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：3787401
自主品牌
已选条件
-
T1773Afatinib Dimaleate；双马来酸盐阿法替尼BIBW2992|||Afatinib|||BIBW 2992MA2|||Afatinib (BIBW2992) Dimaleate；马来酸阿法
Afatinib Dimaleate (BIBW 2992MA2) is an orally bioavailable anilino-quinazoline derivative and inhibitor of the receptor tyrosine kinase (RTK) epidermal growth factor receptor (ErbB; EGFR) family, with antineoplastic activity.
价 格：￥电议型 号：T1773产 地：中国大陆
-
T17729Cl-C6-PEG4-C3-COOH；化合物 T17729Cl-C6-PEG4-C3-COOH
Cl-C6-PEG4-C3-COOH, a PROTAC linker, is a suitable component for synthesizing chloroalkane-containing PROTACs (HaloPROTACs).
价 格：￥电议型 号：T17729产 地：中国大陆
-
T17629Bis-PEG29-acid；化合物 T17629Bis-PEG29-acid
Bis-PEG29-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T17629产 地：中国大陆
-
T17529BCN-PEG3-Biotin；化合物 T17529BCN-PEG3-Biotin
BCN-PEG3-Biotin is a non-cleavable three-unit PEG linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17529产 地：中国大陆
-
T17429Amino-PEG36-acid；化合物 T17429Amino-PEG36-acid
Amino-PEG36-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T17429产 地：中国大陆
-
T173292-Bromo-2,2-dimethyl-acetamido-PEG3-acid；化合物 T173292-Bromo-2,2-dimethyl-acetamido-PEG3-acid
2-Bromo-22-dimethyl-acetamido-PEG3-acid is a polyethylene glycol (PEG) derivative commonly employed as a PEG-based PROTAC linker during PROTAC synthesis[1].
价 格：￥电议型 号：T17329产 地：中国大陆
-
T17299(-)-Indolactam V；化合物 T17299Indolactam V；Indolactam V
(-)-Indolactam V is a PKC activator (Kis: 3.36 nM, 1.03 μM for η-CRD2 , γ-CRD2). (-)-Indolactam V also has the Kds are 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-C1B), 18.9 nM (β-C1A-long), 20.8 nM (α-C1A-long), 137 nM (β-C1B), 138 nM (γ-C1A), 213 nM (γ-C1B). It has antitumor activity.
价 格：￥电议型 号：T17299产 地：中国大陆
-
T17298Zylofuramine；化合物 T17298Zylofuramine
Zylofuramine is a stimulant of psychomotor.
价 格：￥电议型 号：T17298产 地：中国大陆
-
T17297ZXH-3-26；化合物 T17297ZXH-3-26
ZXH-3-26 is a selective degrader of the PROTAC BRD4 (DC50/5h: ~ 5 nM).
价 格：￥电议型 号：T17297产 地：中国大陆
-
T17296Zotatifin；化合物 T17296eFT226；eFT226
Zotatifin is a potent and well-tolerated eIF4A inhibitor. Zotatifin promotes eIF4A binding to specific mRNA sequences with recognition motifs in the 5’-UTRs (IC50=2 nM). Zotatifin effectively reduces viral infectivity by inhibiting SARS-CoV-2 NP protein biogenesis (IC90=37 nM).
价 格：￥电议型 号：T17296产 地：中国大陆
-
T17295ZM39923；化合物 T17295ZM39923
ZM39923 is a JAK3 inhibitor (pIC50: 7.1). ZM39923 also effectively inhibits tissue transglutaminase (IC50: 10 nM).
价 格：￥电议型 号：T17295产 地：中国大陆
-
T17294ZL0454；化合物 T17294ZL0454
ZL0454 is an effective and selective Bromodomain-containing protein 4 inhibitors (IC50: 49 and 32 nM for BD1 and BD2).
价 格：￥电议型 号：T17294产 地：中国大陆
-
T17293ZL006；化合物ZL006ZL006
ZL006 is an effective inhibitor of nNOS/PSD-95 interaction. ZL006 also inhibits NMDA receptor-mediated NO synthesis.
价 格：￥电议型 号：T17293产 地：中国大陆
-
T17292ZK159222；化合物 T17292ZK159222
ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character.
价 格：￥电议型 号：T17292产 地：中国大陆
-
T17291ZK 216348；化合物 T17291(+)-ZK 216348；(+)-ZK 216348
ZK 216348 also binds to Progesterone and mineralocorticoid receptors (IC50s: 20.4 nM and 79.9 nM, respectively). ZK 216348 is a nonsteroidal selective glucocorticoid receptor agonist (IC50: 20.3 nM). ZK 216348 has an anti-inflammatory activity similar to Prednisolone.
价 格：￥电议型 号：T17291产 地：中国大陆
-
T17284Zardaverine；扎达维林BY 290|||B 84290；BY 290|||B 84290
Zardaverine (BY 290) is an orally available, selective and potent PDE3/4 inhibitor with bronchodilator activity and anti-hepatocarcinogenic activity.Zardaverine´s action in platelets is mediated by PDE III isoenzymes and can be used in studies of acute renal failure and chronic airflow obstruction.
价 格：￥电议型 号：T17284产 地：中国大陆
-
T17246VU0529331；化合物 T17246VU0529331
VU0529331 is a modestly selective non-GIRK1-containing G protein-gated, inwardly-rectifying, potassium channel activator (EC50s: 5.1 μM and 5.2 μM for GIRK2 and GIRK1/2 in HEK293 cells, respectively). It is also effective on the GIRK4 homomeric channel.
价 格：￥电议型 号：T17246产 地：中国大陆
-
T17229Verubulin化合物 T17229MPC 6827
Verubulin is a microtubule-disrupting agent with potent and broad-spectrum in vitro and in vivo cytotoxic activities.
价 格：￥电议型 号：T17229产 地：中国大陆
-
T17129Tos-PEG3；化合物 T17129Tos-PEG3
Tos-PEG3, a PEG-based PROTAC linker, is suitable for synthesizing PROTACs and 3´-aminooxy oligonucleotide solid supports[1].
价 格：￥电议型 号：T17129产 地：中国大陆
-
T17059Tetrahydrouridine；四氢尿苷NSC 112907|||NSC112907|||NSC-112907；NSC 112907|||NSC112907|||四氢尿苷|||NSC-112907
Tetrahydrouridine (NSC-112907; THU) is a multidrug resistance modulator. It can be used in cancer treatment to make tumor cells more sensitive to radiation therapy. THU is a competitive cytidine deaminase(CDA) inhibitor that inhibits deamination in the catabolism of cytotoxic deoxycytidine analogs such as ara-C and Gemcitabine.
价 格：￥电议型 号：T17059产 地：中国大陆
