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T15241ER-000444793
ER-000444793 is a potent mitochondrial permeability transition pore (mPTP) opening inhibitor and it also inhibits mPTP (IC50: 2.8 μM).
价 格：￥电议型 号：T15241产 地：中国大陆
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T15047DacisteineN,S-Diacetyl-L-cysteine
Dacisteine is an inhibitor of New Delhi metallo-beta-lactamase-1 (NDM-1, IC50 = 1000 μM).
价 格：￥电议型 号：T15047产 地：中国大陆
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T1500Xylazine hydrochloride丙泊酚杂质J；Xylazine HCl；BAY 1470 hydrochloride
Xylazine hydrochloride is an adrenergic alpha-2 agonist used as a sedative, analgesic and centrally acting muscle relaxant in veterinary medicine
价 格：￥电议型 号：T1500产 地：中国大陆
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T14943CGP60474
CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC. CGP60474 is also a highly potent anti-endotoxemic agent and inhibits cyclin-dependent kinase (CDK) potently.
价 格：￥电议型 号：T14943产 地：中国大陆
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T14797Bromo-PEG3-C2-acid溴代-三聚乙二醇-羧酸
Bromo-PEG3-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T14797产 地：中国大陆
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T14792Bromo-PEG2-CH2-Boc乙酸叔丁酯-二聚乙二醇-溴代
Bromo-PEG2-CH2-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T14792产 地：中国大陆
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T1479Isosorbide dinitrate硝酸异山梨酯；Sorbide nitrate；Sorbidnitrate；Nitrosorbide；Isordil
Isosorbide dinitrate is a vasodilator used in the treatment of angina pectoris.
价 格：￥电议型 号：T1479产 地：中国大陆
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T14782BrilaroxazineRP5063
Brilaroxazine is a potent multimodal dopamine/5-HT modulator. Brilaroxazine is a partial agonist of dopamine D2, D3, and D4 receptors, 5-HT1A (Ki =1.5 nM) and 5-HT2A (Ki = 2.5 nM), and has antagonist activity 5-HT2B, and 5-HT7 receptors with Kis of 0.19 n
价 格：￥电议型 号：T14782产 地：中国大陆
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T1478Ondansetron hydrochloride dihydrate盐酸昂丹司琼；GR 38032；SN 307；Ondansetron hydrochloride；NSC 665799
Ondansetron hydrochloride is a competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.
价 格：￥电议型 号：T1478产 地：中国大陆
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T14779BRD7389
BRD7389 is an inducer of insulin expression in pancreatic α-cells and a specific inhibitor of RSK family kinase (IC50s: 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3).
价 格：￥电议型 号：T14779产 地：中国大陆
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T14778BRD6989
BRD6989 is an analog of the natural product cortistatin A (dCA). Which inhibits CDK8 and upregulates IL-10. BRD6989 inhibits the kinase activity of recombinant CDK8 or CDK19 complexes. BRD6989 selectively binds a complex of CDK8 with an IC50 of ~200 nM.
价 格：￥电议型 号：T14778产 地：中国大陆
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T14776BRD4 Inhibitor-10
BRD4 Inhibitor-10 is an inhibitor of BRD4-BD1 (IC50: 8 nM).
价 格：￥电议型 号：T14776产 地：中国大陆
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T14775Bragsin26-methoxy-5-nitro-2-(trifluoromethyl)chromen-4-one；Bragsin 2
Bragsin2 is a hydration-resistant cell penetrant, selective and non-competitive inhibitor of Afr guanine nucleotide exchange factor BRAG2 that inhibits Arf GTPase activation, with an IC50 of 3 μM. Bragsin2 binds at the interface between the pleckstrin hom
价 格：￥电议型 号：T14775产 地：中国大陆
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T14767BP 897 hydrochloride
BP 897 is a potent and selective agonist of dopamine D3 receptor and it is a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors. Which shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).
价 格：￥电议型 号：T14767产 地：中国大陆
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T14766BPH-715
BPH-715 inhibits the liver-stage growth of P. falciparum with an IC50 of 10 μM for P. falciparum exoerythrocytic forms in HepG2 cells.
价 格：￥电议型 号：T14766产 地：中国大陆
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T14765BOS-172722
BOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint(IC50 of 2 nM).
价 格：￥电议型 号：T14765产 地：中国大陆
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T1476Pramipexole普拉克索；SND 919
Pramipexole is a selective dopamine receptor agonist used in the therapy of Parkinson disease. Pramipexole therapy is associated with a low rate of transient serum enzyme elevations during treatment but has not been implicated in cases of clinically appar
价 格：￥电议型 号：T1476产 地：中国大陆
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T1475Fesoterodine fumarateToviaz；SPM 907；富马酸非索罗定
Fesoterodine Fumarate is the fumarate salt form of fesoterodine, a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties. Fesoterodine is rapidly hydrolyzed in vivo into its active metabolite 5-hydroxymethyl
价 格：￥电议型 号：T1475产 地：中国大陆
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T14746Boc-NH-PEG4-CH2COOHN-叔丁氧羰基-四聚乙二醇-乙酸
Boc-NH-PEG4-CH2COOH is a cleavable ADC linker used as a linker for antibody-drug conjugates (ADC)[1].
价 格：￥电议型 号：T14746产 地：中国大陆
