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产品数：86101
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T4490PF-01247324PF 01247324；PF01247324
PF-01247324 is a selective and orally bioavailable Nav1.8 channel blocker (IC50: 196 nM).
价 格：￥电议型 号：T4490产 地：中国大陆
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T4478CID 16020046C390-0219
CID16020046 is a selective GPR55 antagonist, inhibiting GPR55 constitutive activity with IC50 of 0.15 μM in yeast.
价 格：￥电议型 号：T4478产 地：中国大陆
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T4477Domatinostat tosylate4SC-202 tosylate；4SC-202
4SC-202 is a selective inhibitor of class I HDAC for HDAC1/2/3 (IC50: 1.20/1.12/0.57 μM). It also displays inhibitory activity against Lysine-specific demethylase 1 (LSD1).
价 格：￥电议型 号：T4477产 地：中国大陆
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T4475JNJ-632
JNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator.
价 格：￥电议型 号：T4475产 地：中国大陆
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T4474Asunaprevir阿那匹韦；BMS-650032
Asunaprevir is an effective hepatitis C virus (HCV) NS3 protease inhibitor.
价 格：￥电议型 号：T4474产 地：中国大陆
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T4473IbiglustatSAR402671；Venglustat；GZ402671
Ibiglustat is a potent and selective Glucosylceramide synthase inhibitor and ceramide glucosyltransferase inhibitor. Ibiglustat blocks the formation of glucosylceramide (GL-1), a key intermediate in the synthesis of GL-3. Ibiglustat is potentially useful
价 格：￥电议型 号：T4473产 地：中国大陆
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T4472NMS-P118
NMS-P118 is a potent, selective and orally available Inhibitor of PARP-1 for cancer therapy.
价 格：￥电议型 号：T4472产 地：中国大陆
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T4471E7449UNII-9X5A2QIA7C
E7449 is a potent PARP1 and PARP2 inhibitor and also inhibits TNKS1 and TNKS2, with IC50s of 2.0, 1.0, ～50 and ～50 nM for PARP1, PARP2, TNKS1 and TNKS2, respectively, using 32P-NAD+ as substrate.
价 格：￥电议型 号：T4471产 地：中国大陆
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T4470Pyridostatin TFA
Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay, which targets a series of proto-oncogenes including c-kit, K-ras and Bcl-2.
价 格：￥电议型 号：T4470产 地：中国大陆
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T4463Rucaparib瑞卡帕布；AG014699；PF-01367338；AG-14447
Rucaparib is an inhibitor of PARP with Ki of 1.4 nM for PARP1 in a cell-free assay, and also shows binding affinity to eight other PARP.
价 格：￥电议型 号：T4463产 地：中国大陆
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T4387evobrutinibM2951；MSC2364447C
Evobrutinib, also known as M-2951 and MSC-2364447C, is a highly selective inhibitor of the Bruton´s tyrosine kinase (BTK), which is important in the development and functioning of various immune cells including B -lymphocytes and macrophages. PreClinical
价 格：￥电议型 号：T4387产 地：中国大陆
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T4347ML355
ML355, a specific, effective 12-Lipoxygenase(12-LOX) inhibitors(IC50=0.34 μM), possess favorable ADME properties.
价 格：￥电议型 号：T4347产 地：中国大陆
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T4338USP7/USP47 inhibitorUSP7/47 inhibitor-1
USP7/USP47 inhibitor is a selective ubiquitin-specific protease 7/47 (USP7/USP47) inhibitor, with EC50s of 0.42 μM and 1.0 μM, respectively.
价 格：￥电议型 号：T4338产 地：中国大陆
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T4311HAMNONSC111847
HAMNO is a protein interaction inhibitor of replication protein A (RPA).
价 格：￥电议型 号：T4311产 地：中国大陆
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T4298JNJ-47965567JNJ-479655
JNJ-47965567 is a selective antagonist of the purinergic receptor P2X subtype 7 (P2X7), a ligand-gated ion channel(with pKis of 7.9 and 8.7 for human and rat P2X7, respectively).
价 格：￥电议型 号：T4298产 地：中国大陆
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T4267Tulathromycin A托拉菌素 A；Tulathromycin；Draxxin；CP 472295
Tulathromycin A is a macrolide antibiotic.
价 格：￥电议型 号：T4267产 地：中国大陆
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T4247I-CBP112 hydrochloride
I-CBP112 is a selective inhibitor of the bromodomain-containing transcription factors. I-CBP112 (1 mM) has little activity against other bromodomains. I-CBP112 targets the CBP/p300 bromodomains. I-CBP112 significantly reduced the leukemia-initiating poten
价 格：￥电议型 号：T4247产 地：中国大陆
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T4210SAR-20347SAR20347；SAR 20347
SAR-20347 is an inhibitor of TYK2, JAK1/2/3 (IC50: 0.6/23/26/41 nM).
价 格：￥电议型 号：T4210产 地：中国大陆
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T41247Thioperamide maleateMR-12842 maleate
Thioperamide maleate is an effective and selective antagonist of H3 receptor (Ki = 4.3 nM) for inhibition of [3H]histamine synthesis (Ki = 31 nM).
价 格：￥电议型 号：T41247产 地：中国大陆
