maleimidocapronic acid, an alkyl chain-based PROTAC linker, is utilized in the synthesis of PROTACs (proteolysis-targeting chimeras).
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1-Bromo-6-chlorohexane
1-Chloro-6-bromohexane, 6-Chlorohexyl bromide, Hexane, 1-bromo-6-chloro-, 6-Bromohexyl Chloride
T407286294-17-3
1-Bromo-6-chlorohexane (Hexane, 1-bromo-6-chloro-) is used as PROTAC linker.
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dBET6
T51301950634-92-0
dBET6 is a selective and cell-permeable degrader of BET based on PROTAC (IC50: 14 nM). It has antitumor activity.
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BSJ-4-116
T91172519823-34-6
BSJ-4-116 is a highly potent and selective CDK12 degrader (PROTAC) with an IC50 of 6 nM. It downregulates DDR genes through a premature termination of transcription, primarily through increasing poly(adenylation).
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Hydroxy-PEG6-Boc
T15537361189-64-2
Hydroxy-PEG7-Boc, a PEG-based PROTAC linker, is utilized in PROTAC synthesis [1].
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NH2-PEG6-Boc
T163151286281-32-0
NH2-PEG6-Boc is a PEG-based PROTAC linker used in PROTAC synthesis[1] and a non-cleavable 6-unit PEG ADC linker for antibody-drug conjugates (ADCs) synthesis[2].
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Propargyl-PEG3-acid
T166051347760-82-0
Propargyl-PEG3-acid is a non-cleavable (3-unit PEG) ADC linker and a PEG-based PROTAC linker, used to synthesize 6-OHDA-PEG3-yne, a compound containing 6-OHDA and Propargyl-PEG3-acid[1].
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2,3,4,6-Tetra-o-acetyl-alpha-galactosylpyranosyl bromide
2-3-4-6-tetra-o-acetyl-alpha-galactosylpyranosyl-bromide
T17326529493-92-3
2,3,4,6-Tetra-O-acetyl-alpha-galactosylpyranosyl bromide (2-3-4-6-tetra-o-acetyl-alpha-galactosylpyranosyl-bromide) is an alkyl chain-based PROTAC linker used in PROTAC synthesis.
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Biotin-PEG6-Boc
Biotin-PEG6-t-butyl ester
T175911352814-07-3
Biotin-PEG6-Boc (Biotin-PEG6-t-butyl ester) is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
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Boc-NH-C6-Br
T17654142356-33-0
Boc-NH-C6-Br is a cleavable linker used in antibody-drug conjugates (ADC).
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Boc-NH-PEG6-CH2COOH
T17681391684-36-9
Boc-NH-PEG6-CH2COOH is a PEG-based PROTAC linker employed in PROTAC synthesis.
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Thalidomide-O-amido-C6-NH2 TFA
E3 Ligase Ligand-Linker Conjugates 25 Trifluoroacetate, Cereblon Ligand-Linker Conjugates 11 TFA, E3 Ligase Ligand-Linker Conjugates 25 TFA
T179191950635-14-9
Thalidomide-O-amido-C6-NH2 TFA (Cereblon Ligand-Linker Conjugates 11 TFA) is a synthesized E3 ligase ligand-linker conjugate comprising a Thalidomide-based cereblon ligand and a linker.
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(S,R,S)-AHPC-PEG2-NH2 hydrochloride
VH032-PEG2-NH2 hydrochloride, VHL Ligand-Linker Conjugates 3 hydrochloride, E3 ligase Ligand-Linker Conjugates 6
T179242097973-72-1
(S,R,S)-AHPC-PEG2-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 6) is a synthesized E3 ligase ligand-linker conjugate that includes the (S,R,S)-AHPC based VHL ligand and a 2-unit PEG linker used in the synthesis of PROTAC.
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OTs-C6-OBn
T18513126519-80-0
OTs-C6-OBn, an alkyl chain-based PROTAC linker, is utilized in the synthesis of PROTAC SGK3 degrader-1[1].
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Thalidomide-O-amido-C6-NH2 hydrochloride
T188162376990-31-5
Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, integrating a Thalidomide-based cereblon ligand with a linker, suitable for PROTAC synthesis.
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Azido-C6-OH
T38953146292-90-2
Azido-C6-OH is a cleavable ADC linker utilized for the synthesis of antibody-drug conjugates (ADCs).
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Thalidomide 4'-ether-alkylC2-amine hydrochloride
halidomide-linker 6
T400302341840-99-9
Thalidomide 4'-ether-alkylC2-amine hydrochloride (halidomide-linker 6) is a synthesized E3 ligase ligand-linker conjugate.
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Thalidomide-O-C6-NH2 hydrochloride
4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride
T400312245697-88-3
Thalidomide-O-C6-NH2 hydrochloride (4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride) is a synthesized E3 ligase ligand-linker conjugate.
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PEG6-(CH2CO2H)2
T823277855-76-6
PEG6-(CH2CO2H)2 is a symmetric PEG PROTAC linker.
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BET-IN-6
T105222570470-39-0
BET-IN-6, a ligand with potent and high affinity for inhibiting BRD2 BRD4, plays a crucial role in the synthesis of PROTAC BRD2 BRD4 degrader-1 [1], targeting the protein BRD2 4.
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CDK ligand for PROTAC
T10734
CDK ligand for PROTAC is a CDK inhibitor with antitumor activity. It has been used to design PROTAC CDK4/6 degraders.
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CDK ligand for PROTAC hydrochloride
T10734L
CDK ligand for PROTAC hydrochloride is a CDK inhibitor with antitumor activity. It has been used to design PROTAC CDK4/6 degraders.
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XY028-133
T133612229974-73-4
XY028-133 is a PROTAC-based CDK4 6 degrader for the study of tumors.
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