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T5209INH14；化合物INH14INH14
INH14 is a novel inhibitor of the IKKα/β-dependent TLR inflammatory response (IC50s: 8.97/3.59 μM for IKKα/IKKβ).
价 格：￥电议型 号：T5209产 地：中国大陆
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T5208BAY-8002；化合物BAY-8002BAY8002|||BAY 8002；BAY8002|||BAY 8002
BAY-8002 is a potent dual MCT1/2 inhibitor (IC50 values are 3, 8, and 12 nM at rat (C6), human (DLD-1) and mouse (4T1) MCT1 respectively).
价 格：￥电议型 号：T5208产 地：中国大陆
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T5207LIT927；化合物LIT-927LIT 927|||LIT-927；LIT 927|||LIT-927
LIT927 (LIT-927) is an orally active CXCL12 neutraligand (Ki: 267 nM for CXCL12 binding to CXCR4).
价 格：￥电议型 号：T5207产 地：中国大陆
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T5206DAAO inhibitor-1；DAAO抑制剂1DAAO inhibitor-1
DAAO inhibitor-1 is a potent D-amino acid oxidase (DAAO) inhibitor (IC50: 0.12 μM).
价 格：￥电议型 号：T5206产 地：中国大陆
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T5203Sodium Tartrate；酒石酸钠Sodium Tartrate
Sodium Tartrate is a food additive, used as an emulsifier and binding agent in food products.
价 格：￥电议型 号：T5203产 地：中国大陆
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T5202Imidazole咪唑Glyoxaline|||1,3-Diaza-2,4-cyclopentadiene|||1,3-diazole|||咪唑
Imidazole is a planar 5-membered ring and a highly polar compound. It has been used extensively as a corrosion inhibitor. Imidazole is incorporated into many important biological molecules.
价 格：￥电议型 号：T5202产 地：中国大陆
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T4988Boceprevir；波普瑞韦SCH 503034|||EBP 520；SCH 503034|||EBP 520|||波普瑞韦
Boceprevir (SCH 503034) is a novel, potent, highly selective, orally bioavailable HCV NS3 protease inhibitor with Ki of 14 nM in both enzyme assay and EC90 of 350 nM in cell-based replicon assay.
价 格：￥电议型 号：T4988产 地：中国大陆
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T4817Methylmalonic acid；甲基丙二酸NSC 25201|||MMA|||Isosuccinic acid|||Methylpropanedioic acid|||Methylmalonat
Methylmalonic acid (Isosuccinic acid) is a dicarboxylic acid that can be derived from methylmalonyl-coenzyme A. It is an indicator of Vitamin B-12 deficiency in cancer.
价 格：￥电议型 号：T4817产 地：中国大陆
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T4696BMS202 hydrochloride (1675203-84-5(free base))；化合物BMS202 hydrochloridePD-1/PD-L1 inhibitor 2 hydroch
BMS202 hydrochloride (1675203-84-5(free base)) (PD-1/PD-L1 inhibitor 2 hydrochloride) is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophysical studies demonstrate that BMS202 binds directly to PD-L1. Binding of BMS202 promotes PD-L1 dimerisation and blocks the PD-L1/ PD1 interaction.
价 格：￥电议型 号：T4696产 地：中国大陆
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T4520Berberine chloride (hydrate)化合物 T4520Natural Yellow 18 chloride hydrate|||盐酸小檗碱水合物
Berberine chloride (hydrate) is an alkaloid from Hydrastis canadensis L., Berberidaceae and also found in many other plants. It is relatively toxic to parenterally but has been used orally for various fungal and parasitic infections and an anti-diarrheal.
价 格：￥电议型 号：T4520产 地：中国大陆
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T40520Thiophene-2Thiophene-2Thiophene-2|||TP2
Thiophene-2 (TP2) is a targeted inhibitor of polyketide synthase 13 (Pks13), specifically designed to disrupt mycolic acid biosynthesis. By doing so, it effectively induces rapid cell death in mycobacteria. Thiophene-2 demonstrates notable anti-tuberculosis activity and exhibits a minimum inhibitory concentration (MIC) value of 1 μM against Mycobacterium tuberculosis.
价 格：￥电议型 号：T40520产 地：中国大陆
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T39520Vamifeport；化合物 VamifeportVIT-2763；VIT-2763
Vamifeport (VIT-2763) is a novel orally active inhibitor that targets iron transport proteins and reduces markers of hemolysis in the SCD Townes model.VIT-2763 improves anemia and erythropoiesis, ameliorates vascular inflammation, and can be studied in β-thalassemia.
价 格：￥电议型 号：T39520产 地：中国大陆
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T38594MK-5204；MK-5204MK-5204
MK-5204 is an orally active β-1,3-glucan synthesis inhibitor.
价 格：￥电议型 号：T38594产 地：中国大陆
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T38520Benzyl-PEG8-Ots；Benzyl-PEG8-OtsBenzyl-PEG8-Ots；Benzyl-PEG8-Ots
Benzyl-PEG8-Ots is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T38520产 地：中国大陆
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T37520DL-Glutamic acid；DL-谷氨酸DL-Glutamic acid
DL-Glutamic acid, the conjugate acid of Glutamic acid, serves as a crucial metabolite. In comparison to the α and β polymorphs of L-Glutamic acid´s second phase, DL-Glutamic acid exhibits enhanced stability[1].
价 格：￥电议型 号：T37520产 地：中国大陆
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T37131MS 15203；MS 15203MS 15203
Potent and selective GPR171 partial agonist (EC50 = 90 nM; 28% inhibition of forskolin activated adenylyl cyclase activity in rat hypothalamic memebranes). Exhibits minimal binding to a panel of ~70 GPCRs and 10 other receptors (<22% of radioligand displaced from the target receptors). Increases neuronal activity in the paraventricular nucleus. Increases food intake and body weight in mice.
价 格：￥电议型 号：T37131产 地：中国大陆
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T36520COR659；化合物COR659COR659
COR659 is a 2-acylaminothiophene derivative able to suppress alcohol and chocolate self-administration in rats, likely via positive allosteric modulation of the GABAB receptor and antagonism/inverse agonism at the cannabinoid CB1 receptor.
价 格：￥电议型 号：T36520产 地：中国大陆
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T3571SU5201；化合物NSC 247030NSC 247030；NSC 247030
SU5201 (NSC 247030) is a biochemical.
价 格：￥电议型 号：T3571产 地：中国大陆
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T35520Aflatoxin G1-13C17；Aflatoxin G1-13C17Aflatoxin G1-13C17；Aflatoxin G1-13C17
Aflatoxin G1-13C17is intended for use as an internal standard for the quantification of aflatoxin G1by GC- or LC-MS. Aflatoxin G1is a mycotoxin that has been found inA. terricola.1
价 格：￥电议型 号：T35520产 地：中国大陆
