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T7378BRD9539Histone Methyltransferase,chromatin,PRC2,BRD9539,G9a,senescent,BRD-9539,BRD 9539,inhibit,H3K9
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM
价 格：￥电议型 号：T7378产 地：中国大陆
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T6859I-BRD9cancer,inhibit,Epigenetic Reader Domain,bromodomain-containing protein 7(BRD7),bromodomain and
I-BRD9 is the first selective cellular inhibitor for BRD9 with pIC50 of 7.3.
价 格：￥电议型 号：T6859产 地：中国大陆
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T8342BRD9876Kinesin,microtubule,Inhibitor,BRD9876,BMSC,multiple,myeloma,α4-α6,CD34,tyrosine,ATP,MM1S,G2/M
BRD9876 is a selective inhibitor of MM1S growth.
价 格：￥电议型 号：T8342产 地：中国大陆
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T31221LdBRD9 HCl
dBRD9 HCl is a PROTAC composed of the BRD9 inhibitor BI 7273 conjugated to the cereblon E3 ligase ligand pomalidomide . dBRD9 HCl is a potent and selective degrader of BRD9 (IC50 = 56.6 nM in MOLM-13 cells). dBRD9 HCl does not degrade BRD4 or BRD7 at concentrations up to 5 μM. dBRD9 HCl displays antiproliferative effects in human AML cell lines.
价 格：￥电议型 号：T31221L产 地：中国大陆
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T12560PROTAC BRD9 Degrader-1PROTAC BRD9 Degrader-1
PROTAC BRD9 Degrader-1 is a lead PROTAC BRD9 chemical degrader with IC50 of 13.5 nM.
价 格：￥电议型 号：T12560产 地：美洲
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T8342BRD98766-叔丁基-2,3-二氰基萘6-叔丁基-2,3-二氰基萘
BRD9876 is a selective inhibitor of MM1S growth.
价 格：￥电议型 号：T8342产 地：中国大陆
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T82821BRD9 Degrader-1；化合物 BRD9 Degrader-1BRD9 Degrader-1
BRD9 Degrader-1 functions as a BRD9 degrader, demonstrating micromolar binding affinity towards BRD9 and nanomolar affinity for the ternary complex involving BRD9 and VCB [1].
价 格：￥电议型 号：T82821产 地：中国大陆
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T81385PROTAC BRD9 Degrader-2；化合物 PROTAC BRD9 Degrader-2PROTAC BRD9 Degrader-2
PROTAC BRD9 Degrader-2 is a bifunctional compound designed for the targeted degradation of BRD9 in cancer research applications.
价 格：￥电议型 号：T81385产 地：中国大陆
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T81384PROTAC BRD9 Degrader-3；化合物 PROTAC BRD9 Degrader-3PROTAC BRD9 Degrader-3
PROTAC BRD9 Degrader-3 is a bifunctional degrader targeting BRD9, utilized in cancer research.
价 格：￥电议型 号：T81384产 地：中国大陆
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T81383PROTAC BRD9 Degrader-5；化合物 PROTAC BRD9 Degrader-5PROTAC BRD9 Degrader-5
PROTAC BRD9 Degrader-5 is a proteolysis targeting chimera (PROTAC) designed for the specific degradation of Bromodomain-containing protein 9 (BRD9).
价 格：￥电议型 号：T81383产 地：中国大陆
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T81382PROTAC BRD9 Degrader-7；化合物 PROTAC BRD9 Degrader-7PROTAC BRD9 Degrader-7
PROTAC BRD9 Degrader-7 is a selective and orally active BRD9 degrader with a DC50 of 1.02 nM and demonstrates superior pharmacokinetics, evidenced by a Cmax of 3436.95 ng/mL [1].
价 格：￥电议型 号：T81382产 地：中国大陆
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T77975PROTAC BRD9 Degrader-6；化合物 PROTAC BRD9 Degrader-6PROTAC BRD9 Degrader-6
PROTAC BRD9 Degrader-6, with an IC50 value of 0.13 nM, is a potent degrader of BRD9 suitable for research on BAF complex-related disorders [1].
价 格：￥电议型 号：T77975产 地：中国大陆
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T77936PROTAC BRD9 Degrader-4；化合物 PROTAC BRD9 Degrader-4PROTAC BRD9 Degrader-4
PROTAC BRD9 Degrader-4 is a bifunctional degrader targeting BRD9, designed for cancer research applications.
价 格：￥电议型 号：T77936产 地：中国大陆
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T74256PROTAC BRD9-binding moiety 5；化合物 PROTAC BRD9-binding moiety 5PROTAC BRD9-binding moiety 5
PROTAC BRD9-binding moiety 5, a selective binder of BRD9 with an IC50 value of 4.20 μM, is utilized in PROTAC synthesis and exhibits antiproliferative activity against cancer cells [1].
价 格：￥电议型 号：T74256产 地：中国大陆
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T7378BRD9539；化合物BRD9539BRD9539
BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM
价 格：￥电议型 号：T7378产 地：中国大陆
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T6859I-BRD9；化合物I-BRD9GSK602；GSK602
I-BRD9 (GSK602) is the first selective cellular inhibitor for BRD9 with pIC50 of 7.3.
价 格：￥电议型 号：T6859产 地：中国大陆
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T60603BRD9500；化合物 BRD9500BRD9500
BRD9500 is an orally active inhibitor of phosphodiesterases 3 (PDE3) with IC 50 s of 10 and 27 nM for PDE3A and PDE3B, respectively. BRD9500 is active in an SK-MEL-3 xenograft model of cancer [1].
价 格：￥电议型 号：T60603产 地：中国大陆
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T35480dBRD9-A；dBRD9-AdBRD9-A；dBRD9-A
Potent BRD9 degrader. Selectively binds BRD9 and elicits near complete degradation of BRD9 at nanomolar concentrations. Inhibits growth of synovial sarcoma cells in vitro and tumor progression in a synovial sarcoma xenograft mouse model.
价 格：￥电议型 号：T35480产 地：中国大陆
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T31221LdBRD9 HCl；化合物dBRD9盐酸盐dBRD9 HCl(2170679-45-3 Free base)；dBRD9 HCl(2170679-45-3 Free base)
dBRD9 HCl is a PROTAC composed of the BRD9 inhibitor BI 7273 conjugated to the cereblon E3 ligase ligand pomalidomide . dBRD9 HCl is a potent and selective degrader of BRD9 (IC50 = 56.6 nM in MOLM-13 cells). dBRD9 HCl does not degrade BRD4 or BRD7 at concentrations up to 5 μM. dBRD9 HCl displays antiproliferative effects in human AML cell lines.
价 格：￥电议型 号：T31221L产 地：中国大陆
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T31221dBRD9化合物dBRD9dBRD-9|||dBRD 9
dBRD9 is a PROTAC. dBRD9 is a double-acting molecule, partially containing Bromodomain-containing protein 9 (BRD9), ligand that recruits the cereblon E3 ubiquitin ligase. Ligand that recruits the cereblon E3 ubiquitin ligase. dBRD9 can inhibit the degradation of BRD9 in MOLM-13 cells, and the IC50 is 104 nM.
价 格：￥电议型 号：T31221产 地：中国大陆
