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T10563L2BM635 mesylate (1493762-74-5 free base)；化合物 T10563L2BM635 mesylate；BM635 mesylate
BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
价 格：￥电议型 号：T10563L2产 地：中国大陆
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T10563LBM635 hydrochloride (1493762-74-5 free base)；化合物 T10563LBM635 hydrochloride；BM635 hydrochloride
BM635 hydrochloride is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
价 格：￥电议型 号：T10563L产 地：中国大陆
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T10560P2X3 antagonist 34；化合物 T10560BLU-5937；BLU-5937
P2X3 antagonist 34, a potent, selective, and orally active antagonist, targets the P2X3 homotrimeric receptor, exhibiting IC50s of 25 nM, 92 nM, and 126 nM for human, rat, and guinea pig P2X3 receptors respectively. It shows reduced activity against P2X2/3 heterotrimeric receptors across human, rat, and guinea pig models. Notably, this compound demonstrates a significant anti-tussive effect without altering taste[1].
价 格：￥电议型 号：T10560产 地：中国大陆
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T10538LBI-9321 trihydrochloride；化合物 T10538LBI-9321 trihydrochloride
BI-9321 trihydrochloride is a selective and cellular active nuclear receptor-binding SET domain 3 (NSD3)-PWWP1 domain antagonist (Kd: 166 nM). BI-9321 is inactive against NSD2-PWWP1 and NSD3-PWWP2.
价 格：￥电议型 号：T10538L产 地：中国大陆
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T10538BI-9321；化合物 T10538BI-9321
BI-9321 is a selective and cellular active nuclear receptor-binding SET domain 3 (NSD3)-PWWP1 domain antagonist (Kd: 166 nM). BI-9321 is inactive against NSD2-PWWP1 and NSD3-PWWP2.
价 格：￥电议型 号：T10538产 地：中国大陆
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T10537BI-749327；化合物BI-749327BI-749327
BI-749327 is a high selectivity and orally bioavailable antagonist of TRPC6 (IC50s: 13 nM, 19 nM and 15 nM for mouse, human and guinea pig TRPC6).
价 格：￥电议型 号：T10537产 地：中国大陆
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T10493Beclabuvir；贝拉布韦BMS-791325；BMS-791325
Beclabuvir (BMS-791325) is a potent NS5A replication complex inhibitor that inhibits the activity of the NS5B protein expressed by HCV genotypes 1, 2, 4, and 5 and is used in the study of HCV infection.
价 格：￥电议型 号：T10493产 地：中国大陆
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T10393AT-007；化合物AT-007AT-007
AT-007 is an orally active CNS penetrant Aldose Reductase inhibitor for the treatment of Galactosemia (IC50: 100 pM). It reduces toxic galactitol levels and prevents disease complications in GALT deficiency rats.
价 格：￥电议型 号：T10393产 地：中国大陆
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T1024Roflumilast；罗氟司特B9302-107|||BYK 20869|||APTA 2217|||BY 217；罗氟司特|||B9302-107|||BYK 20869|||APTA 2217|
Roflumilast (APTA 2217) is an orally available, long-acting inhibitor of phosphodiesterase (PDE) type 4 (PDE4), with anti-inflammatory and potential antineoplastic activities. Upon administration, roflumilast and its active metabolite roflumilast N-oxide selectively and competitively bind to and inhibit PDE4, which leads to an increase of both intracellular levels of cyclic-3´, 5´-adenosine monophosphate (cAMP) and cAMP-mediated signaling.
价 格：￥电议型 号：T1024产 地：中国大陆
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T10093LE1R；化合物 T10093LE1R
E1R is a positive sigma-1 receptor (Sig1R PAM) allosteric modulator. It has a cognition-enhancing activity.
价 格：￥电议型 号：T10093L产 地：中国大陆
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T10093(2R,3R)-E1R；化合物 T10093(2R,3R)-E1R
(2R,3R)-E1R is an enantiomer of E1R. (2R,3R)-E1R is a sigma-1 receptor positive allosteric modulator for the treatment of cognition/memory disorders.
价 格：￥电议型 号：T10093产 地：中国大陆
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T09845-Fluorouracil；5-氟脲嘧啶5-FU|||Fluorouracil|||NSC 19893|||5-Fluoracil；5-FU|||Fluorouracil|||5-氟脲嘧啶|||NS
5-Fluorouracil (5-FU) is a uracil analog, an inhibitor of DNA synthesis. 5-Fluorouracil has antitumor activity and affects pyrimidine synthesis through inhibition of thymidylate synthase. 5-Fluorouracil causes apoptosis and autophagy.
价 格：￥电议型 号：T0984产 地：中国大陆
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T0939Phenytoin；苯妥英Diphenylhydantoin|||5,5-Diphenylhydantoin；苯妥英|||Diphenylhydantoin|||5,5-Diphenylhydanto
Phenytoin (5,5-Diphenylhydantoin) is a hydantoin derivative and a non-sedative antiepileptic agent with anticonvulsant activity. Phenytoin potentially acts by promoting sodium efflux from neurons located in the motor cortex reducing post-tetanic potentiation at synapses. The reduction of potentiation prevents cortical seizure foci spreading to adjacent areas, stabilizing the threshold against hyperexcitability. In addition, this agent appears to reduce sensitivity of muscle spindles to stretch c
价 格：￥电议型 号：T0939产 地：中国大陆
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T0938Thiabendazole；噻菌灵2-(4-Thiazolyl)benzimidazole；2-(4-Thiazolyl)benzimidazole|||噻菌灵
Thiabendazole (2-(4-Thiazolyl)benzimidazole) is a benzimidazole derivative with anthelminthic property.
价 格：￥电议型 号：T0938产 地：中国大陆
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T0937Riboflavin；维生素B2Vitamin B2|||E101；Vitamin B2|||维生素B2|||E101
Riboflavin (E101) is a micronutrient that occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as flavin mononucleotide and flavin-adenine dinucleotide.
价 格：￥电议型 号：T0937产 地：中国大陆
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T0935Butylated hydroxytoluene；2,6-二叔丁基对甲酚BHT FCC/NF；BHT FCC/NF|||2,6-二叔丁基对甲酚
Butylated hydroxytoluene (BHT FCC/NF) is an antioxidant widely used in food, cosmetics and industrial liquids. It is a ferroptosis inhibitor.
价 格：￥电议型 号：T0935产 地：中国大陆
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T0934Nicotinamide；烟酰胺Nicotinic acid amide|||Vitamin B3|||Niacinamide|||Vitamin PP；Nicotinic acid amide|||
Niacinamide is an important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
价 格：￥电议型 号：T0934产 地：中国大陆
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T0933D-(+)-Glucono-1,5-lactone葡萄糖酸内酯Gluconic acid lactone|||Delta-Gluconolactone|||Gluconolactone|||葡萄糖酸内
D-(+)-Glucono-1,5-lactone (Gluconolactone) is a naturally-occurring food additive used as a sequestrant, an acidifier, or a curing, pickling, or leavening agent. It is a cyclic ester of D-gluconic acid. Pure gluconolactone is a white odorless crystalline powder.
价 格：￥电议型 号：T0933产 地：中国大陆
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T0932Cefixime；头孢克肟FK-027|||Cefspan|||Cefiximum|||Cephoral|||FR-17027|||CL-284635；FK-027|||头孢克肟|||Cefspan|
Cefixime (FR-17027) is a broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell wall synthesis by disrupting peptidoglycan synthesis, resulting in a reduction in bacterial cell wall stability and bacterial cell lysis. Stable in the presence of a variety of beta-lactamases, this agent is more active against gram-
价 格：￥电议型 号：T0932产 地：中国大陆
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T0930Sulfadiazine；磺胺嘧啶Sulphadiazine；Sulphadiazine|||磺胺嘧啶
Sulfadiazine (Sulphadiazine) is a synthetic pyrimidinyl sulfonamide derivative, short-acting bacteriostatic Sulfadiazine inhibits bacterial folic acid synthesis by competing with para-aminobenzoic acid. It is used in combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections.
价 格：￥电议型 号：T0930产 地：中国大陆
