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：3615876
自主品牌
已选条件
-
T6259DizocilpineMK-801；地佐环平
MK-801 (Dizocilpine) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM.
价 格：￥电议型 号：T6259产 地：中国大陆
-
T6061LMK-235LMK235；LMK 235
LMK-235 is a potent HDAC inhibitor, and is used in cancer research.
价 格：￥电议型 号：T6061产 地：中国大陆
-
T6035Odanacatib奥达卡替；奥当卡替；MK-0822
Odanacatib is an inhibitor of cathepsin K with potential anti-osteoporotic activity.
价 格：￥电议型 号：T6035产 地：中国大陆
-
T6032BirabresibMK-8628；OTX015 （MK 8628/Birabresib）；OTX-015
Birabresib is a synthetic, small molecule inhibitor of the BET (Bromodomain and Extra-Terminal) family of bromodomain-containing proteins 2, 3 and 4 with potential antineoplastic activity.
价 格：￥电议型 号：T6032产 地：中国大陆
-
T6013Z-VAD(OMe)-FMKZ-Val-Ala-Asp(OMe)-FMK；Z-VAD-FMK
Z-VAD(OMe)-FMK is a cell-permeable and irreversible pan-caspase inhibitor. It inhibits cleavage of PARP, preventing apoptosis when used at 10-50 μM.
价 格：￥电议型 号：T6013产 地：中国大陆
-
T6005Z-DEVD-FMKCaspase-3 Inhibitor
Z-DEVD-FMK is a selective, irreversible Caspase-3 inhibitor, and also exhibits effective inhibition activity on caspase-6, caspase-7, caspase-8, and caspase-10.
价 格：￥电议型 号：T6005产 地：中国大陆
-
T5954Methyldopa hydrateL-甲基多巴；L-(-)-α-Methyldopa hydrate；Methyldopa Sesquihydrate；MK-351 hydrate；Alpha-Me
Alpha-Methyldopa Sesquihydrate is a DOPA decarboxylase inhibitor and indirect α2-adrenergic receptor agonist used to treat hypertension. It inhibits the sympathetic nervous system, decreases production of dopamine, norepinephrine, and epinephrine, and exh
价 格：￥电议型 号：T5954产 地：中国大陆
-
T5863Indinavir sulfate硫酸茚地那韦；MK-639 sulfate；L735524 sulfate
Indinavir is a HIV protease inhibitor.It inhibits the HIV-1 protease with an IC50 value of 0.41 nM and Ki value of 0.24 nM.
价 格：￥电议型 号：T5863产 地：中国大陆
-
T5836Eprinomectin依普菌素；MK-397
Eprinomectin is an avermectin with anthelmintic and insecticidal activities.
价 格：￥电议型 号：T5836产 地：中国大陆
-
T5632SuvecaltamideMK-8998
MK-8998 as potent inhibitors of T-type calcium channels.
价 格：￥电议型 号：T5632产 地：中国大陆
-
T5396Letermovir莱莫维韦；MK-8828；AIC246
Letermovir (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.
价 格：￥电议型 号：T5396产 地：中国大陆
-
T5152MKT-077MKT077；MKT 077；FJ-776
MKT-077 is a cationic rhodacyanine dye that demonstrates antiproliferative activity against cancer cell lines (EC50s: 1.4-2.2 μM in vitro) through its ability to inhibit members of the Hsp70 family of molecular chaperones.
价 格：￥电议型 号：T5152产 地：中国大陆
-
T5099GefapixantAF219；RO 4926219；MK-7264
Gefapixant is a P2X3 receptor (P2X3R) antagonist with IC50 of ~30 nM at recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors.
价 格：￥电议型 号：T5099产 地：中国大陆
-
T4999Ertugliflozin埃格列净；PF-04971729；MK-8835
PF-04971729 (Ertugliflozin) is a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2).
价 格：￥电议型 号：T4999产 地：中国大陆
-
T4991Ertapenem sodiumL-749345；MK-826；厄他培南钠；尔他培南钠
Ertapenem sodium is a new long-acting 1-β-methyl carbapenem antibiotic with a broad antibacterial spectrum including common aerobic and anaerobic bacteria and organisms with extended-spectrum β-lactamases.
价 格：￥电议型 号：T4991产 地：中国大陆
-
T4598BMS-5LIMKi 3；BMS5；BMS 5
BMS-5 is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.
价 格：￥电议型 号：T4598产 地：中国大陆
-
T4547GrazoprevirMK-5172
MK-5172 is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Ki of 0.01 nM (gt1a), 0.08 nM (gt2a), 0.90 nM (gt3a), 0.01 nM (gt1b), 0.15 nM (gt2b), respectively.
价 格：￥电议型 号：T4547产 地：中国大陆
-
T4544ElbasvirMK-8742
Elbasvir is an inhibitor of nonstructural protein 5A (NS5A) of hepatitis C virus (HCV) being developed as a component of treatment regimens for chronic HCV infection.
价 格：￥电议型 号：T4544产 地：中国大陆
-
T4442MK2-IN-1 hydrochlorideMK2 Inhibitor；MK 25
MK2-IN-1 is a highly selective, non-ATP competitive inhibitor of p38/mitogen-activated protein kinase-activated protein kinase 2 (MAPKAPK2 or MK2, IC50: 0.11 μM) [1].
价 格：￥电议型 号：T4442产 地：中国大陆
-
T4106MK-8617MK8617；MK 8617
MK-8617 is an orally available HIF PHD1 3 pan-inhibitor, inhibiting PHD1/2/3 (IC50: 1.0/1.0/14 nM).
价 格：￥电议型 号：T4106产 地：中国大陆
