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T11332FUBP1–IN-1FUBP1–IN-1
FUBP1 - in-1, with an IC50 value of 11.0 M, is an effective FUSE binding protein 1 (FUBP1) inhibitor that can interfere with the binding of FUBP1 to its SINGLE-strand target DNA FUSE sequence.
价 格：￥电议型 号：T11332产 地：美洲
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T12366PARP14 inhibitor H10PARP14 inhibitor H10
PARP14 inhibitor H10 is a selective inhibitor against PARP14 with IC50 of 490 nM
价 格：￥电议型 号：T12366产 地：美洲
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T12579PTP1B-IN-9PTP1B-IN-9
PTP1B-IN-9 is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.
价 格：￥电议型 号：T12579产 地：美洲
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T13252(S)-Rasagiline(S)-Rasagiline,TVP1022,S-PAI
(S)-Rasagiline is rasagiline S-isomer,and is an agent of anti-Parkinson .
价 格：￥电议型 号：T13252产 地：美洲
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T140222OH-BNPP12OH-BNPP1
2OH-BNPP1 is an inhibitor of BUB1 kinase. Which is a Ser/Thr kinase. It is used for the treatment of cancer.
价 格：￥电议型 号：T14022产 地：美洲
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T14297AP1867AP1867
AP1867 is a FKBP12F36V-directed ligand. Which is Synthesized.
价 格：￥电议型 号：T14297产 地：美洲
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T14298RimiducidRimiducid,AP1903,
Rimiducid (AP1903) is a dimerizer agent that acts by cross-linking the FKBP domains. Rimiducid (AP1903) dimerizes the Caspase 9 suicide switch. And it rapidly induces apoptosis.
价 格：￥电议型 号：T14298产 地：美洲
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T16790RotigaptideRotigaptide,ZP123,
Rotigaptide is a novel and specific modulator of Cx43 and is a potent AAP. Rotigaptide prevents the uncoupling of Cx43-mediated gap junction communication and normalizes cell-to-cell communication during acute metabolic stress.
价 格：￥电议型 号：T16790产 地：美洲
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T16833S1P1 Agonist IIIS1P1 Agonist III
S1P1 Agonist III is an effective and orally active S1P1 agonist (EC50: 18 nM).
价 格：￥电议型 号：T16833产 地：美洲
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T1759OTSSP167OTSSP167,MELK inhibitor,OTS167
MELK Inhibitor OTS167 is an orally available inhibitor of maternal embryonic leucine zipper kinase (MELK) with potential antineoplastic activity.
价 格：￥电议型 号：T1759产 地：美洲
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T1932B-AP15B-AP15,NSC 687852,
B-AP15(NSC687852) is a selective inhibitor of the deubiquitinating enzymes Usp14 and UCHL5 of the 26S proteasome. It blocks the deubiquitinating activity of the 26S proteasome.
价 格：￥电议型 号：T1932产 地：美洲
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T1985WHI-P154WHI-P154,Jak3 inhibitor ii,
WHI-P154 is a potent JAK3 inhibitor.
价 格：￥电议型 号：T1985产 地：美洲
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T2032WHI-P180WHI-P180,Janex 3,
WHI-P180 is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respectively.
价 格：￥电议型 号：T2032产 地：美洲
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T2045WHI-P131WHI-P131,Jak3 inhibitor I,JANEX-1
Janex-1 is a cell-permeable, reversible, effective, ATP-competitive, and selective inhibitor of JAK3 (IC50: 78 μM); little inhibitory against JAK1/2, or Zap/Syk or SRC tyrosine kinases.
价 格：￥电议型 号：T2045产 地：美洲
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T21531 nM-PP11 nM-PP1,PP1 Analog II,
1NM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors.
价 格：￥电议型 号：T2153产 地：美洲
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T2385IpragliflozinIpragliflozin,ASP1941,
Ipragliflozin is under investigation in Type 2 Diabetes and Diabetes Mellitus, Type 2.
价 格：￥电议型 号：T2385产 地：美洲
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T2415PP121PP121
PP-121 is a multi-targeted inhibitor of PDGFR (IC50: 2 nM), Hck (IC50: 8 nM), mTOR (IC50: 10 nM), VEGFR2(IC50: 12 nM), Src (IC50: 14 nM) and Abl (IC50: 18 nM) , also inhibits DNA-PK (IC50: 60 nM).
价 格：￥电议型 号：T2415产 地：美洲
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T2429GZD824 DimesylateGZD824 Dimesylate,HQP1351,
GZD824 Dimesylate is a novel orally bioavailable Bcr-Abl inhibitor for Bcr-Abl(WT) and Bcr-Abl(T315I).
价 格：￥电议型 号：T2429产 地：美洲
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T4587MirificinMirificin,Puerarin Apioside,BCP10902
Puerarin has been investigated for the treatment of Alcohol Abuse.
价 格：￥电议型 号：T4587产 地：美洲
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T6196PP1PP1,EI 275,AGL 1872
PP1, a specific and effective Src inhibitor, is with IC50 for Lck/Fyn is 5 nM/ 6 nM, respectively.
价 格：￥电议型 号：T6196产 地：美洲
