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：3847357
自主品牌
已选条件
-
T6767TCS7010Aurora Kinase,inhibit,TCS 7010,Apoptosis,TCS-7010,TCS7010,Inhibitor
Aurora A Inhibitor I is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.
价 格：￥电议型 号：T6767产 地：中国大陆
-
T6676SofosbuvirPSI7977,inhibit,Inhibitor,HCV,PSI 7977,Hepatitis C virus,Sofosbuvir,GS-7977,GS7977
Sofosbuvir is a uridine monophosphate analog inhibitor of hepatitis C virus (HCV) polymerase NS5B that is used as an antiviral agent in the treatment of chronic hepatitis C.
价 格：￥电议型 号：T6676产 地：中国大陆
-
T9906IpilimumabBMS734016,MDX010,Ipilimumab,inhibit,BMS-734016,BMS 734016,Inhibitor,MDX 010,MDX-010
Ipilimumab anti-CTLA-4) is an immunomodulatory monoclonal antibody directed against the cell surface antigen CTLA-4 and also a type of immune checkpoint inhibitor.
价 格：￥电议型 号：T9906产 地：中国大陆
-
T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：中国大陆
-
T8774MS7972inhibit,Inhibitor,MDM-2/p53,MS-7972,MS7972,MS 7972
MS7972 is CREBBP inhibitor that blocks human p53 and CREB binding protein association. MS7972 can almost completely block this BRD interaction at 50 μM
价 格：￥电议型 号：T8774产 地：中国大陆
-
T10893CS-722 Free baseCS722 Free base,CS 722 Free base
CS-722 Free base is a synthetic central muscle relaxant with muscle relaxant activity and inhibitory effect on spinal reflex. CS-722 Free base may inhibit spontaneous inhibitory post-synaptic current and excitatory post-synaptic current in hippocampal culture by inhibiting sodium current and calcium current.
价 格：￥电议型 号：T10893产 地：中国大陆
-
TP1107LMas7 acetate(145854-59-7 free base)Mas7 acetate(145854 59 7 free base),Mas-7 acetate(145854-59-7 fre
Mas7 acetate, a structural analogue of mastoparan is a known activator of heterotrimeric Gi-proteins and its downstream effectors.
价 格：￥电议型 号：TP1107L产 地：中国大陆
-
T6131PimasertibN-[(2S)-2,3-二羟基丙基]-3-[(2-氟-4-碘苯基)氨基]-4-吡啶甲酰胺；MSC1936369B；AS703026；SAR 245509
Pimasertib is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
价 格：￥电议型 号：T6131产 地：中国大陆
-
T2699BMS 777607BMS777607；BMS-777607；BMS 817378
BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：中国大陆
-
T2419BMS-794833BMS794833
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.
价 格：￥电议型 号：T2419产 地：中国大陆
-
T2349BMS-754807BMS 754807；BMS754807
Dual IGF-1R/InsR Inhibitor BMS-754807 is an oral small molecule inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (InsR) tyrosine kinases with potential antineoplastic activity.
价 格：￥电议型 号：T2349产 地：中国大陆
-
T2349BMS-754807BMS-754807,BMS754807,BMS 754807
Dual IGF-1R/InsR Inhibitor BMS-754807 is an oral small molecule inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (InsR) tyrosine kinases with potential antineoplastic activity.
价 格：￥电议型 号：T2349产 地：美洲
-
T2419BMS794833BMS794833
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2; a prodrug of BMS-817378.
价 格：￥电议型 号：T2419产 地：美洲
-
T2699BMS-777607BMS-777607,BMS777607,BMS 777607
BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 nM). BMS-777607 has been investigated for the basic science of Malignant Solid Tumour.
价 格：￥电议型 号：T2699产 地：美洲
-
T6131PimasertibPimasertib,MSC1936369B,AS703026
Pimasertib is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
价 格：￥电议型 号：T6131产 地：美洲
-
T6420BMS-707035BMS-707035,BMS707035,BMS 707035
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格：￥电议型 号：T6420产 地：美洲
-
T8774MS7972；化合物MS7972MS7972
MS7972 is CREBBP inhibitor that blocks human p53 and CREB binding protein association. MS7972 can almost completely block this BRD interaction at 50 μM
价 格：￥电议型 号：T8774产 地：中国大陆
-
T83741S7 TFA；化合物 S7 TFALeu-Ser-Leu-Iso-Thr-Arg-Leu-OH；Leu-Ser-Leu-Iso-Thr-Arg-Leu-OH
S7, a peptide antagonist of the IL-6 receptor, concentration-dependently inhibits IL-6 binding to its receptor. At 50 ?M, S7 suppresses IL-6-triggered elevations in VEGF levels within C-33 A cervical cancer cells and RPMI-8226 B cell lymphocytes. It significantly reduces tumor volume in a C-33 A cervical cancer mouse xenograft model with IL-6 overexpression, following a dosage regimen of 50 mg/kg bi-daily. Moreover, when linked to cysteine on lipid nanoparticles (LNPs) encapsulating doxorubicin,
价 格：￥电议型 号：T83741产 地：中国大陆
-
T83492[His7] Corazonin；化合物 [His7] Corazonin[His7] Corazonin
[His7] Corazonin, a neurohormone in Locusta migratoria, stimulates dark pigmentation in the insect´s cuticle and epidermis [1].
价 格：￥电议型 号：T83492产 地：中国大陆
-
T79326MRS7925；化合物 MRS7925MRS7925
MRS7925 (Compound 43) serves as a potent antagonist of the 5-HT2B receptor, with an inhibition constant (Ki) of 17 nM, and is utilized in the study of fibrosis [1].
价 格：￥电议型 号：T79326产 地：中国大陆
