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:3541335
已选条件
-
T70708U 92032;化合物 U 92032U 92032
U 92032 is a T-channel antagonist and antioxidant that inhibits lipid peroxidation.
价 格:¥电议型 号:T70708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
-
T70328HDM-201 succinate;化合物 HDM-201 succinateHDM-201 succinate
HDM-201 succinate is an orally bioavailable human double minute 2 homolog (HDM2) inhibitor with potential antineoplastic activity.
价 格:¥电议型 号:T70328产 地:中国大陆
-
T70327OD38;化合物 OD38OD38
OD38 is a novel potent and selective receptor-interacting protein kinase 2 (ripk2) inhibitor
价 格:¥电议型 号:T70327产 地:中国大陆
-
T70326Mevidalen HBA;化合物 Mevidalen HBAMevidalen HBA
Mevidalen, also known as LY3154207, is a novel, potent, and subtype selective human D1 positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50 = 3 nM). In contrast to orthosteric agonists, LY3154207 showed a distinct pharmacological profile without a bell-shaped dose-response relationship or tachyphylaxis in preclinical models. Identification of a crystalline form of free LY3154207 from the discovery lots was not successful. Instead, a novel cocrystal form with superi
价 格:¥电议型 号:T70326产 地:中国大陆
-
T70325Mifanertinib;化合物 MifanertinibMifanertinib
Mifanertinib is a potent tyrosine kinase inhibitor with antineoplastic activity [1] .
价 格:¥电议型 号:T70325产 地:中国大陆
-
T70324EGFR-IN-557;化合物 EGFR-IN-557EGFR-IN-557
EGFR-IN-557 is an EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis.
价 格:¥电议型 号:T70324产 地:中国大陆
-
T70323Diethanolamine Fusidate;化合物 Diethanolamine FusidateDiethanolamine Fusidate
Diethanolamine Fusidate is a bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid. This product inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA.
价 格:¥电议型 号:T70323产 地:中国大陆
-
T70322Valbenazine dihydrochloride;化合物 Valbenazine dihydrochlorideValbenazine dihydrochloride
Valbenazine dihydrochloride inhibits vesicular monoamine transporter 2 (VMAT2); used to treat tardive dyskinesia.
价 格:¥电议型 号:T70322产 地:中国大陆
-
T70321CBB3001;化合物 CBB3001CBB3001
CBB3001 is a selective lysine-specific histone demethylase LSD1 inhibitor.
价 格:¥电议型 号:T70321产 地:中国大陆
-
T70320GNLPT-IN-1;化合物 GNLPT-IN-1GNLPT-IN-1
GNLPT-IN-1 is an inhibitor of gram-negative lipoprotein trafficking.
价 格:¥电议型 号:T70320产 地:中国大陆
-
T7032Eupatorin;半齿泽兰素Eupatorin
Eupatorin has antiproliferative and antiangiogenic effects. Eupatorin has antiproliferative and cytostatic effects on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism. Eupatorin-induced cell death is mediated by both the extrinsic and the intrinsic apoptotic pathways and through a mechanism dependent on reactive oxygen species generation. Eupatorin also has meaningful anti-inflammatory property.
价 格:¥电议型 号:T7032产 地:中国大陆
-
T70093JTP 103237;化合物 JTP 103237JTP 103237
JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.
价 格:¥电议型 号:T70093产 地:中国大陆
-
T70087EPZ032597;化合物EPZ032597EPZ032597
EPZ032597 is a novel selective inhibitor of SMYD2 with an IC50 of 16 nM. EPZ032597 has anticancer activity and can be used to prevent and treat pancreatic cancer.
价 格:¥电议型 号:T70087产 地:中国大陆
-
T70032NCI-006;化合物 NCI-006NCI-006
NCI-006 is a potent new inhibitor of lactate dehydrogenase (LDH) that disrupts tumor growth in mice. LDH inhibition slows tumor growth but rapidly redirects pyruvate to support mitochondrial metabolism. Inhibiting both mitochondrial complex 1 and LDH suppresses metabolic plasticity of glycolytic tumors in vivo, significantly prolonging tumor growth inhibition.
价 格:¥电议型 号:T70032产 地:中国大陆
-
T7000Tiagabine hydrochloride盐酸噻加宾NO328 hydrochloride|||盐酸噻加宾|||NO050328 hydrochloride|||TGB hydrochloride
Tiagabine hydrochloride (NO050328 hydrochloride) is the hydrochloride salt form of tiagabine, a nipecotic acid derivative with anticonvulsant property. A selective gamma-aminobutyric acid (GABA) reuptake inhibitor.
价 格:¥电议型 号:T7000产 地:中国大陆
-
T6S0325Glycitein;黄豆黄素Glycetein;黄豆黄素|||Glycetein
1. Gycitein has weak estrogenic activity. 2. Glycitein (Glycetein) inhibits glioma cell invasion through down-regulation of MMP-3 and MMP-9 gene expression.
价 格:¥电议型 号:T6S0325产 地:中国大陆
-
T69645BRD20322;化合物 BRD20322BRD20322
BRD20322 is a novel potent inhibitor of spCas9, disrupting spCas9-DNA binding and exerting dose and temporal control of spCas9 in human cell lines.
价 格:¥电议型 号:T69645产 地:中国大陆
-
T69368GKK1032B;化合物 GKK1032BGKK1032B
GKK1032B is a fungal metabolite that has antiproliferative and antibacterial activities. GKK1032B inhibits the growth of HeLa S3 cervical and MCF-7 breast cancer cells and Vero cells. It also inhibits the growth of B. subtilis and M. tuberculosis.
价 格:¥电议型 号:T69368产 地:中国大陆
-
T69032Org 6582;化合物 Org 6582Org 6582
Org 6582 inhibits 3-hydroxytryptamine reuptake.
价 格:¥电议型 号:T69032产 地:中国大陆