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：3856017
自主品牌
已选条件
-
T68241Wy 27127；化合物 Wy 27127Wy 27127
Wy 27127 is an alpha 2-adrenoceptors antagonist that has estimated potency based on ability to block clonidine-induced inhibition of electrically-evoked contractions of the rat isolated vas deferens.
价 格：￥电议型 号：T68241产 地：中国大陆
-
T68127Picenadol；哌西那朵LY-150720|||LY150720|||LY 150720；LY-150720|||LY150720|||LY 150720
Picenadol (LY 150720) is a racemic mixture of N-methyl-4-phenylpiperidine derivatives with agonist-antagonist opioid properties.Picenadol has central analgesic activity.
价 格：￥电议型 号：T68127产 地：中国大陆
-
T671271H-1,2,4-Triazole-1-carboximidamide hydrochloride；化合物 1H-1,2,4-Triazole-1-carboximidamide hydrochlor
1H-1,2,4-Triazole-1-carboximidamide hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T67127 and the CAS number is 19503-26-5.
价 格：￥电议型 号：T67127产 地：中国大陆
-
T661272-(Aminomethyl)benzonitrile hydrochloride；化合物 2-(Aminomethyl)benzonitrile hydrochloride2-(Aminomethy
2-(Aminomethyl)benzonitrile hydrochloride is a useful organic compound for research related to life sciences. The catalog number is T66127 and the CAS number is 1134529-25-1.
价 格：￥电议型 号：T66127产 地：中国大陆
-
T65127Sodium phosphate dibasic dodecahydrate；化合物 Sodium phosphate dibasic dodecahydrateSodium phosphate di
Sodium phosphate dibasic dodecahydrate is a useful organic compound for research related to life sciences and the catalog number is T65127.
价 格：￥电议型 号：T65127产 地：中国大陆
-
T64127VT-1598；化合物 VT-1598VT-1598
VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.
价 格：￥电议型 号：T64127产 地：中国大陆
-
T63127PDGFRα/FLT3-ITD-IN-3；化合物 PDGFRα/FLT3-ITD-IN-3PDGFRα/FLT3-ITD-IN-3
PDGFRα/FLT3-ITD-IN-3 (Compound 18d) is a potent inhibitor of PDGFRα (IC50: 0.153 μM), FLT3 (IC50: 0.004 μM) and PDGFRα/FLT3-ITD-IN-3 has the potential to be studied in acute myeloid leukaemia or chronic eosinophilic leukaemia. .
价 格：￥电议型 号：T63127产 地：中国大陆
-
T6290Tanespimycin；坦螺旋霉素17-AAG|||CP 127374|||NSC 330507|||KOS 953；坦螺旋霉素|||17-AAG|||CP 127374|||NSC 330507|
Tanespimycin (KOS 953) (17-AAG) is an inhibitor of Hsp90 that selectively inhibits BT474 tumor cell Hsp90 (IC50: 5 nM).
价 格：￥电议型 号：T6290产 地：中国大陆
-
T62618SPH3127；化合物 SPH3127SPH3127
SPH3127 (DRI 18) is a potent, orally active, novel direct renin inhibitor with IC50 values of 0.4 nM and 0.45 nM for recombinant human-renin and human plasma renin activity, respectively. SPH3127 has an anti-hypertensive effect and can be used to study hypertension.
价 格：￥电议型 号：T62618产 地：中国大陆
-
T62127AMPA-IN-1；化合物 AMPA-IN-1AMPA-IN-1
AMPA-IN-1 is a potent inhibitor of AMPA receptors, a widely expressed receptor in the brain with a central role in the regulation of rapid excitatory synaptic transmission and synaptic plasticity. 14).
价 格：￥电议型 号：T62127产 地：中国大陆
-
T61971CHMFL-PI4K-127；化合物 CHMFL-PI4K-127CHMFL-PI4K-127
CHMFL-PI4K-127 (compound 15g) is a highly selective inhibitor of PfPI4K (Plasmodium falciparum PI4K kinase) with oral activity (IC50=0.9 nM). CHMFL-PI4K-127 shows strong inhibitory activity against Plasmodium falciparum 3D7 (EC50=25.1 nM). CHMFL-PI4K-127 has anti-malaria effect.
价 格：￥电议型 号：T61971产 地：中国大陆
-
T6179Moxalactam sodium salt拉氧头孢钠Latamoxef sodium|||6059 S|||拉氧头孢钠|||Moxalactam Disodium|||LY-127935|||Ant
Moxalactam sodium salt (LY-127935) is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosathan cephalosporins.
价 格：￥电议型 号：T6179产 地：中国大陆
-
T6154SU11274；化合物SU11274Met Kinase Inhibitor|||PKI-SU11274；Met Kinase Inhibitor|||PKI-SU11274
SU11274 (Met Kinase Inhibitor)(IC50=10 nM) is a specific Met inhibitor. It shows no significant effects on PGDFRβ, EGFR or Tie2.
价 格：￥电议型 号：T6154产 地：中国大陆
-
T61279TS010；化合物 TS010TS010
TS010 is a highly potent inhibitor of GLO-I, with an IC50 value of 0.57 μM. It holds significant promise for advancements in cancer research [1].
价 格：￥电议型 号：T61279产 地：中国大陆
-
T61278Aminopeptidase-IN-1；氨基肽酶-IN1Aminopeptidase-IN-1
Aminopeptidase-IN-1 is a potent inhibitor of insulin-regulated aminopeptidase (IRAP) (Ki: 7.7 μM).Aminopeptidase-IN-1 can be used in studies of cognitive and memory disorders.
价 格：￥电议型 号：T61278产 地：中国大陆
-
T61277mGluR2 modulator 4；化合物 mGluR2 modulator 4mGluR2 modulator 4
mGluR2 modulator 4 (compound 47) is a highly potent positive allosteric modulator of mGluR2, exhibiting an EC 50 value of 0.8 μM. It holds the potential for investigating antipsychotic properties [1].
价 格：￥电议型 号：T61277产 地：中国大陆
-
T61276CB1R Allosteric modulator 2；化合物 CB1R Allosteric modulator 2CB1R Allosteric modulator 2
CB1R Allosteric modulator 2 (compound 18) is a potent allosteric modulator of the CB1R receptor. It exhibits negative modulation of the functional activity of orthosteric ligands (NAM) at CB1Rs, as demonstrated in previous studies [1].
价 格：￥电议型 号：T61276产 地：中国大陆
-
T61275TRPM4-IN-2；化合物TRPM4-IN-2NBA；NBA
TRPM4-IN-2 (NBA), also known as NBA, is a highly effective inhibitor of transient receptor potential melastatin 4 (TRPM4). Its inhibitory potency is represented by an IC 50 value of 0.16 μM. This compound serves as a valuable tool in the investigation of prostate cancer and colorectal cancer [1] [2].
价 格：￥电议型 号：T61275产 地：中国大陆
-
T61274PC190723；化合物 PC190723PC190723
PC190723 (Compound 2), an inhibitor of the FtsZ bacterial cell division protein, demonstrates potent efficacy with an IC50 value of 55 ng/ml. Additionally, it showcases notable anti-staphylococcal activity, characterized by Minimum Inhibitory Concentration (MIC) values of 1 μg/ml against both Methicillin-Sensitive Staphylococcus aureus (MSSA) and Methicillin-Resistant Staphylococcus aureus (MRSA) [1].
价 格：￥电议型 号：T61274产 地：中国大陆
-
T61272EGFR/HER2-IN-7；化合物 EGFR/HER2-IN-7EGFR/HER2-IN-7
EGFR/HER2-IN-7 is a highly selective and potent anticancer compound specifically designed to target MCF-7 breast cancer cells. It functions as a dual inhibitor, targeting both EGFR/HER2 kinases and DHFR (dihydrofolate reductase). Its inhibitory activities are measured with IC50 values of 0.18 μM for EGFR, 0.146 μM for HER2, and 0.907 μM for DHFR [1].
价 格：￥电议型 号：T61272产 地：中国大陆
