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T29078Ursodeoxycholic acid sodium；熊去氧胆酸钠盐UDCA Na|||UDCA sodium|||Sodium Ursodeoxycholate|||Ursodiol sodium
Ursodeoxycholic acid sodium (Sodium Ursodeoxycholate) is a naturally occurring secondary bile acid with anti-inflammatory and cytoprotective activities. Ursodeoxycholic acid sodium acts as signaling molecule, exerting its effects by interacting with bile acid activated receptors,
价 格：￥电议型 号：T29078产 地：中国大陆
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T29077Urolinin；化合物 T29077nWWK-Tyr(3-NO2)-Abu；nWWK-Tyr(3-NO2)-Abu
Urolinin is a linear peptidic Urotensin-II Receptor Agonist with low nanomolar potency as well as improved metabolic stability. Urolinin is a hexameric UIIR agonist with an EC50 of 4.75 nM and a metabolic stability of 1319 min, 6.3-fold higher than wild-type U-II.
价 格：￥电议型 号：T29077产 地：中国大陆
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T29076Uredepa；化合物 T29076AB100|||AB 100|||AB-100|||Urdepa|||Avinar；AB100|||AB 100|||AB-100|||Urdepa|||Avina
Uredepa may be has antineoplastic properties.
价 格：￥电议型 号：T29076产 地：中国大陆
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T29075UR-7247；化合物 T29075UR7247；UR7247
UR-7247 is an angiotensin type 1 receptor antagonist with a very long plasma elimination half-life.
价 格：￥电议型 号：T29075产 地：中国大陆
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T29074UR-3216；化合物 T29074UR-3216
UR-3216, a prodrug, is a selective and orally active platelet surface glycoprotein (GPIIb/IIIa) receptor antagonist. UR-3216 is the very tight binding of its active metabolite to platelets (Ki for resting platelets is < 1 nM). UR-2992, the active form of UR-3216, binds to platelets for a long period of time, while the unbound drug is rapidly cleared.
价 格：￥电议型 号：T29074产 地：中国大陆
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T29073UR-2922；化合物 T29073UR2922|||UR-2922|||UR 2922|||UR 2922|||UR2922|||UR 2922；UR2922|||UR-2922|||UR 2922
UR-2922 is an oral antagonist of platelet GPIIb/IIIa. UR-2922 possessed a high affinity for the human platelet receptor (K(d) <1 nM) and a slow dissociation rate (k(off)= 90 min) in vitro. UR-2922 induced no ligand-induced binding sites (LIBS) expression or prothrombotic activity in human platelets.
价 格：￥电议型 号：T29073产 地：中国大陆
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T29072UR-1505；化合物 T29072UR1505|||UR 1505；UR1505|||UR 1505
UR-1505 is a nuclear factor of activated T cells (NF-AT) inhibitor. UR-1505 acts by inhibiting T cell activation depending on T cell receptor signaling pathway. Furthermore, the antiproliferative effects of UR-1505 are not a consequence of decreased cell viability.
价 格：￥电议型 号：T29072产 地：中国大陆
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T29071UR13870；化合物 UR13870Org 48762-0|||POLB 001|||UR-13870|||UR 13870；Org 48762-0|||POLB 001|||UR-13870|||
UR-13870 (Org 48762-0) is an orally active and selective inhibitor of p38 mitogen-activated protein kinase (MAPK), which prevents bone damage in collagen-induced arthritis in mice.
价 格：￥电议型 号：T29071产 地：中国大陆
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T29070Uproleselan；化合物 T29070Uproleselan
Uproleselan has antithrombotic and antineoplastic properties.
价 格：￥电议型 号：T29070产 地：中国大陆
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T2907Tanshinone I；丹参酮ITanshinone A；丹参酮I|||Tanshinone A
Tanshinone I (Tanshinone A), an active principle isolated from the herbal medicine Salvia miltiorrhiza, displays cytotoxicity against tumor cells.
价 格：￥电议型 号：T2907产 地：中国大陆
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T29069Uprifosbuvir；化合物 T29069MK3682|||IDX21437|||IDX 21437|||MK 3682|||IDX-21437|||MK-3682；MK3682|||IDX214
Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.
价 格：￥电议型 号：T29069产 地：中国大陆
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T29068UPCDC-30245；化合物 T29068UPCDC 30245；UPCDC 30245
UPCDC30245 is an AAA ATPase p97 allosteric inhibitor.
价 格：￥电议型 号：T29068产 地：中国大陆
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T29067LUpacicalcet HCl；乌帕西卡塞盐酸盐Upacicalcet HCl(1333218-50-0 Free base)；Upacicalcet HCl(1333218-50-0 Free ba
Upacicalcet HCl is an intravesical calcium mimetic that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on calcium-sensitive receptors in parathyroid cell membranes, thereby lowering PTH levels in the blood.Upacicalcet HCl can be used for the treatment of blood Upacicalcet HCl is a novel compound for the treatment of secondary hyperparathyroidism, targeting amino acid-binding sites of calcium-sensitive receptors. binding sites.
价 格：￥电议型 号：T29067L产 地：中国大陆
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T29067Upacicalcet；乌帕卡塞PLS-240|||SK-1403|||AJT-240；PLS-240|||SK-1403|||AJT-240
Upacicalcet (AJT-240) is an intraventricular calcium mimetic, a SHPT available for human hemodialysis, that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on parathyroid cell membrane calcium-sensitive receptors, thereby lowering blood levels of PTH.Upacicalcet is an orthosteric modulator of calcium-sensitive receptors and prevents adenine-induced secondary vascular calcification and bone disease in a rat model of adenine-induced secondary hyperparathyroidism.
价 格：￥电议型 号：T29067产 地：中国大陆
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T29066UNC9995；化合物 T29066UNC-9995|||UNC 9995；UNC-9995|||UNC 9995
UNC9995 is a β-Arrestin-Biased Dopamine D2 Receptor agonist (β-Arrestin, EC50 = 120 nM; Emax = 88%).
价 格：￥电议型 号：T29066产 地：中国大陆
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T29065UNC9994；化合物 T29065UNC-9994|||UNC 9994；UNC-9994|||UNC 9994
UNC9994 is a β-arrestin-biased dopamine D? receptor agonist (β-arrestin EC50 = 50 nM; Emax = 97%) with robust in vivo antipsychotic drug-like activities.
价 格：￥电议型 号：T29065产 地：中国大陆
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T29064UNC9975；化合物 T29064UNC-9975；UNC-9975
UNC9975 is an analog of aripiprazole and a β-arrestin-biased D2R agonist.
价 格：￥电议型 号：T29064产 地：中国大陆
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T29063UNC-4219 TFA；化合物 T29063UNC4219|||UNC-4219|||UNC 4219；UNC4219|||UNC-4219|||UNC 4219
UNC4219 is a negative control compound for UNC3866, a potent antagonist of the methyllysine (Kme) reading function of the Polycomb CBX and CDY families of chromodomains.
价 格：￥电议型 号：T29063产 地：中国大陆
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T29062UNC3133；化合物 T29062UNC 3133|||UNC-3133；UNC 3133|||UNC-3133
UNC3133 is a potent and selective Mer tyrosine kinase (MerTK) inhibitor with IC50 Mer 3.0 nM; Axl 17nM; Tyro 3.31 nM; FLT3 6.6 nM; PO Cmax = 0.023; IV T1/2 = 1.59 h, %F = 16. Mer tyrosine kinase (MerTK) is aberrantly elevated in various tumor cells and has a normal anti-inflammatory role in the innate immune system. Inhibition of MerTK may provide dual effects against these MerTK-expressing tumors through reducing cancer cell survival and redirecting the innate immune response.
价 格：￥电议型 号：T29062产 地：中国大陆
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T29061UNC0006；化合物 T29061UNC 0006|||UNC-0006；UNC 0006|||UNC-0006
UNC0006 is a β-arrestin-biased dopamine D2 ligand.
价 格：￥电议型 号：T29061产 地：中国大陆
