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产品数：86101
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T7703PK11007PK11007,inhibit,MDM-2/p53,Reactive Oxygen Species,Inhibitor,PK 11007,PK-11007
PK11007 is an anti-p53 drug.
价 格：￥电议型 号：T7703产 地：中国大陆
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T8782MitoBloCK-11?(MB-11)MitoBloCK11?(MB11),MitoBloCK 11?(MB 11)
MitoBloCK-11 (MB-11) is a s mall molecule inhibitor of mitochondrial protein import possibly acts through transport protein Seo1, but not Tom70 or Tom20; inhibits precursor proteins that contain hydrophobic segments, confers growth in media lacking uracil in a specific manner and affects zebrafish development.
价 格：￥电议型 号：T8782产 地：中国大陆
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T4459PK11000
PK11000 is a p53 targeting compound, has anti-tumor activities through activation of unstable p53.
价 格：￥电议型 号：T4459产 地：中国大陆
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T3153SerabelisibINK1117；MLN1117；TAK-117
MLN1117 (INK1117) is a p110α/β/γ/δ inhibitor (IC50: 15/4.5/1.9/13.39 μM).
价 格：￥电议型 号：T3153产 地：中国大陆
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T28972Tiaramide hydrochlorideFK 1160；FK-1160；FK1160；NTA-194；tiaramide
Tiaramide hydrochloride is an anti-inflammatory drug that inhibits the action of mediators released from mast cells and has direct smooth muscle relaxant properties.
价 格：￥电议型 号：T28972产 地：中国大陆
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T2125Trametinib曲美替尼；JTP-74057；GSK1120212
Trametinib is an ATP-noncompetitive inhibitor of MEK 1/2 (IC50s: 0.7/0.9 nM). It shows low inhibition for more than 180 kinases, including B-Raf, c-Raf, and MEK5.
价 格：￥电议型 号：T2125产 地：中国大陆
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T1988DuvelisibINK1197；IPI-145；度维利塞
Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：中国大陆
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T11129Duvelisib (R enantiomer)INK1197 R enantiomer；Duvelisib R enantiomer；IPI-145 R enantiomer
Duvelisib R enantiomer is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
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T11129Duvelisib R enantiomerDuvelisib R enantiomer,IPI-145 R enantiomer,INK1197 R enantiomer
Duvelisib R enantiomer is an enantiomer with low activity of Duvelisib and is an inhibitor of PI3K.
价 格：￥电议型 号：T11129产 地：美洲
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T13931TLK117TLK117,TER117,
TLK117 selective inhibits Glutathione S-transferase P1–1 (GSTP1-1)(Ki of 0.4 μM for GSTP).
价 格：￥电议型 号：T13931产 地：美洲
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T19018K114K114
K114 binds tightly to amyloid fibrils (EC50: 20-30 nM). K114 is an efficient detector of semen-derived enhancer of virus infection (SEVI).
价 格：￥电议型 号：T19018产 地：美洲
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T1988DuvelisibDuvelisib,INK1197,IPI-145
Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：美洲
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T2125TrametinibTrametinib,JTP-74057,GSK1120212
Trametinib is an ATP-noncompetitive inhibitor of MEK 1/2 (IC50s: 0.7/0.9 nM). It shows low inhibition for more than 180 kinases, including B-Raf, c-Raf, and MEK5.
价 格：￥电议型 号：T2125产 地：美洲
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T8424TLK117；化合物 T8424TER117；TER117
TLK117 selective inhibits Glutathione S-transferase P1–1 (GSTP1-1)(Ki of 0.4 μM for GSTP).
价 格：￥电议型 号：T8424产 地：中国大陆
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T8346311(α)-Hydroxynepasaikosaponin k；化合物 11(α)-Hydroxynepasaikosaponin k11(α)-Hydroxynepasaikosaponin k
11(α)-Hydroxynepasaikosaponin K (HOSSc) is a saikosaponin derived from Bupleurum scorzonerifolium Willd [1].
价 格：￥电议型 号：T83463产 地：中国大陆
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T80385K11；化合物 K11K11
K11, an antimicrobial peptide, demonstrates activity against MDR/XDR K. pneumoniae isolates (MIC: 8-512 μg/mL) and inhibits bacterial biofilm formation. It also acts synergistically with various antibiotics (Chloramphenicol, Meropenem, Rifampicin, etc.) to combat drug-resistant K. pneumoniae and exhibits high thermal and wide pH stability [1].
价 格：￥电议型 号：T80385产 地：中国大陆
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T7392Revefenacin；化合物RevefenacinTD-4208|||GSK1160724；TD-4208|||GSK1160724
Revefenacin (TD-4208) is a mAChR antagonist has a high affinity on M3 receptor( Ki : 0.18 nM),and potentially useful for the treatment of respiratory disease.
价 格：￥电议型 号：T7392产 地：中国大陆
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T71654APcK110；化合物 APcK110APcK110
APcK110 is a novel Kit inhibitor . APcK110 inhibits proliferation of the mastocytosis cell line HMC1.2 and the SCF-responsive cell line OCI/AML3 in a dose-dependent manner . APcK110 is a more potent inhibitor of OCI/AML3 proliferation than the clinically used Kit inhibitors imatinib and dasatinib and at least as potent as cytarabine. APcK110 inhibits the phosphorylation of Kit, Stat3, Stat5, and Akt in a dose-dependent fashion, showing activity of APcK110 on Kit and its downstream signaling path
价 格：￥电议型 号：T71654产 地：中国大陆
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T4459PK11000；化合物PK11000PK11000
PK11000 is a p53 targeting compound, has anti-tumor activities through activation of unstable p53.
价 格：￥电议型 号：T4459产 地：中国大陆
