1201 Results for "

linker conjugates for PROTACs

" in MedChemExpress (MCE) Product Catalog:
Products (1201)

1201 Results for "linker conjugates for PROTACs" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-122562
CAS No.: 2231744-29-7
Purity:  98.35%
Target:  

PROTACs Btk

Research Areas:  

Cancer

MT-802 is a BTK PROTAC degrader. MT-802 degrades wild-type BTK (DC50 = 14.6 nM) and BTK mutants including E41K, C481S (DC50 = 14.9 nM), C481R, C481Y, C481T, C481F, L528W, and inhibits their Y223 phosphorylation. BI-4732 can be used for the study of Ibrutinib (HY-10997)-resistant chronic lymphocytic leukemia (CLL). (Pink: BTK ligand (HY-150885), Blue: CRBN Ligand (HY-14658), Black: Linker (HY-141371), E3 ligase ligand-linker conjugate (HY-176340)) .
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4
4 Cited Publications
Cat. No.: HY-123921
CAS No.: 2230821-27-7
Purity:  99.98%
Target:  

PROTACs EGFR

Research Areas:  

Cancer

Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a von Hippel-Lindau ligand via a linker, induces EGFR degradation with DC50s of 11.7 nM and 22.3 nM in HCC827(exon 19 del) and H3255 (L858R mutantion) cells, respectively .
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2
2 Cited Publications
Cat. No.: HY-103604
CAS No.: 2064292-52-8
Purity:  98.06%
Synonyms: VH032-PEG4-NH2 hydrochloride; VHL Ligand-linker conjugates 4 hydrochloride; E3 ligase Ligand-linker conjugates 7
Research Areas:  

Cancer

(S,R,S)-AHPC-PEG4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology.
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2
2 Cited Publications
Cat. No.: HY-103604A
CAS No.: 2010159-57-4
Purity:  95.62%
Synonyms: VH032-PEG4-NH2; VHL Ligand-linker conjugates 4 ; E3 ligase Ligand-linker conjugates 7 Free Base
Research Areas:  

Cancer

(S,R,S)-AHPC-PEG4-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology.
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2
2 Cited Publications
Cat. No.: HY-103601
CAS No.: 1797406-81-5
Purity:  99.93%
Synonyms: VH032-PEG4-N3; VHL Ligand-linker conjugates 5; E3 ligase Ligand-linker conjugates 4
Research Areas:  

Others

(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology. (S,R,S)-AHPC-PEG4-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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1
1 Cited Publications
Cat. No.: HY-128832
Purity:  99.19%
Synonyms: MDM2 Ligand-linker conjugates 1; E3 ligase Ligand-linker conjugates 48
Research Areas:  

Cancer

Nutlin-C1-amido-PEG4-C2-N3 (MDM2 Ligand-Linker Conjugates 1; E3 ligase Ligand-Linker Conjugates 48) is an E3 ligase ligand-linker conjugate that can be used for the synthesis of PROTACs .
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1
1 Cited Publications
Cat. No.: HY-103614
CAS No.: 1950635-16-1
Purity:  99.43%
Synonyms: Cereblon Ligand -linker conjugates 2 TFA; E3 Ligase Ligand-linker conjugates 20 TFA
Thalidomide-O-amido-C8-NH2 TFA (Cereblon Ligand -Linker Conjugates 2 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
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1
1 Cited Publications
Cat. No.: HY-120237
CAS No.: 170572-38-0
Purity:  ≥97.0%
Research Areas:  

Cancer

m-PEG7-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. m-PEG7-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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1
1 Cited Publications
Cat. No.: HY-130408
CAS No.: 184357-46-8
Purity:  ≥97.0%
Research Areas:  

Cancer

m-PEG6-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. m-PEG6-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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1
1 Cited Publications
Cat. No.: HY-W018174
CAS No.: 74654-07-2
Research Areas:  

Cancer

m-PEG3-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. m-PEG3-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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1
1 Cited Publications
Cat. No.: HY-W040214
CAS No.: 85030-56-4
Research Areas:  

Cancer

m-PEG4-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. m-PEG4-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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1
1 Cited Publications
Cat. No.: HY-126885
CAS No.: 2144395-59-3
Purity:  95.06%
Research Areas:  

Cancer

DBCO-PEG5-NHS ester is a PEG/Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. DBCO-PEG5-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . DBCO-PEG5-NHS ester is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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1
1 Cited Publications
Cat. No.: HY-103599
CAS No.: 2010159-45-0
Purity:  99.94%
Synonyms: VH032-PEG2-N3; VHL Ligand-linker conjugates 6; E3 ligase Ligand-linker conjugates 13
Research Areas:  

Cancer

(S,R,S)-AHPC-PEG2-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-PEG2-N3 can be used for the synthesis of PROTACs .
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1
1 Cited Publications
Cat. No.: HY-140844
CAS No.: 2380318-57-8
Purity:  98.02%
Thalidomide-O-PEG4-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. Thalidomide-O-PEG4-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-138632
CAS No.: 2417370-42-2
Purity:  98.23%
PROTAC BRD4 Degrader linker conjugate is a linker-payload conjugate as well as a bifunctional degrader of BRD4 that binds to VHL, consisting of PROTAC and a linker. PROTAC BRD4 Degrader linker conjugate can be conjugated with STEAP1 and CLL1 antibodies to degrade BRD4 protein, with DC50 values of 0.86 nM and 7.6 nM, respectively. PROTAC BRD4 Degrader linker conjugate can be used in research related to prostate cancer and acute myeloid leukemia (BRD4 ligand: (HY-129939); VHL ligand: (HY-125845)) .\n




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Cat. No.: HY-175360
CAS No.: 3098774-65-0
USP7 Ligand-Linker Conjugates 1 is an Target Protein Ligand-Linker Conjugate that incorporates a ligand for USP7 (HY-175359) and a PROTAC linker, which recruits E3 ligases. USP7 Ligand-Linker Conjugates 1 can be used for synthesis of PROTAC USP7 Degrader-1 (HY-175358) .
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Cat. No.: HY-W1006706
CAS No.: 2502189-47-9
Research Areas:  

Cancer

E3 Ligase Ligand-linker Conjugate 157 is the conjugate composed of the E3 ligase ligand and the linker. E3 Ligase Ligand-linker Conjugate 157 can be used for synthesis of PROTAC degrader KT-253 (HY-170451) .
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Cat. No.: HY-175766
CAS No.: 2476319-08-9
CRBN Ligand-Linker Conjugate 2 is a synthesized E3 ligand-linker conjugate that can be used for synthesis of PROTACs, such as FIP22 (HY-175764). FIP22 is a potent and selective IRAK4 PROTAC degrader with anti- atopic dermatitis activity .
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Cat. No.: HY-176918
Research Areas:  

Cancer

K-Ras ligand-Linker Conjugate 8 is a Target Protein Ligand-Linker Conjugate that incorporates a ligand for KRAS (HY-162960) and a PROTAC linker, which recruits E3 ligases. K-Ras ligand-Linker Conjugate 8 can be used for synthesis of PROTAC KRAS(on) degrader ACBI-4 (HY-176792) .
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Cat. No.: HY-175726
CAS No.: 3094183-96-4
Research Areas:  

Cancer

BRAF ligand-Linker Conjugate 1 is a target protein ligand-linker conjugate that can be used to synthesize PROTAC CST905(HY-175435) .
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