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：3602173
自主品牌
已选条件
-
T16355NSC781406；化合物NSC781406NSC781406
NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).
价 格：￥电议型 号：T16355产 地：中国大陆
-
T16354NSC745885；化合物 T16354NSC745885
NSC745885 is an effective down-regulator of EZH2 via proteasome-mediated degradation. NSC745885 is also an effective anti-tumor agent that displays selective toxicity against multiple cancer cell lines but not normal cells. NSC745885 offers possibilities for the study of advanced bladder and oral squamous cell carcinoma (OSCC) cancers.
价 格：￥电议型 号：T16354产 地：中国大陆
-
T16353Meseclazone；美西拉宗W2395|||NSC297623；美西拉宗|||W2395|||NSC297623
Meseclazone has anti-inflammatory, analgesic, and antipyretic activity. Meseclazone shows inhibitory potency of secondary phase ADP aggregation.
价 格：￥电议型 号：T16353产 地：中国大陆
-
T16352NSC23925；化合物 T16352NSC23925
NSC23925 is a selective and effective inhibitor of P-glycoprotein (Pgp).
价 格：￥电议型 号：T16352产 地：中国大陆
-
T16351NSC16168；化合物 T16351NSC16168
NSC16168 inhibits DNA repair and potentiates CDDP efficacy in cancer. NSC16168 is a specific ERCC1-XPF inhibitor (IC50: 0.42 μM).
价 格：￥电议型 号：T16351产 地：中国大陆
-
T16350NSC-87877；化合物NSC-87877NSC-87877
NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50=0.318 μM, 0.355 μM of shp2 and shp1, respectively).It also inhibits dual-specificity phosphatase 26 (DUSP26).
价 格：￥电议型 号：T16350产 地：中国大陆
-
T16349NSC-60339；化合物NSC-60339NSC-60339
NSC-60339 is an inhibitor of efflux pump, and a substrate of AcrAB-TolC, is a polybasic terephthalic acid derivative studied as a potential cancer chemotherapeutic agent.
价 格：￥电议型 号：T16349产 地：中国大陆
-
T1632Amitraz双甲脒BTS-27419|||NSC 324552|||双甲脒
Amitraz (NSC 324552) is a white monoclinic crystals. Melting point 187-189°F (86-87°C). Insoluble in water. Used as an acaricide, insecticide and treatment of demodectic mange in dogs.
价 格：￥电议型 号：T1632产 地：中国大陆
-
T16191N-(Azido-PEG3)-N-Fluorescein-PEG3-acid；化合物 T16191N-(Azido-PEG3)-N-Fluorescein-PEG3-acid
N-(Azido-PEG3)-N-Fluorescein-PEG3-acid is a PEGylated PROTAC linker incorporating azide, fluorescein, and carboxylic acid functional groups.
价 格：￥电议型 号：T16191产 地：中国大陆
-
T16183N-(Azido-PEG2)-N-Fluorescein-PEG3-acid；化合物 T16183N-(Azido-PEG2)-N-Fluorescein-PEG3-acid
N-(Azido-PEG2)-N-Fluorescein-PEG3-acid is a polyethylene glycol (PEG)-derived PROTAC linker specifically designed for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16183产 地：中国大陆
-
T1618Dipyridamole；双嘧达莫Persantin|||Dypyridamole|||Dipyridamol|||NSC-515776|||Dipyudamine；Persantin|||Dypyr
Dipyridamole (Persantin) is a Platelet Aggregation Inhibitor. The physiologic effect of dipyridamole is by means of Decreased Platelet Aggregation.
价 格：￥电议型 号：T1618产 地：中国大陆
-
T1616Cefotiam hydrochloride；盐酸头孢替安Pansporin|||SCE-963 hydrochloride|||Pansporine|||Cefotiam dihydrochlori
Cefotiam hydrochloride (SCE-963 hydrochloride) is the hydrochloride salt form of cefotiam, a third-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity. Cefotiam binds to penicillin-binding proteins (PBPs), transpeptidases that are responsible for crosslinking of peptidoglycan. By preventing crosslinking of peptidoglycan, cell wall integrity is lost and cell wall synthesis is halted.
价 格：￥电议型 号：T1616产 地：中国大陆
-
T1610Metaxalone；美他沙酮Skelaxin|||Methaxalonum|||Zorane|||NSC170959|||AHR438；Skelaxin|||Methaxalonum|||美他沙酮|
Metaxalone (Methaxalonum) (marketed by King Pharmaceuticals under the brand name Skelaxin ) is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions.
价 格：￥电议型 号：T1610产 地：中国大陆
-
T1601Lomustine；洛莫司汀CCNU|||NSC 79037；CCNU|||NSC 79037|||洛莫司汀
Lomustine (NSC-79037) is an alkylating agent of value against both hematologic malignancies and solid tumors.
价 格：￥电议型 号：T1601产 地：中国大陆
-
T1595Nevirapine；奈韦拉平NSC 641530|||BI-RG 587|||NVP；NSC 641530|||奈韦拉平|||BI-RG 587|||奈伟拉平|||NVP
Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor. In combination with other antiretroviral drugs, nevirapine reduces HIV viral loads and increases CD4 counts, thereby retarding or preventing the damage to the immune system and reducing the risk of developing AIDS.
价 格：￥电议型 号：T1595产 地：中国大陆
-
T1593Ezetimibe；依泽替米贝SCH 58235；依泽替米贝|||SCH 58235
Ezetimibe (SCH 58235) is a Dietary Cholesterol Absorption Inhibitor. The physiologic effect of ezetimibe is by means of Decreased Cholesterol Absorption.
价 格：￥电议型 号：T1593产 地：中国大陆
-
T1591Ancitabine hydrochloride盐酸环胞苷NSC 145668 HCl|||盐酸环胞苷|||Cyclocytidine hydrochloride|||Cyclo-CMP hydroc
Ancitabine hydrochloride (NSC 145668 HCl) is the hydrochloride salt of a cytarabine congener prodrug with antineoplastic activity. Upon administration, ancitabine is slowly hydrolyzed into cytarabine. Subsequently, cytarabine is converted to the triphosphate form within the cell and then competes with cytidine for incorporation into DNA. Because the arabinose sugar sterically hinders the rotation of the molecule within DNA, DNA replication ceases, specifically during the S phase of the cell cycl
价 格：￥电议型 号：T1591产 地：中国大陆
-
T1571Estriol；雌三醇NSC-12169|||Oestriol；NSC-12169|||Oestriol|||雌三醇
Estriol (Oestriol) is a hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, a large amount of estriol is produced by the PLACENTA.
价 格：￥电议型 号：T1571产 地：中国大陆
-
T15634JYL 1421化合物JYL 1421SC 0030
JYL 1421 (SC 0030) is an antagonist of TRPV1 receptor (IC50 = 8 nM).
价 格：￥电议型 号：T15634产 地：中国大陆
-
T1559Betamethasone dipropionate；二丙酸倍他米松Diprolene AF|||SCH 11460|||Betamethasone 17,21-dipropionate|||Dipr
Betamethasone Dipropionate is the 17, 21-dipropionate ester of betamethasone, a synthetic glucocorticoid with metabolic, immunosuppressive and anti-inflammatory actions. Betamethasone dipropionate (SCH 11460) binds to specific intracellular glucocorticoid receptors and subsequently binds to DNA to modify gene expression. The synthesis of certain anti-inflammatory proteins is induced while the synthesis of certain inflammatory mediators is inhibited. As a result, there is an overall reduction in
价 格：￥电议型 号：T1559产 地：中国大陆
