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T16841SAR-260301SAR-260301
SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM).
价 格：￥电议型 号：T16841产 地：美洲
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T19301DUPADUPA
DUPA selectively delivers cytotoxic drugs to prostate cancer cells [1][2], belonging to the glutamate class, as a targeted part of drug coupling.
价 格：￥电议型 号：T19301产 地：美洲
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T2301SB202190SB202190,FHPI,
SB 202190 is a selective and cell-permeable inhibitor of p38 MAPK (IC50s: 50/100 nM for p38α/p38β).
价 格：￥电议型 号：T2301产 地：美洲
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T2369RociletinibRociletinib,AVL-301,CNX-419
Rociletinib is an orally available small molecule, irreversible inhibitor of epidermal growth factor receptor (EGFR) with potential antineoplastic activity.
价 格：￥电议型 号：T2369产 地：美洲
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T2441TAS-301TAS-301,TAS301,TAS 301
TAS-301, an inhibitor of smooth muscle cell migration and proliferation, inhibits intimal thickening after balloon injury to rat carotid arteries.
价 格：￥电议型 号：T2441产 地：美洲
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T2466Osu-03012Osu-03012,Osu03012,Osu 03012
AR-12 is an orally bioavailable, small-molecule, celecoxib-derived inhibitor of phosphoinositide-dependent kinase-1 (PDK1) with potential antineoplastic activity.
价 格：￥电议型 号：T2466产 地：美洲
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T5301Crotonic acidCrotonic acid,alpha-butenoic acid,
Crotonic acid is fatty acid formed by the action of fatty acid synthases from acetyl-CoA and malonyl-CoA precursors. It is involved in the fatty acid biosynthesis. It is also found in water extracts from carrot seeds (Daucus carota L.).
价 格：￥电议型 号：T5301产 地：美洲
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T5394PrulifloxacinPrulifloxacin,NM441,AF 3012
Prulifloxacin is a broad-spectrum fluoroquinolone antibiotic. It Inhibits bacterial DNA synthesis by inhibiting the activity of bacterial DNA topoisomerase II and IV.
价 格：￥电议型 号：T5394产 地：美洲
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T6006RomidepsinRomidepsin,FR 901228,NSC 630176
Romidepsin is an intravenously administered histone deacetylase inhibitor and antineoplastic agent that is approved for use in refractory or relapsed cutaneous and peripheral T cell lymphomas.
价 格：￥电议型 号：T6006产 地：美洲
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T6301TosedostatTosedostat,CHR-2797,
CHR-2797 is an orally bioavailable inhibitor of the M1 family of aminopeptidases with potential antineoplastic activity. CHR-2797 is converted intracellularly into a poorly membrane-permeable active metabolite (CHR-79888) which inhibits the M1 family of a
价 格：￥电议型 号：T6301产 地：美洲
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T84301PT-179；化合物 PT-179PT-179
PT-179 is a novel IMiD derivative, a molecular gel.
价 格：￥电议型 号：T84301产 地：中国大陆
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T8426Encequidar；化合物EncequidarHM30181|||HM30181A；HM30181|||HM30181A
Encequidar (HM30181A) is a potent and selective P-glycoprotein inhibitor.
价 格：￥电议型 号：T8426产 地：中国大陆
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T838944A7C-301-Nurr1 Agonist；化合物 4A7C-301-Nurr1 Agonist4A7C-301-Nuclear Receptor-Related 1；4A7C-301-Nuclea
The compound 4A7C-301-Nurr1 agonist is a specific agonist for the nuclear receptor-related 1 (Nurr1). By binding to the Nurr1 ligand-binding domain with an IC50 value of 48.22 nM, it enhances the transcriptional activity of both Nurr1-LBD and the full-length Nurr1, as demonstrated in reporter assays using SK-N-BE(2)C human neuroblastoma cells, with EC50 values of 6.53 and 50-70 ?M, respectively. Additionally, administration of 4A7C-301-Nurr1 agonist at a dosage of 5 mg/kg per day has been shown
价 格：￥电议型 号：T83894产 地：中国大陆
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T8359Lanreotide acetate；化合物Lanreotide acetateLanreotide acetate (108736-35-2 free base)|||BIM 23014 (acet
Lanreotide acetate (BIM 23014 acetate) is a somatostatin analogue with antineoplastic activity, used for carcinoid syndrome
价 格：￥电议型 号：T8359产 地：中国大陆
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T833284A7C-301；化合物 4A7C-3014A7C-301
4A7C-301, a Nurr1 agonist, exhibits potent neuroprotective effects in vitro and markedly mitigates neuropathological abnormalities while enhancing motor and olfactory functions in male mouse models with AAV2-mediated α-synuclein overexpression. This compound is applicable in Parkinson’s disease research [1].
价 格：￥电议型 号：T83328产 地：中国大陆
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T833015,7-Dimethoxy-2,3-phenanthrenediol；化合物 5,7-Dimethoxy-2,3-phenanthrenediol5,7-Dimethoxy-2,3-phenanthr
5,7-Dimethoxy-2,3-phenanthrenediol exhibits estrogenic activity by promoting the proliferation of MCF-7 cells and enhancing the expression of ERβ within this cell line [1].
价 格：￥电议型 号：T83301产 地：中国大陆
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T83019Antiproliferative agent-38；化合物 Antiproliferative agent-38Antiproliferative agent-38
Antiproliferative Agent-38 (COM 18), a tetracyclic compound, features a reactive ring nitrogen (likely the quinoline moiety) that resists N-alkylation. Despite its classification, it neither exhibits anti-malarial properties nor inhibits cancer cell proliferation [1].
价 格：￥电议型 号：T83019产 地：中国大陆
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T83018Antiproliferative agent-39；化合物 Antiproliferative agent-39Antiproliferative agent-39
Antiproliferative Agent-39 (Compound 12) effectively inhibits the proliferation of various cancer cell lines, including A549, SNU-638, Col2, HT1080, and MCF-7, with respective IC50 values of 11, 25, 14, 11, and 6.3 μM [1].
价 格：￥电议型 号：T83018产 地：中国大陆
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T83017Antiproliferative agent-40；化合物 Antiproliferative agent-40Antiproliferative agent-40
Antiproliferative agent-40 (Compound 9) effectively inhibits the proliferation of HT1080 and MCF-7 cancer cells, displaying IC50 values of 52 μM and 8.2 μM, respectively [1].
价 格：￥电议型 号：T83017产 地：中国大陆
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T83016Antiproliferative agent-41；化合物 Antiproliferative agent-41Antiproliferative agent-41
Antiproliferative Agent-41 (Compound 14), classified as indanorine [1], functions as an antiproliferative compound.
价 格：￥电议型 号：T83016产 地：中国大陆
