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
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:3717967
已选条件
-
T70370PF-06658607;化合物 PF-06658607PF-06658607
PF-06658607 is an alkynylated irreversible Brutons tyrosine kinase (BTK) inhibitor.
价 格:¥电议型 号:T70370产 地:中国大陆
-
T70377-Acetoxy-4-methylcoumarin;7-乙酰氧基-4-甲基香豆素MU-Ac;7-乙酰氧基-4-甲基香豆素|||MU-Ac
7-Acetoxy-4-methylcoumarin is a fluorogenic substrate for carboxylesterase yielding a blue fluorescent solution upon cleavage. The compound has been used in aprotic media, a cell membrane environmental mimic, to study superoxide and related oxyl-radical reactions of model biological membranes dispersed in aqueous media. Due to the ability for AchE to cleave and activate 7-Acetoxy-4-methylcoumarin, the fluorogenic substrate has been used to study the AchE inhibitor Tacrine·HCl (sc-200172). The co
价 格:¥电议型 号:T7037产 地:中国大陆
-
T70329SH-11037;化合物 SH-11037SH-11037
SH-11037 is a novel potent seh inhibitor, effectively blocking key angiogenic properties of human retinal endothelial cells (hrecs), inhibiting choroidal sprouting and significantly suppressing cnv lesion volume
价 格:¥电议型 号:T70329产 地:中国大陆
-
T70037AJG-049 free base;化合物 AJG-049 free baseAJG-049 free base
AJG-049 free base is a calcium channel antagonist that inhibits L-type Ca2+ channels via diltiazem-binding site(s).
价 格:¥电议型 号:T70037产 地:中国大陆
-
T69678WUN40378;化合物 WUN40378WUN40378
WUN40378 is compound first reported in PCT Int. Appl. (2019), WO 201909959, in which it was described as CBFβ-?RUNX1 inhibitor. WUN40378 is very similar to Ro 5-3335 but with an F instead of Cl. WUN40378 is also analog of Ro 24-7429. This product has no formal name at the moment. For the convenience of communication, a temporary code name was therefore proposed according to MedKoo Chemical Nomenclature (see web page: https://www.medkoo.com/page/naming).
价 格:¥电议型 号:T69678产 地:中国大陆
-
T69037Azaperone dimaleate;化合物 Azaperone dimaleateAzaperone dimaleate
Azaperone dimaleate is a dopamine antagonist.
价 格:¥电议型 号:T69037产 地:中国大陆
-
T68037LCBS-1114 HCl;CBS-1114盐酸盐N-Phenylbenzamidrazone hydrochloride|||cbs-1114 HCl(46721-85-1 Free base);N-
CBS-1114 HCl (N-Phenylbenzamidrazone hydrochloride) is a 5-lipoxygenase inhibitor and an anti-inflammatory compound in a good eye-permeable model.CBS-1114 HCl maintains and improves cardiac function, attenuates cardiac dysfunction, as well as reduces epicardial adipose tissue and/or pericardial adipose tissue in subjects with cardiovascular disease.
价 格:¥电议型 号:T68037L产 地:中国大陆
-
T670371-(3-Carboxy-2-pyridyl)-4-methyl-2-phenylpiperazine;化合物 1-(3-Carboxy-2-pyridyl)-4-methyl-2-phenylpip
1-(3-Carboxy-2-pyridyl)-4-methyl-2-phenylpiperazine is a useful organic compound for research related to life sciences. The catalog number is T67037 and the CAS number is 61338-13-4.
价 格:¥电议型 号:T67037产 地:中国大陆
-
T6626PF-3758309;化合物PF3758309PF-309|||PF-03758309|||PF 3758309;PF-309|||PF-03758309|||PF 3758309
PF-3758309 (PF-03758309) (IC50=1.3 nM), a pyrrolopyrazole inhibitor of PAK4, has effective ATP-competition.
价 格:¥电议型 号:T6626产 地:中国大陆
-
T66037(R)-Tetrahydropapaverine hydrochloride;(R)-Tetrahydropapaverine 盐酸盐(R)-Tetrahydropapaverine hydrochl
(R)-Tetrahydropapaverine hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T66037 and the CAS number is 54417-53-7.
价 格:¥电议型 号:T66037产 地:中国大陆
-
T6521GSK 2830371化合物GSK2830371GSK2830371
GSK 2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM.
价 格:¥电议型 号:T6521产 地:中国大陆
-
T65037Boc-Gly-OtBu;化合物 Boc-Gly-OtBuBoc-Gly-OtBu
Boc-Gly-OtBu is a useful organic compound for research related to life sciences. The catalog number is T65037 and the CAS number is 111652-20-1.
价 格:¥电议型 号:T65037产 地:中国大陆
-
T6438Cefoselis Sulfate硫酸头孢噻利FK 037 Sulfate|||FK-037|||硫酸头孢噻利
Cefoselis Sulfate (FK 037 Sulfate) is a widely used beta-lactam antibiotic.
价 格:¥电议型 号:T6438产 地:中国大陆
-
T64311KUSC-5037;化合物 KUSC-5037KUSC-5037
KUSC-5037 is a potent inhibitor of HIF-1 with an IC50 value of 1.2 μM. KUSC-5037 exhibits inhibitory effects on mitochondrial respiratory complex V and FoF1ATP synthase.
价 格:¥电议型 号:T64311产 地:中国大陆
-
T64037CYP3A4-IN-2;化合物 CYP3A4-IN-2CYP3A4-IN-2
CYP3A4-IN-2 is a specific inhibitor of cytochrome P450 3A4 (CYP3A4) (IC50: 0.055 μM). CYP3A4-IN-2 is a ritonavir analogue with a more hydrophobic R2 side group and stronger inhibition than ritonavir. CYP3A4-IN-2 is capable of acting as an immunosuppressive and antiviral agent.
价 格:¥电议型 号:T64037产 地:中国大陆
-
T63705UNC0379 TFA;化合物 UNC0379 TFAUNC0379 TFA
UNC0379 TFA is a selective, substrate competitive inhibitor of lysine methyltransferase SETD8 (KMT5A) (IC50: 7.3 μM) and exhibits good selectivity for 15 other methyltransferases.
价 格:¥电议型 号:T63705产 地:中国大陆
-
T63072ETP-47037;化合物 ETP-47037ETP-47037
ETP-47037 is a potent inhibitor of the PI3Kα isoform (IC50: 0.99 nM) and inhibits the PI3Kβ (IC50: 49.2 nM), PI3Kδ (IC50: 7.13 nM) and PI3Kγ (IC50: 49.1 nM) isoforms. ETP-47037 has potential for telomere protection chemoregulation studies.
价 格:¥电议型 号:T63072产 地:中国大陆
-
T63037hDHODH-IN-10;化合物 hDHODH-IN-10hDHODH-IN-10
hDHODH-IN-10 is a selective, orally active, potent hDHODH inhibitor (IC50: 10.9 nM) that forms hydrogen bonds with key residues Arg136 and Gln47. hDHODH-IN-10 inhibits the proliferation of cancer cells and can be used to study cancers (e.g. AML, colon cancer).
价 格:¥电议型 号:T63037产 地:中国大陆
-
T6254Idasanutlin;依达奴林RG7388|||Ro 5503781;RG7388|||Ro 5503781|||依达奴林
Idasanutlin (Ro 5503781) (RG-7388) is an effective and specific p53-MDM2 inhibitor (IC50: 6 nM).
价 格:¥电议型 号:T6254产 地:中国大陆
-
T62037BNS-22;化合物 BNS-22BNS-22
BNS-22 is a catalytic inhibitor of DNA topoisomerase II ( TOP2 ). BNS-22 shows the IC 50 values of 2.8 μM and 0.42 μM for human TOP2α and TOP2β, respectively. BNS-22 induces abnormal division and shows anti-proliferative activity.
价 格:¥电议型 号:T62037产 地:中国大陆