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T11826LCH-7749944GNF-PF-2356
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis. LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.
价 格：￥电议型 号：T11826产 地：中国大陆
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T0373LErlotinib hydrochlorideNSC 718781；OSI-744；Erlotinib HCl；CP-358774；盐酸埃罗替尼
Erlotinib is an EGFR inhibitor (IC50: 2 nM). It is used for the treatment of non-small cell lung cancer.
价 格：￥电议型 号：T0373L产 地：中国大陆
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T0373Erlotinib埃罗替尼；NSC 718781；OSI-744；R1415；CP358774
Erlotinib is an EGFR inhibitor (IC50: 2 nM). It is used for the treatment of non-small cell lung cancer.
价 格：￥电议型 号：T0373产 地：中国大陆
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T0091Alfuzosin hydrochloride盐酸阿夫唑嗪；Alfuzosin HCl；SL 77499-10
Alfuzosin hydrochloride is an α1 adrenergic receptor antagonist. It applies to treat benign prostatic hyperplasia (BPH).
价 格：￥电议型 号：T0091产 地：中国大陆
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T0091Alfuzosin hydrochlorideAlfuzosin hydrochloride,SL 77499-10,Alfuzosin HCl
Alfuzosin hydrochloride is an?α1 adrenergic receptor?antagonist. It applies to treat benign prostatic hyperplasia (BPH).
价 格：￥电议型 号：T0091产 地：美洲
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T0373LErlotinib hydrochlorideErlotinib hydrochloride,NSC 718781,CP-358774
Erlotinib is an EGFR inhibitor (IC50: 2 nM). It is used for the treatment of non-small cell lung cancer.
价 格：￥电议型 号：T0373L产 地：美洲
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T11826LCH-7749944LCH-7749944,GNF-PF-2356,
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis.?LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.?
价 格：￥电议型 号：T11826产 地：美洲
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T12193NCGC00247743NCGC00247743
NCGC00247743 is an inhibitor of histone lysine demethylase KDM4.
价 格：￥电议型 号：T12193产 地：美洲
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T12774RSV-IN-1RSV-IN-1
RSV-IN-1 is an inhibitor of human respiratory syncytical virus (hRSV)(IC50 of 0.11 μM).
价 格：￥电议型 号：T12774产 地：美洲
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T13774ML390ML390
ML390 exerts its potent differentiation effect on multiple leukemia models.
价 格：￥电议型 号：T13774产 地：美洲
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T14774Bragsin1Bragsin1
Bragsin1 is a potent, selective and noncompetitive inhibitor of the ArfGEF BRAG2. Which inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin1 has no effect on the Sec7 domain of human ArfGEFs. Anti-cancer activity[1]. Bragsin1 binds to PH domain
价 格：￥电议型 号：T14774产 地：美洲
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T16774RO-9187RO-9187
RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).
价 格：￥电议型 号：T16774产 地：美洲
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T1774SB 742457SB 742457,GSK-742457,RVT-101
SB742457 is a highly selective 5-HT6 receptor antagonist, used in trials studying the treatment of Alzheimer´s Disease.
价 格：￥电议型 号：T1774产 地：美洲
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T2302CNX-774CNX-774,CNX774,CNX 774
CNX-774 is a highly specific, irreversible, and orally active BTK inhibitor (IC50<1 nM).
价 格：￥电议型 号：T2302产 地：美洲
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T5537IDF-11774IDF-11774
IDF-11774 is a HIF-1 inhibitor.It reduces hif-1α HRE luciferase activity (IC50 = 3.65 μM).
价 格：￥电议型 号：T5537产 地：美洲
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T57747-demethylsuberosin7-demethylsuberosin,Demethylsuberosin,
7-demethylsuberosin is a coumarin compound isolated from Angelica gigas Nakai,and has anti-inflammatory activity,and exhibited inhibitory effects on PGE2 production with the IC50 values of 9.42 μM.
价 格：￥电议型 号：T5774产 地：美洲
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T8776FEMA 4774；化合物FEMA 4774S9632；S9632
FEMA 4774 (S9632) is a positive allosteric modulator of T1R2/T1R3. FEMA4774 shows obvious enhancement of the sweetness of sucrose in sensory evaluation tests
价 格：￥电议型 号：T8776产 地：中国大陆
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T8774MS7972；化合物MS7972MS7972
MS7972 is CREBBP inhibitor that blocks human p53 and CREB binding protein association. MS7972 can almost completely block this BRD interaction at 50 μM
价 格：￥电议型 号：T8774产 地：中国大陆
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T8576P18IN011；化合物P18IN011P18IN011 - CAS 77408-67-4 - Calbiochem；P18IN011 - CAS 77408-67-4 - Calbiochem
P18IN011 (P18IN011 - CAS 77408-67-4 - Calbiochem) is a novel inhibitor of p18(INK4C).
价 格：￥电议型 号：T8576产 地：中国大陆
