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T10773CF53CF-53,CF53
CF53 is a highly potent, selective and orally active inhibitor of BET protein, with a Ki of <1 nM, Kd of 2.2 nM and an IC50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2, BRD3, BRD4, and BRDT BET proteins with high affinities, very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo.
价 格：￥电议型 号：T10773产 地：中国大陆
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T22667CID 5951923Krüppel-like factor,CID-5951923,CID5951923,KLF5,inhibit,cancer,factor,KLF,transcription,I
CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.
价 格：￥电议型 号：T22667产 地：中国大陆
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TN1684Ginsenoside F5Ginsenoside F-5,inhibit,Ginsenoside F5,leukemia,Ginsenoside F 5,Inhibitor,Apoptosis,pr
Ginsenoside F5 is a natural product from Panax ginseng C. A. Mey, remarkably inhibits the growth of HL-60 cells by the apoptosis pathway
价 格：￥电议型 号：TN1684产 地：中国大陆
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T8499eCF506eCF 506,eCF506,Inhibitor,Src,eCF-506,inhibit
eCF506 is a potent and selective inhibitor of SRC (IC50 < 0.5 nM)
价 格：￥电议型 号：T8499产 地：中国大陆
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T8840PF-543 hydrochlorideNrf-2,PF543 hydrochloride,anti-cancer,sphingosine-competitive,S1P,Sphingosine Ki
PF-543 inhibits SphK1 with a K(i) of 3.6 nM, is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform.
价 格：￥电议型 号：T8840产 地：中国大陆
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T60037SR15006growth,inhibit,KLF5,SR 15006,Krüppel-like factor,SR15006,colorectal cancer cells,cycle,Inhibi
SR15006 is Krüppel-like factor 5 (KLF5) inhibitor (IC50 = 41.6 nM).
价 格：￥电议型 号：T60037产 地：中国大陆
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T6097GNF-5837GNF5837；GNF 5837
GNF-5837 is a specific, and orally bioavailable pan-TRK inhibitor for TrkA/TrkB (IC50: 8/12 nM).
价 格：￥电议型 号：T6097产 地：中国大陆
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T5465PF-5274857PF5274857；PF-5274857 freebase；PF 5274857
PF-5274857 is an effective and selective hedgehog signaling pathway inhibitor (IC50: 5.8 nM and a Ki: 4.6 nM). PF-5274857 is a potentially attractive clinical candidate for the treatment of tumor types including brain tumors and brain metastasis driven by
价 格：￥电议型 号：T5465产 地：中国大陆
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T24784SF5SF 5；SF-5
SF5 is an inhibitor of the apoptosis pathway through JNK-p53-caspase apoptotic cascade.
价 格：￥电议型 号：T24784产 地：中国大陆
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T2465PF-562271PF562271；PF 562271
PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).
价 格：￥电议型 号：T2465产 地：中国大陆
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T2262ItanapracedCHF5074；CSP-1103
CHF5074, a γ-secretase modulator, reduces Aβ42/40 secretion (IC50: 3.6/18.4 μM).
价 格：￥电议型 号：T2262产 地：中国大陆
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T20804Bensulfuron-methyl苄嘧磺隆；F 5384；DPX 84；F-5384；F5384
Bensulfuron-methyl is a broad-spectrum herbicide for broadleaf weeds in paddy fields.
价 格：￥电议型 号：T20804产 地：中国大陆
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T1803GNF-5GNF 5；GNF5
GNF-5 is a specific non-ATP competitive inhibitor of Bcr-Abl (IC50: 0.22±0.1 uM, Wild-type Abl). It is an analog of GNF-2 with improved pharmacokinetic properties.
价 格：￥电议型 号：T1803产 地：中国大陆
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T15202EF-5EF5；2-Nitroimidazole
EF-5 is a agent of hypoxia labeling. It is used to identify hypoxia in cells.
价 格：￥电议型 号：T15202产 地：中国大陆
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T1222Trifluoperazine dihydrochlorideUrinox；SKF5019；Trifluoperazine 2HCl；盐酸三氟拉嗪
Trifluoperazine Dihydrochloride is a potent dopamine D2 receptor inhibitor used as an antipsychotic and an antiemetic.
价 格：￥电议型 号：T1222产 地：中国大陆
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T1028MoxonidineBDF5895；莫索尼定；莫索尼啶
Moxonidine is a selective agonist at the imidazoline receptor subtype 1, acting as an antihypertensive drug.
价 格：￥电议型 号：T1028产 地：中国大陆
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T1028MoxonidineMoxonidine,BDF5895,
Moxonidine is a selective agonist at the imidazoline receptor subtype 1， acting as an antihypertensive drug.
价 格：￥电议型 号：T1028产 地：美洲
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T10773CF53CF53
CF53 is a highly potent, selective, and orally active inhibitor of BET protein (Ki: <1 nM, Kd: 2.2 nM, IC50: 2 nM for BRD4 BD1).
价 格：￥电议型 号：T10773产 地：美洲
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T1222Trifluoperazine dihydrochlorideTrifluoperazine dihydrochloride,SKF5019,Urinox
Trifluoperazine Dihydrochloride is a potent dopamine D2 receptor inhibitor used as an antipsychotic and an antiemetic.
价 格：￥电议型 号：T1222产 地：美洲
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T140525-IAF5-IAF,5-Iodoacetamidofluorescein,
5-IAF is a fluoresceine idoacetamide derivate.
价 格：￥电议型 号：T14052产 地：美洲
