首页 工具
登录
购物车
PROTAC Selection

PROTAC Selection

Cat. No. Product Name CAS No. Purity Chemical Structure
T13834 PROTAC BRD4 Degrader-2
化合物 T13834
2185795-53-1 98%
TargetMol Chemical Structure PROTAC BRD4 Degrader-2
PROTAC BRD4 Degrader-2 is an efficacious degrader of PROTAC BRD4(BRD4 BD1,IC50 of 14.2 nM).
T11975 PROTAC Mcl1 degrader-1
化合物 T11975
2163793-38-0 98%
TargetMol Chemical Structure PROTAC Mcl1 degrader-1
PROTAC Mcl1 degrader-1 induces the ubiquitination and proteasomal degradation of Mcl-1 by introducing the E3 ligase cereblon (CRBN)-binding ligand pomalidomide t...
T18636 PROTAC ERα Degrader-1
化合物 T18636
T18636 98%
TargetMol Chemical Structure PROTAC ERα Degrader-1
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 ...
T13786 MZP-55
化合物 T13786
2010159-48-3 98%
TargetMol Chemical Structure MZP-55
MZP-55 is a selective BRD3/4 degrader based on PROTAC technology(Brd4BD2 with Kd of 8 nM)
T13657 DMCL1-2
化合物 T13657
2351218-88-5 98%
TargetMol Chemical Structure dMCL1-2
dMCL1-2 is a potent and selective myeloid leukemia 1 (MCL1) degrading agent based on PROTAC, which binds to MCL1 with a KD of 30 nM. dmcl-2 activates the apoptos...
T12552 PROTAC CDK2/9 Degrader-1
化合物 T12552
2408641-24-5 98%
TargetMol Chemical Structure PROTAC CDK2/9 Degrader-1
PROTAC CDK2/9 Degrader-1 is a potent CDK2 and CDK9 dual degrader(DC50 of 62 nM and 33 nM).
T18604 PROTAC CRBN Degrader-1
化合物 T18604
2358775-70-7 98%
TargetMol Chemical Structure PROTAC CRBN Degrader-1
PROTAC CRBN Degrader-1 is a chemical compound consisting of a cereblon (CRBN) ligand binding group, a linker, and a von Hippel-Landau (VHL) binding group. It fun...
T18680 SD-36
化合物 SD-36
2429877-44-9 98%
TargetMol Chemical Structure SD-36
SD-36, a potent and efficacious PROTAC STAT3 degrader (Kd=~50 nM), exhibits high specificity for STAT3 over other STAT members. It effectively targets both wild-...
T13887 SJF620
化合物 T13887
2376187-16-3 98%
TargetMol Chemical Structure SJF620
SJF620 is a potent degrader of PROTAC BTK(DC50 : 7.9 nM).
T13782 MS432
化合物 T13782
T13782 98%
TargetMol Chemical Structure MS432
MS432 is a highly selective PD0325901-based VHL-recruiting PROTAC degrader for MEK1 and MEK2.
T17543 BI-3663
化合物 T17543
2341740-84-7 98%
TargetMol Chemical Structure BI-3663
BI-3663 is a highly selective PTK2/FAK PROTAC, with cereblon ligands to hijack E3 ligases for PTK2 degradation. BI-3663 inhibits PTK2 with an IC50 of 18 nM. BI-3...
T13105 TD-428
化合物 T13105
T13105 98%
TargetMol Chemical Structure TD-428
TD-428 is a highly specific degrader of BRD4(DC50 of 0.32 nM). TD-428 is a BET PROTAC, which comprises TD-106 (a CRBN ligand) linked to JQ1 (a BET inhibitor). TD...
T17926 (S,R,S)-AHPC-PEG6-C4-Cl
化合物 T17926
1835705-59-3 98%
TargetMol Chemical Structure (S,R,S)-AHPC-PEG6-C4-Cl
(S,R,S)-AHPC-PEG6-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 6-unit PEG linker. (S,R,S)-AHPC-PEG6-C4-Cl is capa...
T13840 PROTAC FAK degrader 1
化合物 T13840
2301916-69-6 98%
TargetMol Chemical Structure PROTAC FAK degrader 1
PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM).
T13930 TL13-12
化合物 T13930
2229037-04-9 98%
TargetMol Chemical Structure TL13-12
TL13-12 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: 0.69 nM).
T13833 PROTAC BRD4 Degrader-1
化合物 T13833
2133360-00-4 98%
TargetMol Chemical Structure PROTAC BRD4 Degrader-1
PROTAC BRD4 Degrader-1 is an efficacious degrader of BRD4(BRD4 BD1,IC50 of 41.8 nM).
T13743 JH-XI-10-02
化合物 T13743
2209085-22-1 98%
TargetMol Chemical Structure JH-XI-10-02
JH-XI-10-02 causes proteasomal degradation, does not affect CDK8 mRNA levels. JH-XI-10-02 shows no effect on CDK19. JH-XI-10-02 is a potent and selective degrade...
T13845 PROTAC PARP1 degrader
化合物 T13845
2369022-68-2 98%
TargetMol Chemical Structure PROTAC PARP1 degrader
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 μ...
T12907 SIAIS178
化合物 T12907
2376047-73-1 98%
TargetMol Chemical Structure SIAIS178
SIAIS178 is a potent and selective degrader of BCR-ABL based on PROTAC technology (IC50 of 24 nM).
T14318 ARCC-4
化合物 T14318
1973403-00-7 98%
TargetMol Chemical Structure ARCC-4
ARCC-4 is an enzalutamide-based von Hippel-Lindau (VHL)-recruiting AR PROTAC and outperforms enzalutamide and it is a low-nanomolar androgen receptor (AR) degrad...
PROTAC BRD4 Degrader-2
T13834
PROTAC BRD4 Degrader-2 is an efficacious degrader of PROTAC BRD4(BRD4 BD1,IC50 of 14.2 nM).
PROTAC Mcl1 degrader-1
T11975
PROTAC Mcl1 degrader-1 induces the ubiquitination and proteasomal degradation of Mcl-1 by introducing the E3 ligase cereblon (CRBN)-binding ligand pomalidomide t...
PROTAC ERα Degrader-1
T18636
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 ...
MZP-55
T13786
MZP-55 is a selective BRD3/4 degrader based on PROTAC technology(Brd4BD2 with Kd of 8 nM)
dMCL1-2
T13657
dMCL1-2 is a potent and selective myeloid leukemia 1 (MCL1) degrading agent based on PROTAC, which binds to MCL1 with a KD of 30 nM. dmcl-2 activates the apoptos...
PROTAC CDK2/9 Degrader-1
T12552
PROTAC CDK2/9 Degrader-1 is a potent CDK2 and CDK9 dual degrader(DC50 of 62 nM and 33 nM).
PROTAC CRBN Degrader-1
T18604
PROTAC CRBN Degrader-1 is a chemical compound consisting of a cereblon (CRBN) ligand binding group, a linker, and a von Hippel-Landau (VHL) binding group. It fun...
SD-36
T18680
SD-36, a potent and efficacious PROTAC STAT3 degrader (Kd=~50 nM), exhibits high specificity for STAT3 over other STAT members. It effectively targets both wild-...
SJF620
T13887
SJF620 is a potent degrader of PROTAC BTK(DC50 : 7.9 nM).
MS432
T13782
MS432 is a highly selective PD0325901-based VHL-recruiting PROTAC degrader for MEK1 and MEK2.
BI-3663
T17543
BI-3663 is a highly selective PTK2/FAK PROTAC, with cereblon ligands to hijack E3 ligases for PTK2 degradation. BI-3663 inhibits PTK2 with an IC50 of 18 nM. BI-3...
TD-428
T13105
TD-428 is a highly specific degrader of BRD4(DC50 of 0.32 nM). TD-428 is a BET PROTAC, which comprises TD-106 (a CRBN ligand) linked to JQ1 (a BET inhibitor). TD...
(S,R,S)-AHPC-PEG6-C4-Cl
T17926
(S,R,S)-AHPC-PEG6-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 6-unit PEG linker. (S,R,S)-AHPC-PEG6-C4-Cl is capa...
PROTAC FAK degrader 1
T13840
PROTAC FAK degrader 1 is a selective and potent degrader of focal adhesion kinase (Fak) (IC50 of 6.5 nM).
TL13-12
T13930
TL13-12 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: 0.69 nM).
PROTAC BRD4 Degrader-1
T13833
PROTAC BRD4 Degrader-1 is an efficacious degrader of BRD4(BRD4 BD1,IC50 of 41.8 nM).
JH-XI-10-02
T13743
JH-XI-10-02 causes proteasomal degradation, does not affect CDK8 mRNA levels. JH-XI-10-02 shows no effect on CDK19. JH-XI-10-02 is a potent and selective degrade...
PROTAC PARP1 degrader
T13845
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 μ...
SIAIS178
T12907
SIAIS178 is a potent and selective degrader of BCR-ABL based on PROTAC technology (IC50 of 24 nM).
ARCC-4
T14318
ARCC-4 is an enzalutamide-based von Hippel-Lindau (VHL)-recruiting AR PROTAC and outperforms enzalutamide and it is a low-nanomolar androgen receptor (AR) degrad...
1 2 3 4 5 6
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼