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T74161Iboxamycin；化合物 IboxamycinIboxamycin
Iboxamycin, a promising antibiotic candidate, features a fused bicyclic amino acid residue. It is orally bioavailable and has demonstrated safety and efficacy against both Gram-positive and Gram-negative bacterial infections in mouse models [1] [2].
价 格：￥电议型 号：T74161产 地：中国大陆
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T7385WT-161；化合物WT-161WT-161
WT161 is a potent and selective inhibitor of HDAC6 (IC50:0.40 nM).
价 格：￥电议型 号：T7385产 地：中国大陆
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T73161HadAB-IN-1；化合物 HadAB-IN-1HadAB-IN-1
HadAB-IN-1, a potent inhibitor of the HadAB enzyme complex, exhibits significant activity by restraining mycolic acid biosynthesis in Mycobacterium tuberculosis (Mtb), with an inhibitory concentration (IC 50) value of 0.03 μM. This compound is utilized in tuberculosis (TB) research.
价 格：￥电议型 号：T73161产 地：中国大陆
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T71619ST72；化合物 ST72ST72
ST72 is a potent inhibitor of FP2. ST72 exhibited strong growth inhibition of chloroquine-sensitive (3D7; EC50 = 2.8 ?M) and chloroquine-resistant (RKL-9; EC50 = 6.7 ?M) strains of Plasmodium falciparum
价 格：￥电议型 号：T71619产 地：中国大陆
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T71618Oxocarbazate；化合物 OxocarbazateOxocarbazate
Oxocarbazate, also known as CID23631927, is an inhibitor of human cathepsin L. In the cathepsin L inhibition assay, The oxocarbazate caused a time-dependent 17-fold drop in IC50 from 6.9 nM (no preincubation) to 0.4 nM (4-h preincubation). Slowly reversible inhibition was demonstrated in a dilution assay. CID23631927 demonstrate activity in blocking both SARS-CoV (IC50 = 273 nM) and Ebola virus (IC50 = 193 nM) entry into human embryonic. CID 23631927 was a subnanomolar, slow-binding, reversible
价 格：￥电议型 号：T71618产 地：中国大陆
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T71617NCQ-469；化合物 NCQ-469NCQ-469
NCQ-469 is a metabolite of remoxipride and a dopamine D2 receptor antagonist.
价 格：￥电议型 号：T71617产 地：中国大陆
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T71616Adaprolol；化合物 AdaprololAdaprolol
Adaprolol is a beta-adrenergic antagonist. Enantiomers of Adaprolol may be used in the treatment of Glaucoma or other ailments of the eye.
价 格：￥电议型 号：T71616产 地：中国大陆
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T71614FR 900452；化合物 FR 900452FR 900452
FR 900452 is a platelet activating factor antagonist from fermentatiion products of Streptomyces phaeofaciens.
价 格：￥电议型 号：T71614产 地：中国大陆
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T71613MK-8712；化合物 MK-8712MK-8712
MK-8712 is a monobactam beta-lactamase inhibitor.
价 格：￥电议型 号：T71613产 地：中国大陆
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T71612SU086；化合物 SU086SU086
SU086 an inhibitor of HSP90, impairs glycolysis and represents a treatment strategy for advanced prostate cancer
价 格：￥电议型 号：T71612产 地：中国大陆
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T71611αSyn-IN-576755；化合物 αSyn-IN-576755αSyn-IN-576755
αSyn-IN-576755 is a novel inhibitor of αSyn fibrillization, blocking fibril growth and suppressing A53T αSyn neurotoxicity.
价 格：￥电议型 号：T71611产 地：中国大陆
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T71610Docosylferulate；化合物 DocosylferulateDocosylferulate
Docosylferulate is a biochemical that has been studied for its inhibition on Hep G2 cells and anti-tumor activities.
价 格：￥电议型 号：T71610产 地：中国大陆
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T71226Opc 15161；化合物 Opc 15161Opc 15161
Opc 15161 is a degradation product of OPC-15160 and superoxide inhibitor.
价 格：￥电议型 号：T71226产 地：中国大陆
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T71161Thiorphan disulfide；化合物 Thiorphan disulfideThiorphan disulfide
Thiorphan disulfide is an impurity of Racecadotril -- an antidiarrheal and enkephalinase inhibitor that reduces the amount of water and electrolytes absorbed into the intestine.
价 格：￥电议型 号：T71161产 地：中国大陆
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T70161Berotralstat HCl；化合物 Berotralstat HClBerotralstat HCl
Berotralstat HCl is a novel selective inhibitor of plasma kallikrein, blocking the enzymatic activity of plasma kallikrein in releasing bradykinin, the major biologic peptide that promotes swelling and pain associated with attacks of HAE.
价 格：￥电议型 号：T70161产 地：中国大陆
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T69961CJ-15161 (free base)；化合物 CJ-15161 (free base)CJ-15161 (free base)
CJ-15161 (free base), an opioid κ-receptor agonist, is undergoing development with Pfizer as an analgesic agent.
价 格：￥电议型 号：T69961产 地：中国大陆
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T69960CJ-15161 hydrochloride；化合物 CJ-15161 hydrochlorideCJ-15161 hydrochloride
CJ-15161 hydrochloride is the salt form of CJ-15161 (free base), an opioid κ-receptor agonist, is undergoing development with Pfizer as an analgesic agent.
价 格：￥电议型 号：T69960产 地：中国大陆
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T69161Hexamethonium bromide dihydrate；化合物 Hexamethonium bromide dihydrateHexamethonium bromide dihydrate
Hexamethonium bromide dihydrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant.
价 格：￥电议型 号：T69161产 地：中国大陆
