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T71742SMases D inhibitor-1；化合物 SMases D inhibitor-1SMases D inhibitor-1
SMases D inhibitor-1 is a novel inhibitor of loxosceles sphingomyelinases d (smases d)
价 格：￥电议型 号：T71742产 地：中国大陆
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T71661HIF-1α inhibitor-1；化合物 HIF-1α inhibitor-1HIF-1α inhibitor-1
HIF-1α inhibitor-1 is a HIF-1 alpha inhibitor.
价 格：￥电议型 号：T71661产 地：中国大陆
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T68594NFAT:AP-1 inhibitor-10；化合物 NFAT:AP-1 inhibitor-10NFAT:AP-1 inhibitor-10
NFAT:AP-1 inhibitor-10 is a novel inhibitor of the NFAT:AP-1:DNA interaction on the ARRE-2 element, binding to DNA in a sequence-selective manner and inhibiting the transcription of the Il2 gene and several other cyclosporin A-sensitive cytokine genes important for the effector immune response.
价 格：￥电议型 号：T68594产 地：中国大陆
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T67928NDH-1 inhibitor-1；NDH-1抑制剂-1NDH-1 inhibitor-1
NDH-1 inhibitor-1 is an effective NDH-1 inhibitor, which can inhibit bovine SMP (mitochondrial granules), potato SMP and Escherichia coli, with pI50 values of <4, 5.40, 6.15 ?M, respectively.
价 格：￥电议型 号：T67928产 地：中国大陆
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T67755Protein kinase G inhibitor-1；化合物 Protein kinase G inhibitor-1Protein kinase G inhibitor-1
Protein kinase G inhibitor-1 is a potent Protein kinase G inhibitor, IC50= 0.9 uM.
价 格：￥电议型 号：T67755产 地：中国大陆
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T6583MG-101；钙蛋白酶抑制剂IALLN|||Ac-LLnL-CHO|||Calpain inhibitor I|||Calpain inhibitor-1|||MG101；ALLN|||Ac-LLnL
MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
价 格：￥电议型 号：T6583产 地：中国大陆
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T64291sEH inhibitor-1；化合物 sEH inhibitor-1sEH inhibitor-1
sEH inhibitor-1 (compound TCPU) is a potent, orally active inhibitor of soluble epoxide hydrolase (sEH) with IC50 values of 0.4 and 5.3 nM for human and murine she, respectively.
价 格：￥电议型 号：T64291产 地：中国大陆
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T64131HIV-1 inhibitor-17；化合物 HIV-1 inhibitor-17HIV-1 inhibitor-17
HIV-1 inhibitor-18 is a potent inhibitor of the HIV-1 capsid and is able to act on the HIV-1 NL4-3 strain (EC50: 2.57 μM). HIV-1 inhibitor-18 exhibits some cytotoxicity with an MT-4CC50 value of >8.55.
价 格：￥电议型 号：T64131产 地：中国大陆
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T6409ALK kinase inhibitor-1；化合物SAR348830SAR348830；SAR348830
SAR348830 is an ALK inhibitor, targeting anaplastic lymphoma kinase.
价 格：￥电议型 号：T6409产 地：中国大陆
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T63963HIV-1 inhibitor-14；化合物 HIV-1 inhibitor-14HIV-1 inhibitor-14
HIV-1 inhibitor-14 is a potent, broad-spectrum inhibitor of HIV-1 non-nucleoside reverse transcriptase (RT) (IC50=0.14 μM for HIV-1 RT). HIV-1 inhibitor-14 inhibits both wild-type and drug-resistant HIV-1 strains (EC50: 5.79-28.3 nM).
价 格：￥电议型 号：T63963产 地：中国大陆
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T63853Aurora kinase inhibitor-10；化合物 Aurora kinase inhibitor-10Aurora kinase inhibitor-10
Aurora kinase inhibitor-10 is an orally active Aurora B inhibitor (IC50: 8 nM) that exhibits antitumour effects.
价 格：￥电议型 号：T63853产 地：中国大陆
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T63687HIV-1 inhibitor-18；化合物 HIV-1 inhibitor-18HIV-1 inhibitor-18
HIV-1 inhibitor-18 is a potent inhibitor of the HIV-1 capsid that acts against the HIV-1 NL4-3 strain (EC50: 5.14 μM) and exhibits some cytotoxicity (MT-4CC50>9.51).
价 格：￥电议型 号：T63687产 地：中国大陆
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T63677HIV-1 inhibitor-13；化合物 HIV-1 inhibitor-13HIV-1 inhibitor-13
HIV-1 inhibitor-13 is an orally active HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI) with an IC50 value of 0.14 μM against HIV-1 RT. HIV-1 inhibitor-13 is active against HIV-1 resistant strains (EC50: 2.85-18.0 nM).
价 格：￥电议型 号：T63677产 地：中国大陆
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T63363HIV-1 inhibitor-19；化合物 HIV-1 inhibitor-19HIV-1 inhibitor-19
HIV-1 inhibitor-19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase (NNRTI) that acts on L100I, K103N and V106A/F227L mutant strains with EC50s of 7.3 nM, 9.2 nM and 21.0 nM, respectively.
价 格：￥电议型 号：T63363产 地：中国大陆
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T63352BRD4 Inhibitor-18；化合物 BRD4 Inhibitor-18BRD4 Inhibitor-18
BRD4 Inhibitor-18 is a potent BRD4 inhibitor (IC50: 110 nM) with a hydrophobic acetylcyclopentane side chain. BRD4 Inhibitor-18 significantly reduces the proliferation of MV-4-11 cells with high BRD4 levels, inhibits G0/G1 cycle activity, and promotes apoptosis. The inhibition of G0/G1 cycle activity and apoptosis were also observed.
价 格：￥电议型 号：T63352产 地：中国大陆
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T63302BRD4 Inhibitor-19；化合物 BRD4 Inhibitor-19BRD4 Inhibitor-19
BRD4 inhibitors -19 are BET inhibitors that act on BRD4-BD1 (IC50: 55 nM) and can be used to study multiple myeloma.
价 格：￥电议型 号：T63302产 地：中国大陆
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T63235KRAS inhibitor-14；化合物 KRAS inhibitor-14KRAS inhibitor-14
KRAS inhibitor-14 is a potent inhibitor of KRAS G12C (IC50: 0.249 μM). KRAS inhibitor-14 exhibited p-ERK inhibition in MIA PaCA-2, A549 cells with IC50s of 1.12, >33.3 μM, respectively. KRAS inhibitor-14 has potential to be investigated in pancreatic, colorectal and lung cancers.
价 格：￥电议型 号：T63235产 地：中国大陆
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T63164KRAS inhibitor-13；化合物 KRAS inhibitor-13KRAS inhibitor-13
KRAS inhibitor-13 (compound 5-6) is a potent inhibitor of KRAS G12C (IC50: 0.883 μM). KRAS inhibitor-13 has a p-ERK inhibitory effect in MIA PaCA-2, A549 cells with IC50 values of 5.9 and >100 μM respectively. KRAS inhibitor-13 has potential to be studied in pancreatic, colorectal and lung cancers.
价 格：￥电议型 号：T63164产 地：中国大陆
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T62981KRAS inhibitor-17；化合物 KRAS inhibitor-17KRAS inhibitor-17
KRAS inhibitor-17 (compound 3-9) is a potent inhibitor of KRAS G12C (IC50: 3.37 μM). KRAS inhibitor-17 exhibits p-ERK inhibition with IC50 = 9.25 μM in MIA PaCA-2 cells and >33.3 μM in A549 cells. KRAS inhibitor-17 has the potential to be studied in pancreatic, colorectal and lung cancers.
价 格：￥电议型 号：T62981产 地：中国大陆
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T62784KRAS inhibitor-18；化合物 KRAS inhibitor-18KRAS inhibitor-18
KRAS inhibitor-18 (compound 3-10) is a potent inhibitor of KRAS G12C (IC50: 4.74 μM). KRAS inhibitor-18 exhibited p-ERK inhibition in MIA PaCA-2, A549 cells with IC50s of 66.4, 11.1 μM respectively. KRAS inhibitor-18 has potential for pancreatic, colorectal and lung cancer studies.
价 格：￥电议型 号：T62784产 地：中国大陆
