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T1278AstemizoleParalergin；Histaminos；Laridal；阿司咪唑
Astemizole is a synthetic piperidinyl-benzimidazol derivative with antiallergic properties, acts as a reversible competitive inhibitor of histamine H1 receptors, with less anticholinergic effects compared to related agents. It is a long-acting, non-sedati
价 格：￥电议型 号：T1278产 地：中国大陆
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T12719RG7834RO 7020322
RG7834 is a highly selective and orally bioavailable inhibitor of HBV(HBsAg and HBeAg and HBV DNA with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells).
价 格：￥电议型 号：T12719产 地：中国大陆
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T12718LRG7800RO6885247
RG7800 has the potential for spinal muscular atrophy treatment. RG7800 is an SMN2 splicing modifier.
价 格：￥电议型 号：T12718L产 地：中国大陆
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T12678(Rac)-Telmesteine3,4-Thiazolidinedicarboxylic Acid 3-Ethyl Ester；3-(Ethoxycarbonyl)thiazolidine-4-ca
(Rac)-Telmesteine is an inhibitor of protease and is thus a suitable enzyme stabilizer.
价 格：￥电议型 号：T12678产 地：中国大陆
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T12578(E,E)-RAMB4PTP1B-IN-8
PTP1B-IN-8 is a potent and selective inhibitor of protein tyrosine phosphatase-1B (PTP1B).
价 格：￥电议型 号：T12578产 地：中国大陆
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T12478LPinacidilP1134；S 1230；P 1134；P-1134；S-1230
Pinardil (P-1134, S-1230) is a guanidine that opens potassium channels and directly dilates peripheral blood vessels in small arteries, lowering blood pressure and peripheral resistance and producing fluid retention.
价 格：￥电议型 号：T12478L产 地：中国大陆
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T1240Flumazenil氟马西尼；Ro 15-1788
Flumazenil antagonizes the benzodiazepine binding site of the gamma-aminobutyric acid (GABA)/benzodiazepine receptor complex in the central nervous system (CNS), thereby preventing the chloride channel opening events and inhibiting neuronal hyperpolarizat
价 格：￥电议型 号：T1240产 地：中国大陆
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T11836Lefamulin acetate醋酸来法莫林；BC-3781 acetate
Lefamulin acetate (BC-3781 acetate) is the first semi-synthetic pleuromutilin for systemic treatment of bacterial infections in humans. Lefamulin acetate (BC-3781 acetate) inhibits protein synthesis by binding to the peptidyl transferase center of the 50S
价 格：￥电议型 号：T11836产 地：中国大陆
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T11782KRN2 bromide
KRN2 bromide is a selective inhibitor of nuclear factor of activated T cells , with an IC50 of 0.1 μM.
价 格：￥电议型 号：T11782产 地：中国大陆
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T1178TemozolomideNSC 362856；TMZ；TZM；CCRG 81045；替莫唑胺
Temozolomide is a DNA alkylating agent interfering with DNA replication.
价 格：￥电议型 号：T1178产 地：中国大陆
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T11578LEncequidar mesylateHM30181 mesylate；HM30181A mesylate
Encequidar mesylate is a competitive P-glycoprotein inhibitor.
价 格：￥电议型 号：T11578L产 地：中国大陆
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T11571HLY784-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine
HLY78 targets the DIX domain of Axin, is an activator of the Wnt/β-catenin signaling pathway and can enhance Axin-LRP6 binding to promote Wnt signaling.
价 格：￥电议型 号：T11571产 地：中国大陆
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T11318Dopexamine hydrochlorideFPL60278AR；盐酸多培沙明
Dopexamine hydrochloride is a β2-adrenergic receptor agonist.
价 格：￥电议型 号：T11318产 地：中国大陆
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T11078Deschloroclozapine
Deschloroclozapine, a metabolite of Clozapine, is a highly potent muscarinic DREADDs agonist. Deschloroclozapine binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively.
价 格：￥电议型 号：T11078产 地：中国大陆
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T10988LDegarelix acetate(214766-78-6 free base)
Degarelix acetate is a competitive and reversible antagonist of gonadotropin-releasing hormone receptor (GnRHR) .
价 格：￥电议型 号：T10988L产 地：中国大陆
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T1095SparfloxacinCI-978；Zagam；AT-4140；PD 131501；司帕沙星
Sparfloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase, thereby inhibiting DNA replication and transcription.
价 格：￥电议型 号：T1095产 地：中国大陆
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T10814Cinacalcet metabolite M4Rarechem AL BW 1078；3-三氟甲基苯丙胺
Cinacalcet metabolite M4 is a metabolite of Cinacalcet. Cinacalcet is an allosteric agonist of Ca receptor.
价 格：￥电议型 号：T10814产 地：中国大陆
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T10789Chitosan oligosaccharideCOS；壳聚糖低聚乳酸酯
Chitosan oligosaccharide, an oligomer of β-(1→4)-linked D-glucosamine, activates AMPK and inhibits inflammatory signaling pathways.
价 格：￥电议型 号：T10789产 地：中国大陆
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T1078Sulfadimethoxine磺胺二甲氧嗪；Sulphadimethoxine
Sulfadimethoxine is a sulfanilamide that is used as an anti-infective agent.
价 格：￥电议型 号：T1078产 地：中国大陆
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T10353APX-115 free baseEwha-18278 free base
APX-115 free base (Ewha-18278 free base) is a potent, orally active pan NADPH oxidase （Nox) inhibitor (Kis: 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2, and Nox4). APX-115 effectively prevents kidney injury.
价 格：￥电议型 号：T10353产 地：中国大陆
