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产品数：86101
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T71118NEP-28；化合物 NEP-28NEP-28
NEP-28 is an AR agonist. NEP28 is a new SARM exhibiting high selectivity for androgen receptor. NEP28 showed tissue-selective effect equivalent to or higher than existing SARMs. In addition, the administration of NEP28 increased the activity of neprilysin, a known Aβ-degrading enzyme.
价 格：￥电议型 号：T71118产 地：中国大陆
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T71117AZD5248；化合物 AZD5248AZD5248
AZD-5248 is a potent, selective, first generation, oral inhibitor of dipeptidyl peptidase 1 (DPP1).
价 格：￥电议型 号：T71117产 地：中国大陆
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T71116MPT0B098；化合物 MPT0B098MPT0B098
MPT0B098 is a potent microtubule inhibitor through binding to the colchicine-binding site of tubulin. MPT0B098 is active against the growth of various human cancer cells, including chemoresistant cells with IC50 values ranging from 70 to 150 nmol/L. MPT0B098 arrests cells in the G2?–M phase and subsequently induces cell apoptosis. In addition, MPT0B098 effectively suppresses VEGF-induced cell migration and capillary-like tube formation of HUVECs. Distinguished from other microtubule inhibitors,
价 格：￥电议型 号：T71116产 地：中国大陆
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T71115Formoterol HCl；化合物 Formoterol HClFormoterol HCl
Formoterol HCl is a long-acting beta-2 adrenergic agonist (LABA).
价 格：￥电议型 号：T71115产 地：中国大陆
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T71114Mivazerol；化合物 MivazerolMivazerol
Mivazerol is an alpha 2-adrenoceptor agonist.
价 格：￥电议型 号：T71114产 地：中国大陆
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T71113Minnelide free acid；化合物 Minnelide free acidMinnelide free acid
Minnelide is an effective therapy against pancreatic cancer. Minnelide Inhibits Androgen Dependent, Castration Resistant Prostate Cancer Growth by Decreasing Expression of Androgen Receptor Full Length and Splice Variants. Minnelide reduced tumor volume in multiple models of pancreatic cancer. Minnelide was a more effective drug against pancreatic cancer models. It effectively reduced tumor burden and tumor related morbidity in different unique but complementary mouse models. It reduced metastat
价 格：￥电议型 号：T71113产 地：中国大陆
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T71112SAR156497；化合物 SAR156497SAR156497
SAR156497 is an exquisitely selective Aurora A, B, and C inhibitor with in vitro and in vivo efficacy with IC50 = 0.5 nM (Aurora A); 1 nM (Aurora B / incenp); 3 nM (Aurora C / incenp) respectively SAR156497 combines high in vitro potency with satisfactory metabolic stability and limited CYP 3A4 and PDE3 inhibition. In vitro, SAR156497 displayed high antiproliferative activity on a large panel of tumor cell lines without correlation with any particular genetic signature or Aurora kinases expressi
价 格：￥电议型 号：T71112产 地：中国大陆
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T71111Famitinib malate；化合物 Famitinib malateSHR1020 malate；SHR1020 malate
Famitinib malate (SHR1020) is an orally active multi-targeted kinase inhibitor that effectively inhibits the activity of c-kit, VEGFR-2, and PDGFRβ with IC50 values of 2.3 nM, 4.7 nM, and 6.6 nM, respectively. It induces cell apoptosis and demonstrates potent antitumor activity in human gastric cancer cells and xenografts, making it a valuable compound for cancer research.
价 格：￥电议型 号：T71111产 地：中国大陆
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T71110Nanatinostat TFA；化合物 Nanatinostat TFANanatinostat TFA
Nanatinostat, also known as Tractinostat, CHR-3996 and VRx-3996, is an orally bioavailable, second-generation hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inhibitor CHR-3996 inhibits HDAC, resulting in an accumulation of highly acetylated histones, the induction of chromatin remodeling, and the selective transcription of tumor suppressor genes; these events may result in the inhibition of tumor cell division and the induction of tumor
价 格：￥电议型 号：T71110产 地：中国大陆
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T7111Tenofovir Disoproxil；替诺福韦酯GS 4331|||Bis(POC)-PMPA；替诺福韦酯|||GS 4331|||Bis(POC)-PMPA
Tenofovir Disoproxil (GS 4331) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.
价 格：￥电议型 号：T7111产 地：中国大陆
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T7108Omberacetam；化合物NoopeptSGS-111|||Noopept|||GVS-111；SGS-111|||Noopept|||GVS-111
Omberacetam (Noopept) is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models by a mechanism similar to other related racetam compounds.
价 格：￥电议型 号：T7108产 地：中国大陆
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T70969FR 111142；化合物 FR 111142FR 111142
FR 111142 is an angiogenesis inhibitor produced by the fungus Scolecobasidium arenarium.
价 格：￥电议型 号：T70969产 地：中国大陆
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T70111GT-2394；化合物 GT-2394GT-2394
GT-2394 is a histamine H3 receptor agonist.
价 格：￥电议型 号：T70111产 地：中国大陆
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T69585GMC-1111 free base；化合物 GMC-1111 free baseGMC-1111 free base
GMC-1111 free base is a dopamine partial agonist and stabilizer.
价 格：￥电议型 号：T69585产 地：中国大陆
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T69584GMC-1111 dihydrochloride；化合物 GMC-1111 dihydrochlorideGMC-1111 dihydrochloride
GMC-1111 dihydrochloride is a dopamine partial agonist and stabilizer.
价 格：￥电议型 号：T69584产 地：中国大陆
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T69484CGC 11144；化合物 CGC 11144CGC 11144
CGC 11144 is a Polyamine analogue inhibit tumor growth in vitro and in vivo.
价 格：￥电议型 号：T69484产 地：中国大陆
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T69483CGC 11150；化合物 CGC 11150CGC 11150
CGC 11150 is a polyamine analogue inhibit tumor growth in vitro and in vivo.
价 格：￥电议型 号：T69483产 地：中国大陆
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T68989ICI-111075；化合物 ICI-111075ICI-111075
ICI-111075 is a methane inhibitor.
价 格：￥电议型 号：T68989产 地：中国大陆
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T68627Ono 11119；化合物 Ono 11119Ono 11119
Ono 11119 is a thromboxane A2 antagonist.
价 格：￥电议型 号：T68627产 地：中国大陆
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T68037LCBS-1114 HCl；CBS-1114盐酸盐N-Phenylbenzamidrazone hydrochloride|||cbs-1114 HCl(46721-85-1 Free base)；N-
CBS-1114 HCl (N-Phenylbenzamidrazone hydrochloride) is a 5-lipoxygenase inhibitor and an anti-inflammatory compound in a good eye-permeable model.CBS-1114 HCl maintains and improves cardiac function, attenuates cardiac dysfunction, as well as reduces epicardial adipose tissue and/or pericardial adipose tissue in subjects with cardiovascular disease.
价 格：￥电议型 号：T68037L产 地：中国大陆
