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T74202Hispaglabridin A；化合物 Hispaglabridin AHispaglabridin A
Hispaglabridin A, an effective antioxidant, inhibits lipid peroxidation [1].
价 格：￥电议型 号：T74202产 地：中国大陆
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T742013′-Hydroxy-4′-O-methylglabridin；化合物 3′-Hydroxy-4′-O-methylglabridin3′-Hydroxy-4′-O-methylglabridin
3′-Hydroxy-4′-O-methylglabridin effectively prevents NADH-dependent peroxidation, exhibiting potent antioxidant properties [1].
价 格：￥电议型 号：T74201产 地：中国大陆
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T74200Glicophenone；化合物 GlicophenoneGlicophenone
Glicophenone, an antibacterial agent, demonstrates minimum inhibitory concentrations (MICs) of 32 μg/mL against multiple strains, including MRSA OM481, MRSA OM505, MRSA OM584, MRSA OM623, and MSSA 209P [1].
价 格：￥电议型 号：T74200产 地：中国大陆
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T7420Valifenalate；霜霉灭Valiphenal|||IR5885；霜霉灭|||Valiphenal|||IR5885
Valifenalate (IR5885) is antifungal agent, effective against various types of mildew
价 格：￥电议型 号：T7420产 地：中国大陆
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T7392Revefenacin；化合物RevefenacinTD-4208|||GSK1160724；TD-4208|||GSK1160724
Revefenacin (TD-4208) is a mAChR antagonist has a high affinity on M3 receptor( Ki : 0.18 nM),and potentially useful for the treatment of respiratory disease.
价 格：￥电议型 号：T7392产 地：中国大陆
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T7379320-Carboxy-Leukotriene B4；化合物 20-Carboxy-Leukotriene B420-Carboxy-Leukotriene B4
20-Carboxy-Leukotriene B4 (20-COOH LTB4), a metabolite of Leukotriene B4 (LTB4), exhibits high affinity binding to the BLT1 receptor. It notably inhibits LTB4-mediated neutrophil responses, including migration, degranulation, and leukotriene biosynthesis [1].
价 格：￥电议型 号：T73793产 地：中国大陆
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T73420SP-471P；化合物 SP-471PSP-471P
SP-471P is a potent inhibitor of dengue virus (DENV) protease, exhibiting half-maximal effective concentrations (EC50) of 5.9 μM for DENV1, 1.4 μM for DENV2, 5.1 μM for DENV3, and 1.7 μM for DENV4, with a cytotoxic concentration (CC50) greater than 100 μM. Additionally, SP-471P effectively reduces DENV viral RNA synthesis [1].
价 格：￥电议型 号：T73420产 地：中国大陆
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T7277SB 242084；化合物SB 242084 dihydrochloride hydrateSB 242084 dihydrochloride hydrate；6 - 氯-2,3 - 二氢- 5 -甲
SB 242084 dihydrochloride hydrate is a psychoactive drug and research chemical which acts as a selective antagonist for the 5HT2C receptor.
价 格：￥电议型 号：T7277产 地：中国大陆
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T72663(Rac)-Etavopivat；化合物 (Rac)-Etavopivat(Rac)-FT-4202；(Rac)-FT-4202
(Rac)-Etavopivat ((Rac)-FT-4202), an isomer of Etavopivat, is an orally active activator of erythrocyte pyruvate kinase-R (PKR) used in studies related to sickle cell disease and other haemoglobinopathies [1].
价 格：￥电议型 号：T72663产 地：中国大陆
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T72420MTK458；化合物 MTK458Mitophagy activator 1|||EP-0035985；Mitophagy activator 1|||EP-0035985
MTK458 (EP-0035985) is an orally active and brain-permeable PINK1 activator that promotes pathological clearance of alpha-synuclein and reduces pUb in a PFF inoculation model.MTK458 induces pathological alpha-synuclein clearance by stimulating dimerization and stabilization of the PINK1/TOM complex.MTK458 may be used in Parkinson´s disease research.
价 格：￥电议型 号：T72420产 地：中国大陆
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T71420RO314724；化合物 RO314724RO314724
RO314724 is a HDAC inhibitor. RO314724 is also a a reversible, tightly binding, MMP inhibitor with a Ki of 26 nm. Matrix metalloproteinases (MMPs) belong to the key enzymes of the proteolytic destruction of cartilage matrix during chronic rheumatic diseases. Ro314724 displayed MMP-proteoglycanase inhibitory activity both in vitro and ex vivo and proved to be not harmful to the morphology, viability and proteoglycan biosynthesis of bovine articular cartilage explants.
价 格：￥电议型 号：T71420产 地：中国大陆
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T70420PHA 543613 hydrochloride；化合物 PHA 543613 hydrochloridePHA 543613 hydrochloride
PHA-543613 hydrochloride acts as a potent and selective agonist for the α7 subtype of neural nicotinic acetylcholine receptors, with a high level of brain penetration and good oral bioavailability. It is under development as a possible treatment for cognitive deficits in schizophrenia.
价 格：￥电议型 号：T70420产 地：中国大陆
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T69431A-420983；化合物 A-420983A-420983
A-420983 is a novel potent Lck inhibitor, exhibiting oral efficacy in animal models of delayed-type hypersensitivity and organ transplant rejection.
价 格：￥电议型 号：T69431产 地：中国大陆
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T69420Vestipitant；化合物 VestipitantVestipitant
Vestipitant, also known as GW597599, is one of the most potent and selective NK(1) receptor antagonists ever discovered, showing appropriate pharmacokinetic properties and in vivo activity. Its actions support the utility of NK(1) receptor blockade in the alleviation of anxiety and, possibly, depression. It is under development as a potential antiemetic and anxiolytic drug, and as a treatment for tinnitusand insomnia.
价 格：￥电议型 号：T69420产 地：中国大陆
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T68984AF-399/42018025；化合物 AF-399/42018025AF-399/42018025
AF-399/42018025 is a CC chemokine receptor 4 (CCR4) antagonist.
价 格：￥电议型 号：T68984产 地：中国大陆
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T6828ZL0420；化合物ZL0420ZL0420
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格：￥电议型 号：T6828产 地：中国大陆
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T67822LUlodesine；化合物UlodesineBCX4208；BCX4208
Ulodesine (BCX4208) is a purine nucleoside phosphorylase (PNP) inhibitor that inhibits PNP with an IC50 value of 2.293 nM/L. Ulodesine may be used to study hyperuricaemia.
价 格：￥电议型 号：T67822L产 地：中国大陆
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T674202-(((6-(Difluoromethoxy)-1H-benzo[d]imidazol-2-yl)sulfonyl)methyl)-3,4-dimethoxypyridine 1-oxide；化合物
2-(((6-(Difluoromethoxy)-1H-benzo[d]imidazol-2-yl)sulfonyl)methyl)-3,4-dimethoxypyridine 1-oxide is a useful organic compound for research related to life sciences. The catalog number is T67420 and the CAS number is 953787-55-8.
价 格：￥电议型 号：T67420产 地：中国大陆
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T66420(1R,2S)-2-Phenylcyclopropanamine；化合物 (1R,2S)-2-Phenylcyclopropanamine(1R,2S)-2-Phenylcyclopropanamin
(1R,2S)-2-Phenylcyclopropanamine is a useful organic compound for research related to life sciences. The catalog number is T66420 and the CAS number is 3721-26-4.
价 格：￥电议型 号：T66420产 地：中国大陆
