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T76308Gastric Inhibitory Polypeptide (1-30), porcine；化合物 Gastric Inhibitory Polypeptide (1-30), porcineGas
Gastric Inhibitory Polypeptide (1-30), porcine, deficient in the 12 C-terminal amino acids of the natural gastric inhibitory polypeptide (GIP), demonstrates biological activity through the enhancement of insulin and somatostatin release [1].
价 格：￥电议型 号：T76308产 地：中国大陆
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T76084Parathyroid Hormone (1-34), human, biotinylated；化合物 Parathyroid Hormone (1-34), human, biotinylatedP
Parathyroid Hormone (1-34), human, biotinylated serves as a probe targeting the parathyroid hormone receptor. It is utilized in the analysis of interactions between parathyroid hormone and its receptors within living cells and facilitates the purification of hormone-receptor complexes using affinity columns [1] [2].
价 格：￥电议型 号：T76084产 地：中国大陆
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T76061Parathyroid hormone (1-34) (rat) acetate；化合物 Parathyroid hormone (1-34) (rat) acetateParathyroid hor
Parathyroid hormone (1-34) (rat) (acetate) is a parathyroid hormone variant that enhances the structure of both cortical and cancellous bones. It is utilized in osteoporosis research [1] [2].
价 格：￥电议型 号：T76061产 地：中国大陆
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T76041GIP (1-30) amide,human acetate；化合物 GIP (1-30) amide,human acetateGIP (1-30) amide,human acetate
GIP (1-30) amide, human acetate is a fragment of glucose-dependent insulinotropic polypeptide (GIP), an incretin hormone that plays a crucial role in stimulating insulin secretion and mitigating postprandial glycemic excursions. This compound has been shown to enhance insulin secretion in a dose-dependent manner across concentrations of 10^-9 to 10^-6 M [1].
价 格：￥电议型 号：T76041产 地：中国大陆
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T76005LSuper-TDU (1-31) (TFA)；化合物 Super-TDU (1-31) (TFA)Super-TDU (1-31) (TFA)
Super-TDU (1-31) TFA, a peptide fragment of Super-TDU, acts as an inhibitor of the YAP-TEAD complex. Demonstrating potent anti-tumor activity, it effectively suppresses tumor growth in a gastric cancer mouse model [1] [2].
价 格：￥电议型 号：T76005L产 地：中国大陆
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T76005Super-TDU (1-31)；化合物 Super-TDU (1-31)Super-TDU (1-31)
Super-TDU (1-31), a peptide fragment of Super-TDU, acts as an inhibitor of the YAP-TEAD complex. Demonstrating potent anti-tumor activity, it effectively suppresses tumor growth in a gastric cancer mouse model [1] [2].
价 格：￥电议型 号：T76005产 地：中国大陆
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T75867Parathyroid Hormone (1-34), bovine TFA；化合物 Parathyroid Hormone (1-34), bovine TFAParathyroid Hormone
Parathyroid Hormone (1-34), bovine TFA, a potent agonist of the parathyroid hormone (PTH) receptor, elevates calcium and inorganic phosphate levels in vivo. This compound is employed in osteoporosis research [1].
价 格：￥电议型 号：T75867产 地：中国大陆
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T7562β-Amyloid (31-35)；异亮氨酰-异亮氨酰-甘氨酰-亮氨酰-蛋氨酸β-Amyloid 31-35(TFA)|||β-Amyloid 31-35；异亮氨酰-异亮氨酰-甘氨酰-亮氨酰-蛋氨酸|
β-Amyloid (31-35) (β-Amyloid 31-35) is the shortest sequence of native Amyloid-β peptide.
价 格：￥电议型 号：T7562产 地：中国大陆
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T75401D-galactosyl-β1-3-N-acetyl-D-hexosamine phosphorylase (BiGalHexNAcP)；化合物 D-galactosyl-β1-3-N-acetyl-
D-galactosyl-β1-3-N-acetyl-D-hexosamine phosphorylase (BiGalHexNAcP), belonging to the CAZy glycoside hydrolase family GH112, plays a pivotal role in biochemical research. This enzyme catalyzes the phosphorolysis of lacto-n-biose and galacto-n-biose, yielding Gal-1-P and the corresponding N-acetyl-D-hexosamine [1].
价 格：￥电议型 号：T75401产 地：中国大陆
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T70377BAY 61-3606 HCl；化合物 BAY 61-3606 HClBAY 61-3606 HCl
BAY 61-3606 HCl is a cell-permeable, reversible inhibitor of spleen tyrosine kinase. BAY 61-3606 HCl can inhibit degranulation and block cytokine release from mast cells. Oral administration of BAY 61-3606 to rats was shown to suppress antigen-induced passive cutaneous anaphylactic reaction, bronchoconstriction, and bronchial edema. It can also sensitize MCF-7 breast cancer cells to TNF-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis by inhibiting Cdk9. This compound has been used i
价 格：￥电议型 号：T70377产 地：中国大陆
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T69590ONO-AE1-329；化合物 ONO-AE1-329ONO-AE1-329
ONO-AE1-329 is a novel agonist of the prostaglandin PGE2 receptor EP4.
价 格：￥电议型 号：T69590产 地：中国大陆
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T68129L1Picumeterol FA；吡库特罗甲酸盐Picumeterol FA(130641-36-0 Free base)；Picumeterol FA(130641-36-0 Free base)
picumeterol FA is a potent and selective β2-adrenergic receptor agonist. In in vitro and in vivo tests, picumeterol FA produces long-lasting airway smooth muscle relaxation. picumeterol FA is a pure R-enantiomer and can be used to improve lung function and reduce airway hyperresponsiveness in patients with asthma.
价 格：￥电议型 号：T68129L1产 地：中国大陆
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T68022LSulotroban potassium；磺曲苯钾盐BM 13177 potassium|||Sulotroban potassium(72131-33-0 Free base)；BM 13177 p
Sulotroban potassium is a small molecule thromboxane A2 receptor (TXA2R) antagonist that can be used to study myocardial infarction and thrombosis.
价 格：￥电议型 号：T68022L产 地：中国大陆
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T6776BAY 61-3606 dihydrochloride；化合物BAY-61-3606BAY 61-3606|||BAY-61-3606 dihydrochloride；BAY 61-3606|||BA
BAY 61-3606 dihydrochloride (BAY 61-3606) is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
价 格：￥电议型 号：T6776产 地：中国大陆
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T62822CT1-3；化合物 CT1-3CT1-3
CT1-3 is a potent anti-cancer agent. CT1-3 regulates the JNK/Bcl-2/Bax/XIAP pathway, which induces mitochondria-mediated apoptosis. CT1-3 regulates the E-cadherin/Snail axis to inhibit epithelial mesenchymal transition (EMT) potentials in human cancer cells (HCCs) and suppresses tumourigenesis. CT1-3 has anti-tumour effects in mouse models and does not show significant hepatotoxicity or nephrotoxicity.
价 格：￥电议型 号：T62822产 地：中国大陆
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T5146Eptifibatide acetate (148031-34-9 free base)；依菲巴特醋酸盐Eptifibatide acetate；Eptifibatide acetate|||依菲巴特
Eptifibatide acetate (148031-34-9 free base) (Eptifibatide acetate) , an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class, is a cyclic heptapeptide constructed from 6 amino acids and a mercaptopropionyl residue.
价 格：￥电议型 号：T5146产 地：中国大陆
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T46062119738-71-3；化合物2119738-71-32119738-71-3
Compound 2119738-71-3 interacts with the FAK receptor.
价 格：￥电议型 号：T4606产 地：中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base))；化合物UNC2025 2HClUNC2025 2HCl (1429881-91-3(free base))
UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of 0.8/0.74 nM for Mer/Flt3.
价 格：￥电议型 号：T4419产 地：中国大陆
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T4417LDC-4297 HCl (1453834-21-3(free base))；化合物LDC-4297 HClLDC-4297 HCl (1453834-21-3(free base))
LDC4297 is a potent and selective CDK7 inhibitor with an IC50 of 0.13 nM.
价 格：￥电议型 号：T4417产 地：中国大陆
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T4263BAY 61-3606；化合物BAY 61-3606Syk inhibitor IV；2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺|||Syk inhi
BAY 61-3606 (Syk inhibitor IV) is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (Ki= 7.5 nM), exhibiting no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
价 格：￥电议型 号：T4263产 地：中国大陆
