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:3552913
已选条件
-
TP1549LNY-BR-1 p904 A2 acetate(347142-73-8 free base)NY-BR-1 p-904 A2 acetate(347142-73-8 free base),NYBR1
T-cell clones specific for this NY-BR-1 epitope (p904) can recognize breast tumor cells expressing NY-BR-1.
价 格:¥电议型 号:TP1549L产 地:中国大陆
-
T11079NMI 8739
NMI 8739 is an agonist of D2 autoreceptor. NMI 8739 reduces NO production and elicits concentration-dependent suppression of CCL-20, MCP-1 and IL-6 release.
价 格:¥电议型 号:T11079产 地:中国大陆
-
T1730NPS-2143SB-262470A,Inhibitor,NPS-2143,NPS2143,inhibit,Calcium-sensing receptor,CaSR
NPS-2143 is a novel potent and selective antagonist of Ca(2+) receptor.
价 格:¥电议型 号:T1730产 地:中国大陆
-
T7598Calcium N5-methyltetrahydrofolateinhibit,NSC 173328,Calcium N5methyltetrahydrofolate,Antifolate,NSC-
Calcium N5-methyltetrahydrofolate is the calcium salt of levomefolic acid, which has been proposed for treatment of cardiovascular disease and advanced cancers such as breast and colorectal cancers
价 格:¥电议型 号:T7598产 地:中国大陆
-
T17315(±)-CPSI-1306
(±)-CPSI-1306 is a macrophage migration inhibitory factor (MIF) antagonist and can be used in studies about non-insulin-dependent diabetes mellitus (NIDDM) and the prevention of the deleterious cutaneous effects of acute and chronic UVB exposure.
价 格:¥电议型 号:T17315产 地:中国大陆
-
T6785BI-847325BI 847325,inhibit,Apoptosis,MEK,MAPKK,MAP2K,Inhibitor,Aurora Kinase,Mitogen-activated prote
BI-847325 is a selective dual inhibitor of MEK and aurora kinases (AK) with IC50 values of 4 and 15 nM for human MEK2 and AK-C, respectively.
价 格:¥电议型 号:T6785产 地:中国大陆
-
TN1073Nuezhenidic acidinhibit,Inhibitor,Nuezhenidic acid
Nuezhenidic acid is a natural product, posseses inhibitory activities against influenza A virus.
价 格:¥电议型 号:TN1073产 地:中国大陆
-
T6S1373Casticininhibit,Inhibitor,Casticin,STAT
1. Vitexicarpin can significantly reduce vascular inflammation, through inhibition of ROS-NF-κB pathway in vascular endothelial cells. 2. Vitexicarpin may become a potential leading drug in the therapy of prostate carcinoma.
价 格:¥电议型 号:T6S1373产 地:中国大陆
-
T13739Isopropylidenylacetyl-marmesin
Isopropylidenylacetyl-marmesin is a natural product derived from the roots of Notopterygium incisum and Ferulago bracteata.
价 格:¥电议型 号:T13739产 地:中国大陆
-
T6734WZ8040HER1,WZ 8040,mutated,WZ8040,Inhibitor,phosphorylation,EGFR,NSCLC,Epidermal growth factor recep
WZ8040 is a novel mutant-selective irreversible EGFRT790M inhibitor, does not inhibit ERBB2 phosphorylation (T798I).
价 格:¥电议型 号:T6734产 地:中国大陆
-
TP1273FLAG peptideInhibitor,FLAG peptide,inhibit
FLAG peptide is an eight amino acids peptide (Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys) with an enterokinase-cleavage site used for the purification of recombinant proteins.
价 格:¥电议型 号:TP1273产 地:中国大陆
-
TN6735Bigelovininhibit,Autophagy,Inhibitor,Retinoic acid receptors,Bigelovin,Retinoid X receptors,Apoptosi
Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.
价 格:¥电议型 号:TN6735产 地:中国大陆
-
T8737GR 125743h5-HT1B,cognitive disorder,h5-HT1D,cardiovascular,GR-125743,GR125743,inhibit,Parkinson’s di
GR 125743 is a novel antagonist of 5-HT1B/1D receptor.
价 格:¥电议型 号:T8737产 地:中国大陆
-
TN6733Kansuiphorin CKansuiphorin C,inhibit,Inhibitor
Kansuiphorin C is a natural product with a number of bioactivity. KPC could ameliorate malignant ascites by modulating gut microbiota mainly containing the increase of Lactobacillus and the decrease of Helicobacter and related carbohydrate and amino acid metabolism.
价 格:¥电议型 号:TN6733产 地:中国大陆
-
T7080CCT245737CCT245737,Inhibitor,CCT 245737,inhibit,Checkpoint Kinase (Chk),CCT-245737
CCT245737 is an orally active and selective Chk1 inhibitor (IC50: 1.3 nM); CCT245737 shows much less activity against Chk2 (IC50: 2440 nM).
价 格:¥电议型 号:T7080产 地:中国大陆
-
T7391SAR407899SAR 407899,Rho-associated kinase,ROK,Rho-kinase,ROCK,Rho-associated protein kinase,SAR40789
SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
价 格:¥电议型 号:T7391产 地:中国大陆
-
T11014DFP00173AQP,Inhibitor,human,isoforms,erythrocytes,selective,homologous,DFP 00173,glycerol,DFP-00173,
DFP00173 is a potent and selective aquaporin 3 (AQP3) inhibitor. DFP00173 inhibits mouse and human AQP3 with IC50 of ~0.1-0.4 μM. Compared with the homologous AQP subtypes AQP7 and AQP9, DFP00173 is selective for AQP3.
价 格:¥电议型 号:T11014产 地:中国大陆
-
T7322TheliatinibATP-competitive,inhibit,EGFR,ERK,cancer,esophageal,Epidermal growth factor receptor,HMPL-
Theliatinib, a potent and highly selective EGFR inhibitor, with anti-tumor activity. Ki of 0.05 nM for wild type EGFR, and IC50s of 3 and 22 nM for EGFR and EGFR T790M/L858R mutant, respectively.
价 格:¥电议型 号:T7322产 地:中国大陆
-
T7734BETA-CFT sulfateBETACFT sulfate,BETA CFT sulfate
BETA-CFT sulfate is a chemical compound.
价 格:¥电议型 号:T7734产 地:中国大陆
-
T27328FL104FL104
FL104 is a potent agonist of small-molecule urotensin II receptor, pEC50= 7.11.
价 格:¥电议型 号:T27328产 地:中国大陆