Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T13834 | PROTAC BRD4 Degrader-2
化合物 T13834
|
2185795-53-1 | 98% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
SJF620 is a potent degrader of PROTAC BTK(DC50 : 7.9 nM). | ||||
T13782 | MS432
化合物 T13782
|
T13782 | 98% |
|
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% |
|
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% |
|
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% |
|
(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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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... |