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:3765174
已选条件
-
T82307Glp-His-Pro-Gly-NH2;化合物 Glp-His-Pro-Gly-NH2pGlu-His-Pro-Gly-NH2;pGlu-His-Pro-Gly-NH2
pGlu-His-Pro-Gly-NH2, also known as Glp-His-Pro-Gly-NH2, is a tetrapeptide that promotes the release of gonadotropin, luteinizing hormone (LH), and follicle-stimulating hormone (FSH) [1] [2].
价 格:¥电议型 号:T82307产 地:中国大陆
-
T81413pppApG;化合物 pppApGpppApG
pppApG serves as an initial substrate for the synthesis of vRNA (viral RNA) and cRNA (complementary RNA), with applications in influenza virus research [1].
价 格:¥电议型 号:T81413产 地:中国大陆
-
T81370Protegrin-1;化合物 Protegrin-1PG1;PG1
Protegrin-1, an antimicrobial peptide, exhibits antimicrobial activity [1].
价 格:¥电议型 号:T81370产 地:中国大陆
-
T81150SLSLSPG;化合物 SLSLSPGSLSLSPG
SLSLSPG, a common variant in immunoglobulin G (IgG) [1], is derived from the C-terminal end of the heavy chain of human Igγ-1.
价 格:¥电议型 号:T81150产 地:中国大陆
-
T81126SORT-PGRN interaction inhibitor 2;化合物 SORT-PGRN interaction inhibitor 2SORT-PGRN interaction inhibit
SORT-PGRN Interaction Inhibitor 2 is a compound that downregulates SORT1 protein expression and enhances extracellular progranulin (PGRN) secretion in various mammalian cell lines, and is utilized in the study of neurological diseases [1].
价 格:¥电议型 号:T81126产 地:中国大陆
-
T7948HPGDS inhibitor 2化合物GSK-2894631AGSK-2894631A
HPGDS inhibitor 2 (GSK-2894631A) is a potent, selective hematopoietic prostaglandin D synthase (h-pgds) inhibitor, IC50 = 9.9 nm.
价 格:¥电议型 号:T7948产 地:中国大陆
-
T79363APG-2449;化合物 APG-2449APG-2449
APG-2449 is an orally active inhibitor targeting ALK, ROS1, and FAK, demonstrating antitumor efficacy in mouse models of non-small cell lung cancer (NSCLC) [1].
价 格:¥电议型 号:T79363产 地:中国大陆
-
T79106SORT-PGRN interaction inhibitor 3;化合物 SORT-PGRN interaction inhibitor 3SORT-PGRN interaction inhibit
SORT-PGRN Interaction Inhibitor 3 (Compound 13), with an IC50 value of 0.17 μM, acts as an inhibitor of the SORT-PGRN interaction, and is utilized in the study of neurodegenerative diseases [1].
价 格:¥电议型 号:T79106产 地:中国大陆
-
T79096IPG7236;化合物 IPG7236IPG7236
IPG7236, a selective CCR8 antagonist, demonstrates notable tumor suppression in a mouse xenograft model of human breast cancer and is applicable in cancer research [1].
价 格:¥电议型 号:T79096产 地:中国大陆
-
T78584Prostaglandin D3;化合物 Prostaglandin D3PGD3;PGD3
Prostaglandin D3 (PGD3) functions as an inhibitor of platelet aggregation and modulates autonomic neurotransmission in humans [1].
价 格:¥电议型 号:T78584产 地:中国大陆
-
T7858215-keto-Prostaglandin E2;化合物 15-keto-Prostaglandin E215-keto-PGE2;15-keto-PGE2
15-keto-Prostaglandin E2, an endogenous metabolite, inhibits STAT3 activation through binding to Cys259 and regulates breast cancer cell growth and progression. Additionally, it binds and stabilizes the EP2 and EP4 receptors, activates PPAR-γ, and promotes fungal growth [1] [2] [3].
价 格:¥电议型 号:T78582产 地:中国大陆
-
T78030GRGESP;化合物 GRGESPGRGESP
GRGESP is a collagen gel contraction inhibitor that impedes the spreading of human fibroblasts within collagen gels and significantly reduces gel contraction, thus serving as a valuable agent for research in connective tissue morphogenesis [1].
价 格:¥电议型 号:T78030产 地:中国大陆
-
T7730Aminopterin氨基蝶呤APGA|||氨基蝶呤|||4-Aminofolic acid
Aminopterin (4-Aminofolic acid) is a synthetic folic acid derivative whose metabolite is a competitive inhibitor of dihydrofolate reductase
价 格:¥电议型 号:T7730产 地:中国大陆
-
T76369CEDAEVFKDSMVPGEK;化合物 CEDAEVFKDSMVPGEKCEDAEVFKDSMVPGEK
CEDAEVFKDSMVPGEK, the peptide sequence corresponding to the rat vanilloid receptor subtype 1 (VR1), facilitates the detection and mapping of VR1 distribution [1].
价 格:¥电议型 号:T76369产 地:中国大陆
-
T76201LEESGGGLVQPGGSMK TFA;化合物 LEESGGGLVQPGGSMK TFALEESGGGLVQPGGSMK TFA
LEESGGGLVQPGGSMK TFA, a proteolysis peptide component of Infliximab, serves for the quantitative analysis of the latter. Infliximab is a chimeric monoclonal IgG1 antibody, binding specifically to TNF-α [1].
价 格:¥电议型 号:T76201产 地:中国大陆
-
T75848PG106 TFA;化合物 PG106 TFAPG106 TFA
PG106 TFA is a potent, selective antagonist of the human melanocortin 3 (hMC3) receptor, displaying an IC50 value of 210 nM, while exhibiting negligible activity at the hMC4 receptors (EC50 = 9900 nM) and hMC5 receptor [1].
价 格:¥电议型 号:T75848产 地:中国大陆
-
T75847PG-931 TFA;化合物 PG-931 TFAPG-931 TFA
PG-931 TFA, a potent and selective agonist of the melanocortin 4 (MC4) receptor (IC50=0.58 nM) compared to the hMC3R (IC50=55 nM) and hMC5R (IC50=2.4 nM), is an analog of SHU 9119. This compound has demonstrated efficacy in reversing hemorrhagic shock and preventing multiple organ damage in vivo [2].
价 格:¥电议型 号:T75847产 地:中国大陆
-
T75756PGLa TFA;化合物 PGLa TFAPGLa TFA
PGLa TFA, a 21-residue antimicrobial peptide from the magainin family of antibiotic peptides found in frog skin and its secretions [1], serves as a representative member of this bioactive group.
价 格:¥电议型 号:T75756产 地:中国大陆
-
T75347Blue FPG-A trisodium;化合物 Blue FPG-A trisodiumBlue FPG-A trisodium
Blue FPG-A trisodium, a structural isomer of Reactive Blue 2 (RB2) components [1], serves as a selective antagonist for both P2X1 and P2Y1 receptors, boasting IC50 values of 35.5 μM and 2.6 μM, respectively.
价 格:¥电议型 号:T75347产 地:中国大陆
-
T75113GLPG2534;化合物GLPG2534GLPG-2534;GLPG-2534
GLPG2534 is an orally active, selective and potent IRAK4 inhibitor with anti-inflammatory activity. GLPG2534 inhibits human and mouse IRAK4 and could be used to study psoriasis and atopic dermatitis.
价 格:¥电议型 号:T75113产 地:中国大陆