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:3763256
已选条件
-
T8418DCLK1-IN-1DCLK1 IN 1,signaling,PDAC,KRAS,cancer,low,ERK,Inhibitor,selective,DCLK1IN1,inhibit,DCLK-1-
DCLK1-IN-1 is a selective and in vivo-compatible chemical probe of the DCLK1 kinase domain .
价 格:¥电议型 号:T8418产 地:中国大陆
-
T9353OXOMEMAZINEhistamine H1-receptor,OXOMEMAZINE,Histamine Receptor,inhibit,phenothiazine,antimuscarinic
Oxomemazine is a phenothiazine-based histamine H1-receptor blocker with pronounced antimuscarinic activity. Oxomemazine is a selective antagonist of mycotoxins M1 receptors, showing high (Ki=84 nM, M1 receptors) and low (Ki=1.65 μM, M2 receptors) affinity sites 20 times the difference[1]. Oxomemazine is an antihistamine and anticholinergic agent used in studies related to cough studies[2].
价 格:¥电议型 号:T9353产 地:中国大陆
-
TN2315XanthopurpurinXanthopurpurin,Inhibitor,inhibit,Purpuroxanthin
Xanthopurpurin shows antiviral activity. Xanthopurpurin can effectively inhibit rotavirus multiplication by promoting virus-induced apoptosis in MA-104 cells. Xanthopurpurin shows mainly strong inhibition of collagen-induced platelet aggregation.
价 格:¥电议型 号:TN2315产 地:中国大陆
-
T28743Seglitide acetate
Seglitide acetate is a selective agonist of sst2 somatostatin receptor.
价 格:¥电议型 号:T28743产 地:中国大陆
-
T7126Hydroquinineinhibit,Hydroquinine,Inhibitor
Hydroquinine, is an organic compound and as a cinchona alkaloid closely related to quinine.
价 格:¥电议型 号:T7126产 地:中国大陆
-
T6S1683DemethoxycurcuminBacterial,Inhibitor,Autophagy,Demethoxycurcumin,inhibit,Apoptosis
1. Demethoxycurcumin has antioxidant activity. 2. Demethoxycurcumin has anti-inflammatory activity. 3. Demethoxycurcumin has anti-proliferative activity. 4. Demethoxycurcumin has anti-acanthamoebic effect. 5. Demethoxycurcumin is a potential additive natural product in combination with chemotherapeutic agents in drug-resistant cancers. 6. Demethoxycurcumin inhibits energy metabolic and oncogenic signaling pathways through AMPK activation in triple-negative breast cancer cells.
价 格:¥电议型 号:T6S1683产 地:中国大陆
-
T8047Menthyl acetate5-aminolevulinic,Menthyl,ALA,permeation,acid,Inhibitor,inhibit,l-menthol,Menthyl acet
(1R)-(-)-Menthyl acetate is a derivative of L-menthol.
价 格:¥电议型 号:T8047产 地:中国大陆
-
TJS03186-Hydroxy-4-methylcoumarinInhibitor,6 Hydroxy 4 methylcoumarin,inhibit,6Hydroxy4methylcoumarin
Growth inhibition of human U937 cells by [3H]thymidine incorporation assay
价 格:¥电议型 号:TJS0318产 地:中国大陆
-
T7703PK11007PK11007,inhibit,MDM-2/p53,Reactive Oxygen Species,Inhibitor,PK 11007,PK-11007
PK11007 is an anti-p53 drug.
价 格:¥电议型 号:T7703产 地:中国大陆
-
T9059Fmoc-Phe(4-CN)-OHFmoc Phe(4 CN) OH,Inhibitor,FmocPhe(4CN)OH,inhibit
Fmoc-Phe(4-CN)-OH?is an N-Fmoc protected phenylalanine derivative and potentially useful synthetic intermediate
价 格:¥电议型 号:T9059产 地:中国大陆
-
TN2117Pulsatilloside EChinensioside B,inhibit,Pulsatilloside E,Inhibitor
Pulsatilloside E is a natural product isolated from the roots of Pulsatilla chinensis (Ranunculaceae).
价 格:¥电议型 号:TN2117产 地:中国大陆
-
TWS1293Angelic anhydrideAngelic anhydride,Inhibitor,inhibit
Angelic Anhydride is a reagent in the improved synthesis of angelate esters, which are the active chemical behind the strong pain-relieving and spasmolytic action of extracts from the plant butterbur.
价 格:¥电议型 号:TWS1293产 地:中国大陆
-
T9975GPR183GPR183 antagonist-1,SAE-14,inhibit,SAE 14,SAE14,HL-60,GPR183,Inhibitor,GPR183 antagonist SAE-1
GPR183 is a chemotactic receptor known for its role in the maturation of B cells, and the endogenous ligand is the oxysterol 7α,25-dihydroxycholesterol (7α,25-OHC). GPR183 can be used in research on inflammatory bowel disease (IBD).
价 格:¥电议型 号:T9975产 地:中国大陆
-
T8998AA41612AA41612,AA-41612,Inhibitor,inhibit,AA 41612
AA41612 is a novel antagonist of melanopsin-mediated phototransduction.
价 格:¥电议型 号:T8998产 地:中国大陆
-
TN1926Methyl caffeateinhibit,stress,antimicrobial,Bacterial,antimycobacterial,Methyl caffeate,α-glucosidas
Methyl caffeate acid
价 格:¥电议型 号:TN1926产 地:中国大陆
-
T6975Sarcosineinhibit,dysfunction,schizophrenia,Endogenous Metabolite,Sarcosine,Inhibitor,cognitive,depre
Sarcosine is a competitive inhibitor of the type I glycine transporter (GlyT1) and an N-methyl-D-aspartate receptor (NMDAR) co-agonist.
价 格:¥电议型 号:T6975产 地:中国大陆
-
T8836CY5-SE triethylamine saltoligonucleotides,reactive,dye,amino-groups,inhibit,CY-5-SE triethylamine sa
Fluorolink Cy5 triethanolamine salt is a hydrophilic amine-reactive fluorescent probe. It displays excitation/emission maxima of 646/662 nm, respectively. Cy5-SE-conjugated ligands have been used in the characterization of hematopoietic tumor microenvironments.
价 格:¥电议型 号:T8836产 地:中国大陆
-
TJS03145,7-Dihydroxy-4-methylcoumarinBacterial,inhibit,Fungal,Inhibitor,5,7Dihydroxy4methylcoumarin,5,7 Dih
5,7-Dihydroxy-4-methylcoumarin inhibits human neutrophil oxidative metabolism and elastase activity. 5,7-Dihydroxy-4-methylcoumarin has in vitro platelet antiaggregatory property. 5,7-Dihydroxy-4-methylcoumarin shows inhibition of the cyclooxygenase pathway.
价 格:¥电议型 号:TJS0314产 地:中国大陆
-
T9124Laninamivir octanoateH2N2,CS8958,H3N2,inhaled,CS 8958,Laninamivir octanoate,neuraminidase,inhibit,An
Laninamivir octanoate is a long acting influenza neuraminidase (NA) inhibitor which shows superior anti-influenza virus activity.
价 格:¥电议型 号:T9124产 地:中国大陆
-
T7103idalopirdine5-HT Receptor,Serotonin Receptor,Lu AE-58054,idalopirdine,Inhibitor,inhibit,5-hydroxytry
Idalopirdine, a selective 5-HT6 receptor antagonist( Ki : 0.83 nM),as a treatment for Alzheimer´s disease.
价 格:¥电议型 号:T7103产 地:中国大陆