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：3565207
自主品牌
已选条件
-
T18610PROTAC FKBP Degrader-3；化合物 T18610PROTAC FKBP Degrader-3
PROTAC FKBP Degrader-3 is a PROTAC that comprises a FKBP ligand binding group, a linker and an VHL binding group. PROTAC FKBP Degrader-3 is a potent FKBP degrader[1].
价 格：￥电议型 号：T18610产 地：中国大陆
-
T18597dFKBP-1；化合物 T18597dFKBP-1
dFKBP-1 is a potent and PROTAC-based FKBP12 degrader. dFKBP-1 incorporates the ligand SLF of FKBP12, the Thalidomide based cereblon ligand and a linker[1].
价 格：￥电议型 号：T18597产 地：中国大陆
-
T1794Micafungin sodium；米卡芬净钠Mycamine Sodium|||FK 463|||FK463 Sodium；Mycamine Sodium|||FK 463|||FK463 Sodi
Micafungin sodium (FK 463) is the sodium salt form of micafungin, a semi-synthetic echinocandin derived from a natural product of the fungus Coleophoma empetri with antifungal activity.
价 格：￥电议型 号：T1794产 地：中国大陆
-
T15285FK706；化合物 T15285FK706
FK706 is a slow-binding and competitive human neutrophil elastase inhibitor (IC50: 83 nM; Ki: 4.2 nM). FK706 also inhibits mouse neutrophil elastase and porcine pancreatic elastase (IC50s: 22 nM and 100 nM, respectively). FK706 has an anti-inflammatory effect.
价 格：￥电议型 号：T15285产 地：中国大陆
-
T14365AZ PFKFB3 26；化合物AZ PFKFB3 26AZ PFKFB3 26
AZ PFKFB3 26 is an effective and selective PFKFB3 inhibitor with an IC50 of 23 nM. The IC50s for PFKFB1 and PFKFB2 are 2.06 and 0.384 μM, respectively.
价 格：￥电议型 号：T14365产 地：中国大陆
-
T1422Nilvadipine；尼伐地平FK235|||FR34235|||ARC029；FK235|||FR34235|||尼伐地平|||ARC029
Nilvadipine (FK235), a calcium channel blocker (CCB), is utilized for treatment of hypertension.
价 格：￥电议型 号：T1422产 地：中国大陆
-
T13914SLF-amido-C2-COOH；化合物 T13914PROTAC FKBP12-binding moiety 1；PROTAC FKBP12-binding moiety 1
SLF-amido-C2-COOH is a synthetic ligand for FKBP (SLF), and can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T13914产 地：中国大陆
-
T13694FKBP12 PROTAC RC32；化合物 T13694RC32；RC32
FKBP12 PROTAC RC32 contains conjugation of Rapamycin and a ligand for an E3 ubiquitin ligase.FKBP12 PROTAC RC32 (RC32) is a potent FKBP12 degrader based on PROTAC technology.
价 格：￥电议型 号：T13694产 地：中国大陆
-
T124984Kushenol F；化合物 Kushenol FKushenol F
Kushenol F is a useful organic compound for research related to life sciences and the catalog number is T124984.
价 格：￥电议型 号：T124984产 地：中国大陆
-
T11941Manitimus；玛尼莫司FK778；FK778
Manitimus (FK778) is an inhibitor of dehydroorotate dehydrogenase and an immunosuppressant with immunosuppressive and antiproliferative activity, prevents vascular remodeling after mechanical endothelial injury, and can be used to study immune dysfunction.
价 格：￥电议型 号：T11941产 地：中国大陆
-
T11293(±)-Fabesetron hydrochloride；化合物 T11293FK1052 hydrochloride；FK1052 hydrochloride
FK1052 hydrochloride is a potent 5-HT3 and 5-HT4 receptor dual antagonist.
价 格：￥电议型 号：T11293产 地：中国大陆
-
T11292FKBP12 PROTAC dTAG-7；化合物 T11292dTAG-7；dTAG-7
FKBP12 PROTAC dTAG-7 (dTAG-7) is a heterobifunctional compound that selectively degrades the BET bromodomain transcriptional co-activator BRD4 by connecting BET bromodomains to the E3 ubiquitin ligase CRBN. Additionally, it serves as a degrader of FKBP12F36V when FKBP12F36V is expressed in-frame with a targeted protein.
价 格：￥电议型 号：T11292产 地：中国大陆
-
T11291FKBP12 PROTAC dTAG-13；化合物 T11291dTAG-13；dTAG-13
FKBP12 PROTAC dTAG-13 (dTAG-13) is a degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 (dTAG-13) also is a selective degrader of BET bromodomain transcriptional co-activator BRD4 by bridging BET bromodomains to an E3 ubiquitin ligase CRBN. FKBP12 PROTAC dTAG-13 (dTAG-13) is a PROTAC-based heterobifunctional degrader.
价 格：￥电议型 号：T11291产 地：中国大陆
-
T11290FK-448 Free base；化合物 T11290FK-448 Free base
FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.
价 格：￥电议型 号：T11290产 地：中国大陆
-
T10055(Iso)-FK-480；化合物 CHEMBL333994CHEMBL333994；CHEMBL333994
(Iso)-FK-480 is a novel orally available cholecystokinin A (CCK-A) antagonist for investigational treatment of chronic pancreatitis.
价 格：￥电议型 号：T10055产 地：中国大陆
-
T0932Cefixime；头孢克肟FK-027|||Cefspan|||Cefiximum|||Cephoral|||FR-17027|||CL-284635；FK-027|||头孢克肟|||Cefspan|
Cefixime (FR-17027) is a broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell wall synthesis by disrupting peptidoglycan synthesis, resulting in a reduction in bacterial cell wall stability and bacterial cell lysis. Stable in the presence of a variety of beta-lactamases, this agent is more active against gram-
价 格：￥电议型 号：T0932产 地：中国大陆
-
T0133Cefdinir；头孢地尼FK-482|||CI-983|||PD 134393；FK-482|||头孢地尼|||CI-983|||PD 134393
Cefdinir (FK-482) is a semi-synthetic, broad-spectrum antibiotic in the third generation of the cephalosporin class, proven effective for common bacterial infections of the ear, sinus, throat and skin.
价 格：￥电议型 号：T0133产 地：中国大陆
