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T8517Belinostat；贝利司他PX105684|||PXD101|||PXD-101；PX105684|||PXD101|||贝利司他|||PXD-101
Belinostat (PXD101) is an inhibitor of hydroxamic acid-type histone deacetylase (HDAC, IC50 of 27 nM in HeLa cell extracts),and with antineoplastic activity.
价 格：￥电议型 号：T8517产 地：中国大陆
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T8401Efonidipine hydrochloride monoethanolate；盐酸依福地平一乙醇盐NZ-105 hydrochloride monoethanolate；NZ-105 hydroc
Efonidipine hydrochloride monoethanolate (NZ-105 hydrochloride monoethanolate) is a Ca(2+)-channel Blocker, Enhances the Production of Dehydroepiandrosterone Sulfate in NCI-H295R Human Adrenocortical Carcinoma Cells
价 格：￥电议型 号：T8401产 地：中国大陆
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T8380Bendamustine；宾达氮芥SDX105；SDX105|||宾达氮芥
Bendamustine (SDX105) for the treatment of Non-Hodgkin Lymphomas and Chronic Lymphocytic Leukemia
价 格：￥电议型 号：T8380产 地：中国大陆
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T83105Antennapedia Peptide FAM-labeled；化合物 Antennapedia Peptide FAM-labeledAntennapedia Peptide FAM-labele
Antennapedia Peptide FAM-labeled, a fluorophore-tagged peptide, functions as a molecular probe in cancer research [1].
价 格：￥电议型 号：T83105产 地：中国大陆
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T83011Antitumor agent-105；化合物 Antitumor agent-105Antitumor agent-105
Antitumor Agent-105 (Compound 37) exhibits antitumor activity, demonstrating inhibition of A549, H1299, H460, HCT116, and MDA-MB-231 cells with respective IC50 values of 6.7, 8.3, 4.3, 4.4, and 6.7 μM [1].
价 格：￥电议型 号：T83011产 地：中国大陆
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T82900Bemfivastatin hemicalcium；化合物 Bemfivastatin hemicalciumPPD 10558 hemicalcium；PPD 10558 hemicalcium
Bemfivastatin hemicalcium (PPD 10558), an orally active HMG-CoA reductase inhibitor, serves as a lipid-lowering agent. It amplifies liver extract activity and exhibits no-observed adverse effect levels (NOAEL) at dosages of ≥320 mg/kg/d for rat developmental toxicity, ≥12.5 mg/kg/d for rabbit maternal toxicity, and ≥25 mg/kg/d for rabbit developmental toxicity. This compound is utilized in research concerning hypercholesterolemic myalgia in patients intolerant to statins.
价 格：￥电议型 号：T82900产 地：中国大陆
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T82105ICMT-IN-38；化合物 ICMT-IN-38ICMT-IN-38
ICMT-IN-38 (Compound 42) is an ICMT inhibitor, demonstrating an IC50 value of 0.049 μM [1].
价 格：￥电议型 号：T82105产 地：中国大陆
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T81747MS6105；化合物 MS6105MS6105
MS6105 is a chimeric LDH protein hydrolysis-targeted PROTAC that degrades LDHA and LDHB efficiently, with its activity contingent on both time and the ubiquitin-proteasome system, exhibiting anticancer properties [1]. Additionally, as a click chemistry reagent possessing an Alkyne group, MS6105 can partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with Azide-bearing molecules.
价 格：￥电议型 号：T81747产 地：中国大陆
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T81105SREBP/SCAP-IN-1；化合物 SREBP/SCAP-IN-1SREBP/SCAP-IN-1
SREBP/SCAP-IN-1 (compound 10b) serves as a selective inhibitor of SREBP/SCAP [1].
价 格：￥电议型 号：T81105产 地：中国大陆
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T81059SWELYYPLRANL-NH2；化合物 SWELYYPLRANL-NH2SWELYYPLRANL-NH2
SWELYYPLRANL-NH2 is a dual antagonist of E-cadherin and N-cadherin, effectively inhibiting the binding of phage clones to both E-cad/Fc and N-cad/Fc chimeric proteins with IC50 values of 0.7 μM and 0.09 μM, respectively. This compound also impedes cell aggregation and has potential applications in enhancing drug delivery by increasing epithelial and endothelial permeability barriers [1].
价 格：￥电议型 号：T81059产 地：中国大陆
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T81058SWELYYPLRANL-NH2 TFA；化合物 SWELYYPLRANL-NH2 TFASWELYYPLRANL-NH2 TFA
SWELYYPLRANL-NH2 TFA acts as an antagonist to both E-cadherin and N-cadherin, with inhibitory effects on phage clone binding to E- or N-cad/Fc chimeric proteins, exhibiting IC50 values of 0.7 μM and 0.09 μM, respectively. Additionally, it disrupts cell aggregation and is utilized to enhance drug delivery by increasing the permeability of epithelial and endothelial barriers [1].
价 格：￥电议型 号：T81058产 地：中国大陆
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T81057Swertiaside；化合物 SwertiasideSwertiaside
Swertiaside, a natural product isolated from Swertia mussotii Franch [1], is a chemical compound.
价 格：￥电议型 号：T81057产 地：中国大陆
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T81056SWTX-143；化合物 SWTX-143SWTX-143
SWTX-143, a novel covalent inhibitor, specifically and irreversibly binds to the palmitoylation pocket of all four TEAD isoforms, inhibiting the transcriptional activity of the YAP/TAZ-TEAD complex and demonstrating antitumor activity [1].
价 格：￥电议型 号：T81056产 地：中国大陆
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T81055Szechenyin A；化合物 Szechenyin ASzechenyin A
Szechenyin A, a constituent of the Tibetan medicinal plant Gentianae Szechenyii Spray, exhibits various pharmacological properties.
价 格：￥电议型 号：T81055产 地：中国大陆
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T81054T-1-MCPAB；化合物 T-1-MCPABT-1-MCPAB
T-1-MCPAB, a VEGFR-2 inhibitor with an IC50 of 0.135 ?M, effectively suppresses MCF7 cell migration and has applications in cancer research [1].
价 格：￥电议型 号：T81054产 地：中国大陆
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T81053T3SS-IN-3；化合物 T3SS-IN-3T3SS-IN-3
T3SS-IN-3 (compound F-24) serves as an inhibitor specific to the type III secretion system (T3SS), significantly reducing the transcription of the hrpY gene while not impeding bacterial growth [1].
价 格：￥电议型 号：T81053产 地：中国大陆
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T81052T988C；化合物 T988C(+)-T988C；(+)-T988C
T988C, a heptacyclic epidithiodioxopiperazine (ETP) natural product, exhibits potent cytotoxicity against cultured P388 leukemia cells [1].
价 格：￥电议型 号：T81052产 地：中国大陆
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T81051Talaroenamine F；化合物 Talaroenamine FTalaroenamine F
Talaroenamine F exhibits antimicrobial activity against Bacillus cereus, demonstrating a minimum inhibitory concentration (MIC) of 0.85 μg/mL.
价 格：￥电议型 号：T81051产 地：中国大陆
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T81050Talizumab；化合物 TalizumabTNX 901|||Anti-Human IgE Fc Recombinant Antibody；TNX 901|||Anti-Human IgE Fc
Talizumab (TNX 901), a humanized IgG1 monoclonal antibody, targets IgE [1].
价 格：￥电议型 号：T81050产 地：中国大陆
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T8105Indole-3-carboxaldehyde；3-吲哚甲醛3-Formylindole；3-Formylindole|||3-吲哚甲醛
1H-Indole-3-carboxaldehyde (3-Formylindole), also known as 3-formylindole or 3-indolealdehyde, belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 1H-Indole-3-carboxaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 1H-Indole-3-carboxaldehyde has been detected, but not quantified in, several different f
价 格：￥电议型 号：T8105产 地：中国大陆
