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产品数:86101
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TN67063-demethylcolchicinecarrageenin,3 demethylcolchicine,inhibit,Inhibitor,scavenging,colchicine,3-Demet
3-demethylcolchicine is a natural product isolated from Gloriosa superba.Inhibitory effect on the polymerization of purified bovine brain tubulin.
价 格:¥电议型 号:TN6706产 地:中国大陆
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T7839Lasofoxifene Tartrateosteoporosis,inhibit,Estrogen Receptor/ERR,arthritis,CP 336156,endocrine resist
Lasofoxifene Tartrate is a third-generation, non-steroidal selective estrogen receptor modulator.
价 格:¥电议型 号:T7839产 地:中国大陆
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T99683-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride3Piperidinyl(1pyrrolidinyl)methanone hydrochlori
3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
价 格:¥电议型 号:T9968产 地:中国大陆
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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
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TQ0019RR6inhibit,RR 6,RR6,RR-6,Inhibitor
RR6 acts as a selective, reversible, and competitive vanin inhibitor at nanomolar concentration.
价 格:¥电议型 号:TQ0019产 地:中国大陆
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TQ027427-Hydroxycholesterol27Hydroxycholesterol,LXR,Liver X receptor,Inhibitor,Estrogen Receptor/ERR,Endog
27-Hydroxycholesterol is a selective modulator of estrogen receptor and an agonist of the liver X receptor.
价 格:¥电议型 号:TQ0274产 地:中国大陆
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T60554Schnurri-3 inhibitor-1
Schnurri-3 inhibitor-1 is a potent inhibitor of schnurri-3, an essential regulator of adult bone formation. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in Shn3FFL (osteoblast cell line, AC50= 2.09 μM). Schnurri-3 inhibitor-1 has research value in osteoporosis.
价 格:¥电议型 号:T60554产 地:中国大陆
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TN1705GlycyrrhisoflavoneGlycyrrhisoflavone
Glycyrrhisoflavone is a tyrosinase inhibitor with anti-inflammatory effects. Glycyrrhisoflavone inhibits α-glucosidase and monoamine oxidase.
价 格:¥电议型 号:TN1705产 地:中国大陆
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T7299β-Estradiol 17-acetateβ Estradiol 17 acetate,Estrogen Receptor/ERR,Inhibitor,βEstradiol 17acetate,in
beta-estradiol 17-acetate is a metabolite of estradiol.
价 格:¥电议型 号:T7299产 地:中国大陆
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T6947PiperlongumineExtracellular signal regulated kinases,Ferroptosis,Bacterial,Inhibitor,inhibit,Apoptos
Piperlongumine is a natural alkaloid from Piper longum L. It selectively kills cancer cells and strengthens the level of reactive oxygen species (ROS).
价 格:¥电议型 号:T6947产 地:中国大陆
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T6541Ibutilide FumarateIbutilide,antiarrhythmia agent,Potassium Channel,inhibit,Inhibitor,long QT syndrom
Ibutilide Fumarate is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval.
价 格:¥电议型 号:T6541产 地:中国大陆
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T6S1597Mulberroside AMulberroside A,Tumor Necrosis Factor Receptor,inhibit,TNF Receptor,Tyrosinase,TNFR,Inh
1. Mulberroside has nephroprotective, hypoglycemic, and antidiabetic effects. 2. Mulberroside A is a glycosylated stilbene of oxyresveratrol; thus, the deglycosylation of Mulberroside A resulted in enhanced inhibition of melanogenesis. 3. Mulberroside A has anti-inflammatory antiapoptotic effects. by decreasing the expressions of tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6 and inhibiting the activation of NALP3, caspase-1, and nuclear factor-κB and the phosphorylation of extra
价 格:¥电议型 号:T6S1597产 地:中国大陆
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T8349Cyclofenilmaturation,inhibit,Cyclofenil,Zika,FSH,Estrogen Receptor/ERR,Influenza Virus,replication,I
Cyclofenil is an estrogen antagonist, has anti-dengue-virus activity
价 格:¥电议型 号:T8349产 地:中国大陆
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T9756AZD-9574PPAR,Peroxisome proliferator-activated receptors,breast cancer,inhibit,AZD-9574,HRR,HRR-defi
AZD-9574 is a selective inhibitor of PARP1 at the sites of SSBs. AZD-9574 exhibits anti-cancer activities and can be used in studies about HRD+ breast cancer and advanced solid malignancies.
价 格:¥电议型 号:T9756产 地:中国大陆
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TMA1644Segetalin BInhibitor,inhibit,Segetalin B,Estrogen Receptor/ERR
Segetalin B is a natural product from Vaccaria segetalis (Neck.) Garcke, has estrogen-like activity.
价 格:¥电议型 号:TMA1644产 地:中国大陆
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TN7163Methyl 4-bromopyrrole-2-carboxylate
Methyl 4-bromopyrrole-2-carboxylate is a marine derived natural products found in Lissodendoryx sp.
价 格:¥电议型 号:TN7163产 地:中国大陆
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T8970ML162p62,Glutathione Peroxidase,GPX4,ML-162,Nrf2,anticancer,HRAS,Ferroptosis,Inhibitor,inhibit,ML 16
ML162 is an inhibitor of GPX4 that is selectively lethal to mutant RAS oncogene-expressing cell lines (IC50s = 25 and 578 nM for HRASG12V-expressing and wild-type BJ fibroblasts, respectively)
价 格:¥电议型 号:T8970产 地:中国大陆
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TMA2394DL-alpha-TocopherolFerroptosis,Inhibitor,inhibit,DL alpha Tocopherol,DLalphaTocopherol
Antioxidant.
价 格:¥电议型 号:TMA2394产 地:中国大陆
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T6620Ospemifeneinhibit,Ospemifene,Inhibitor,Estrogen Receptor/ERR
Ospemifene is a new selective non-hormonal estrogen receptor modulator (SERM) that is used for the treatment of moderate to severe dyspareunia, a symptom of vulvar and vaginal atrophy, due to menopause. FDA approved on February 26, 2013.
价 格:¥电议型 号:T6620产 地:中国大陆
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T67754(3Z)-5-(pyridin-3-yl)-3-[(1H-pyrrol-2-yl)methylidene]-2,3-dihydro-1H-indol-2-one(3Z)5(pyridin3yl)3[(
(3Z)-5-(pyridin-3-yl)-3-[(1H-pyrrol-2-yl)methylidene]-2,3-dihydro-1H-indol-2-one is a potent, selective and orally active FLT3 inhibitor, with IC50s of ?40, 8, and 4 nM for FLT3-WT, FLT3-D835Y, and FLT3-D835H, respectively.
价 格:¥电议型 号:T67754产 地:中国大陆