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Cat. No. Product Name Target Signaling Pathways
T39727 ERα degrader-2

ERK MAPK
ERα degrader-2 是一种具有选择性和有效性的雌激素受体 (SERD)降解剂,具有抗癌活性,抑制 ERα,对雌激素受体降解的 EC50 值为 0.3 nM。ERα degrader-2 可用于预防和治疗 HER 阳性乳腺癌。
T13721 Homo-PROTAC cereblon degrader 1

Others; Ligand for E3 Ligase Others; PROTAC
Homo-PROTAC cereblon degrader 1 (compound 15a) 是一种高效 cereblon 降解剂,对 IKZF1 和 IKZF3 的影响很小。
T13722 Homo-PROTAC pVHL30 degrader 1

Others; Ligand for E3 Ligase Others; PROTAC
Homo-PROTAC pVHL30 degrader 1 是一种基于 PROTAC 的 pVHL30 降解剂。
T9236 WSB1 Degrader 1

Others; E1/E2/E3 Enzyme Others; Ubiquitination
WSB1 Degrader 1 是具有口服活性的 WSB1降解剂,具有抗癌活性。
T69753 HDAC6 degrader 9c

HDAC Chromatin/Epigenetic; DNA Damage/DNA Repair
HDAC6 degrader 9c 是一种小分子组蛋白脱乙酰酶 6 (HDAC6) 降解剂,可用于研究癌症或其他疾病。
T4207 (S,R,S)-AHPC hydrochloride

VHL Ligand 1 hydrochloride,ULM-1,Protein degrader 1 hydrochloride

Others; Ligand for E3 Ligase Others; PROTAC
(S,R,S)-AHPC hydrochloride (Protein degrader 1 hydrochloride) 是基于 VH032 的 VHL 配体,可用于募集 von Hippel-Lindau (VHL) 蛋白。它能够利用 linker 与靶蛋白配体连接,得到 PROTAC 分子。
T37329 PROTAC IDO1 Degrader-1

PROTAC IDO1 Degrader-1

PROTAC IDO1 Degrader-1 is the first potent IDO1 (indoleamine 2,3-dioxygenase 1) degrader that hijacks IDO1 to CRBN E3 ligase to introduce IDO1 into UPS and eventually achieve ubiquitination and degradation (DC50=2.84 μM). PROTAC IDO1 Degrader-1 moderately improves the tumor-killing activity of H ER2 CAR-T cells[1]. PROTAC IDO1 Degrader-1 (compound 2c) (10 μM; 24 hours) notably decreases IDO1 level induced by IFN-γ[1].PROTAC IDO1 Degrader-1 and IFN-γ (5 ng/mL) are incubated with HeLa cells for 24...
T40072 PROTAC BRD4 Degrader-9

PROTAC BRD4 Degrader-9

PROTAC BRD4 Degrader-9 (compound 8a) is a novel chemical compound consisting of ligands for von Hippel-Lindau and BRD4, connected by a PROTAC moiety. This compound can effectively degrade the BRD4 protein in PC3 prostate cancer cells. When conjugated with STEAP1 and CLL1 antibodies, PROTAC BRD4 Degrader-9 exhibits potent activity, with respective DC50 values of 0.86 nM and 7.6 nM.
T39902 PROTAC IRAK4 degrader-5

PROTAC IRAK4 degrader-5

PROTAC IRAK4 degrader-5 is a Cereblon-based IRAK4 degrader.
T36242 PROTAC BRD4 Degrader-5

PROTAC BRD4 Degrader-5

PROTAC BRD4 Degrader-5 is a PROTAC-based BRD4 degrader. PROTAC BRD4 Degrader-5 can potent degrade BRD4 in HER2 positive and negative breast cancer cell lines[1].
T40073 PROTAC BRD4 Degrader-10

PROTAC BRD4 Degrader-10

PROTAC BRD4 Degrader-10, also known as compound 8b, is a dual ligand-based PROTAC that combines ligands for von Hippel-Lindau and BRD4. To degrade the BRD4 protein in PC3 prostate cancer cells, PROTAC BRD4 Degrader-10 can be conjugated with STEAP1 and CLL1 antibodies, with respective DC 50 values of 1.3 nM and 18 nM.
T40074 PROTAC BRD4 Degrader-15

PROTAC BRD4 Degrader-15

PROTAC BRD4 Degrader-15 is a chemical compound consisting of a PROteolysis TArgeting Chimera (PROTAC) linked to ligands specific to von Hippel-Lindau and BRD4. It exhibits an IC50 of 7.2 nM for BRD4 BD1 and 8.1 nM for BRD4 BD2. Additionally, PROTAC BRD4 Degrader-15 demonstrates potent degradation activity against the BRD4 protein in PC3 prostate cancer cells.
T40143 PROTAC CBP/P300 Degrader-1

PROTAC CBP/P300 Degrader-1

PROTAC CBP/P300 Degrader-1 is an effective compound that degrades CBP/P300 in a potent manner. It significantly reduces cell viability in various cancer cell lines.
T39920 PROTAC IRAK4 degrader-3

PROTAC IRAK4 degrader-3

PROTAC IRAK4 degrader-3 is a PROTAC-induced IRAK4 degrader based on von Hippel-Lindau.
T36628 PROTAC BRD4 Degrader-8

PROTAC BRD4 Degrader-8

PROTAC BRD4 Degrader-8 is a potent BRD4 inhibitor, with IC50s of 1.1 nM and 1.4 nM for BRD4 BD1 and BD2, respectively. PROTAC BRD4 Degrader-8 is capable of potently degrading the BRD4 protein in PC3 prostate cancer cells[1]. PROTAC BRD4 Degrader-8 (compound 8; 6 days) inhibits the proliferation of PC3 prostate cancer cells, with an IC50 of 28 nM[1].PROTAC BRD4 Degrader-8 (4 h) suppresses MYC gene transcript in MV4-11 AML cells, with an IC50 of 11 nM[1].PROTAC BRD4 Degrader-8 (4 h) potently degra...
T39903 PROTAC IRAK4 degrader-6

PROTAC IRAK4 degrader-6

PROTAC IRAK4 degrader-6 is a potent Cereblon-based compound designed to degrade interleukin-1 receptor-associated kinase 4 (IRAK4).
T39901 PROTAC IRAK4 degrader-4

PROTAC IRAK4 degrader-4

PROTAC IRAK4 degrader-4 (US20190192668A1, compound I-127) is a Cereblon-based PROTAC specifically designed to target and degrade interleukin-1 receptor-associated kinase 4 (IRAK4).
T40250 SHP2 protein degrader-1

SHP2 protein degrader-1

SHP2 protein degrader-1 is a highly efficient allosteric inhibitor targeting SHP2. It effectively induces degradation of SHP2 protein, resulting in cell apoptosis. This compound shows promising potential for studying diseases associated with SHP2.
T39996 PROTAC CDK9 degrader-4

PROTAC CDK9 degrader-4

PROTAC CDK9 degrader-4 is a potent and efficacious chemical compound designed specifically to degrade CDK9, a protein involved in transcription regulation. This compound effectively targets and reduces the levels of CDK9, thereby modulating transcriptional activity.
T40075 PROTAC BRD4 Degrader-13

PROTAC BRD4 Degrader-13

PROTAC BRD4 Degrader-13 (compound 9d) is a bioactive compound that functions as a proteolysis targeting chimera (PROTAC), linking ligands for von Hippel-Lindau and BRD4 proteins. In the context of PC3 prostate cancer cells, this compound effectively degrades the BRD4 protein through conjugation with STEAP1 and CLL1 antibodies. The degradation of BRD4 protein is achieved with remarkable potency, exhibiting a DC 50 of 0.025 nM and 6.0 nM when combined with STEAP1 and CLL1 antibodies, respectively.
T36256 LC-2

LC 2,PROTAC KRASG12C Degrader-LC-2,LC2

PROTACs PROTAC
LC-2 (PROTAC KRASG12C Degrader-LC-2) 是一种新型基于von Hippel-Lindau的内源性 KRAS G12C 的 PROTAC 降解剂,DC50 在 0.25 和 0.76 μM 之间。LC-2 是一种与 MRTX849 共价结合 KRAS G12C 并招募 E3 连接酶 VH的 PROTAC,诱导 KRAS G12C 快速持续降解。LC-2 对纯合和杂合子 KRAS G12C 细胞系 MAPK 信号有抑制作用。
T8745 PROTAC BRAF-V600E degrader-1

Compound 23

Raf MAPK
PROTAC BRAF-V600E degrader-1 (Compound 23) 选择性地诱导 BRAF-V600E 的降解,而不是野生型 BRAF。
T40112 PROTAC PD-1/PD-L1 degrader-1

PROTAC PD-1/PD-L1 degrader-1

PROTAC PD-1/PD-L1 degrader-1, a Cereblon E3 ligand-based compound, is a PD-1/PD-L1 PROTAC that effectively inhibits the interaction between PD-1 and PD-L1 with an IC50 value of 39.2 nM. It successfully restores the suppressed immune response in a co-culture model consisting of Hep3B/OS-8/hPD-L1 cells and CD3 T cells. Additionally, this compound moderately decreases PD-L1 protein levels through a lysosome-dependent mechanism.
T39685 PCSK9 degrader 1

PCSK9 degrader 1 is a selective proprotein convertase substilisin-like/kexin type 9 (PCSK9) degrader. PCSK9 degrader 1 does not affect PCSK9 function.
T39837 PROTAC ERRα Degrader-3

PROTAC ERRα Degrader-3 is a highly effective and selective von Hippel-Lindau-based ligand that efficiently degrades the ERRα protein. At a concentration of 30 nM, this compound exhibits a remarkable degradation capability, reducing the ERRα protein levels by >80%. Importantly, PROTAC ERRα Degrader-3 shows no activity against the ERRβ and ERRγ proteins.
T5439 BRD4 degrader AT1

Epigenetic Reader Domain Chromatin/Epigenetic
BRD4 degrader AT1 是基于 PROTAC 技术的高选择性 Brd4 降解剂,在细胞中对 Brd4BD2 的 Kd 为 44 nM。
T13845 PROTAC PARP1 degrader

Others Others
PROTAC PARP1 degrader is a degrader of PARP1 based on the PROTAC technology. PROTAC PARP1 degrader at 10 μM at 24 h inhibits MDA-MB-231 cell line (IC50 of 6.12 μM).
T36243 PROTAC RIPK degrader-6

PROTAC RIPK degrader-6 (example 1) is a PROTAC designed for the targeted degradation of RIP Kinase, featuring a RIP2 kinase inhibitor connected through a linker to a cereblon binder[1].
T39374 PROTAC BET Degrader-10

PROTAC BET Degrader-10 (WO2017007612A1, example 37) is a highly efficient and selective small molecule compound designed to degrade BET protein BRD4. PROTAC BET Degrader-10 functions by utilizing specific ligands that connect Cereblon and BRD4, with a DC 50 value of 49 nM.
T18609 PROTAC ERRα Degrader-2

Others Others
PROTAC ERRα Degrader-2 is a compound consisting of an MDM2 ligand binding group, a linker, and an estrogen-related receptor alpha (ERRα) binding group. This compound is designed to specifically degrade estrogen-related receptor alpha (ERRα), acting as an ERRα degrader[1].
T12560 PROTAC BRD9 Degrader-1

Epigenetic Reader Domain Chromatin/Epigenetic
PROTAC BRD9 Degrader-1 is a lead PROTAC BRD9 chemical degrader with IC50 of 13.5 nM.
T18632 PROTAC MDM2 Degrader-2

Others Others
PROTAC MDM2 Degrader-2 is a compound designed utilizing PROTAC technology, functioning as a MDM2 degrader. Comprised of a highly potent inhibitor targeting MDM2, a linker, and the MDM2 ligand for E3 ubiquitin ligase, this compound facilitates the degradation of MDM2[1].
T18631 PROTAC MDM2 Degrader-1

Others Others
PROTAC MDM2 Degrader-1 is a chemical compound that utilizes PROTAC technology to degrade MDM2. This compound is comprised of a highly effective MDM2 inhibitor, a linker, and the MDM2 ligand for E3 ubiquitin ligase[1].
T18635 PROTAC RAR Degrader-1

Others Others
PROTAC RAR Degrader-1 comprises a cIAP1 ligand binding group, a linker and a RAR ligand binding group. PROTAC RAR Degrader-1 is an RAR degrader. Maximal RAR degradation at 30 μM concentration in HT1080 cells. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers (SNIPERs)[1].
T5438 PROTAC CDK9 Degrader-1

CDK Cell Cycle/Checkpoint
PROTAC CDK9 Degrader-1 是一种选择性 CDK9 降解剂,是由Cereblon 配体和CDK 配体相连的PROTAC。
T13833 PROTAC BRD4 Degrader-1

Epigenetic Reader Domain Chromatin/Epigenetic
PROTAC BRD4 Degrader-1 is an efficacious degrader of BRD4(BRD4 BD1,IC50 of 41.8 nM).
T18634 PROTAC MDM2 Degrader-4

Others Others
PROTAC MDM2 Degrader-4 is a compound designed using PROTAC technology to degrade MDM2. It combines a powerful MDM2 inhibitor, a linker, and the MDM2 ligand for E3 ubiquitin ligase[1].
T12553 PROTAC EED degrader-1

Others Others
PROTAC EED degrader-1 is a PROTAC targeting EED (pKD = 9.02), is a inhibitor of polycomb repressive complex 2 (PRC2) with pIC50 of 8.17.
T13847 PROTAC SGK3 degrader-1

SGK3-PROTAC1

SGK Metabolism
PROTAC SGK3 degrader-1 (SGK3-PROTAC1) 是一种靶向 SGK3 且与 VH032 VHL 结合配体的 PROTAC 偶联物,可诱导内源性 SGK3 降解。PROTAC SGK3 degrader-1 可抑制GDC0941诱导的癌细胞增殖。
T13849 PROTAC BET Degrader-1

Epigenetic Reader Domain Chromatin/Epigenetic
PROTAC BET Degrader-1 is a potent degrader of BET based on PROTAC.
T18610 PROTAC FKBP Degrader-3

Others Others
PROTAC FKBP Degrader-3 is a PROTAC that comprises a FKBP ligand binding group, a linker and an VHL binding group. PROTAC FKBP Degrader-3 is a potent FKBP degrader[1].
T12554 PROTAC EED degrader-2

Others Others
PROTAC EED degrader-2 is a PROTAC targeting EED (pKD of 9.27),is a inhibitor of polycomb repressive complex 2 (PRC2) with pIC50 of 8.11.
T18636 PROTAC ERα Degrader-1

Others Others
PROTAC ERα Degrader-1 is a chemical compound. It consists of a ubiquitin E3 ligase binding group, a linker, and a protein binding group. This compound serves as a degrader of estrogen receptor-alpha (ERα).
T18605 PROTAC ERα Degrader-2

Others Others
PROTAC ERα Degrader-2 comprises a cIAP1 ligand binding group, a linker and an estrogen receptor α (ERα) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers (SNIPERs)[1].
T13842 PROTAC IRAK4 degrader-1

Others Others
PROTAC IRAK4 degrader-1 is a degrader of PROTAC interleukin-1 receptor-associated kinase 4 (IRAK4).
T13840 PROTAC FAK degrader 1

Others Others
PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM).
T12555 PROTAC FLT-3 degrader 1

Others Others
PROTAC FLT-3 degrader 1 is a PROTAC FLT-3 degrader of internal tandem duplication (ITD)(IC50 0.6 nM),with anti-proliferative activity.
T12556 PROTAC B-Raf degrader 1

Raf MAPK
PROTAC B-Raf degrader 1 is a proteolysis targeting chimera (PROTAC) for the degradation of B-Raf,PROTAC B-Raf degrader 1 With anti-cancer activity.
T13835 PROTAC BRD4 Degrader-3

Epigenetic Reader Domain Chromatin/Epigenetic
PROTAC BRD4 Degrader-3 is an efficacious degrader of PROTAC BRD4.
T13834 PROTAC BRD4 Degrader-2

Epigenetic Reader Domain Chromatin/Epigenetic
PROTAC BRD4 Degrader-2 is an efficacious degrader of PROTAC BRD4(BRD4 BD1,IC50 of 14.2 nM).

化合物

ERα degrader-2
Cat.No: T39727
Synonym:
Target: ERK
Homo-PROTAC cereblon degrader 1
Cat.No: T13721
Synonym:
Target: Others, Ligand for E3 Ligase
Homo-PROTAC pVHL30 degrader 1
Cat.No: T13722
Synonym:
Target: Others, Ligand for E3 Ligase
WSB1 Degrader 1
Cat.No: T9236
Synonym:
Target: Others, E1/E2/E3 Enzyme
HDAC6 degrader 9c
Cat.No: T69753
Synonym:
Target: HDAC
(S,R,S)-AHPC hydrochloride
Cat.No: T4207
Synonym: VHL Ligand 1 hydrochloride,ULM-1,Protein degrader 1 hydrochloride
Target: Others, Ligand for E3 Ligase
PROTAC IDO1 Degrader-1
Cat.No: T37329
Synonym: PROTAC IDO1 Degrader-1
Target:
PROTAC BRD4 Degrader-9
Cat.No: T40072
Synonym: PROTAC BRD4 Degrader-9
Target:
PROTAC IRAK4 degrader-5
Cat.No: T39902
Synonym: PROTAC IRAK4 degrader-5
Target:
PROTAC BRD4 Degrader-5
Cat.No: T36242
Synonym: PROTAC BRD4 Degrader-5
Target:
PROTAC BRD4 Degrader-10
Cat.No: T40073
Synonym: PROTAC BRD4 Degrader-10
Target:
PROTAC BRD4 Degrader-15
Cat.No: T40074
Synonym: PROTAC BRD4 Degrader-15
Target:
PROTAC CBP/P300 Degrader-1
Cat.No: T40143
Synonym: PROTAC CBP/P300 Degrader-1
Target:
PROTAC IRAK4 degrader-3
Cat.No: T39920
Synonym: PROTAC IRAK4 degrader-3
Target:
PROTAC BRD4 Degrader-8
Cat.No: T36628
Synonym: PROTAC BRD4 Degrader-8
Target:
PROTAC IRAK4 degrader-6
Cat.No: T39903
Synonym: PROTAC IRAK4 degrader-6
Target:
PROTAC IRAK4 degrader-4
Cat.No: T39901
Synonym: PROTAC IRAK4 degrader-4
Target:
SHP2 protein degrader-1
Cat.No: T40250
Synonym: SHP2 protein degrader-1
Target:
PROTAC CDK9 degrader-4
Cat.No: T39996
Synonym: PROTAC CDK9 degrader-4
Target:
PROTAC BRD4 Degrader-13
Cat.No: T40075
Synonym: PROTAC BRD4 Degrader-13
Target:
LC-2
Cat.No: T36256
Synonym: LC 2,PROTAC KRASG12C Degrader-LC-2,LC2
Target: PROTACs
PROTAC BRAF-V600E degrader-1
Cat.No: T8745
Synonym: Compound 23
Target: Raf
PROTAC PD-1/PD-L1 degrader-1
Cat.No: T40112
Synonym: PROTAC PD-1/PD-L1 degrader-1
Target:
PCSK9 degrader 1
Cat.No: T39685
Synonym:
Target:
PROTAC ERRα Degrader-3
Cat.No: T39837
Synonym:
Target:
BRD4 degrader AT1
Cat.No: T5439
Synonym:
Target: Epigenetic Reader Domain
PROTAC PARP1 degrader
Cat.No: T13845
Synonym:
Target: Others
PROTAC RIPK degrader-6
Cat.No: T36243
Synonym:
Target:
PROTAC BET Degrader-10
Cat.No: T39374
Synonym:
Target:
PROTAC ERRα Degrader-2
Cat.No: T18609
Synonym:
Target: Others
PROTAC BRD9 Degrader-1
Cat.No: T12560
Synonym:
Target: Epigenetic Reader Domain
PROTAC MDM2 Degrader-2
Cat.No: T18632
Synonym:
Target: Others
PROTAC MDM2 Degrader-1
Cat.No: T18631
Synonym:
Target: Others
PROTAC RAR Degrader-1
Cat.No: T18635
Synonym:
Target: Others
PROTAC CDK9 Degrader-1
Cat.No: T5438
Synonym:
Target: CDK
PROTAC BRD4 Degrader-1
Cat.No: T13833
Synonym:
Target: Epigenetic Reader Domain
PROTAC MDM2 Degrader-4
Cat.No: T18634
Synonym:
Target: Others
PROTAC EED degrader-1
Cat.No: T12553
Synonym:
Target: Others
PROTAC SGK3 degrader-1
Cat.No: T13847
Synonym: SGK3-PROTAC1
Target: SGK
PROTAC BET Degrader-1
Cat.No: T13849
Synonym:
Target: Epigenetic Reader Domain
PROTAC FKBP Degrader-3
Cat.No: T18610
Synonym:
Target: Others
PROTAC EED degrader-2
Cat.No: T12554
Synonym:
Target: Others
PROTAC ERα Degrader-1
Cat.No: T18636
Synonym:
Target: Others
PROTAC ERα Degrader-2
Cat.No: T18605
Synonym:
Target: Others
PROTAC IRAK4 degrader-1
Cat.No: T13842
Synonym:
Target: Others
PROTAC FAK degrader 1
Cat.No: T13840
Synonym:
Target: Others
PROTAC FLT-3 degrader 1
Cat.No: T12555
Synonym:
Target: Others
PROTAC B-Raf degrader 1
Cat.No: T12556
Synonym:
Target: Raf
PROTAC BRD4 Degrader-3
Cat.No: T13835
Synonym:
Target: Epigenetic Reader Domain
PROTAC BRD4 Degrader-2
Cat.No: T13834
Synonym:
Target: Epigenetic Reader Domain
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