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T001-00000001ML251
ML251 is a potent novel nanomolar inhibitor of T. brucei and T. cruzi phosphofructokinase[1]. ML251 inhibits T. brucei PFK (IC50=0.37 μM) and T. cruzi PFK (IC50=0.13 μM). ML251 can be used for the research of parasite[1].
价 格：￥电议型 号：T001-00000001产 地：中国大陆
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T0031L2ZiprasidoneZiprasidone,CP-88059,Geodon
Ziprasidone?is an a typical antipsychotic used in the treatment of schizophrenia and bipolar disorder. Use of?ziprasidone?has not been consistently associated with serum enzyme elevations and has yet to be linked to instances of clinically apparent acute
价 格：￥电议型 号：T0031L2产 地：美洲
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T0182L2(±) Clopidogrel hydrogen sulfate(±) Clopidogrel hydrogen sulfate,Iscover,Clopidogrel hydrogen sulfat
Clopidogrel, an antiplatelet agent pharmacologically and structurally analogous to ticlopidine, is used to inhibit blood clots in various conditions such as cerebrovascular disease, peripheral vascular disease, and coronary artery disease.
价 格：￥电议型 号：T0182L2产 地：美洲
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T0375L2Atropine sulfateAtropine sulfate,Sulfatropinol,Atropette
Atropine sulfate is a competitive antagonist for muscarinic acetylcholine receptor.
价 格：￥电议型 号：T0375L2产 地：美洲
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T05662-Methylbenzhydrol2-Methylbenzhydrol
2-Methylbenzhydrol is used as pharmaceutical intermediates.
价 格：￥电议型 号：T0566产 地：美洲
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T06342-Acetyl-4-butyramidophenol2-Acetyl-4-butyramidophenol
2-Acetyl-4-butyramidophenol is gray crystalline powder.
价 格：￥电议型 号：T0634产 地：美洲
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T06712-Naphthol2-Naphthol,Betanaphthol,
2-Naphthol is an isomer of 1-naphthol, differing by the location of the hydroxyl group on the naphthalene ring.
价 格：￥电议型 号：T0671产 地：美洲
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T0683MevastatinMevastatin,ML236B,Compactin
Mevastatin is an HMG-CoA reductase inhibitor that was initially isolated from the mold Pythium ultimum. Mevastatin was the first statin to enter clinical trials.
价 格：￥电议型 号：T0683产 地：美洲
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T1008520(S)-Hydroxycholesterol20(S)-Hydroxycholesterol,20α-Hydroxycholesterol,
20(S)-hydroxyCholesterol is an allosteric activator of the oncoprotein smoothened (Smo) that activates the hedgehog signaling pathway with an EC50 of 3 μM in NIH3T3 cells.
价 格：￥电议型 号：T10085产 地：美洲
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T1008624-Hydroxycholesterol24-Hydroxycholesterol
24-Hydroxycholesterol is a natural sterol, which serves as a positive allosteric modulator of NMDA receptors, and a potent activator of the transcription factors LXR.
价 格：￥电议型 号：T10086产 地：美洲
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T1008824R-Calcipotriol24R-Calcipotriol,PRI 2202,
24R-Calcipotriol(PRI 2202) is an impurity of Calcipotriol which is a ligand of VDR-like receptors.
价 格：￥电议型 号：T10088产 地：美洲
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T10252L2ADU-S100 ammonium saltADU-S100 ammonium salt,MIW815 ammonium salt,ML RR-S2 CDA ammonium salt
ADU-S100 ammonium salt is an stimulator of interferon genes (STING) activator.
价 格：￥电议型 号：T10252L2产 地：美洲
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T10358L2Netarsudil mesylateNetarsudil mesylate,AR-13324 (mesylate),
Netarsudil mesylate is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP) reduction.
价 格：￥电议型 号：T10358L2产 地：美洲
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T10485PROTAC Bcl2 degrader-1PROTAC Bcl2 degrader-1
PROTAC Bcl2 degrader-1 is a PROTAC, which potently and selectively induces the degradation of Mcl-1 (IC50: 11.81 μM) and Bcl-2 (IC50: 4.94 μM; DC50: 3.0 μM).
价 格：￥电议型 号：T10485产 地：美洲
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T10802-Aminoethanethiol2-Aminoethanethiol,2-Mercaptoethylamine,Cysteamine
Cysteamine is a Cystine Depleting Agent. The mechanism of action of cysteamine is as a Cystine Disulfide Reduction.
价 格：￥电议型 号：T1080产 地：美洲
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T10833CL264CL264
CL264, a specific agonist of TLR7, is used for innate immune signals research.
价 格：￥电议型 号：T10833产 地：美洲
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T10994L2Deltasonamide 2 (TFA)Deltasonamide 2 (TFA)
Deltasonamide 2 TFA is competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
价 格：￥电议型 号：T10994L2产 地：美洲
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T12006MetarrestinMetarrestin,ML246,
Metarrestin is a first-in-class perinucleolar compartment inhibitor with a favorable PK profile, which effectively suppresses metastasis.?Metarrestin disrupts the nucleolar structure and inhibits RNA polymerase (Pol) I transcription, at least in part by i
价 格：￥电议型 号：T12006产 地：美洲
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T12076LML218ML218
ML218 inhibits the burst activity in the subthalamic nucleus (STN) neurons. ML218 is an effective, selective, and orally active inhibitor of T-type Ca2+ channel (Cav3.1, Cav3.2, Cav3.3) (IC50s: 310 nM and 270 nM for Cav3.2 and Cav3.3, respectively). ML218
价 格：￥电议型 号：T12076L产 地：美洲
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T12266L2Ilginatinib hydrochlorideIlginatinib hydrochloride,NS-018 hydrochloride,
Ilginatinib hydrochloride is a highly active and orally bioavailable inhibitor of JAK2.
价 格：￥电议型 号：T12266L2产 地：美洲
