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
工商认证 【已认证】
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：3286706
自主品牌
已选条件
-
T3S0208Hederagenin 28-O-beta-D-glucopyranosyl ester；常春苷元-28-BETA-D-吡喃葡萄糖苷Hederagenin-28-beta-D-glucopyranos
Hederagenin-28-beta-D-glucopyranoside, a triterpene saponin isolated from Ilex cornuta, protects cardiac myocytes against H2O2-induced damage.
价 格：￥电议型 号：T3S0208产 地：中国大陆
-
T3S0205β-Hederin；β-常春藤素Beta-Hederin；Beta-Hederin|||β-常春藤素
1. β-Hederin has antileishmanial activity. 2. β-Hederin has apoptotic effect on breast cancer cells, it could be a promising candidate for chemotherapy of breast cancer.
价 格：￥电议型 号：T3S0205产 地：中国大陆
-
T3S0195Nootkatone诺卡酮诺卡酮|||努特卡酮,诺卡酮
1. Nootkatone can provide effective tick control. 2. (+)-Nootkatone has antiallergic, anti-inflammatory, and antiplatelet activities. 3. Nootkatone can prevent obesity and improve physical performance through AMPK activation in skeletal muscle and liver.
价 格：￥电议型 号：T3S0195产 地：中国大陆
-
T3S0175Gardenia yellow；西红花苷 Ialpha-Crocin|||Crocin I|||Crocine；alpha-Crocin|||Crocin I|||Crocine|||西红花苷 I||
Gardenia yellow (Crocin I) has anti atherosclerosis and hypolipidemic effects.
价 格：￥电议型 号：T3S0175产 地：中国大陆
-
T3S0165Atractylone；苍术酮Atractylon；Atractylon|||苍术酮
Atractylone (Atractylon) has the functions of protecting liver, lowering blood sugar, antibacterial, anti-tumor and anti-virus.
价 格：￥电议型 号：T3S0165产 地：中国大陆
-
T3S0156Atractyloside potassium salt；苍术苷钾盐Atractyloside Dipotassium Salt；Atractyloside Dipotassium Salt|||苍术
1. Atractyloside potassium salt (Atractyloside Dipotassium Salt) inhibits oxidative phosphorylation by blocking the transfer of adenosine nucleotides through the mitochondrial membrane.
价 格：￥电议型 号：T3S0156产 地：中国大陆
-
T3S0153Xanthatin苍耳亭苍耳亭|||叶黄制菌素
1. Xanthatin has cytotoxic activity. 2. Xanthatin has antibacterial and antifungal activies against MRSA. 3. Xanthatin may have therapeutic potential against NSCLC. 4. Xanthatin can inhibit murine melanoma B16-F1 cell proliferation possibly associated with activation of Wnt/β-catenin pathway and its activity against melanoma tumor might also be relevant to inhibition of angiogenesis.
价 格：￥电议型 号：T3S0153产 地：中国大陆
-
T3S0137Bavachalcone；补骨脂查耳酮Bavachalcone
Bavachalcone is a major bioactive compounds isolated from Psoralea corylifolia L. it may be useful as a therapeutic drug for bone resorption-associated diseases.Bavachalcone can protect the endothelial function by increasing AMPK activity and MnSOD expression and reducing mitochondrial oxidative stress.
价 格：￥电议型 号：T3S0137产 地：中国大陆
-
T3S0128Hydroprotopine氢化物碱氢化原阿片碱|||氢化物碱
Hydroprotopine, treatment for coronary heart disease and angina, and the treatment effect is remarkable.
价 格：￥电议型 号：T3S0128产 地：中国大陆
-
T3S0081Oxypeucedanin；氧化前胡素(+-)-Oxypeucedanin|||Oxypeucadanin；(+-)-Oxypeucedanin|||氧化前胡素|||Oxypeucadanin
1. Oxypeucedanin ((+-)-Oxypeucedanin) has novel anticancer effect, mediated via induction of G2-M cell cycle arrest and apoptosis in human prostate carcinoma DU145 cells. 2. Oxypeucedanin is a kind of open-channel blocker of the hKv1.5 channel and it prolongs the APD; therefore, it is an excellent candidate as an antiarrhythmic drug for atrial fibrillation.
价 格：￥电议型 号：T3S0081产 地：中国大陆
-
T3S0057Dihydrochelerythrine；二氢白屈菜红碱12,13-Dihydrochelerythrine；12,13-Dihydrochelerythrine|||二氢白屈菜红碱
1. Dihydrochelerythrine (12,13-Dihydrochelerythrine) is nontoxic up to 5μM concentration. 2. Dihydrochelerythrine has antifungal activity against pathogenic plant fungi. 3. Dihydrochelerythrine has potential application in the therapy of serious infection caused by I. multifiliis. 4. Dihydrochelerythrine affects cell cycle distribution, activates mitochondrial apoptotic pathway, and induces apoptosis and necrosis in HL-6 cells.
价 格：￥电议型 号：T3S0057产 地：中国大陆
-
T3S0027Picropodophyllotoxin；苦鬼臼毒素AXL 1717|||Picropodophyllin；AXL 1717|||Picropodophyllin|||苦鬼臼毒素
Picropodophyllotoxin (AXL 1717) is a cyclolignan alkaloid found in the mayapple plant family (Podophyllum peltatum), and a small molecule inhibitor of the insulin-like growth factor 1 receptor (IGF1R) with potential antineoplastic activity. Picropodophyllotoxin (AXL 1717) specifically inhibits the activity and downregulates the cellular expression of IGF1R without interfering with activities of other growth factor receptors, such as receptors for insulin, epidermal growth factor, platelet-derive
价 格：￥电议型 号：T3S0027产 地：中国大陆
-
T3S0013Ethyl trans-caffeate；咖啡酸乙酯Ethyl caffeate|||Caffeic Acid Ethyl Ester；咖啡酸乙酯|||Ethyl caffeate|||Caffeic
1. Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) has anti-inflammatory activity. 2. Ethyl trans-caffeate may as a promising natural compound for future application in chronic liver disease. 3. Ethyl trans-caffeate is a potent chemopreventive compound against skin carcinogenesis caused by solar UV exposure. 4. Ethyl trans-caffeate is the high-resolution structures of representative inhibitors in complex with human pancreatic α-amylase. 5. Ethyl trans-caffeate strongly inhibits neoplastic transf
价 格：￥电议型 号：T3S0013产 地：中国大陆
-
T3S0012coniferyl ferulate；阿魏酸松柏酯coniferyl ferulate
Coniferyl ferulate is a strong inhibitor of glutathione S-transferase (GST) isolated from Radix Angelicae sinensis. It shows strong inhibition of human placental GST (IC50: 0.3 μM). It also reverses multidrug resistance and downregulates P-glycoprotein.
价 格：￥电议型 号：T3S0012产 地：中国大陆
-
T3S0006(E)-Ferulic acid methyl ester；(E)-阿魏酸甲酯Methyl ferulate|||Methyl (E)-ferulate；Methyl ferulate|||Methy
(E)-Ferulic acid methyl ester (Methyl (E)-ferulate) is a possible inhibitor of the mitogen activated phosphor kinase pathway, it could be a potential anti-inflammatory agent isolated for the first time in medicinal plant S. tuberosa. (E)-Ferulic acid methyl ester has promising anthelmintic activity against Haemonchus contortus.
价 格：￥电议型 号：T3S0006产 地：中国大陆
-
T3986SF2523；化合物SF2523SF2523
SF2523 is a highly selective and potent inhibitor.
价 格：￥电议型 号：T3986产 地：中国大陆
-
T39299(3S,4S)-PF-06459988；(3S,4S)-PF-06459988(3S,4S)-PF-06459988
(3S, 4S)-PF-06459988 is the less active S enantiomer of PF-06459988, which is a potent irreversible inhibitor of T790M mutant epidermal growth factor receptor (EGFR). PF-06459988 exhibits excellent selectivity against EGFR wild-type due to its minimally reactive electrophile, which reduces the likelihood of off-target labeling.
价 格：￥电议型 号：T39299产 地：中国大陆
-
T38986Fitusiran；FitusiranALN-AT3SC|||SAR439774；ALN-AT3SC|||SAR439774
Fitusiran (ALN-AT3SC) is a small interfering RNA compound designed to selectively bind to antithrombin (AT) messenger RNA in the liver, leading to decreased AT production. By doing so, Fitusiran enhances thrombin generation, making it a promising candidate for hemophilia research.
价 格：￥电议型 号：T38986产 地：中国大陆
-
T38854sFTX-3.3；sFTX-3.3sFTX-3.3
sFTX-3.3 is a calcium ion channel antagonist, exhibiting IC50 values of approximately 0.24 mM and 0.70 mM against P-type and N-type channels respectively.
价 格：￥电议型 号：T38854产 地：中国大陆
-
T38683SCD1 inhibitor-3；化合物SCD1 inhibitor-3SCD1-IN-3|||SCD1 inhibitor-3|||SCD1 inhibitor 17a；SCD1-IN-3|||SC
SCD1 inhibitor-3 (ML-270) is a highly effective and orally available compound that inhibits SCD1 with remarkable safety. SCD1 inhibitor-3 demonstrates strong potential for research in metabolic diseases, including obesity, type II diabetes, and dyslipidemia, as well as various skin conditions like acne and cancer.
价 格：￥电议型 号：T38683产 地：中国大陆
