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T11888LtaS-IN-1
LtaS-IN-1 is an effective inhibitor of Lipoteichoic acid synthesis in multidrug-resistant (MDR) E. faecium and by altering the cell wall morphology. LtaS-IN-1 is against Enterococcus spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/m
价 格：￥电议型 号：T11888产 地：中国大陆
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T11829LDH-IN-1
LDH-IN-1 is a pyrazole-based human lactate dehydrogenase (LDH) inhibitor(IC50s of 32 and 27 nM for LDHA and LDHB, respectively).
价 格：￥电议型 号：T11829产 地：中国大陆
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T11820LAT1-IN-12-氨基-2-去甲菠烷羧酸；BCH
LAT1-IN-1 (BCH) significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis. is a selective and competitive inhibitor of large neutral amino acid transporter 1 (LAT1).
价 格：￥电议型 号：T11820产 地：中国大陆
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T11634IL-15-IN-1
IL-15-IN-1 is a selective and potent Interleukin 15 (IL-15) inhibitor, inhibiting the proliferation of IL-15-dependent cells (IC50: 0.8 μM).
价 格：￥电议型 号：T11634产 地：中国大陆
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T11630IFN alpha-IFNAR-IN-1 hydrochloride
IFN alpha-IFNAR-IN-1 hydrochloride is an inhibitor of the interaction between IFN-α and IFNAR. IFN alpha-IFNAR-IN-1 hydrochloride inhibits MVA-induced IFN-α responses by BM-pDCs with IC50 of 2-8 μM.
价 格：￥电议型 号：T11630产 地：中国大陆
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T11616IDO-IN-13GS-4361
IDO-IN-13 is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).
价 格：￥电议型 号：T11616产 地：中国大陆
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T11615IDO-IN-12
IDO-IN-12 is an inhibitor of indoleamine 2,3-dioxygenase (IDO).
价 格：￥电议型 号：T11615产 地：中国大陆
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T11580Heme Oxygenase-1-IN-1HO-1-IN-1
HO-1-IN-1 is a heme oxygenase 1 (HO-1) inhibitor (IC50: 250 nM).
价 格：￥电议型 号：T11580产 地：中国大陆
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T11546hDHODH-IN-1
hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.
价 格：￥电议型 号：T11546产 地：中国大陆
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T11538Hck-IN-1
Hck-IN-1 is a selective Nef-dependent Hck inhibitor (IC50s: 2.8 μM and >20 μM for Nef:Hck complex and Hck) with antiretroviral activity. Hck-IN-1 is a direct and wide HIV-1 Nef antagonist with an IC50 of 100-300 nM for wild-type HIV-1 replication.
价 格：￥电议型 号：T11538产 地：中国大陆
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T11505GSTO1-IN-1
GSTO1-IN-1 is a potent glutathione S-transferase omega 1 inhibitor (GSTO1; IC50: 31 nM).
价 格：￥电议型 号：T11505产 地：中国大陆
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T11373GCN2-IN-1A-92
GCN2-IN-1 (A-92) is a potent general control nonderepressible 2 kinase (GCN2) inhibitor with an IC50 of 0.3-3 μM in the cell assay and an IC50 of <0.3 μM in the enzyme assay.
价 格：￥电议型 号：T11373产 地：中国大陆
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T11368GATA4-NKX2-5-IN-1
GATA4-NKX2-5-IN-1 exhibits no activity on the protein kinases involved in the regulation of GATA4 phosphorylation, and it modulates the hypertrophic agonist-induced cardiac gene expression.GATA4-NKX2-5-IN-1 ?dose-dependently inhibits the GATA4–NKX2-5 tran
价 格：￥电议型 号：T11368产 地：中国大陆
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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：中国大陆
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T11267FASN-IN-1TVB-2460
FASN-IN-1 is a fatty acid synthase (FASN) inhibitor.
价 格：￥电议型 号：T11267产 地：中国大陆
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T11224RineterkibERK-IN-1
Rineterkib is an inhibitor of RAF and ERK1/2 activating mutations in the MAPK pathway.
价 格：￥电议型 号：T11224产 地：中国大陆
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T11221ERAP1-IN-1
ERAP1-IN-1 is an endoplasmic reticulum aminopeptidase 1 (ERAP1) inhibitor. ERAP1-IN-1 competitively inhibits ERAP1 activity towards a nonamer peptide representative of physiological substrates.
价 格：￥电议型 号：T11221产 地：中国大陆
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T11110DUB-IN-1
DUB-IN-1, with an IC50 value of 0.24 for USP8, is an active inhibitor of ubiquitin-specific protease (USPs).
价 格：￥电议型 号：T11110产 地：中国大陆
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T11020DHODH-IN-11
DHODH-IN-11 is a leflunomide derivative and weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.
价 格：￥电议型 号：T11020产 地：中国大陆
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