459 Results for "

PROTAC compound

" in MedChemExpress (MCE) Product Catalog:
Products (459)

459 Results for "PROTAC compound" in MCE Product Catalog:

Cat. No.: HY-153673
CAS No.: 2911615-06-8
Target:  

PROTACs IRAK

Research Areas:  

Inflammation/Immunology Cancer

PROTAC IRAK4 degrader-8 (Compound 2) is a PROTAC degrader that targets IRAK4 by recruiting cereblon. PROTAC IRAK4 degrader-8 inhibits IRAK4 kinase activity with an IC50 of 15.5 nM. PROTAC IRAK4 degrader-8 suppresses IL-6 production in immune cells. PROTAC IRAK4 degrader-8 can be used in the research of inflammatory diseases, immune diseases and cancers .
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Cat. No.: HY-107444
CAS No.: 1603845-36-8
Purity:  99.64%
Research Areas:  

Cancer

PROTAC HER3-binding moiety 1 (compound 1b) is a Her3 Ligand for PROTAC .
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Cat. No.: HY-178797
CAS No.: 3080678-98-1
Target:  

PROTACs LRRK2

PROTAC LRRK2 Degrader-3 (compound 6) is a PROTAC LRRK2 degrader with a DC50 of 0.17 nM. PROTAC LRRK2 Degrader-3 can be used for research in Parkinson’s disease and inflammation .
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Cat. No.: HY-161616
CAS No.: 3010273-13-6
Research Areas:  

Cancer

ATR-IN-30 (Compound 5) is a selective ATR ligand, and can be used for synthesis of ATR PROTACs, such as PROTAC ATR degrader-2 (HY-161615) .
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Cat. No.: HY-128527
CAS No.: 2158322-29-1
PROTAC ER Degrader-3 is an intermediate for synthesis of PAC. PAC, consists the ADCs linker and PROTACs, conjugated to an antibody. PAC extracts from patent WO2017201449A1, compound LP2. PAC conjugated to an antibody is a more marked estrogen receptor-alpha (ERα) degrader compared to PROTAC (without Ab) .
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Cat. No.: HY-160221
CAS No.: 2505495-83-8
Research Areas:  

Cancer

PROTAC AR Degrader-7 (compound 99) is a PROTAC targeting androgen receptor with an IC50 value of 3 nM .
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Cat. No.: HY-107445
CAS No.: 2097512-23-5
Research Areas:  

Cancer

PROTAC BRD9-binding moiety 1 is a compound that binds to BRD9, and used for inhibiting BRD9 activity, based on PROTAC.
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Cat. No.: HY-159608
CAS No.: 3035210-39-7
Target:  

PROTACs E1/E2/E3 Enzyme

Research Areas:  

Cancer

PROTAC Cbl-b-IN-1 (compound 64) is a potent Cbl-b PROTAC degrader with a DC50 of less than 30 nM. PROTAC Cbl-b-IN-1 can be used for cancer research .
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Cat. No.: HY-155072
CAS No.: 3049086-75-8
Target:  

PROTACs Btk

Research Areas:  

Cancer

PROTAC BTK degraders-5(compound 3e) is a selective BTK PROTAC degrader with a DC50 value of 7.0 nM in JeKo-1 cells. PROTAC BTK degraders-5 has no off-target effect on degrading CRBN neosubstates. PROTAC BTK degraders-5 has anti-proliferation effect on various lymphoma tumor cells and can be used in chronic lymphoid malignancies research .
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Cat. No.: HY-130500
CAS No.: 1346502-15-5
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Br-PEG3-CH2COOH (compound 28) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
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Cat. No.: HY-162245
CAS No.: 3024266-69-8
Target:  

PROTACs SWI/SNF Complex

Research Areas:  

Cancer

PROTAC SMARCA2 degrader-3 is a PROTAC degrader of the SWI/SNF ATPase subunits, SMARCA2. PROTAC SMARCA2 degrader-3 has anticancer effects (WO2023244764A1; Compound 153) .
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Cat. No.: HY-170769
CAS No.: 2769753-49-1
Research Areas:  

Cancer

FLT3 Ligand-Linker Conjugate 1 (compound 7) contains the FLT3 ligand and a PROTAC linker, which can recruit the E3 ligase VHL. FLT3 Ligand-Linker Conjugate 1 can be used to synthesize the PROTAC RSS0680 (HY-148062). PROTAC RSS0680 is a bifunctional compound that targets protein degradation of kinases .
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Cat. No.: HY-177729
Research Areas:  

Cancer

PROTAC BRD9 Degrader-9 (Compound 16) is an efficient and selective targeting BRD9 PROTAC degrader. PROTAC BRD9 Degrader-9 does not cause significant cytotoxicity. PROTAC BRD9 Degrader-9 can be used for cancer research
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Cat. No.: HY-153820
CAS No.: 2086300-61-8
Research Areas:  

Cancer

PROTAC BRD4 Degrader-20 (Compound 195) is a PROTAC degrader that targets BRD4 for degradation by recruiting VHL. PROTAC BRD4 Degrader-20 is applicable to the research of diffuse large B-cell lymphoma .
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Cat. No.: HY-160264
Research Areas:  

Cancer

PROTAC ER Degrader-12 (Compound 70) is an estrogen receptor PROTAC degrader (DC50: <10 nM), and inhibits MCF-7 proliferation (DC50: <10 nM). PROTAC ER Degrader-12 has anticancer effect .
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Cat. No.: HY-161749
CAS No.: 3049802-45-8
Research Areas:  

Cancer

PROTAC ALK degrader-1 (compound B1) is an ALK degrader based on PROTACs, with the DC50 of 26 nM in H3122 EML4-ALK. PROTAC ALK degrader-1 can be used to synthesis PROTAC ALK degrader-2 (HY-161750) with superior bioavailability .
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Cat. No.: HY-163851
Target:  

PROTACs HIV

Research Areas:  

Infection

PROTAC Vif degrader-1 (Compound L15) is a Vif PROTAC degrader. PROTAC Vif degrader-1 has antiviral activity against HIV-1 (EC50: 33.35 μM against HIV-1IIIB) .
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Cat. No.: HY-164306
CAS No.: 2923686-62-6
Target:  

PROTACs PARP

Research Areas:  

Cancer

PROTAC PARP1 degrader-2 (Compound 72) is a PROTAC degrader for PARP with a DC50<10 nM in MDA-MB-231 cell. PROTAC PARP1 degrader-2 inhibits the cell viability of MDA-MB-436 with an IC50 <100 nM .
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Cat. No.: HY-168057
CAS No.: 3024971-78-3
Target:  

PROTACs CDK

Research Areas:  

Cancer

PROTAC CDK2 Degrader-1 (Compound 41) is a PROTAC degrader for cyclin-dependent kinase 2 (CDK2). PROTAC CDK2 Degrader-1 inhibits the phosphorylation of RB protein in CDK2 dependent cell line OVCAR3 with an IC50 of 100-500 nM .
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Cat. No.: HY-128528
PROTAC ER Degrader-2 is an intermediate for synthesis of PAC. PAC, consists the ADCs linker and PROTACs, conjugated to an antibody. PAC extracts from patent WO2017201449A1, compound LP2. PAC conjugated to an antibody is a more marked estrogen receptor-alpha (ERα) degrader compared to PROTAC (without Ab) .
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