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:3777660
已选条件
-
T82701CMV pp65(13-27);化合物 CMV pp65(13-27)CMV pp65(13-27)
CMV pp65(13-27) is a bioactive peptide derived from the 65k lower matrix phosphoprotein of the human cytomegalovirus, specifically comprising amino acid residues 13 to 27. It includes a nine-amino-acid sequence (LGPISGHVL) that corresponds to the consensus binding motif for the major histocompatibility complex H2-Dd T-cell epitope.
价 格:¥电议型 号:T82701产 地:中国大陆
-
T81754mP6;化合物 mP6Myr-FEEERA-OH;Myr-FEEERA-OH
mP6 (Myr-FEEERA-OH), a myristoylated peptide, selectively inhibits Gα 13´s interaction with integrin β 3 while preserving talin-dependent integrin function. Additionally, mP6 impedes the GTPase activity of Rac1, Rap1, and Rab7, effectively reducing the infection of CHO-A24 cells [1].
价 格:¥电议型 号:T81754产 地:中国大陆
-
T81578p60c-src substrate II, phosphorylated;化合物 p60c-src substrate II, phosphorylatedp60c-src substrate II
Phosphorylated p60c-src substrate II is a pentapeptide and a phosphorylated polypeptide form of p60c-src substrate II. Phosphorylation is a critical post-translational modification (post-translationmodification) vital for biological regulatory processes [1].
价 格:¥电议型 号:T81578产 地:中国大陆
-
T81577P60v-src(137-157);化合物 P60v-src(137-157)P60v-src(137-157)
P60v-src(137-157) is a synthetic peptide that serves as an inhibitor of the tyrosine kinase activity of p60 v-src, with an IC50 value of 7.5 μM [1] [2].
价 格:¥电议型 号:T81577产 地:中国大陆
-
T81356PTBP1-RNA-binding inhibitor P6 TFA;化合物 PTBP1-RNA-binding inhibitor P6 TFAPTBP1 α3-helix derived pept
PTBP1-RNA-binding inhibitor P6 (PTBP1 α3-helix derived peptide P6) TFA is a stapled peptide that acts as an inhibitor for the splicing factor PTBP1, targeting the alternative splicing events this protein regulates. It operates by binding to RNA via PTBP1´s RNA recognition motif [1].
价 格:¥电议型 号:T81356产 地:中国大陆
-
T81217SAP6;化合物 SAP6SAP6
SAP6 is a bioactive peptide that inhibits virus entry into cells.
价 格:¥电议型 号:T81217产 地:中国大陆
-
T80686γ-AA peptide P6;化合物 γ-AA peptide P6γ-AA peptide P6
γ-AA peptide P6 acts as a potent activator of E6 associated protein (E6AP), facilitating both its self-ubiquitination and the ubiquitination of E6AP substrates in vitro reconstituted reactions. Furthermore, γ-AA peptide P6 amplifies substrate ubiquitination within the cell, thereby expediting their proteasomal degradation [1].
价 格:¥电议型 号:T80686产 地:中国大陆
-
T76617(D-Trp6)-LHRH free acid;化合物 (D-Trp6)-LHRH free acid(D-Trp6)-LHRH free acid
(D-Trp6)-LHRH free acid is a luteinizing hormone-releasing hormone ( LHRH ) agonist [1] .
价 格:¥电议型 号:T76617产 地:中国大陆
-
T76427(D-Pro2,D-Trp6,8,Nle10)-Neurokinin B;化合物 (D-Pro2,D-Trp6,8,Nle10)-Neurokinin B(D-Pro2,D-Trp6,8,Nle10)
(D-Pro2,D-Trp6,8,Nle10)-Neurokinin B functions as a competitive antagonist to the Neurokinin B receptor, exhibiting a pA2 value of 5.5. Notably, it does not affect Substance P or Neurokinin A [1].
价 格:¥电议型 号:T76427产 地:中国大陆
-
T76402[Glp6] Substance P (6-11);化合物 [Glp6] Substance P (6-11)[Glp6] Substance P (6-11)
[Glp6] Substance P (6-11) is an analogue of the native peptide, Substance P (6-11), known to act on ´septide-sensitive´ tachykinin receptors, thereby stimulating the formation of [3H]-inositol monophosphate ([3H]-IP1) in rat urinary bladder, as evidenced by references [1] [2].
价 格:¥电议型 号:T76402产 地:中国大陆
-
T76391p60c-src substrate II;化合物 p60c-src substrate IIp60c-src substrate II
P60c-src substrate II is a potent pentapeptide substrate for the tyrosine kinase pp60c-src [1].
价 格:¥电议型 号:T76391产 地:中国大陆
-
T743666BrCaQ-C10-TPP;化合物 6BrCaQ-C10-TPP6BrCaQ-C10-TPP
6BrCaQ-C10-TPP, a potent inhibitor of the mitochondrial heat shock protein TRAP1, exhibits antiproliferative activity against various human cancer cells, with an IC50 range of 0.008-0.30 μM. Additionally, it induces disturbances in mitochondrial membranes [1].
价 格:¥电议型 号:T74366产 地:中国大陆
-
T740336-Me-ATP;化合物 6-Me-ATP6-Me-ATP
6-Me-ATP (N6-Methyl-ATP), a N6-modified adenosine triphosphate (ATP) derivative, exhibits strong binding affinity for glycogen synthase kinase 3 (GSK3) and acts as the phosphate group donor in GSK3β-catalyzed phosphorylation of its substrate peptide [1].
价 格:¥电议型 号:T74033产 地:中国大陆
-
T71381Exp6803;化合物 Exp6803Exp6803
Exp6803 is an Angiotensin II receptor antagonist.
价 格:¥电议型 号:T71381产 地:中国大陆
-
T68626JCP678;化合物 JCP678JCP678
JCP678 is an irreversible serine hydrolases inhibitor.
价 格:¥电议型 号:T68626产 地:中国大陆
-
T6584MG 149化合物MG149MG149|||Tip60 HAT inhibitor
MG 149 (Tip60 HAT inhibitor) is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).
价 格:¥电议型 号:T6584产 地:中国大陆
-
T649466-HAP;化合物 6-HAP6-HAP
6-HAP is a useful organic compound for research related to life sciences and the catalog number is T64946.
价 格:¥电议型 号:T64946产 地:中国大陆
-
T6091CP-673451;化合物CP673451CP-673451
CP-673451 is a specific inhibitor of PDGFRα/β (IC50: 10/1 nM) with antiangiogenic and antitumor activity and the selectivity is higher 450-fold than other angiogenic receptors.
价 格:¥电议型 号:T6091产 地:中国大陆
-
T60661CP681301;化合物 CP681301CP681301
CP681301 is a potent inhibitor of CDK5 with antiproliferative activity. CP681301 exhibits anti-tumor activity in Drosophila. CP681301 decreases the expression of CD133, OLIG2, SOX2, KI67, pCDK5 protein level in Glioma stem cells (GSCs). CP681301 reduces self-renewal in mouse glioma xenografts [1].
价 格:¥电议型 号:T60661产 地:中国大陆
-
T5400Q203;化合物Q203IAP6|||Telacebec;IAP6|||Telacebec
Q203 (Telacebec) is a novel potent anti-tuberculosis agent targeting cytochrome b subunit qcrB and inhibits M. tuberculosis H37Rv (MIC50: 2.7 nM).
价 格:¥电议型 号:T5400产 地:中国大陆