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：3547323
自主品牌
已选条件
-
T1615Irbesartan厄贝沙坦；SR-47436；BMS-186295
Irbesartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of irbesartan is as an Angiotensin 2 Receptor Antagonist.
价 格：￥电议型 号：T1615产 地：中国大陆
-
T16144MRX-2843UNC2371
MRX-2843 is a potent and orally active inhibitor of MERTK and FLT3(IC50s of 1.3 nM and 0.64 nM, respectively).
价 格：￥电议型 号：T16144产 地：中国大陆
-
T16143MRTX-1257
MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse, with free fraction exposures well above the
价 格：￥电议型 号：T16143产 地：中国大陆
-
T16140MRS 1754
MRS 1754 is a selective antagonist radioligand for the A2B adenosine receptor. It has a very low affinity for A1 and A3 receptors of both humans and rats.
价 格：￥电议型 号：T16140产 地：中国大陆
-
T16136MRS-1706
MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1, and A3 receptors respectively. MRS-1706 is an effective and selective adenosine A2B receptor inverse agonist.
价 格：￥电议型 号：T16136产 地：中国大陆
-
T16133MRK-560
MRK-560 is an effective and brain-penetrant inhibitor of γ-secretase.
价 格：￥电议型 号：T16133产 地：中国大陆
-
T16130Mps1-IN-3
Mps1-IN-3 is an effective and selective inhibitor of MPS1 kinase (IC50: 50 nM).
价 格：￥电议型 号：T16130产 地：中国大陆
-
T1613Hydralazine hydrochloride盐酸肼屈嗪；Hydralazine HCl；Apresoline
Hydralazine Hydrochloride is the hydrochloride salt of hydralazine, a phthalazine derivative with antihypertensive and potential antineoplastic activities. Hydralazine alters intracellular calcium release and interferes with smooth muscle cell calcium inf
价 格：￥电议型 号：T1613产 地：中国大陆
-
T16129MPI_5a
MPI_5a is an effective and selective inhibitor of HDAC6 (IC50=36 nM). MPI_5a weakly inhibits other HDAC isoforms and it also inhibits acyl-tubulin accumulation in cells (IC50: 210 nM).
价 格：￥电议型 号：T16129产 地：中国大陆
-
T16128MP-A08
MP-A08 is a highly selective ATP competitive inhibitor of sphingosine kinase (SPHK1) that targets both SphK1 and SphK2 (Ki: 6.9 ± 0.8 μM and 27 ± 3 μM, respectively).
价 格：￥电议型 号：T16128产 地：中国大陆
-
T16125MMV390048
MMV390048 is an antimalarial agent and is a representative of a new chemical class of Plasmodium PI4K inhibitor (Kdapp=0.3 μM). MMV390048 binds to the ATP binding site of Plasmodium PI4K and does not bind to other P. falciparum and human kinases apart fro
价 格：￥电议型 号：T16125产 地：中国大陆
-
T16124MMP13-IN-3
MMP13-IN-3 is >1000 selective over other MMPs. MMP13-IN-3 is an effective, selective, and orally active MMP-13 inhibitor (IC50=1 nM) for the potential treatment of osteoarthritis.
价 格：￥电议型 号：T16124产 地：中国大陆
-
T1612Neostigmine methyl sulfateNormastigmin；Syntostigmin；Hodostin；甲基硫酸新斯的明；甲硫酸新斯的明
Hodostin is a reversible inhibitor of acetylcholinesterase, can not cross the blood-brain barrier, used in the treatment of myasthenia gravis.
价 格：￥电议型 号：T1612产 地：中国大陆
-
T16118MLS0315771
MLS0315771 is an effective and biologically active competitive phosphomannose isomerase (MPI) inhibitor (IC50: ~1 μM and a Ki: 1.4 μM).
价 格：￥电议型 号：T16118产 地：中国大陆
-
T16116MLN-4760
MLN-4760 is an angiotensin-converting (ACE2) inhibitor(human ACE2;IC50=0.44 nM). It also has excellent selectivity (>5000-fold) versus related enzymes including human testicular ACE (IC50, >100 μM) and bovine carboxypeptidase A (CPDA; IC50, 27 μM).
价 格：￥电议型 号：T16116产 地：中国大陆
-
T16115MLi-2
MLi-2 is a structurally novel, highly potent, and selective LRRK2 kinase inhibitor with central nervous system activity. MLi-2 exhibits exceptional potency in a purified LRRK2 kinase assay in vitro (IC50 = 0.76 nM), a cellular assay monitoring dephosphory
价 格：￥电议型 号：T16115产 地：中国大陆
-
T16110ML418
ML418 is a potent, selective and CNS penetrating Kir7.1 potassium channel blocker (IC50 = 310 nM), and also potently inhibits Kir6.2/SUR1.
价 格：￥电议型 号：T16110产 地：中国大陆
-
T1611Isotretinoin异维A酸；13-cis-Retinoic acid
Isotretinoin binds to and activates nuclear retinoic acid receptors (RARs); activated RARs serve as transcription factors that promote cell differentiation and apoptosis. Isotretinoin is a naturally-occurring retinoic acid with potential antineoplastic ac
价 格：￥电议型 号：T1611产 地：中国大陆
-
T16104ML-9
ML-9 suppresses MLCK, PKA, and PKC activity with Ki values of 4, 32, and 54 μM, respectively. ML-9 is a selective and effective inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK), and stromal interaction molecule 1 (STIM1) activity. ML-9 c
价 格：￥电议型 号：T16104产 地：中国大陆
-
T16102ML-792
ML-792 is a specific small ubiquitin-like modifier (SUMO)-activating enzyme (SAE) inhibitor. Compared with NAE/NEDD8 and UAE/ubiquitin (IC50s of 32 μM and >100 μM, respectively), ML-792 is an effective and selective inhibitor of SAE/SUMO1 and SAE/SUMO2 in
价 格：￥电议型 号：T16102产 地：中国大陆
