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Epigenetic Reader Domain

Epigenetic reader domains can be thought of as effector proteins that recognize and are recruited to specific epigenetic marks.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T82821 BRD9 Degrader-1 98%
BRD9 Degrader-1
BRD9 Degrader-1 functions as a BRD9 degrader, demonstrating micromolar binding affinity towards BRD9 and nanomolar affinity for the ternary complex involving BRD...
T10520 BET-IN-2 2104688-91-5 98%
BET-IN-2
BET-IN-2 is a BET inhibitor (IC50: 52 nM for BRD4-BD1).
T13849 PROTAC BET Degrader-1 2093386-22-0 98%
PROTAC BET Degrader-1
PROTAC BET Degrader-1 is a potent degrader of BET based on PROTAC.
T14512 BAZ2-ICR 1665195-94-7 98%
BAZ2-ICR
BAZ2-ICR is an epigenetic chemical probe and it also is a potent, selective, cell active and orally active BAZ2A/B bromodomains inhibitor with IC50s of 130 nM an...
T11597 IACS-9571 1800477-30-8 98%
IACS-9571
IACS-9571 is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
T15443 GSK8814 1997369-78-4 98%
GSK8814
GSK8814 is a selective and ATAD2/2B bromodomain chemical probe and inhibitor (binding constant pKd=8.1 and a pKi=8.9 in BROMOscan). GSK8814 displays 500-fold sel...
T15397 GNE-049 1936421-41-8 98%
GNE-049
GNE-049 is a highly potent and selective inhibitor of CBP (IC50: 1.1 nM in TR-FRET assay). GNE-049 also inhibits BRET and BRD4(1) (IC50s: 12 nM and 4200 nM, resp...
T17294 ZL0454 2229042-77-5 98%
ZL0454
ZL0454 is an effective and selective Bromodomain-containing protein 4 inhibitors (IC50: 49 and 32 nM for BD1 and BD2).
T13835 PROTAC BRD4 Degrader-3 2313234-00-1 98%
PROTAC BRD4 Degrader-3
PROTAC BRD4 Degrader-3 is an efficacious degrader of PROTAC BRD4.
T13785 MZP-54 2010159-47-2 98%
MZP-54
MZP-54 is a selective degrader of BRD3/4 based on PROTAC technology(Kd of 4 nM for Brd4BD2)
T12560 PROTAC BRD9 Degrader-1 2097971-01-0 98%
PROTAC BRD9 Degrader-1
PROTAC BRD9 Degrader-1 is a lead PROTAC BRD9 chemical degrader with IC50 of 13.5 nM.
T11291 FKBP12 PROTAC dTAG-13 2064175-41-1 98%
FKBP12 PROTAC dTAG-13
FKBP12 PROTAC dTAG-13 (dTAG-13) is a degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 (dTAG-13) al...
T13850 PROTAC BET degrader-3 T13850 98%
PROTAC BET degrader-3
PROTAC BET Degrader-3 is a potent degrader OF BET based on PROTAC.
T15399 GNE-207 2158266-58-9 98%
GNE-207
GNE-207 is a selective and orally bioavailable inhibitor of the bromodomain of CBP (IC50: 1 nM). It has a selective index of >2500-fold against BRD4 (1). GNE-207...
T17297 ZXH-3-26 2243076-67-5 98%
ZXH-3-26
ZXH-3-26 is a selective degrader of the PROTAC BRD4 (DC50/5h: ~ 5 nM).
T13977 (R)-UT-155 2031161-54-1 98%
(R)-UT-155
(R)-UT-155 is a selective androgen receptor degrader (SARD) ligand.
T72096 Eleven-Nineteen-Leukemia Protein IN-1 2894121-68-5 98%
Eleven-Nineteen-Leukemia Protein IN-1
Eleven-Nineteen-Leukemia Protein IN-1 is a potent inhibitor of the ENL YEATS domain, exhibiting an IC50 of 14.5 nM. It binds to the ENL protein, consequently inc...
T72097 Eleven-Nineteen-Leukemia Protein IN-2 2894121-78-7 98%
Eleven-Nineteen-Leukemia Protein IN-2
Eleven-Nineteen-Leukemia Protein IN-2 (compound 23), an ENL inhibitor, exhibits an IC50 of 10.7 nM and is utilized for leukemia research [1].
T72098 Eleven-Nineteen-Leukemia Protein IN-3 2894121-83-4 98%
Eleven-Nineteen-Leukemia Protein IN-3
Eleven-Nineteen-Leukemia Protein IN-3, an orally active ENL YEATS domain inhibitor, exhibits potent activity with an IC50 of 15.4 nM. It downregulates MYC expres...
T72722 Physachenolide C 791117-61-8 98%
Physachenolide C
Physachenolide C, a selective BET inhibitor, induces apoptosis and arrests the cell cycle at the G0-G1 phase, exhibiting antitumor activity [1].
BRD9 Degrader-1
T82821
BRD9 Degrader-1 functions as a BRD9 degrader, demonstrating micromolar binding affinity towards BRD9 and nanomolar affinity for the ternary complex involving BRD...
BET-IN-2
T10520
BET-IN-2 is a BET inhibitor (IC50: 52 nM for BRD4-BD1).
PROTAC BET Degrader-1
T13849
PROTAC BET Degrader-1 is a potent degrader of BET based on PROTAC.
BAZ2-ICR
T14512
BAZ2-ICR is an epigenetic chemical probe and it also is a potent, selective, cell active and orally active BAZ2A/B bromodomains inhibitor with IC50s of 130 nM an...
IACS-9571
T11597
IACS-9571 is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
GSK8814
T15443
GSK8814 is a selective and ATAD2/2B bromodomain chemical probe and inhibitor (binding constant pKd=8.1 and a pKi=8.9 in BROMOscan). GSK8814 displays 500-fold sel...
GNE-049
T15397
GNE-049 is a highly potent and selective inhibitor of CBP (IC50: 1.1 nM in TR-FRET assay). GNE-049 also inhibits BRET and BRD4(1) (IC50s: 12 nM and 4200 nM, resp...
ZL0454
T17294
ZL0454 is an effective and selective Bromodomain-containing protein 4 inhibitors (IC50: 49 and 32 nM for BD1 and BD2).
PROTAC BRD4 Degrader-3
T13835
PROTAC BRD4 Degrader-3 is an efficacious degrader of PROTAC BRD4.
MZP-54
T13785
MZP-54 is a selective degrader of BRD3/4 based on PROTAC technology(Kd of 4 nM for Brd4BD2)
PROTAC BRD9 Degrader-1
T12560
PROTAC BRD9 Degrader-1 is a lead PROTAC BRD9 chemical degrader with IC50 of 13.5 nM.
FKBP12 PROTAC dTAG-13
T11291
FKBP12 PROTAC dTAG-13 (dTAG-13) is a degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 (dTAG-13) al...
PROTAC BET degrader-3
T13850
PROTAC BET Degrader-3 is a potent degrader OF BET based on PROTAC.
GNE-207
T15399
GNE-207 is a selective and orally bioavailable inhibitor of the bromodomain of CBP (IC50: 1 nM). It has a selective index of >2500-fold against BRD4 (1). GNE-207...
ZXH-3-26
T17297
ZXH-3-26 is a selective degrader of the PROTAC BRD4 (DC50/5h: ~ 5 nM).
(R)-UT-155
T13977
(R)-UT-155 is a selective androgen receptor degrader (SARD) ligand.
Eleven-Nineteen-Leukemia Protein IN-1
T72096
Eleven-Nineteen-Leukemia Protein IN-1 is a potent inhibitor of the ENL YEATS domain, exhibiting an IC50 of 14.5 nM. It binds to the ENL protein, consequently inc...
Eleven-Nineteen-Leukemia Protein IN-2
T72097
Eleven-Nineteen-Leukemia Protein IN-2 (compound 23), an ENL inhibitor, exhibits an IC50 of 10.7 nM and is utilized for leukemia research [1].
Eleven-Nineteen-Leukemia Protein IN-3
T72098
Eleven-Nineteen-Leukemia Protein IN-3, an orally active ENL YEATS domain inhibitor, exhibits potent activity with an IC50 of 15.4 nM. It downregulates MYC expres...
Physachenolide C
T72722
Physachenolide C, a selective BET inhibitor, induces apoptosis and arrests the cell cycle at the G0-G1 phase, exhibiting antitumor activity [1].
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TargetMol