当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型:会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
易推广会员:5年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
企业类型:生产商 【已认证】
注册资金:人民币万 【已认证】
产品数:86101
参观次数:3368203
已选条件
-
T8139Sulfamethoxazole sodiumAntibiotic,infection,Sulfamethoxazole sodium,Trimethoprim,pathogen,Inhibitor,
Sulfamethoxazole sodium is a sulfonamide bacteriostatic antibiotic
价 格:¥电议型 号:T8139产 地:中国大陆
-
T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格:¥电议型 号:T6951产 地:中国大陆
-
T11358gamma-secretase modulator 1
gamma-secretase modulator 1 is a modulator of γ secretase and can be used in studies about the treatment of Alzheimer´s disease.
价 格:¥电议型 号:T11358产 地:中国大陆
-
T8423ML417neuroprotection,dopaminergic,β-arrestin,ML417,ML-417,translocation,phosphorylation,neurons,ML 4
ML417 is a selective and brain penetrant agonist of D3 Dopamine (EC50 : 38 nM).
价 格:¥电议型 号:T8423产 地:中国大陆
-
TN2260Taxifolin 7-O-rhamnosideInhibitor,Taxifolin 7Orhamnoside,Taxifolin 7 O rhamnoside,inhibit
Taxifolin 7-O-rhamnoside is a natural product from Hypericum japonicum.
价 格:¥电议型 号:TN2260产 地:中国大陆
-
T6S1572Sauchinoneantioxidant,LPS,Diastereomeric,TNF-α,iNOS,anti-inflammatory,lignan,COX-2,inhibit,Nuclear f
1. Sauchinone is a useful adjunctive treatment for bacterial infection. 2. Sauchinone, an active lignan found in Saururus chinensis, to regulate the activation of HSCs, to prevent liver fibrosis, and to inhibit oxidative stress in vivo and in vitro. 3. Sauchinone diminishes LPS-induced neutrophil activation and acute lung injury. 4. Sauchinone-induced HO-1 expression plays a key role in the vascular protective effects of Sauchinone in HUVEC. 5. Sauchinone protects skin keratinocytes through inhi
价 格:¥电议型 号:T6S1572产 地:中国大陆
-
T6778BDA-366Inhibitor,BDA-366,Antitumor,Bcl-2 Family,inhibit,Bcl2-BH4 domain,Anticancer,BDA 366,Antiapopt
BDA-366 is a potent Bcl2 antagonist, binding Bcl2-BH4 domain with high affinity and selectivity (Ki = 3.3 nM). BDA-366 induces conformational change in Bcl2 that abrogates its antiapoptotic function, converting it from a survival molecule to a cell death inducer. BDA-366 suppresses growth of lung cancer cells[1].
价 格:¥电议型 号:T6778产 地:中国大陆
-
TP1417LSakamototide substrate peptide acetateSakamototide substrate peptide acetate
Sakamototide substrate peptide acetate is a peptide substrate of AMPK kinase family and can be used for the determination of kinase activity.
价 格:¥电议型 号:TP1417L产 地:中国大陆
-
T8016N-MethylbenzylamineN-Methylbenzylamine,inhibit,N Methylbenzylamine,NMethylbenzylamine,Inhibitor
N-Benzylmethylamine is an Alkaloids
价 格:¥电议型 号:T8016产 地:中国大陆
-
TN3500beta-Amyroneantifungal,AChE,COX-2,PI3K-Akt,Anti-inflammatory,Fungal,β-Amyrone,inflammation,CHIKV,Cyc
beta-Amyrone has antifungal activity against Chikungunya virus replication with an EC50 of 86 uM. beta-Amyrone has anti-inflammatory activity through inhibiting the expression of COX-2. beta-Amyrone exhibits anti-α-glucosidase inhibitory activity and moderate AChE activity. β-Amyrone can be used in the research of disease like inflammation, infection, and obesity.
价 格:¥电议型 号:TN3500产 地:中国大陆
-
TP1907L1Dynamin inhibitory peptide, myristoylated acetateDynamin inhibitory peptide, myristoylated acetate
Dynamin inhibitory peptide, myristoylated acetate is a DynaMin inhibitor to interfere with the binding of amphiphysin with dynamin. DynaMin inhibitory peptide, myristoylated TFA is a membrane-permeant form of the peptide that prevents endocytosis.
价 格:¥电议型 号:TP1907L1产 地:中国大陆
-
T22644C2 CeramideC2 Ceramide,C-2 Ceramide
A potent modulator of cell proliferation and differentiation.
价 格:¥电议型 号:T22644产 地:中国大陆
-
T64341H-β-Ala-AMC TFAinhibit,Inhibitor,H β Ala AMC TFA,HβAlaAMC TFA
H-β-Ala-AMC TFA is a substrate for aminopeptidase. Building block for synthesizing the fluorogenic vanin I substrate pantothenate-AMC.
价 格:¥电议型 号:T64341产 地:中国大陆
-
T10837Clocapramine dihydrochloride hydrateClocapramine dihydrochloride hydrate
Clocapramine dihydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
价 格:¥电议型 号:T10837产 地:中国大陆
-
T6920ON123300Platelet-derived growth factor receptor,AMP-activated protein kinase,ON-123300,ON 123300,FGF
ON123300 is a potent and multi-targeted kinase inhibitor for CDK4/Ark5/PDGFRβ/FGFR1/RET/Fyn (IC50: 3.9/5/26/26/9.2/11 nM).
价 格:¥电议型 号:T6920产 地:中国大陆
-
T9945MNK8?MNK-8,HepG2,Bcl-2 Family,STAT3 inhibitor,inhibit,MNK8,MNK8?,Antimigratory agent,Inhibitor,STAT,
3-methyl-6- (naphthalen-1-yl)pyrimidine-2,4(1H, 3H)-dione is a potent STAT3 inhibitor that reduces the ability of STAT3 to bind to DNA and also has a good growth inhibition effect on liver cancer cells [1].
价 格:¥电议型 号:T9945产 地:中国大陆
-
TN2437SerotoninInhibitor,Endogenous Metabolite,Serotonin,5-hydroxytryptamine Receptor,inhibit,Serotonin Re
5-hydroxytryptamine is a natural product from animals
价 格:¥电议型 号:TN2437产 地:中国大陆
-
T22297Clindamycin hydrochloride monohydrate
Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylo
价 格:¥电议型 号:T22297产 地:中国大陆
-
TQ0251(Z)-2-decenoic acidbacteria,inhibit,biofilm,response,gram-positive,unsaturated,(Z) 2 decenoic acid,(
(Z)-2-decenoic acid is an unsaturated short-chain fatty acid secreted by Pseudomonas aeruginosa. It can induce a dispersion response in biofilms formed by gram-negative and gram-positive bacteria. (Z)-2-decenoic acid can inhibit biofilm development.
价 格:¥电议型 号:TQ0251产 地:中国大陆