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:3878696
已选条件
-
T6300DegrasynDegrasyn,WP1130,
Degrasyn (WP1130), a specific deubiquitinase (DUB: USP5, UCH-L1, USP9x, USP14, and UCH37) inhibitor, also inhibits Bcr/Abl, which is a JAK2 transducer (without affecting 20S proteasome) and activator of transcription (STAT).
价 格:¥电议型 号:T6300产 地:美洲
-
T8857LJP-1586 HCl;LJP-1586盐酸盐LJP 1586|||LJP-1586 hydrochloride|||LJP-1586|||LJP1586;LJP 1586|||LJP-1586 h
LJP-1586 HCl, a highly selective inhibitor of vascular adhesion protein-1 (VAP-1), exhibits antiinflammation effect by reducing adhesion molecule expression and immune cell infiltration after intracerebral hemorrhage (ICH).
价 格:¥电议型 号:T8857产 地:中国大陆
-
T8655SR-717;化合物SR-717immunity|||MPYS|||MITA|||inhibit|||SR-717|||ISG-THP1|||Inhibitor|||SR 717|||mimetic|
SR-717 is a cGAMP analog, a non-nucleoside STING agonist that induces a "closed" activation conformation of STING. SR-717 has antitumor activity and promotes activation of immune cells and cross-presentation of antigens.
价 格:¥电议型 号:T8655产 地:中国大陆
-
T8576P18IN011;化合物P18IN011P18IN011 - CAS 77408-67-4 - Calbiochem;P18IN011 - CAS 77408-67-4 - Calbiochem
P18IN011 (P18IN011 - CAS 77408-67-4 - Calbiochem) is a novel inhibitor of p18(INK4C).
价 格:¥电议型 号:T8576产 地:中国大陆
-
T83928DA ZP1;化合物 DA ZP1DA ZP1
DA ZP1 (diacetylated Zinpyr1), a highly sensitive fluorogenic Zn(II) sensor (KdZn2+= 0.6 nM), efficiently images and isolates pancreatic β-cells and β-like cells in vitro and purifies live stem cell-derived β-like cells. It also enables imaging of transplanted islet grafts and endogenous mouse islets in vivo. DA ZP1 is initially non-fluorescent; however, its interaction with Zn(II) ions triggers hydrolytic cleavage of the acetyl groups, creating a robust fluorescent signal with excitation and em
价 格:¥电议型 号:T83928产 地:中国大陆
-
T83886icFSP1 TFA;化合物 icFSP1 TFAicFSP1 TFA
icFSP1, an inhibitor of ferroptosis suppressor protein 1 (FSP1), promotes condensation and phase separation of FSP1 in cellular environments at 2.5 ?M concentration but does not affect FSP1´s enzymatic function in cell-free assessments (IC50 = > 30 ?M). This compound selectively induces ferroptosis in HT-1080 fibrosarcoma cells in a dose-dependent manner. Furthermore, in vivo studies show that icFSP1 administered at 50 mg/kg significantly reduces both the volume and weight of tumors in a B
价 格:¥电议型 号:T83886产 地:中国大陆
-
T83851Tat-QFNP12 TFA;化合物 Tat-QFNP12 TFATat-QFNP12 TFA
Tat-QFNP12 is a peptide that combines a transcriptional transactivator (Tat) transmembrane domain with an inhibitor targeting the interaction between N-Myc downstream regulated gene 2 (NDRG2) and protein phosphatase Mg2+/Mn2+ dependent 1A (PPM1A). This compound effectively mitigates blood-brain barrier endothelial tight junction disruption caused by elevated levels of matrix metalloproteinase-9 (MMP-9), alleviates cerebral edema, and promotes spontaneous activity along with symmetric limb moveme
价 格:¥电议型 号:T83851产 地:中国大陆
-
T83770Klotho-derived Peptide 1 (56-87) (human) TFA;化合物 Klotho-derived Peptide 1 (56-87) (human) TFAKP1 (56
Klotho-derived peptide 1 (KP1) (56-87), a peptide originating from the human Klotho protein, disrupts TGF-β signaling by binding to TGF-β receptor types 1 and 2 (TGFBR1 and TGFBR2; Kds = 1.41 and 14.6 ?M, respectively). Preincubation with KP1 at a concentration of 10 ?g/ml hinders the TGF-β-induced escalation of fibronectin and α-smooth muscle actin (α-SMA) levels in NRK-49F rat fibroblasts. Furthermore, in vivo studies reveal that KP1, administered at 1 mg/kg per day, preferentially accumulates
价 格:¥电议型 号:T83770产 地:中国大陆
-
T83743VPM-p15 TFA;化合物 VPM-p15 TFAT1V/F3Phe(4-Me);T1V/F3Phe(4-Me)
VPM-p15, a synthetic peptide agonist targeting the adhesion G protein-coupled receptor (GPCR) G2 (ADGRG2)—an orphan GPCR implicated in male infertility—facilitates cAMP accumulation in HEK293 cells expressing human ADGRG2, demonstrating efficacy with an EC50 value of 1.41 ?M.
价 格:¥电议型 号:T83743产 地:中国大陆
-
T83742SBP1 TFA;化合物 SBP1 TFASpike Binding Peptide 1;Spike Binding Peptide 1
Spike Binding Peptide 1 (SBP1), representing amino acids 21-43 of angiotensin-converting enzyme 2 (ACE2), has been utilized in a novel approach involving lipid nanoparticles (LNPs) encapsulated with oseltamivir phosphate and conjugated to SBP1. This formulation aims to investigate the possibility of achieving a controlled, long-term in vivo release of oseltamivir phosphate. Furthermore, a 2% concentration of SBP1 immobilized on crosslinked networks composed of hydroxy acrylate and ethylxanthate
价 格:¥电议型 号:T83742产 地:中国大陆
-
T83735Pap12-6 TFA;化合物 Pap12-6 TFAPap12-6 TFA
Pap12-6, an antibacterial peptide originating from the first twelve N-terminal amino acids of papiliocin found in P. xuthus larvae, exhibits activity against a range of eight Gram-negative bacteria (e.g., E. coli, P. aeruginosa, S. syphimurium with MIC50s=4-8 ?M) and Gram-positive bacteria (e.g., S. aureus, methicillin-resistant S. aureus 3126, B. subtilis, and S. epidermidis with MIC50s=4-8 ?M), without compromising the viability of human erythrocytes, mouse RAW 264.7 macrophages, human HaCaT k
价 格:¥电议型 号:T83735产 地:中国大陆
-
T83685UFP101 TFA;化合物 UFP101 TFAUFP101 TFA
UFP101 is a synthetic peptide that functions as an antagonist of the nociceptin receptor, demonstrating high affinity with a Ki of 0.06 nM in CHO cells expressing the human receptor. It exhibits selectivity for the nociceptin receptor over the κ-opioid receptor, with a Ki of 204 nM in CHO cells expressing the rat receptor. The compound effectively inhibits GTPγS release from the nociceptin receptor in CHO cell membranes, with an EC50 of 1.86 nM. When administered intracerebroventricularly at a d
价 格:¥电议型 号:T83685产 地:中国大陆
-
T83681IRBP (1-20) (human, rat) TFA;化合物 IRBP (1-20) (human, rat) TFAIRBP1-20|||Interphotoreceptor Retinoid-
Interphotoreceptor retinoid-binding protein (1-20) (IRBP1-20), a dodecapeptide fragment of retinoid-binding protein 3, plays a crucial role in pigment regeneration by facilitating the transport of retinol and retinal between photoreceptor cells and the retinal pigment epithelium. It has been utilized to provoke autoimmune uveoretinitis in C57BL/6 mice, possessing the H-2b haplotype. Furthermore, IRBP1-20 at a concentration of 3 ?M enhances the secretion of IL-4, IL-5, and IL-6 from primary mouse
价 格:¥电议型 号:T83681产 地:中国大陆
-
T83487[Pmp1,Tyr(OEt)2] AVP;化合物 [Pmp1,Tyr(OEt)2] AVP[Pmp1,Tyr(OEt)2] AVP
[Pmp1,Tyr(OEt)2] AVP, a linear analog of the cyclic arginine vasopressin (AVP) antagonist, retains the antagonistic properties of its parent compound while featuring modified phenylalanine (Pmp) and diethyltyrosine (Tyr(OEt)2) components.
价 格:¥电议型 号:T83487产 地:中国大陆
-
T834321-DCP;化合物 1-DCP1-DCP
1-DCP functions as a powerful ethylene antagonist, effectively hindering ethylene´s influence on fruit ripening and senescence [1].
价 格:¥电议型 号:T83432产 地:中国大陆
-
T82743CFP10 (71–85);化合物 CFP10 (71–85)CFP10 (71–85)
CFP10 (71–85) is an immunologically active peptide that induces IFN-γ production and cytotoxic T lymphocyte (CTL) activity in CD4+ and CD8+ T cells from individuals with diverse MHC class II and I expression profiles.
价 格:¥电议型 号:T82743产 地:中国大陆
-
T82370Fructo-oligosaccharide DP13;化合物 Fructo-oligosaccharide DP13Fructo-oligosaccharide DP13
Fructo-oligosaccharide DP13 is an inulin-type fructan that can be isolated from Morinda officinalis [1].
价 格:¥电议型 号:T82370产 地:中国大陆
-
T82369Fructo-oligosaccharide DP14;化合物 Fructo-oligosaccharide DP14Fructo-oligosaccharide DP14
Fructo-oligosaccharide DP14, an oligosaccharide derived from Atractylodes lancea [1], represents a specific polysaccharide subclass with a degree of polymerization of 14.
价 格:¥电议型 号:T82369产 地:中国大陆
-
T82063Integrin signaling inhibitor, mP13;化合物 Integrin signaling inhibitor, mP13Integrin signaling inhibito
Integrin Signaling Inhibitor mP13 is a compound that impedes both inside-out and outside-in integrin-mediated signaling processes, such as fibrinogen binding, platelet adhesion, and clot retraction [1].
价 格:¥电议型 号:T82063产 地:中国大陆
-
T81984Keap1-Nrf2-IN-10;化合物 Keap1-Nrf2-IN-10Keap1-Nrf2-IN-10
Keap1-Nrf2-IN-10 (compound 15) is a potent inducer of NQO1 and efficaciously mitigates oxidative stress in gamma-irradiated mice by reducing MDA and ROS levels, as well as NQO1 in the liver, which enhances the survival rate of these mice [1].
价 格:¥电议型 号:T81984产 地:中国大陆